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  • Stage II melanoma

    Stage II melanoma

    NSG-530-IKC – Advanced Pathophysiology

    Module 3: Discussion

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    Mr. B, a 40-year-old avid long-distance runner previously in good health, presented to his primary provider for a yearly physical examination, during which a suspicious-looking mole was noticed on the back of his left arm, just proximal to the elbow. He reported that he has had that mole for several years, but thinks that it may have gotten larger over the past two years. Mr. B reported that he has noticed itchiness in the area of this mole over the past few weeks. He had multiple other moles on his back, arms, and legs, none of which looked suspicious. Upon further questioning, Mr. B reported that his aunt died in her late forties of skin cancer, but he knew no other details about her illness. The patient is a computer programmer who spends most of the work week indoors. On weekends, however, he typically goes for a 5-mile run and spends much of his afternoons gardening. He has a light complexion, blonde hair, and reports that he sunburns easily but uses protective sunscreen only sporadically Stage II melanoma.

    Physical exam revealed: Head, neck, thorax, and abdominal exams were normal, with the exception of a hard, enlarged, non-tender mass felt in the left axillary region. In addition, a 1.6 x 2.8 cm mole was noted on the dorsal upper left arm. The lesion had an appearance suggestive of a melanoma. It was surgically excised with 3 mm margins using a local anesthetic and sent to the pathology laboratory for histologic analysis. The biopsy came back Stage II melanoma.

    How is Stage II melanoma treated and according to the research how effective is this treatment?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

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    Melanoma

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    Lois Chappell posted Feb 8, 2021 7:45 PM

                    Melanoma is a disease in which cancer cells form in the cells that bring color to  our skin, melanocytes.  Our skin consists of two layers, the dermis, and the epidermis.  Skin cancer begins in the epidermis, which in itself is composed of three distinct layers, squamous cells, basal cells, and melanocytes.  Over the past thirty years, cases of melanoma have increased dramatically (Melanoma Treatment, 2020).  While usually seen in adults, this cancer can also be seen in children tage II melanoma.  Like all cancers, treatment should begin with prevention.  Educating patients and families to prevent and detect skin cancer is essential.  Clinicians can use the history and physical exam, along with the ABCDE ( asymmetry, border, color, diameter, evolving size) screening method to improve outcomes through early detection (Skin Cancer Foundation, 2020).  Treatment of melanoma begins with testing, which may include biopsy, lymph node mapping, CT studies, blood work and additional tests as warranted.   Standard treatment for melanoma includes surgery, chemotherapy, radiation, and immunotherapy.  Newer treatments include vaccine therapy.  Like all cancers, prevention and a healthy lifestyle are essential to best outcomes.           PDQ Adult Treatment Editorial Board.  May 2020. 
    Melanoma Treatment:  Patient Version
    .  PDQ Cancer Institute.  Retrieved from           Skin Cancer Foundation.  2020.  Melanoma warning signs, what you need to know about early detection.  Retrieved from  less0 UnreadUnread

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                    https://www.skincancer.org/skin-cancer-information/melanoma/melanoma-warning -signs-and-images.

                    https://www.ncbi.nlm.gov/books/NBK6950.

    References

                    While most often found in the trunk, head and neck on men, women tend to develop melanoma on the arms and legs.  Risk factors are numerous and include fair complexion, light hair (red or blonde) and eye color (blue, green), exposure to sun or artificial light, genetics, moles, personal history of melanoma, family history of melanoma, history of sunburns with blistering, and being white (Melanoma Treatment, 2020).

    Stage II Melanoma discussion Week 3
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    Aina Oluwo posted Feb 3, 2021 7:21 PM

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    Stage 11 MelanomaAccording to Melanoma Research Alliance (2021), the staging of melanomas can be divided into three that is; 
    Stage IIA Melanoma:
    this is when the tumor is more than 1.0 millimeter and less than 2.0 millimeters thick with ulceration (broken skin) or more than 2.0 and less than 4.0 millimeters without broken skin. Mr. B’s tumor measurements, which are 1.6 x 2.8cm, falls under stage IIA. In Stage IIB Melanoma, the tumor is more than 2.0 millimeters and less than 4.0 millimeters thick with broken skin (ulceration) or more than 4.0 millimeters without ulceration. Stage IIC Melanoma, the tumor is more than 4.0 millimeters thick with broken skin (ulceration) Stage II melanoma. In cases whereby the SLNB found cancer, doctors do recommend additional treatment (Adjunct Therapy) with an immune checkpoint inhibitor or targeted therapy drugs, which helps to lower the chances of the melanoma coming back (The American Cancer Society, 2019). Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7th ed.). Elsevier.The American Cancer Society. (2019, August 14). 
    Treatment of melanoma by stage
    . American Cancer Society. Retrieved February 1, 2021, from 
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html
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    View profile card for Aina Oluwo

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    February 8 at 12:00 AM
     by Aina Oluwo

    Ward, W. H., Lambreton, F., Goel, N., Yu, J. Q., & Farma, J. M. (2017, December 21). 
    Clinical presentation and staging of melanoma – cutaneous melanoma – ncbi bookshelf
    . Cutaneous Melanoma: Etiology and Therapy. Retrieved February 1, 2021, from 
    https://www.ncbi.nlm.nih.gov/books/NBK481857/

    Melanoma Research Alliance. (2021, January 1). 
    Stage 2 melanoma
    . Retrieved February 1, 2021, from 
    https://www.curemelanoma.org/about-melanoma/melanoma-staging/stage-2/

    References

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    View profile card for Melissa Morgan

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    February 7 at 8:52 PM
     by Melissa Morgan

    PDQ Adult Treatment Editorial Board. Melanoma Treatment (PDQ®): Health Professional Version. (2021). 
    In: PDQ Cancer Information Summaries [Internet]. Bethesda (MD): National Cancer Institute (US); 2002-,. 

    References

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    Steven Bartos posted Feb 3, 2021 5:34 PM

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    In stage II melanoma, it is considered a locally invasive cancer as it has not spread to other parts of the body. Research by Garbe et al. (2016) concluded that surgical excision is the primary interventional treatment for melanoma. However, risk still remains that melanoma may reoccur even after surgery, so it’s not completely effective. Stage II melanoma is broken down into three subdivisions: stages IIA, IIB, and IIC, going from IIA – IIC respectively as the thickness of the melanoma increases. As far as overall survival rates are concerned, stage IIA has a five-year survival rate of 80%, but for stage IIC this decreases to 53% (Lee et al., 2017). ReferencesKoster, B.D., van den Hout, M., Sluijter, B., Molenkamp, B., Vuylsteke, R., Baars, A., van Leeuwen, P., Scheper, R., van del Tol, M., van den Eertwegh, A., de Gruijil, T. (2017) Local adjuvant treatment with low-dose CpG-B offers durable protection against disease recurrence in clinical stage I-II melanoma: Data from two randomized phase II trials. 
    Clinical Cancer Research
    , 
    23
    (19), 5679 – 5685. https://doi.org/10.1158/1078-0432.CCR-17-0944more1 UnreadUnread5 ViewsViews

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    View profile card for Dennies Jones

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    February 7 at 9:21 AM
     by Dennies Jones

    Lee, A.Y., Droppelmann, N., Panageas, K.S., Zhou, Q., Ariyan, C.E., Brady, M.S., Chapman, P.B., & Coit, D.G. (2017). Patterns and timing of initial relapse in pathologic stage II melanoma patients. 
    Annals of Surgical Oncology
    , 
    24
    (4), 939 – 946. http://dx.doi.org.wilkes.idm.oclc.org/10.1245/s10434-016-5642-0

    Garbe, C., Peris, K., Hauschild, A., Saiag, P., Middleton, M., Basthold, L., Grob, J.J. Malvehy, J., Newton-Bishop, J., Stratigos, A.J., Pehamberger, H., & Eggermont, A.M. (2016) Diagnosis and treatment of melanoma. European consensus-based interdisciplinary guideline – update 2016.  
    European Journal of Cancer
    , 
    63
    (1), 201 – 217. 
    https://doi.org/10.1016/j.ejca.2016.05.005

    Research on adjuvant immunotherapy has shown that this can have some benefit specifically to stage 2 melanoma. It is used after primary treatments such as surgery to lessen the chance of the cancer returning. Interferon (IFN)-α is an immunotherapy agent that was shown to be effective in some randomized trials at improving survival rates (Garbe et al., 2016). In another study, Koster et al. (2017) looked at stage I – II melanoma patients and performed randomized trials to determine whether or not a localized adjuvant low dose CpG-B treatment offers benefit after the tumor is removed. These were phase II trials, but the study found that this specific treatment presented as safe, boosted immunity, was associated with lower rates of melanoma re-occurrence, and improved survival rates.

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    Alfonsina Perez posted Feb 3, 2021 1:34 AM

    Contains unread posts Stage II melanoma

                Melanomas are defined as malignant tumors that come from melanocytic cells (Garbe et al., 2016). Melanoma tumors are mostly found in the skin but can also be found in the eyes and meninges (Garbe et al., 2016). The primary treatment for stage II melanoma is an excisional biopsy (Garbe et al., 2016). In an excisional biopsy, the entire tumor is removed with a wide local incision, as opposed to an incisional biopsy when only a portion of the tumor is removed (Garbe et al., 2016). Whenever possible, an excisional biopsy is the preferred method of tumor removal in the case of melanomas. In cases when the tumors have metastasis or the risk of metastasis or recurrent of cancer may be a risk, adjuvant therapies may be recommended and these include chemotherapy and radiation (Garbe et al., 2016). Another part of the treatment for stage II melanoma is to do a sentinel lymph node biopsy to see if any cancer cells have spread to the lymph nodes (Hieken et al., 2019). ReferencesBrożyna, A. A., Guo, H., Yang, S., Cornelius, L., Linette, G., Murphy, M., . . . Carlson, J. A.(2017). TRPM1 (melastatin) expression is an independent predictor of overall survival inclinical AJCC stage I and II melanoma patients. Journal of Cutaneous Pathology, 44(4),328-337. doi:10.1111/cup.12872Garbe, C., Peris, K., Hauschild, A., Saiag, P., Middleton, M., Bastholt, L., . . . EuropeanAssociation of Dermato-Oncology (EADO). (2016). Diagnosis and treatment ofmelanoma. european consensus-based interdisciplinary guideline – update 2016.European Journal of Cancer (1990), 63, 201-217. doi:10.1016/j.ejca.2016.05.005Hieken, T. J., Kane,John M., I.,II, & Wong, S. L. (2019). The role of completion lymph nodedissection for sentinel lymph node-positive melanoma.
     Annals of Surgical
    Oncology, 26
    (4), 1028-1034. doi:http://dx.doi.org.wilkes.idm.oclc.org/10.1245/s10434-018-6812-zless1 UnreadUnread4 ViewsViews

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    View profile card for Jennifer Bryant

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    February 6 at 6:10 PM
     by Jennifer Bryant

     

                   Patients survival rate after treatment with the various modalities is highly dependent on the stage of the melanoma when diagnosed and the promptness of treatment. Brozyna et al., (2017), found that with surgical intervention patients have a survival rate of 88%. It is important to remember that the like hood of survival is highly dependent on the size of tumor, depth and whether there is metastasis present (Brozyna etal., 2017).

    Melanoma Discussion Post
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    Jennifer Bryant posted Feb 1, 2021 6:22 PM

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    In this case study, Mr. B had a suspicious mole excised and pathohistology reported the tumor as Stage II Melanoma. This means the cancer cells are in both the epidermis and the dermis. Wide local excision of the tumor is the current standard of care. Alternative surgical techniques include Mohs micrographic surgery, a targeted, tissue preserving option. Recurrences due to inadequate excision, resulting in true local recurrence rates of 9% to 15% of the head and neck and 3% on the trunk and proximal extremities (Tolkachjov et al, 2017) Stage II melanoma.        Stang, A.,  Roesch, A., Selma Ugurel, S., (2018) Melanoma, 
    The Lancet
    , 392(10151), 971-      Hruza, G. J., M.D., Roenigk, R. K., M.D., Harmon, C. B., M.D. (2017). Understanding
         Clinic Proceedings, 92
    (8), 1261-1271.less1 UnreadUnread3 ViewsViews

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    View profile card for Aina Oluwo

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    February 6 at 12:15 PM
     by Aina Oluwo

         mohs micrographic surgery: A review and practical guide for the nondermatologist.
     Mayo

    Tolkachjov, S. N., M.D., Brodland, D. G., M.D., Coldiron, B. M., M.D., Fazio, M. J., M.D.,

         984.

    Schadendorf, D., van Akkooi, A., Berking, C., Griewank, K. G., Gutzmer, R., Hauschild, A.,

    American Cancer Society, 2021 
    Cancer Facts and Figures, 2021.

    References

    The hard, enlarged, non-tender mass the left axillary region should be biopsied. Lymph node biopsy is recommended for primary melanomas with a tumor thickness of at least 1.0 mm (Schadendorf et al., 2018). The 5 year survival rate for all stages of skin cancer is 93%. When detected early, such as the case of Mr B, a localized tumor that has not spread beyond the skin where it started, the 5 year survival rate is 99% (American Cancer Society, 2021). Ongoing screening and surveillance should occur due to increased risk factors: family history, personal history, light skin and ongoing UV exposure. Mr. B must be educated in prevention with sunscreen, protective clothing and limited sun exposure.

    Stage II Melanoma
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    Jazmin Jerez-Rivera posted Feb 2, 2021 2:41 PM

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    Melanoma is cancer found in the melanocytes of the skin. Huether et. al. states, “Melanoma the most lethal form of skin cancer, can occur at many sites (2020, p. 280). Evidence suggests that occasional sun exposure leading to sunburn can increase the risk of melanoma. According to the American cancer society surgery to remove the cancerous area is the standard for treating stage II melanoma. Research by Domingues et. al. indicates that tumor excision “includes safety margins of 0.5 cm for in situ melanomas, 1 cm for tumors with a thickness of up to 2 mm, and 2 cm for tumors thicker than 2 mm” (2018, p. 35). There are also recommendations for a sentinel lymph node biopsy to check if the melanoma has spread to lymph nodes in the surrounding area. If cancer cells are found, then the lymph nodes in the area will be surgically removed. Other considerations are chemotherapy, targeted therapy and immunotherapy (Dominges et. al., 2018).References
    ImmunoTargets and therapy
    , 
    7
    , 35–49. 
    https://doi.org/10.2147/ITT.S134842
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html#written_by
    Elsevier.less1 UnreadUnread3 ViewsViews

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    View profile card for Candice Russell

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    February 5 at 8:18 PM
     by Candice Russell

    Huether, S. E., McCance, K. L., Brashers, V. L. (2020). Understanding Pathophysiology (7 Ed.).

    American Cancer Society. (2019). Treatment of Melanoma Skin Cancer, by Stage.

    Domingues, B., Lopes, J. M., Soares, P., & Pópulo, H. (2018). Melanoma treatment in review Stage II melanoma.

    Mr. B’s melanoma
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    Tallona Boddy posted Feb 2, 2021 7:13 PM

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    Mr. B was diagnosed with a Stage II melanoma. Mr. B’s cancer was first suspected at his annual physical exam with his primary care physician.  Mr. B’s physician initially excised the suspicious mole and sent it to pathology.  Along with a suspicious mole, the physician also noted a non-tender mass in Mr. B’s left axillary region. The American Cancer Society (n.d.) states an additional step for the treatment of Stage II melanoma is to have a sentinel lymph node biopsy (SLNB) performed. Due to Mr. B’s noted non-tender mass in his axillary a SLNB should be discussed with Mr. B to determine if there are cancerous cells in his lymph nodes.  Melanoma Research Alliance (n.d.) states that the prognosis for stage II melanoma does have a high rate of recurrence or metastasis.  In 2018 the 5 year survival rate of localized melanoma (which includes stage II) is 98.4%.  ReferencesMelanoma Research Alliance. (n.d.). Stage 2 melanoma. 
    https://www.curemelanoma.org/about-melanoma/melanoma-staging/stage-2/.
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    View profile card for Jazmin Jerez-Rivera

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    February 5 at 7:56 PM
     by Jazmin Jerez-Rivera

    Utjés, D., Malmstedt, J., Teras, J., Drzewiecki, K., Gullestad, H. P., Ingvar, C., Eriksson, H., & Gillgren, P. (2019). 2-cm versus 4-cm surgical excision margins for primary cutaneous melanoma thicker than 2 mm: long-term follow-up of a multicentre, randomised trial. Lancet (London, England), 394(10197), 471–477. 
    https://doi.org/10.1016/S0140-6736(19)31132-8

    American Cancer Society. (n.d.). Treatment of melanoma by stage. 
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html
    .

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    View profile card for Tallona Boddy

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    February 5 at 3:28 PM
     by Tallona Boddy

    Treatment of melanoma by stage
    . (n.d.). American Cancer Society | Information and Resources about for Cancer: Breast, Colon, Lung, Prostate, Skin. Retrieved February 2, 2021,  
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html

    Stark M. S. (2017). Melanoma treatment guided by a panel of microRNA biomarkers. 
    Melanoma management
    , 
    4
    (2), 75–77. 
    https://doi.org/10.2217/mmt-2017-0006

    Stage 1 & stage 2 melanomas | Mount Sinai – New York
    . (n.d.). Mount Sinai Health System. Retrieved February 2, 2021, 
    https://www.mountsinai.org/locations/waldman-melanoma-center/what-is/stage-1-and-2-melanoma

               doi: 10.15586/codon.cutaneousmelanoma.2017.ch7

    ‌

    The Surveillance, Epidemiology, and End Results (SEER) database provides survival statistics for different forms of cancer Stage II melanoma. SEER tracks 5-year survival rates for melanoma skin cancer, based on how far the cancer has spread. SEER groups cancer into localized, regional, and distant stages. In stage II melanoma, not spread beyond the skin, is considered localized. The five-year relative survival rate in localized SEER staging is 99% (
    Treatment of melanoma by stage
    , 
    n.d.) In the regional stage, cancer that has spread to nearby structures or lymph nodes, the 5-year survival rate is 66% (
    Treatment of melanoma by stage
    , 
    n.d.). The more advanced the cancer, the survival rates continue to decrease. Continued surveillance is important, even after completed treatment, due to high risk of reoccurrence and development of another melanoma. Self-skin assessment is recommended.

    Surgery is the main treatment option in melanoma, if done during early stages, surgery can cure melanoma. Joyce (2017) stated, “surgery remains the mainstay of treatment of primary melanoma, and in the majority of cases it is curative” (p. 92). Wide excision, surgery that removes the melanoma, as well as some of the normal skin around it, is the standard form of treatment for stage II. The width of the excision depends on the thickness and location of the melanoma. If there is lymph node involvement a sentinel lymph node biopsy (SLNB) may be recommended. 
    Treatment of melanoma by stage
    . 
    (n.d.) states “If an SLNB is done and does not find cancer cells in the lymph nodes then no further treatment is needed, although follow-up is still important” (p. 24). If cancer is found in SLNB, additional treatment with an immune checkpoint inhibitor or targeted therapy drugs may be recommended.

                The type of treatment will depend on the stage and location of the melanoma. Three factors used to determine staging of melanoma, consist of the TNM system. T category determines the tumor thickness and the presence or absence of ulceration. N category determines if regional lymph nodes are involved. M determines if distant metastasis has taken place. The American Joint Committee on Cancer (AJCC) made significant revisions to the melanoma TNM staging system. Balch et al. (2003) stated “the new staging system better reflects independent prognostic factors that are used in clinical trials and in reporting the outcomes of various melanoma treatment modalities” (p. 43) Stage II melanoma.

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    Gisselle Mustiga posted Feb 4, 2021 7:44 AM

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    Melanoma is a skin disease that occurs when cancerous or malignant cells are formed in the melanocytes.  The number of individuals with this disease has continued to increase in the United States over the last three decades (Huether et al., 2020). Melanoma is quite common in adults compared to children and adolescents. Some of the notable signs of melanoma include a mole, which tends to changes in size, changes in skin pigmentation, and the presence of other satellite moles. The disease can be examined through skin exams, biopsy, and physical exams. It occurs in five stages;  Stage 0, also known as melanoma in situ, to stage IV. Each stage has preferred and most effective treatment methods. However, it should be noted that melanoma can recur after treatment.
    References
    PDQ Adult Treatment Editorial Board, (2020). Melanoma Treatment (PDQ®), Patient Version. 
    PDQ Cancer Information Summaries [Internet]. Bethesda (MD):
     National Cancer Institute. 
    https://www.ncbi.nlm.nih.gov/books/NBK65950/
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    View profile card for Hilary Szpara

    Last post 
    February 5 at 2:44 PM
     by Hilary Szpara

    Ward, W. H., & Farma, J. M. (2017). Cutaneous Melanoma: Etiology and Therapy [Internet]: 
    Chapter 7; Surgical Management of Melanoma
    . Brisbane (AU):
     Codon Publications. 
    https://www.ncbi.nlm.nih.gov/books/NBK481850/#:~:text=Surgery%20remains%20the%20best%20option,care%20for%20localized%20cutaneous%20melanoma
    .

    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding Pathophysiology 7 th ed
    . Elsevier Mosby. 
    https://www.sendspace.com/file/19s130

    Stage II melanoma tends to extend beyond the skin’s outer layer (epidermis), thus reaching the dermis.  The most effective and best method for treating stage II melanoma is surgery. This involves performing minor surgeries of wider local excisions to get rid of the melanoma and the surrounding normal skin tissues (PDQ Adult Treatment Editorial Board, 2020). This is then followed by skin grafting, which involves taking skins from other parts of the body to replace the removed one Stage II melanoma. The procedure is essential in covering the wound caused by the surgery. Moreover, sentinel lymph node biopsy is recommended in checking the spread of melanoma to the nearby lymph nodes. Close follow-up is also essential in monitoring the patient’s outcomes. This treatment method has a 5-year survival rate of 92%, making it the best option for localized melanoma (Ward & Farma, 2017).

    Module 3- Melanoma
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    Joanne Hogan posted Feb 3, 2021 3:38 PM

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    References

         Although stage II melanoma can be treated surgically, there is recurrence of this cancer even if patients have negative SLNB post-surgery (Koster et al., 2017). The mortality rate for recurrences of this cancer is 48.5%. The 10-year survival rate in early diagnosed (stage I and stage II) localized melanoma is 95%-40%. The survival rate drops to 68% to 40% if the lymph nodes are affected. According to randomized trial study, an immunotherapy, CpG-B has shown to reduce the recurrence of stage I-II melanoma. Moreover, this treatment has shown more survival rate for patients. CpG-B is an immunotherapy injection that is given through intradermal route. The study concluded that CpG-B has the potential to become a safe treatment for stage I and II melanoma. However, long-term randomized trial research is needed in order to make it a standard treatment (Koster et al., 2017).

    Stage II melanoma
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    Melissa Morgan posted Feb 3, 2021 9:35 PM

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    Melanoma is the most serious form of skin cancer that if not caught early has a low survival rate (Huether, McCance & Brashers, 2020). This is because it can spread quickly and metastasizes to other areas of the body. “The morbidity and mortality of this disease vary according to the time of detection and accessibility to treatment” (Gao, et al., 2020, p. 1). Mr. B has light skin, has a family history of skin cancer, spends his weekends running and gardening, and only uses sunscreen sporadically; these are known risk factors for skin cancer. Gao, Y., Li, Y., Niu, X., Wu, Y., Guan, X., Hong, Y., Chen, H., & Song, B. (2020). Identification and Validation of Prognostically Relevant Gene Signature in Melanoma. 
    BioMed Research International
    , 1–29. https://doi-org.wilkes.idm.oclc.org/10.1155/2020/5323614Motofei, I. G. (2019). Malignant Melanoma: Autoimmunity and Supracellular Messaging as New Therapeutic Approaches. 
    Current Treatment Options in Oncology
    , 
    20
    (6), 1–15. https://doi-org.wilkes.idm.oclc.org/10.1007 Stage II melanoma /s11864-019-0643-4 less1 UnreadUnread7 ViewsViews

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    View profile card for Caroline Otto

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    February 5 at 11:33 AM
     by Caroline Otto

    Sun, R., Guo, M., Fan, X., Meng, Q., Yuan, D., Yang, X., Yan, K., & Deng, H. (2020). MicroRNA-148b Inhibits the Malignant Biological Behavior of Melanoma by Reducing Sirtuin 7 Expression Levels. 
    BioMed Research International
    , 1–13. https://doi-org.wilkes.idm.oclc.org/10.1155/2020/9568976

    Huether, S., McCance, K., and Brashers, V.  (2020).  
    Understanding Pathophysiology
     (7
    th
     ed.).  Elsevier.

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    References

    Mr. B’s cancer is stage II and is localized. Therefore, treatment of melanoma involves a wide surgical excision of the primary lesion site if there is no evidence of metastatic disease (Huether, McCance & Brashers, 2020). A biopsy of the peripherally draining lymph node may be necessary if Mr. B’s lesion is greater than 1 mm deep (Huether, McCance & Brashers, 2020). “Lesions on the extremities have the best surgical prognosis” (Huether, McCance & Brashers, 2020, p. 1034). “Except for melanoma in situ, the surgical procedure is generally not enough when it is performed as monotherapy, local recurrence, and/or metastases develop in most patients after a variable period of time” (Motofei, 2019, p. 2). Mr. B has stage II melanoma, so after surgical removal of the lesion, treatment will likely involve either radiation therapy, chemotherapy, immunotherapy, oncolytic viruses, or targeted molecular therapy (Huether, McCance & Brashers, 2020). Mr. B is 40 years old, his lesion is located in his left arm (which has a better surgical prognosis than other areas of the body), is stage II, and the cancer has not metastasized. Whether this treatment will be effective depends on if all the cancerous cells were removed during surgery, and the recurrence or metastasizes of the cancer in the future. “However, despite promising progress in surgical resection, radiotherapy, and chemotherapy of melanoma, long-term survival remains extremely low due to recurrence and metastasis” (Sun, et al., 2020, p. 1).

    Weekk 3 discussion, Stage II Melanoma

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    Beth Certain posted Feb 3, 2021 10:54 PM

    According to the Skin Cancer Foundation (2020), melanoma is diagnosed when suspicious looking tissue is biopsied to determine if cancer cells are present. This is done by sending the biopsy to the lab for analysis. Once the disease is diagnosed, and the type of melanoma has been identified, the next step is identifying the stage of the disease. Mr. B has been diagnosed with stage II melanoma. There are actually three subgroups of melanoma. The melanoma Research Alliance explains the following:
    Stage IIB Melanoma
    : A tumor in this stage is more than 2.0 millimeters and less than 4.0 millimeters thick with broken skin or more than 4.0 millimeters without ulceration.Because we only know Mr. B’s melanoma is stage II and there isn’t any information on the subgroups, the treatment for stage 2 melanoma is removing the tumor surgically. This procedure is a minor surgery using a wide, local incision, which usually cures local melanoma. Your doctor may suggest a sentinel lymph node biopsy to determine if the melanoma has spread to the nearest lymph node. If melanoma is detected in the biopsy, your doctor may recommend a complete “lymph node dissection (this removes all lymph nodes in a specific area of the body, surgically); however, this is not recommended in all instances” (Melanoma Resource Alliance, N.D.).Clinical trials allow patients access to treatments that have the potential to be more beneficial but have yet to be approved by the U.S. FDA Stage II melanoma. Clinical trials expand the understanding of the disease and improve future treatments for all patients. According to the Melanoma Research Alliance, Stage II Melanoma has an intermediate to high risk for recurrence or metastasis with appropriate treatment. As of 2018, there is a 98.4% of a 5-year survival rate for local melanoma to include Stage II. Once there is no evidence of disease following treatment, monthly self-exams should be performed of the skin and lymph nodes. The patient should have full-body skin exams by a trained dermatologist yearly for the rest of the patient’s life. Exams by your doctor should also be in the treatment plan, usually every 6-12 months for the first 5 years. Imaging tests can also be used to monitor for the recurrence of cancer.Melanoma Research Alliance (N.D.). 
    Stage II Melanoma
    . Retrieved fromThe Skin Cancer Foundation. (June, 2020). 
    Melanoma Stages
    . Retrieved from less0 UnreadUnread

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    View profile card for Gisselle Mustiga

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    February 5 at 11:04 AM
     by Gisselle Mustiga

    Melanoma Stages

    https://www.curemelanoma.org/about-melanoma/melanoma-staging/stage
    . February 2, 2021

    References

    Some melanomas have certain features that increase the chance of metastasis and or recurrence. The doctor will determine what type of additional treatment may be needed to help delay or prevent cancer from returning. Adjuvant therapy is used to reduce the risk of melanoma returning.

    Stage IIC Melanoma
    : The melanoma tumor is more than 4.0 millimeters thick with broken skin.

    Stage IIA Melanoma
    : A melanoma tumor more than 1.0 millimeter and less than 2.0 millimeters thick (approximately the size of a new crayon point), with broken skin, or 2.0 to less than 4.0 millimeters without broken skin.

    Stage II Melanoma’s and Adjuvent therapy
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    Caroline Otto posted Feb 5, 2021 10:35 AM

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    The treatment for Stage 2 Melanoma is primarily treated once it has been staged, because if there are other skin melanomas found; the overall treatment will depend on the stage each of them are in.If the melanoma has spread into the lymph node, a complete lymph node dissection would be performed; but this may not be a treatment option in all cases.If a melanoma is suspected of returning, the physician may recommend “adjuvant therapy” which aids in preventing the melanoma from returning. This is usually done after surgery.Interferon (Intron and Sylatron) – This used to be the golden child of treatment, however over the past couple of years, the use of this medication has been discouraged due to the many toxic effects it has on the body and impact on survival.Ipilimumab (Yervoy) – Was the first immune checkpoint inhibitor ever studied in the adjuvant setting.Dabrafenib + Trametinib (Tafinlar + Mekinist)Adjuvent therapy is rapidly changing the way Melanoma is treated and is now considered the standard of care for many patients. Since this therapy is still in its infancy with limited research participants, its overall role in high-risk 2 and stage IIIA is still being defined (Davis, et.al. 2019) Stage II melanoma. Neo-adjuvant Therapy is recommended when the goal is to shrink the melanoma prior to surgery. If the Melanoma is deeper or thicker than 4.0 millimeters thick it more than likely will involve nearby lymph nodes, and this disease has a high risk of recurrence because after surgery there is the risk that some of the melanoma cells may remain in the body.Participation however remains low and this seems to be because of not being aware of programs out there, as well as fear. There are benefits and risks associated to this form of therapy, however paramount is the early access to a potentially better treatment than one that already exists, and it may be free or be offered at no or low cost to the client.Davis, L. E., Shalin, S. C., & Tackett, A. J. (2019). Current state of melanoma diagnosis and treatment. Cancer biology & therapy, 20(11), 1366–1379.
    https://doi.org/10.1080/15384047.2019.1640032
    Trotter, S. C., Sroa, N., Winkelmann, R. R., Olencki, T., & Bechtel, M. (2013). A Global Review of Melanoma Follow-up Guidelines. The Journal of clinical and aesthetic dermatology, 6(9), 18–26.less0 UnreadUnread

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    Moreno Nogueira, J. A., Valero Arbizu, M., & Pérez Temprano, R. (2013). Adjuvant treatment of melanoma. ISRN dermatology, 2013, 545631. 
    https://doi.org/10.1155/2013/545631

    References

    Clinical Trials serves as an additional form of therapy.

    There are many side effects associated with Adjuvent therapy and these adverse effects increase according to patient comorbidities such as; cardiac disease. The research is limited because of the amount of participants that have been studied.

    Pembrolizumab (Keytruda)

    Nivolumab (Opdivo)

    Better outcomes have been demonstrated by the following medications, with less effects, however they are all in their infancy.

    Examples of this are;

    Staging melanomas gives physicians the information to ascertain which ones would most likely metastasize, and which ones would recur. The American Joint Committee on Cancer (AJCC) has identified that the staging of melanomas is not consistent, and many physicians over treat which has resulted in inaccurate numbers of incidence (Trotter, et. Al. 2013).

    Stage 2 Melanoma however is treated by removing the tumor surgically, and adopting a wide local excision. In addition to that, the physician may recommend a “sentinel lymph node biopsy”, to determine if the melanoma has spread to the nearest lymph node (Moreno Nogueira, et. al, 2013).

    Dennies Jones
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    Dennies Jones posted Feb 2, 2021 1:58 PM

    Contains unread posts

       Mr. B was diagnosed with stage II melanoma based on the biopsy. He had the mole for several years and did not think anything of it until his physician noticed it. The mole has gotten larger over the past two years, shown symptoms of itchiness and a family history of skin cancer. Mr. B  will recognize early signs of skin cancer once educated on warning signs, which are any unusual skin condition change, especially a difference in size, borders, or color of a mole or other dark pigmented growth or spot (Huether et al., 2020). He said to have an enlarged, non-tender mass felt in the left axillary region. Even though he was diagnosed with stage II cancer, this could be a potential risk of cancer spreading more profoundly into the skin and entering the lymph nodes, allowing it to metastasize Stage II melanoma. At an early stage (stages I and II), cutaneous melanomas are defined within the American Joint Cancer (AJCC) classification by modern surgical staging by lacking lymph node involvement. High-risk cancer is considered ulcerated, involving the lymph nodes (Polkepovic & Luke, 2020). Polkepovic and Luke (2020) further stated, “thin melanomas (<2mm) accounted for over twice as many deaths from melanoma than thick melanomas (>4mm)” (p. 1167). It shows a higher need for an increased skin assessment and early diagnosis for early stages of Melanomas.           Mr. B’s diagnosis is commonly treated with adjuvant therapy. Surgically removing the cancerous skin with additional treatment of chemotherapy or radiation therapy is most effective.  Surgical treatment alone with high-risk shows an increase in the chance of recurrence in cancer. Melanoma is one highly immunogenic cancer- the immune system can be manipulated against the disease. Because of this, treatment of melanoma is moving to strategies that target the immune system (Khushalani, 2017).  The second way to target melanoma with the immune system is to block suppressive elements. The activity of the T cell is controlled by a series of molecular regulatory interactions, including those between cytotoxic T cell lymphocyte-associated antigen 4 (CTLA-4) and antigen-presenting cells (APC) and between programs death -1 (PD-1) and its primary ligand, PD-L1 on the melanoma cells (Khushalani, 2017). Mr. B will need continuous follow-up and skin assessment for any other skin cancer.References:Huether, Sue E., McCance, Kathryn L… Understanding Pathophysiology – E-Book (p. 169). Elsevier Health Sciences. Kindle Edition.                      less1 UnreadUnread13 ViewsViews

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    View profile card for Alfonsina Perez

    Last post 
    February 4 at 12:20 AM
     by Alfonsina Perez

    Poklepovic, A. S., & Luke, J. J. (2020). Considering adjuvant therapy for stage II melanoma. 
    Cancer (0008543X)
    , 
    126
    (6), 1166–1174. 
    https://doi-org.wilkes.idm.oclc.org/10.1002/cncr.32585

    Khushalan, N. I. (2017). Evolving Strategies in the Treatment of Metastatic Melanoma. 
    Journal of Managed Care Medicine
    , 
    20
    (1), 31–34.

    Module 3 Discussion
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    Hilary Szpara posted Feb 3, 2021 1:53 AM

    Contains unread posts

    For melanoma in stages I-IIIB, surgical removal is the primary treatment. However, depending on the size, thickness, and location of the tumor, safety margins may vary to help prevent regrowth of the tumor (Domingues, Lopez, Soares, & Pópulo, 2018). A systematic review of literature on stage-specific survival of melanoma in Europe revealed that overall survival rates for people with stage I/II was 91.6% for people coming from lower socioeconomic statuses (SES) and went up to 97.3%-98.3% for patients with a middle or high SES. Researchers believed that patients’ SES may lead to differences in early detection, treatment, and follow up (Svedman, Pillas, Taylor, Kaur, Linder, & Hansson, 2016). A systematic review of literature from 2020 suggested that the five-year disease-specific survival rates for patients with stage II melanoma ranged from 63-81%, with most studies reporting a survival rate of over 70% (Miller, Walker, Shui, Brandtmüller, Cadwell, & Scherrer 2020). The same literature review also showed that five-year disease-specific survival rates decreased to 36-63% when the patients had stage III melanoma, with most studies reporting rates of over 50% (Miller et al., 2020). It seems that for the most part, chance of survival with stage II melanoma is high as long as a patient has the appropriate treatment and is able to maintain proper follow up with medical providers.    less1 UnreadUnread7 ViewsViews

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    View profile card for Amandeep Kaur

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    February 3 at 8:51 PM
     by Amandeep Kaur

    Svedman, F. C., Pillas, D., Taylor, A., Kaur, M., Linder, R., & Hansson, J. (2016). Stage-specific survival and recurrence in patients with cutaneous malignant melanoma in Europe – a systematic review of the literature. 
    Clinical Epidemiology
    , 
    8
    , 109–122. https://doi.org/10.2147/CLEP.S99021

    Miller, R., Walker, S., Shui, I., Brandtmüller, A., Cadwell, K., & Scherrer, E. (2020). Epidemiology and survival outcomes in stages II and III cutaneous melanoma: a systematic review. 
    Melanoma Management
    , 
    7
    (1). https://doi.org/10.2217/mmt-2019-0022

    Domingues, B., Lopes, J. M., Soares, P., & Pópulo, H. (2018). Melanoma treatment in review. 
    ImmunoTargets and Therapy
    , 
    7
    , 35–49. https://doi.org/10.2147/ITT.S134842 Stage II melanoma

    Fritzinger NSG530 discussion Wk3
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    Cassie Fritzinger posted Feb 3, 2021 4:21 PM

    Contains unread posts

    According to the American Cancer Society (2021), melanoma is the most serious type of skin cancer and develops in the melanocytes. Melanoma is staged in a system from I-IV with some stages being broken down further into letters based on amount it has spread in the body (American Cancer Society, 2021). Melanoma Stage II is as reported by the American Cancer Society (2021), to be a tumor which is between 1mm and 4mm thick, which may or may not be ulcerated, and the cancer has not spread to the nearby lymph nodes or other body parts. Treatment for melanoma stage 2 includes immunotherapy, targeted drug therapy, wide excision of the melanoma with margins of healthy tissue and it will generally also include a sentinel lymph node biopsy to determine lymph node involvement.The usual treatment for stage 2 Melanoma would include the surgical removal along with a sentinel lymph node biopsy. Provided this determines there is no lymph node involvement treatment provides a favorable survival rate. However, if there is lymph node involvement survival rates decline. The 5-year survival rate for a patient with Stage 2 Melanoma is 99% unless there is lymph node involvement at which point it then decreases to 65% (Godman, 2020).
     
    American Cancer Society. (2021). Melanoma Skin Cancer. Retrieved February 1, 2021, From 
    https://www.cancer.org/cancer/melanoma-skin-cancer.html
      Mayo Clinic. (2021). Melanoma. Retrieved February 1, 2021, From https://www.mayoclinic.org/diseases-conditions/melanoma/diagnosis-treatment/drc-20374888less0 UnreadUnread

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    Godman, H. (2020). What are the Prognosis and Survival Rates for Melanoma by Stage? Healthline. https://www.healthline.com/health/melanoma-prognosis-and-survival-rates

    References

     

    Immunotherapy is a drug therapy which helps the body’s natural immune system fight the cancerous cells by interfering with the cancer cell’s protein which camouflages them from the immune system, which would normally attack the cell. This is typically done after a surgery has been performed to excise the melanoma (Mayo Clinic, 2021). Another form of treatment may include Targeted drug therapy which focuses on a specific weakness of the cancerous cell to cause the cell to die. This is often recommended if the cancer has spread to lymph nodes. For more advanced melanomas Radiation and Chemotherapy may be required due to their advanced and malignant nature (Mayo Clinic, 2021) Stage II melanoma.

    Melanoma
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    Sheryl Dixon posted Feb 2, 2021 6:34 PM

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    Melanoma is a cancer that is the most lethal form that can occur at many sites. The most common is on the skin of the lower legs, between the shoulders and the hips. Although for people with dark skin, its most found under the fingernails, toenails or the palm of their skin. Treatment of Melanoma with no evidence of metastatic disease involves a wide surgical excision of the primary lesion site (Huether, McCance & Brashers, 2020).Five types of standard treatment are used: Surgery, Chemotherapy, Radiation therapy, Immunotherapy, Targeted therapy. Wide excision (
    surgery
     to remove the melanoma and a margin of normal skin around it) is the standard treatment for stage II melanoma. The width of the margin depends on the thickness and location of the melanoma. Because the melanoma may have spread to nearby lymph nodes, many doctors recommend a 
    sentinel lymph node biopsy
     (SLNB) as well.Chemotherapy is a cancer treatment that uses drugs to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. When chemotherapy is taken by mouth or injected into a vein or muscle, the drugs enter the bloodstream and can reach cancer cells throughout the body (systemic chemotherapy). When chemotherapy is placed directly into the cerebrospinal fluid, an organ, or a body cavity such as the abdomen, the drugs mainly affect cancer cells in those areas (regional chemotherapy).Immunotherapy is a treatment that uses the patient’s immune system to fight cancer. Substances made by the body or made in a laboratory are used to boost, direct, or restore the body’s natural defenses against cancer. This cancer treatment is a type of biologic therapy.Signal-transduction inhibitors include:

    BRAF inhibitors
     (
    dabrafenib
    , 
    vemurafenib
    , encorafenib) that block the activity of proteins made by 
    mutant
     
    BRAF
     
    genes
    ; and

    MEK inhibitors (
    trametinib
    , cobimetinib, binimetinib) that block proteins called MEK1 and MEK2 which affect the growth and survival of cancer cells.

    Combinations of BRAF inhibitors and MEK inhibitors used to treat melanoma include:

    Dabrafenib
     plus 
    trametinib
    .

    Vemurafenib
     plus cobimetinib.

    Encorafenib plus binimetinib.

    Oncolytic virus therapy
    : A type of targeted therapy that is used in the treatment of melanoma. Oncolytic virus therapy uses a 
    virus
     that infects and breaks down cancer cells but not normal cells. Radiation therapy or chemotherapy may be given after oncolytic virus therapy to kill more cancer cells. Talimogene laherparepvec is a type of oncolytic virus therapy made with a form of the 
    herpesvirus
     that has been changed in the laboratory. It is injected directly into tumors in the skin and lymph nodes (National Center for Biotechnology Information, 2020). American cancer society, 2021
    Treatment of Melanoma Skin Cancer, by Stage Stage II melanoma
    . Retrieved from 
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html
    National Center for Biotechnology Information
    , 2020. Melanoma
     Treatment
    . Retrieved from https://www.ncbi.nlm.nih.gov/books/NBK65950/

    Huether, S. E., & McCance, K. L. & Brashers, V.L. (2020). 
    Understanding Pathophysiology 
    7th ed. Elsevier Mosby

                                                                                                           References

    Angiogenesis inhibitors
    : A type of targeted therapy that is being studied in the treatment of melanoma. Angiogenesis inhibitors block the growth of new 
    blood vessels
    . In cancer treatment, they may be given to prevent the growth of new blood vessels that tumors need to grow. Early detection is critical to reducing mortality from metastatic disease (Huether, McCance & Brashers, 2020).

    Targeted therapy is a type of treatment that uses drugs or other substances to identify and attack specific cancer cells. Targeted therapies usually cause less harm to normal cells than chemotherapy or radiation therapy do. The following types of targeted therapy are used or being studied in the treatment of melanoma: 
    Signal-transduction inhibitor
     therapy: Signal-transduction inhibitors block 
    signals
     that are passed from one 
    molecule
     to another inside a cell. Blocking these signals may kill cancer cells. They are used to treat some patients with advanced melanoma or tumors that cannot be removed by surgery.

    Radiation therapy is a cancer treatment that uses high-energy x-rays or other types of radiation to kill cancer cells or keep them from growing. External radiation therapy uses a machine outside the body to send radiation toward the area of the body with cancer. External radiation therapy is used to treat melanoma and may also be used as palliative therapy to relieve symptoms and improve quality of life (National Center for Biotechnology Information, 2020).

    A lymph node biopsy of peripherally draining lymph node (sentinel node) is warranted for lesions greater than 1 mm deep. Lesions extremities have the best surgical prognosis. Radiation therapy, chemotherapy, immunotherapy (checkpoint inhibiters that block proteins to stop the immune system from attacking cancer cells and signal transduction), oncolytic viruses and targeted molecular therapy that inhibits gene mutations, in addition to vaccines, are used to treat metastatic disease and have demonstrated long-term improvement in disease outcome.

    The type of treatment(s) your doctor recommends will depend on the stage and location of the melanoma. But other factors can be important as well, such as the risk of the cancer returning after treatment, if the cancer cells have certain gene changes, and your overall health (American cancer society, 2021) Stage II melanoma.

  • melanoma discussion essays

    Mr. B, a 40-year-old avid long-distance runner previously in good health, presented to his primary provider for a yearly physical examination, during which a suspicious-looking mole was noticed on the back of his left arm, just proximal to the elbow. He reported that he has had that mole for several years, but thinks that it may have gotten larger over the past two years. Mr. B reported that he has noticed itchiness in the area of this mole over the past few weeks. He had multiple other moles on his back, arms, and legs, none of which looked suspicious. Upon further questioning, Mr. B reported that his aunt died in her late forties of skin cancer, but he knew no other details about her illness. The patient is a computer programmer who spends most of the work week indoors. On weekends, however, he typically goes for a 5-mile run and spends much of his afternoons gardening. He has a light complexion, blonde hair, and reports that he sunburns easily but uses protective sunscreen only sporadically.

    Physical exam revealed: Head, neck, thorax, and abdominal exams were normal, with the exception of a hard, enlarged, non-tender mass felt in the left axillary region. In addition, a 1.6 x 2.8 cm mole was noted on the dorsal upper left arm. The lesion had an appearance suggestive of a melanoma. It was surgically excised with 3 mm margins using a local anesthetic and sent to the pathology laboratory for histologic analysis. The biopsy came back Stage II melanoma.

    How is Stage II melanoma treated and according to the research how effective is this treatment?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

     

     

    Module 3: Stage II MelanomaMelanoma accounts for 90% of deaths associated with cutaneous tumors due to their increased risk of metastasis and the speed in which they can evolve (Garbe et al., 2016). 10-year tumor specific survival rates range from 75-85% for a primary tumor without metastasis (Garbe et al., 2016). Increase in age, male sex, and tumor locations on the head or neck all decrease prognosis (Garbe et al., 2016).  The 10-year survival rate for those who have lymph node metastasis decreases to 20-40% (Garbe, et al., 2016). If the patient shows 
    BRAF 
    or 
    MEK
     genetic mutations, inhibitors of these genes may be a viable treatment option to lower risk of recurrence. These genes are responsible for cell growth, proliferation, and survival (Garbe et al., 2016). In instances of inoperable melanomas or melanomas with distant metastases, immunotherapeutic drugs may be used to prolong survival or reduce tumor size (Garbe et al., 2016). It is estimated that roughly 45% of people with melanoma have a 
    BRAF
     mutation (Garbe, et al., 2016). Vemurafenib and dabrafenib are examples of oral drugs approved in the US and UK that act on 
    BRAF 
    and 
    MEK
     mutations and use of these is considered the gold standard of care
     
    (Garbe, et al., 2016). These drugs inhibit these mutations and can improve quality of life and increase longevity.ReferencesHuether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7th ed.). Elsevier.
    Stage II melanoma
    . (2020). Melanoma Research Alliance. Retrieved February 3, 2021, from 
    https://curemelanoma.org/about-melanoma/melanoma-staging/stage-2
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    View profile card for Steven Bartos

    Last post 
    February 5 at 1:43 PM
     by Steven Bartos

    Koster, B. D., van den Hout, M. F., Sluijter, B. J., Molenkamp, B. G., Vuylsteke, R. J., Baars, A., van Leeuwen, P. A., Scheper, R. J., Petrousjka van den Tol, M., van den Eertwegh, A. J., & de Gruijl, T. D. (2017). Local adjuvant treatment with low-dose cpg-b offers durable protection against disease recurrence in clinical stage i–ii melanoma: Data from two randomized phase ii trials. 
    Clinical Cancer Research
    , 
    23
    (19), 5679–5686. 
    https://doi.org/10.1158/1078-0432.ccr-17-0944

    Garbe, C., Peris, K., Hauschild, A., Saiag, P., Middleton, M., Bastholt, L., Grob, J.-J., Malvehy, J., Newton-Bishop, J., Stratigos, A. J., Pehamberger, H., & Eggermont, A. M. (2016). Diagnosis and treatment of melanoma. european consensus-based interdisciplinary guideline – update 2016. 
    European Journal of Cancer
    , 
    63
    , 201–217. 
    https://doi.org/10.1016/j.ejca.2016.05.005

    The first line of treatment for melanoma is removal using surgical means (Huether et al., 2020, pp. 1033-1034). The surgical excision will have a large border and a biopsy of the peripheral lymph node will be taken if the lesion is greater than 1mm (Huether et al., 2020, pp. 1033-1034).  Prognosis is increased if the excision a biopsy occurs within 4-6 weeks of diagnosis (Garbe, et al., 2016). If the melanoma meets certain criteria that increases the risk of metastasis, adjuvant therapy can be used. Typically, adjuvant therapy is only used if the lesion is deeper or thicker than 4mm or if there is lymph node involvement (Koster et al., 2017). Patients that meet these criteria have an increased risk of recurrence due to the likelihood of melanoma cells remaining unseen in the body (Koster, et al., 2017). Adjuvant therapies include chemotherapy, the use of interferon-α, 
    BRAF/MEK
     inhibitors, or immunotherapy with antibodies (Garbe, et al., 2016). Of these therapies, the use of interferon- α has shown the most promise in clinical trials (Garbe et al., 2016). Koster (2017) found that the use of low dose immunotherapy agents may reduce the instance of tumor recurrence by 26%. Research is being done on vaccines as well (Koster, et al 2017).

    Stage II melanoma is a grade of skin cancer that extends beyond the epidermis into the dermis of the skin (
    Stage II Melanoma
    , 2020). Typically, at this stage it is still considered a localized melanoma but is more likely to metastasize compared to its stage 0 or stage I counterparts (
    Stage II Melanoma
    , 2020) Melanoma itself is a malignant tumor that involves the melanocytic cells that are responsible for producing melanin (Huether et al., 2020, pp. 1033-1034). These cells begin to malignantly degenerate in the basal layer of the epidermis or the melanocytic nevus (Huether et al., 2020, pp. 1033-1034). While melanoma typically appears on the skin, it can also appear in the eyes, meninges, or mucosal surfaces (Garbe et al., 2016).  Risks for melanoma include familial history, UV exposure, fair hair/skin, geographical location, and others (Huether et al., 2020, pp. 1033-1034).  Mutations in the 
    BRAF
    , 
    RAS
    , 
    NFI
    , or triple wild gene can also contribute to risk (Huether et al, 2020, pp. 1033-1034).

    Module 3, Eleany Yasein
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    Eleany Yasein posted Feb 2, 2021 10:22 PM

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            First acknowledged as a disease during the 1800s, melanoma is a skin cancer that is highly deadly (Davis, Shalin, & Tackett, 2019). However, treatment can be successful during the early stage of this cancer (Davis et al., 2019). The initial treatment for stage II melanoma is by surgical removal of the tissue (American Cancer Society, 2019). After the surgery, it is recommended that patients get a sentinel lymph node biopsy (SLNB) done, in order to detect whether or not the melanoma has spread to the nearby lymph nodes. If cancer is not detected around the lymph nodes, further treatment will not be necessary. However, close follow up will be crucial to the process. If the SLNB detects cancerous cells around the lymph nodes, all the lymph nodes in the area will be surgically eliminated. Moreover, targeted therapy drugs, as well as immune checkpoint inhibitor are recommended in order to reduce the chances of the cancer returning (American Cancer Society, 2019). American Cancer Society. (2019, August 14). 
    Treatment of Melanoma Skin Cancer, by Stage. 
    Retrieved February 02, 2021, from 
    https://www.cancer.org/cancer/melanoma-skin-cancer/treating/by-stage.html
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    View profile card for Caroline Otto

    Last post 
    February 5 at 12:17 PM
     by Caroline Otto

    Koster, D. B., Van den Hout, F.C.M. M., Sluijter, J.R. B., Molenkamp, G. B., Vuylsteke, J.C.L.M. R., Baars, A., Van Leeuwen, A.M. P., Scheper, J. R., Van den Tol, P. M., Van den Eertwegh, J.M. A., & De Gruijl, D. T. (2017, October). Local Adjuvant Treatment with Low-Dose CpG-B Offers Durable Protection against Disease Recurrence in Clinical Stage I–II Melanoma: Data from Two Randomized Phase II Trials.
    Clinical Cancer Research,
    23(19). doi
    :
    10.1158/1078-0432.CCR-17-0944

    Davis, E. L., Shalin, C. S., & Tackett, J. A. (2019). Current state of melanoma diagnosis and treatment. 
    Cancer biology & therapy, 
    20(11),
     
    1366-1379. doi: 
    10.1080/15384047.2019.1640032

  • melanoma

    Mr. B, a 40-year-old avid long-distance runner previously in good health, presented to his primary provider for a yearly physical examination, during which a suspicious-looking mole was noticed on the back of his left arm, just proximal to the elbow. He reported that he has had that mole for several years, but thinks that it may have gotten larger over the past two years. Mr. B reported that he has noticed itchiness in the area of this mole over the past few weeks. He had multiple other moles on his back, arms, and legs, none of which looked suspicious. Upon further questioning, Mr. B reported that his aunt died in her late forties of skin cancer, but he knew no other details about her illness. The patient is a computer programmer who spends most of the work week indoors. On weekends, however, he typically goes for a 5-mile run and spends much of his afternoons gardening. He has a light complexion, blonde hair, and reports that he sunburns easily but uses protective sunscreen only sporadically.

    Physical exam revealed: Head, neck, thorax, and abdominal exams were normal, with the exception of a hard, enlarged, non-tender mass felt in the left axillary region. In addition, a 1.6 x 2.8 cm mole was noted on the dorsal upper left arm. The lesion had an appearance suggestive of a melanoma. It was surgically excised with 3 mm margins using a local anesthetic and sent to the pathology laboratory for histologic analysis. The biopsy came back Stage II melanoma.

    How is Stage II melanoma treated and according to the research how effective is this treatment?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

     

    According to Melanoma Research Alliance (2021), survival rates have improved significantly additional adjunct therapy with Stage II at a 98.4%. This also depends on early detection and treatment.

    When it comes to treatment for Stage II melanoma, the standard treatment is a wide excision, which is a surgery to remove the melanoma and a margin of normal skin around it) is the standard treatment for stage II melanoma. The width of the margin depends on the thickness and location of the melanoma. Sentinel lymph node biopsy (SLNB) is usually recommended when the doctors think the melanoma has spread to nearby lymph nodes. No further treatment is needed if no cancer cells are found in lymph nodes after an SLNB is done, although close follow-up is still essential. On the other hand, if cancer cells are found after SLNB, then a lymph node dissection a procedure where all the lymph nodes in that area are surgically removed. One other option apart from lymph node dissection is to closely watch the lymph node by doing a regular ultrasound.

                Skin cancer can be divided into three main types; melanoma, cancer that forms in melanocytes, basal cell carcinomas (BCC); these cancers are found in the lower part of the epidermis, and squamous cell carcinomas (SCC), which is located in the flat cells form on the surface of the skin (Huether et al., 2020). Out of these three, melanoma is the most lethal form of skin cancer. (Huether et al., 2020). It does occur at most sites, but some places are more common than others (Ward et al., 2017). Cutaneous melanoma is known to be responsible for the majority of skin cancer-related deaths in the United States. Exposure to ultraviolet rays is the most important modifiable risk factor among environmental exposures (Ward et al., 2017).

    Amandeep Kaur
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    Amandeep Kaur posted Feb 3, 2021 6:05 PM

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    Melanoma is a form of skin cancer that develops in melanocytes. Melanocytes are basilar cells of the skin responsible for skin tone (Davis, Shalin, & Tackett, 2019). Individuals who have light skin that does not tan, blond or red hair and light eyes have a high risk of developing melanoma. This is due to the low amount of eumelanin compared to pheomelanin (pigment produced by melanocytes) which protects the skin from the ultraviolet rays of the sun. Pheomelanin can produce more ultraviolet-A-induced reactive oxidative species (ROS), this damages DNA. Stage II melanoma is when the invasion of the skin extends 0.76 – 1.5 mm, and it has spread to lymph nodes. This is indicated by Mr. B’s physical exam. Treatment of melanomas includes surgical resection, chemotherapy, targeted therapies, and immunotherapies. Since this is a stage II tumor oncologists are most likely to initially suggest an excision of the mole with wide margins. Margins should be 2-3 cm whenever it is anatomically possible (PDQ Adult Treatment Editorial Board, 2021). The wide margins are to ensure there are no cancerous cells left on the skin. This was not adequate with Mr. B as there were 3mm margins indicated. A study was conducted to assess the effectiveness of 1 cm and 3 cm margins and it showed that 1 cm margins had a higher rate of local recurrence.  Following the excision, a sentinel lymph node biopsy can be completed of Mr. B’s left axillary region lymph node. This region has a hard, enlarged, non-tender mass. If the lymph node had cancerous cells, the remaining lymph nodes in the region are removed. Studies indicate that these biopsies have a false negative rate of 0%-2%. Targeted therapy can also be used if there is a BRAF mutation; BRAF inhibitors, vemurafenib, dabrafenib (Davis, Shalin, & Tackett, 2019). These drugs are very effective in 50% of individuals with BRAF mutation. However, many individuals do develop resistance to these drugs. Stage II has a higher rate of survival than if the cancer were to metastasize and progress to Stage III or IV.Davis, L. E., Shalin, S. C., & Tackett, A. J. (2019). Current state of melanoma diagnosis and treatment. 
    Cancer biology & therapy
    , 
    20
    (11), 1366–1379.

    9

  • cystic fibrosis Essays

    cystic fibrosis Essays

    NSG-530-IKC – Advanced Pathophysiology

    Module 2: Discussion

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    Melissa, a 12-year-old girl with cystic fibrosis comes to the primary care office with complaints of increased cough and productive green sputum over the last week. She also complains of increasing shortness of breath. She denies sore throat or nasal congestion. On physical examination her temperature is 101 and she has inspiratory wheezes bilaterally. Negative lymphadenopathy noted. Posterior pharynx is pink without exudate. BP 112/72 HR 96 RR 28 cystic fibrosis Essays.

    In cystic fibrosis, the airway microenvironment favors bacterial colonization. In a minimum of 150 words explain the pathophysiological reason for this occurrence.

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

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    Module 2 Discussion
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    Hilary Szpara posted Jan 27, 2021 3:28 AM

    Contains unread posts cystic fibrosis Essays

    The lungs of a person with cystic fibrosis are saturated with sticky mucus, which makes it easier for bacteria to colonize there. The reason that mucus is able to accumulate in the lungs so easily is due to the mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene (Melnik et al., 2019). This mutation of the CFTR gene disrupts the function of the CFTR protein, an ion channel in the lungs which helps to regulate the volume of liquid, in this case mucus, on epithelial cells (Melnik et al., 2019). When the ion channel’s function is disrupted, there is a reduction in chloride secretion and an increase in sodium absorption (Rossi, 2019).  This malfunction in ion movement reduces the thickness of the periciliary layer, which usually acts as a lubricating layer and allows the normally present mucus to move more easily. However, when the thickness of the periciliary layer is decreased, excess mucus is able to build up because the cilia are no longer able to move it out of the lungs (Rossi, 2019). When this excess amount of mucus builds up in the lungs, the ability of the lungs to properly clear out bacteria is diminished (Bhagirath et al., 2016).  Rossi, G. A, Morelli, P., Galietta, L. J., Colin, A. A. (2019). Airway microenvironment alterations and pathogen growth in cystic fibrosis. 
    Pediatric Pulmonology, 54
    (4). 
    https://doi-org.wilkes.idm.oclc.org/10.1002/ppul.24246
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    View profile card for Sheryl Dixon

    Last post 
    February 7 at 2:45 PM
     by Sheryl Dixon

    Melnik, A. V., Vazquez-Baeza, Y., Aksenov, A., A., Hyde, E., McAvoy, A. C., Wang, M., da Silva, R. R., Protsyuk, I., Wu, J. V., Bouslimani, A., Lim, Y. W., Luzzato-Knaan, T., Comstock, W., Quinn, R. A., Wong, R., Humphrey, G., Ackermann, G., Spivey, T., Brouha, S. S., Bandeira, N., Lin, G. Y., Rohwer, F., Conrad, D. J., Alexandriv, T., Knight, R., Dorrestein, P. C., Garg, N. (2019). Molecular and microbial microenvironments in chronically diseased lungs associated with cystic fibrosis. 
    mSystems, 4
    (5), 1-16. https://doi.org/10.1128/ mSystems.00375-19

    Bhagirath, A. Y., Li, Y., Somayajula, D., Dadashi, M., Badr, S., & Duan, K. (2016). Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. 
    BMC pulmonary medicine
    , 
    16
    (1), 174. 
    https://doi.org/10.1186/s12890-016-0339-5

    In healthy lungs, the mucus layer that is present is thin and works with the cilia to carry bacteria that are inhaled back up to the pharynx so that they can be swallowed (Bhagirath et al., 2016). Defects in CFTR are also associated with less efficient recognition and killing of bacteria, lower expressions of cytokines which promote innate immune responses, and lower production of anti-inflammatory proteins (Rossi, 2019). All of these factors together help to create an environment in which bacteria that would normally be expelled from the body or swallowed, are essentially trapped in the thick, sticky mucus, where they are able to thrive and lead to chronic bacterial infections (Melnik et al., 2019) cystic fibrosis Essays.

    Cystic Fibrosis
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    Sheryl Dixon posted Jan 27, 2021 5:40 PM

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    Cystic Fibrosis (CF) is an autosomal recessive disorder that affects the lungs, digestive tract and reproductive organs .CF affects mostly the gastrointestinal (GI) and respiratory systems. The hallmark pathophysiology triad of CF is obstruction, inflammation and infection that are evident throughout the GI tract and within the airways (Heuther, McCane, &Brashers, 2020).         With Melissa complaining of increased coughing and productive green sputum and increased shortness of breath, I saw where in Stanford, Ryan & Solis-Mayo ,2020, stated that CF affects the cells that produce mucus, sweat and digestive juices .It causes these fluids to become thick and sticky which plug the tubes ,ducts and passageways ,traps germs and makes infections more likely.                                                                                                ReferencesHuether, S. E., & McCance, K. L. & Brashers, V.L. (2020). 
    Understanding Pathophysiology 7
    th
     ed.
     Elsevier Mosby.Stanford, G., Ryan, H., & Solis-Moya, A. (2020). 
    Respiratory muscle training for cystic fibrosis.
     
    The Cochrane database of systematic reviews
    , 
    12
    , CD006112. Retrieved from https://doi.org/10.1002/14651858.CD006112.pub5less3 UnreadUnread12 ViewsViews

    12 cystic fibrosis Essays

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    View profile card for Caroline Otto

    Last post 
    January 31 at 11:12 PM
     by Caroline Otto

    Rossi 
    A.G, Morrelli, P.,
     Galietta 
    ,L.J & Collin, A.A. (2019) 
    Airway microenvironment alterations and pathogen growth in cystic fibrosis
    . Retrieved from 
    https://doi.org/10.1002/ppul.24246

            In CF Treatment can help but there is no cure .Respiratory training for CF is one of the intervention, but study still think the intervention is insufficient and that it should be a case by case basis .Treatment is primarily focus on pulmonary health and nutrition and prevention of persistent cycles of lung infection and inflammation ( Heuther, McCane, &Brashers, 2020).

         The complex interplay between the virulent organisms & predominantly 
    Pseudomonas aeruginosa
     including up regulation of virulence genes and utilization of mucin as a nutrient source, modulates the action of pathogens, modifies the CF airway milieu and contributes to the processes leading to airway derangement (Rossi, et.al.2019).

    Cystic Fibrosis
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    Caroline Otto posted Jan 27, 2021 10:52 PM

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    At the center of Cystic fibrosis is the gene mutation CFTCR (cystic fibrosis transmembrane conductance regulator protein), which prevents chloride and water from not being transported correctly across epithelial membranes, specifically found within the lining the inside of our lungs.  The gene mutation causes the lungs to have the inability of clear secretions effectively, thereby speeding up the disease process of Pneumonia.  Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding Pathophysiology 7th
     ed.
    Elsevier Mosby. less2 UnreadUnread5 ViewsViews cystic fibrosis Essays

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    View profile card for Caroline Otto

    Last post 
    January 31 at 10:01 PM
     by Caroline Otto

    Rossi, G. A., Morelli, P., Galietta, L. J., & Colin, A. A. (2019). Airway microenvironment alterations and pathogen growth in cystic fibrosis.
     
    Pediatric pulmonology, 54
    (4), 497–506. 
    https://doi.org/10.1002/ppul.24246

    Ciofu, O., Hansen, C. R., & Høiby, N. (2013). Respiratory bacterial infections in cystic fibrosis. 
    Current opinion in pulmonary medicine, 19
    (3), 251–258. 
    https://doi.org/10.1097/MCP.0b013e32835f1afc

    References:

    The majority of Cystic Fibrosis patients have a bacterial colonization of Pseudomonas (Ciofu, et.al. 2013). Pseudomonas bacterial lies dominantly within these patients’ lungs, and during an activated cycle these patients will produce green sputum which is the clinical sign for Pseudomonas (Rossi, et.al. 2019).   Aggravated external conditions and overgrowth of the bacterial neighbors produce broncho-constriction and friction causing difficulty breathing and further inflammation.

    Our lungs are an enclosed organ filled with little pockets, small airways cystic fibrosis Essays. The inability of the cilia to move in unison with ventilation prevents the clearance of mucous and secretions thereby causing an environment that is warm, wet and favoring of a microenvironment colonized by opportunistic bacterias  Since this environment is one that is continuously imunno-activated, because of induced inflammatory mediators, that destroy immunoglobulin G (IgG), there is an abundance of neutrophils which release oxidants and proteases that directly damage the lung proteins. This direct damage is reflected by a bacterial film that develops over time that resists beta-lactam antibiotics, and causes a constant infection, which feeds the bacterial community now living inside the lungs (Huether, et.al. Pg. 708, 2020).

    Discussion Post 2 – Cystic Fibrosis
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    Jennifer Bryant posted Jan 26, 2021 2:32 PM

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    Cystic fibrosis (CF) is a progressive genetic disease that causes persistent airway infection. This is caused by a gene mutation that affects the functional deficiency of the cystic fibrosis transmembrane regulator (CFTR). Mutations in the CFTR gene affects epithelial innate immune function and airway clearance of the lung. CFTR functions as a chloride channel where it is highly expressed where is regulates chloride ion movement. Defective transport leads to an imbalance, creating thick dehydrated mucus (Useckaite et al, 2020).References
         Pathophysiology
     (7
    th
     ed.).  Elsevier.     neutrophilic inflammation in cystic fibrosis. 
    J Leukoc Biol
    . 2020; 108: 1777– 1785.     Cassidy, H., Dillon, E. T., Brennan, K., Doyle, S. L., Carter, S., Donnelly, S., Linnane,vesicles mediate inflammatory signalling in cystic fibrosis.
     Thorax, 75
    (6), 449-458.less1 UnreadUnread4 Views Views cystic fibrosis Essays

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    View profile card for Melissa Morgan

    Last post 
    January 31 at 9:57 PM
     by Melissa Morgan

         B., McKone, E. F., McNally, P., & Coppinger, J. A. (2020). Increased extracellular

    Useckaite, Z., Ward, M. P., Trappe, A., Reilly, R., Lennon, J., Davage, H., Matallanas, D.,

    Ng, HP, Jennings, S, Wellems, D, et al. Myeloid CFTR loss‐of‐function causes persistent

    Heuther, S., McCance, K., and Brashers, V.  (2020).  
    Understanding

                In CF lungs, the predominant inflammatory cells are neutrophils. Neutrophils are dedicated microbial killer cells that phagocytose invading organisms. An excessive presence of neutrophils mounts an excessive inflammatory response, a vicious cycle causing damage to the airways (Ng et al, 2020). This microenvironment favors bacteria colonization by creating a bacterial biofilm that promotes chronic endobroncial infection (Huether et al, 2020). Melissa presents with common clinical manifestations of bronchiectasis: increased cough, productive green sputum, wheezing and fever.

    Dennies Jones
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    Dennies Jones posted Jan 25, 2021 7:39 PM

    Contains unread posts cystic fibrosis Essays

    Cystic fibrosis, the most common lethal recessive disease in white children, occurs in about 1 in 2500 births. Approximately 1 in 25 whites carry a copy of a mutation that causes cystic fibrosis (Huether et al. 2020). Defective transport of chloride ions leads to a salt imbalance, which results in secretions of abnormally thick, dehydrated mucus (Huether et al.2020). According to Andrade et al.(2018), cystic fibrosis is a progressive disease with lung function deterioration, malnutrition, and progressive exercise limitation. Moore and Mastoridis (2017) state that P.aeruginosa infection in the lower airways correlates with declining lung function. Andrade, R. C., da Silva e Silva, C. M., Diniz da Silva, A. L. L., Haun, S. R., de Souza, V. A., & Ezequiel, D. J. S. (2018). Comparison of respiratory muscle strength, quality of life, and functional capacity among adolescents with cystic fibrosis with different bacteriological profiles. 
    Fisioterapia e Pesquisa
    , 
    25
    (2), 143–150. https://doi-org.wilkes.idm.oclc.org/10.1590/1809-2950/16862525022018Huether, Sue E., McCance, Kathryn L… Understanding Pathophysiology – E-Book (p. 169). Elsevier Health Sciences. Kindle Edition.Moore, J. E., & Mastoridis, P. (2017). Clinical implications of Pseudomonas aeruginosa location in the lungs of patients with cystic fibrosis. 
    Journal of Clinical Pharmacy & Therapeutics
    , 
    42
    (3), 259–267. https://doi-org.wilkes.idm.oclc.org/10.1111/jcpt.12521less1 UnreadUnread8 ViewsViews

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    View profile card for Aina Oluwo

    Last post 
    January 31 at 7:48 PM
     by Aina Oluwo

                        Inflammation of the airway obstructs the airflow, which causes inadequate ventilation. The impairment of pulmonary function is characterized by respiratory infection followed by colonization by bacteria (Andrade et al., 2018). Bacterial colonization is favorable due to its decreased lung function, nutrient-rich mucous pooled in oxygenated areas such as the respiratory tract, thus creating an optimal breeding environment for bacteria. This is a vicious cycle of bacterial infection in cystic fibrosis patients.

    Melissa-Module 2 Cystic Fibrosis
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    Lois Chappell posted Jan 30, 2021 7:24 PM

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         Cystic fibrosis is an example of an inherited recessive disease; this means a person must have a mutation in both copies of the cystic fibrosis transmembrane conductance regulator (CFTR) gene (Cystic Fibrosis Foundation, 2020) to demonstrate the disease.  If a person is born with just one mutated CFTR gene, they are considered a carrier and may give the defective gene to their children (Cystic Fibrosis Foundation, 2020). References     Foundation cystic fibrosis Essays.     https://www.nih.gov/news-events/nih-research-matters/how-cystic-fibrosis-promotes-lung-infections.less1 UnreadUnread5 ViewsViews

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    View profile card for Sheryl Dixon

    Last post 
    January 31 at 4:26 PM
     by Sheryl Dixon

    Wein, H.  (2016).  How cystic fibrosis promotes lung infections.  
    National 
     Institutes of Health
    , 
    Research Matters.
      Retrieved from

    Cystic Fibrosis Foundation (2020).  
    Cystic fibrosis genetics: the basics.
      Retrieved from 
    https://www.cff.org/About-Us/About-the-Cystic-Fibrosis-

         In people with cystic fibrosis disease, the CFTR protein, responsible for the regulation of salt and fluid movement in different areas of the human body is malfunctioning, or, not produced at all, which can  lead to a buildup of thick mucus, that is more acidic and prone to infections (Wein, 2016).  Destruction and malfunction of organs, as well as persistent lung infections can be seen in those diagnosed with cystic fibrosis (Cystic Fibrosis Foundation, 2020).  Medical therapy is aimed at thinning secretions, opening the airway, fighting infections, and aiding digestion (National Institutes of Health, 2020).  There is no cure for cystic fibrosis; pre-pregnancy screening, early diagnosis and treatment of affected individuals is essential to improve clinical outcomes and quality of life.

    Module II Discussion Post: CF
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    Gisselle Mustiga posted Jan 27, 2021 11:32 PM

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    Cystic fibrosis affects at least 30,000 people in the United States. Between 900 -1000 new cases are detected every year cystic fibrosis Essays. One out of 29 people of Caucasian descent is a carrier not affected by the CF gene mutation. In the United States, cystic fibrosis occurs in 1 in 3,400 live births. It occurs in people of racial and ethnic backgrounds, but whites of Nordic descent are generally are more predisposed to this ailment. It is very common for Caucasians of North European origin.ReferencesFinn, K. M., & Mendenhall, F. (2020). Diagnosis of cystic fibrosis: consensus guidelines from the Cystic Fibrosis Foundation. The Journal of pediatrics, 181, S4-S15.less1 UnreadUnread4 ViewsViews

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    View profile card for Jennifer Bryant

    Last post 
    January 31 at 4:06 PM
     by Jennifer Bryant

    Trivedi, B. P. (2020). Breath from Salt: A Deadly Genetic Disease, a New Era in Science, and the Patients and Families Who Changed Medicine Forever. BenBella Books.

    Historically, half of the affected people were diagnosed when they were five months old, but the average diagnosis age is five years, and some people are not diagnosed until they are adults (Finn & Mendenhall, 2020). Early in life, CF patients become infected with a limited spectrum of bacteria, especially P. aeruginosa. New studies now show that decreased depth of periciliary fluid and abnormal hydration of mucus, which impede mucociliary clearance, contribute to initial infection (Trivedi, 2020). Reduced production of the antibacterial molecule nitric oxide, increased bacterial binding sites (e.g., asialo GM-1) on CF airway epithelial cells, and adaptations made by the bacteria to the airway microenvironment, including the production of virulence factors and the ability to organize into a biofilm, contribute to susceptibility to initial bacterial infection. In short, in healthy lungs, there is a thin layer of mucus that helps your body move dirt and bacteria out of the lungs, while in people patients with CF, this mucus is much thicker and clogs the lungs, creating the perfect environment for harmful bacteria cystic fibrosis Essays.

    Eleany Yasein, Module 2
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    Eleany Yasein posted Jan 26, 2021 11:17 PM

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          Cystic fibrosis is an autosomal recessive disorder that can lead to impairment in different organs including lungs, intestines, as well as the pancreas (Fagundes, Vendrusculo & Perez-Ruiv, 2020). It’s also known to be a disease that tends to progress at a fast rate, and is a result of a gene mutation located in the chromosome 7. This chromosome is responsible for encoding the protein cystic fibrosis transmembrane regulator (CFTR). CFTR regulates the movement of many ions including sodium, chloride, and water across the cell membrane (Fagundes et al., 2020). The chromosome mutation affects the function of CFTR. This leads to the imbalance of osmolality and disrupted movement of ions, which affects the intracellular and extracellular movement of salt and water (Kulkarni, Kansra, & Karande, 2019). In the lung, the defective CFTR affects the normal lining of epithelial tissue and cilia that are there to protect the lung. As a result of that, thick mucus that’s sticky will build up, which makes it easier for bacteria to colonize, and difficult for airway clearance. Furthermore, normal inflammatory processes can not occur due to the imbalance of osmolality and the pH (Kiedrowski & Bomberger, 2018).   Fagundes Donadio, M. V., Vendrusculo, F. M., & Pérez-Ruiz, M. (2020). Scoring tools to monitor risk of disease progression in patients with cystic fibrosis. 
    Journal of Thoracic Disease
    , 
    12
    (8), 3940–3943. 
    https://doi-org.wilkes.idm.oclc.org/10.21037/jtd.2020.03.121
    Kulkarni, H., Kansra, S., & Karande, S. (2019). Cystic fibrosis revisited. 
    Journal of Postgraduate Medicine. 
    65(4), 193-196. doi: 
    10.4103/jpgm.JPGM_263_18
    less1 UnreadUnread7 Views Views cystic fibrosis Essays

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    View profile card for Beth Certain

    Last post 
    January 31 at 12:33 AM
     by Beth Certain

    Kiedrowski, R. M., & Bomberger, M. J. (2018, December 20). Viral-Bacterial Co-infections in the Cystic Fibrosis Respiratory Tract.
     Frontiers in Immunology, 
    9(3067), doi: 
    10.3389/fimmu.2018.03067

                                                                                 References

             Cystic fibrosis can cause pulmonary decline due to the cause of inflammation, hyperventilation, mucus being retained, as well as impediment of the airway. Moreover, this disorder can lead to chronic infections caused by bacteria including Staphylococcus aureus and Pseudomonas aeruginosa (Fagundes et al., 2020). The productive green sputum, and fever Melissa is having indicates signs of infection, that are caused by bacteria in the lung, due the progressive of cystic fibrosis. Lastly, the wheezing she is having also indicates airway obstruction, due to air trapping in the lung (Kulkarine et al., 2019).

    Module 2 Discussion
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    Alfonsina Perez posted Jan 26, 2021 9:59 PM

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                 In patients with cystic fibrosis, the airway microenvironment favors bacteria colonization because the mutation in the CFTR can lead to several malfunctions at the cellular level. First, CFTR malfunction can lead to collapse of the cilia which are in charge of moving fluid through the cells (Ribeiro & Lubamba, 2017). Second, thick mucus may adhere to the airways which can then result in chronic inflammation (Ribeiro & Lubamba, 2017). Constant inflammation in the airways and the presence of thick mucus which is not easily moved in and out of the airway provides an ideal environment for bacteria to colonize in the airway of a person with cystic fibrosis.      less1 UnreadUnread6 ViewsViews

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    View profile card for Steven Bartos

    Last post 
    January 30 at 11:41 PM
     by Steven Bartos

    doi:http://dx.doi.org.wilkes.idm.oclc.org/10.3390/ijms18010118 cystic fibrosis Essays

    inflammation.
     International Journal of Molecular Sciences, 18
    (1), 118.

    Ribeiro, C. M. P., & Lubamba, B. A. (2017). Role of IRE1α/XBP-1 in cystic fibrosis airway

    doi:10.1016/S0140-6736(16)00576-6

    Elborn, J. S., Prof. (2016). Cystic fibrosis. The Lancet (British Edition), 388(10059), 2519-2531.

    References

                In our case study for this week, we learn about a 12 year old girl with cystic fibrosis. Elborn (2016) defines cystic fibrosis as an autosomal recessive genetic disorder which affects mainly the respiratory system but can also affect other areas of the body including, pancreas, liver and sweat glands. Cystic fibrosis is caused by a gene mutation, this particular gene is in charge of encoding a chloride conducting membrane which regulates mucus in the airways (Elborn, 2016). As a result of the gene mutation, the cystic fibrosis transmembrane conductance regulator (CFTR) does not effectively regulate mucus production and inflammation which can lead to an over production of mucus affecting epithelial cells (Elborn, 2016).

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    Module 2 Discussion
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    Steven Bartos posted Jan 27, 2021 3:22 PM

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    The pathophysiology of the microenvironment that favors bacterial colonization in cystic fibrosis can be traced down to the genetic level. Cystic fibrosis is a monogenetic autosomal recessive disease caused by a mutated gene, called the cystic fibrosis transmembrane conductance regulator (CFTR). This gene regulates the chloride ion channel in epithelial cells. When the CFTR dysregulates the chloride ion channel, this leads to an imbalance of salt and subsequent thickened mucus and viscous secretions in the bronchi, pancreas, biliary tract, and intestine. Although mucus provides antibacterial defense for the body, its increased viscosity in cystic fibrosis contributes to the harboring of bacteria (De Palma et al., 2020) cystic fibrosis Essays. The airway surface liquid (ASL) is fluid that covers the surface of the airway epithelium. It assists in clearing out bacteria of the airway and overall homeostasis of that environment. When the volume, pH, ionic or nutrient content of the ASL is impaired, this results in dysregulation of antimicrobial activity and leads to subsequent bacterial infection (Haq et al., 2016). New research is looking at how CFTR also regulates a bicarbonate channel, which affects the exchange of chloride and bicarbonate. This exchange is also shown to help regulate the pH levels and overall homeostasis of the epithelial cells in the ASL, as an imbalance would result in worsening of bacterial colonization in the airways of cystic fibrosis (Borowitz, 2015).Borowitz, D. (2015). CFTR, bicarbonate, and the pathophysiology of cystic fibrosis.
    Pediatric Pulmonology
    , 
    50
    (S40), S24 – S25. https://dx.doi.org/10.1002/ppul.23247 Haq, I.J., Gray, M.A., Garnett, J.P., Ward, C., & Brodlie, M. (2016). Airway surface homeostasis in cystic fibrosis: Pathophysiology and therapeutic targets. 
    Thorax
    , 
    71
    (3), 284 – 287. http://dx.doi.org/10.1136/thoraxjnl-2015-207588  less1 UnreadUnread5 ViewsViews

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    View profile card for Jazmin Jerez-Rivera

    Last post 
    January 30 at 12:29 PM
     by Jazmin Jerez-Rivera

    De Palma, F.D.E., Raia, V., Kroemer, G., Maiuri, M.C. (2020). The multifaceted roles of microRNAs in cystic fibrosis. 
    Diagnostics (Basel, Switzerland)
    , 
    10
    (1102), 1 – 19. https://dx.doi.org/10.3390/diagnostics10121102

    References

    Cystic Fibrosis
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    Jazmin Jerez-Rivera posted Jan 26, 2021 7:14 PM

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    Cystic fibrosis is a genetic disorder that affects the cystic fibrosis transmembrane conductance regulator (CFTR) gene (CDC, 2020). A mutation to this gene causes mucus to buildup and thicken in different parts of the body. The systems primarily affected are gastrointestinal, respiratory, and genitourinary systems This thickened mucus can begin to clog pancreatic and biliary ducts which blocks enzymes to break down food and can interfere with nutrient absorption (Brown et.al., 2017). It can also cause greasy and bulky stool.ReferencesKeep them breathing, 
    Journal of the American Academy of Physician Assistants
    , Volume 30, https://www.cdc.gov/genomics/disease/cystic_fibrosis.htmless1 UnreadUnread4 Views Views cystic fibrosis Essays

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    View profile card for Dennies Jones

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    January 29 at 7:20 PM
     by Dennies Jones

    Centers for Disease Control and Prevention. (2020). Cystic Fibrosis.

    Issue 5, 23-27 doi: 10.1097/01.JAA.0000515540.36581.92

    Brown, Sheena D. PhD, MSCR; White, Rachel MMSc, PA-C; Tobin, Phil DHSc, PA-C. (2017).

    In the respiratory system mucus can increase in the airway of the lungs which can be difficult to clear. This is a constant breeding ground for bacteria which produces a hyperactive inflammatory response (Brown et.al., 2017). In the long run, chronic infections persist causing pulmonary exacerbations, and the continual inflammatory response can lead to airway destruction (CDC, 2020).

    Module II Discussion I
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    Beth Certain posted Jan 27, 2021 10:14 PM

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    In cystic fibrosis, the airway microenvironment favors bacterial colonization, explains the pathophysiological reason for this occurrence. 
    The patient, Melissa, has a respiratory infection caused by the complication of thick, sticky mucous from CF. Treatment for these infections varies depending on the patient and their history of CF. Various antibiotics are used to treat respiratory infections. These are used for acute infections. Some patients will be on prophylactic therapy to help prevent life-threatening infections.Bhagirath, A.Y., Somayajula, D., Dadashi, M., Badr. S., & Duan, K. (2016). Cystic fibrosis lungRosenstein, B. (2020). 
    Cystic Fibrosis
    . Merke Manual Professional Versionless1 UnreadUnread3 Views Views cystic fibrosis Essays

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    View profile card for Cassie Fritzinger

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    January 29 at 5:56 PM
     by Cassie Fritzinger

                https://www.merckmanuals.com/professional

    environment and Pseudomonas aeruginosa infection. BMC Pulmonary Medicine, 16(1), 174. 
    https://doi.org/10.1186/s12890-016-0339-5

    References

    Module 2
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    Joanne Hogan posted Jan 26, 2021 6:12 PM

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    Module 2            Being an autosomal recessive disease, the gene is often seen equally in male and female populations. Parents can carry the gene and not always express it but can still pass it on to their children. Roughly ¼ of children from carrier parents will be affected with the disorder (Heuther et al., 2020, pp 54-55). Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7th ed.). Elsevier.Smith, W. D., Bardin, E., Cameron, L., & Edmondson, C. (2017). Current and future therapies for Psuedomonas aeruginosa infection in patients with cystic fibrosis. 
    FEMS Microbiology Letters
    , 
    364
    (14). Retrieved January 25, 2021, from 
    https://doi.org/10.1093/femsle/fnx121
    less1 UnreadUnread6 Views Vie ws cystic fibrosis Essays

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    View profile card for Tallona Boddy

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     by Tallona Boddy

    Rout-Pitt, N., Farrow, N., Parsons, D., & Donnelley, M. (2018). Epithelial mesenchymal transition (emt): A universal process in lung diseases with implications for cystic fibrosis pathophysiology. 
    Respiratory Research
    , 
    19
    (1). Retrieved January 25, 2021, from 
    https://doi.org/10.1186/s12931-018-0834-8

    References

                Cystic fibrosis is a genetic disorder that primarily occurs due to mutations in the cystic fibrosis transmembrane conductance regulator gene (CFTCR) (Rout-Pitt et al., 2018). This gene is responsible for chloride ion transport out of epithelial cells and the mutation that occurs in cystic fibrosis disrupts this transport of chloride ions leading to dehydration of the respiratory tract (Rout-Pitt et al., 2018). Sodium is also absorbed in unregulated amounts by the epithelial sodium channel further leading to dehydration in the respiratory tract (Smith, et al., 2017). Dehydration in airway epithelium leads to chronic inflammation, risk of infection, and the formation of fibrotic tissues (Rout-Pitt et al., 2018).  The dehydrated epithelium causes an increase in viscous secretions that become difficult to clear (Smith et al., 2017). Because the airways have such a high mucus content, this inhibits the body’s ability to clear pathogens from the respiratory tract. One of the more common infections in patients with cystic fibrosis is 
    Pseudomonas aeruginosa
    , which often occurs in children with CF by the age of five (Smith et al., 2017). According to Smith et al. (2017), the normal response of neutrophils during infection often leads to an increased inflammatory response, reducing clearance of the pathogen and creating a cycle that promotes a difficulty to clear the infection and increase the likelihood of reinfection by the same organism cystic fibrosis Essays.

                Cystic fibrosis is an autosomal recessive disease that primarily effects the respiratory and gastrointestinal systems in the body (Huether et al., 2020, pp 54-55).  The lungs and pancreas are primarily affected due to an increase in mucus production leading to clogged pancreatic ducts and lung infections (Huether et al., 2020, pp 54-55). Patients may experience early death due to heart failure or lung disease (Heuther et al., 2020, pp 54-55).

    Fritzinger, NSG 530 Wk 2
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    Cassie Fritzinger posted Jan 27, 2021 12:56 PM

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    Cystic Fibrosis (CF) is an autosomal recessive disease and is the most common fatal genetic disorder. For a person to develop cystic fibrosis both parents must either have or be a carrier of the mutated gene. The disease is characterized as a single gene mutation of the Transmembrane Conductance Regulator Gene (CFTR). The gene protein is located on every body organ which produces mucus, and the mutation inhibits the protein preventing the release of chloride.  Increased chloride levels cause the mucus produced to be thick and sticky, which in turn blocks passages commonly in the lungs and digestive system. This mucociliary clearance is hindered in clearing particles such as bacteria found in the nose and mouth out of the body to get rid of them (NIH, 2020). This disease causes severe damage to the lungs, digestive system and other organs of the body, and improved care has increased the life expectancy of the patient with CF with some living into their 50s (Mayo Clinic, 2020).Patients who have CF develop a biofilm which can be resistant to antibiotics thus any bacteria which would normally be killed by the antibiotics now collect in this localized area causing a chronic local inflammatory response and causing damage to the airway tissue which is second line of defense to infection (Heuther, 2020). While there is no cure for CF, some of the treatment goal is to prevent infections by loosening the mucus from the lungs, treating and preventing intestinal blockages which can be accomplished by many different means such as gene mutation medications,  improved hydration, and organ/disease specific medications. Keeping active, and maintaining a healthy diet and lifestyle is also very important in the prevention of infection for the CF patient (Mayo Clinic, 2020).
     
    Heuther, S. E., McCance, K. L., & Brashers, V. L. (2020). Understanding Pathophysiology (7th ed.). Elsevier.NIH. (2020). National Heart, Lung, and Blood Institute, Cystic fibrosis. Retrieved January 27, 2021 cystic fibrosis Essays. From https://www.nhlbi.nih.gov/health-topics/cystic-fibrosisless1 UnreadUnread6 ViewsViews

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    View profile card for Candice Russell

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    January 28 at 12:49 PM
     by Candice Russell

    Mayo Clinic. (2020). Cystic Fibrosis. Retrieved January 27, 2021. From https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/symptoms-causes/syc-20353700

    References

     

    “Colonization is the ability of a pathogenic microorganism to survive and multiply on or within the human environment” (Heuther, 2020, pg. 197). Microorganisms which are infectious to humans and affect the mucus membranes such as the lungs include bacteria, fungi, and protozoa. Normal microbiome is present on our body surfaces and are colonized. These normal microbiomes normally do not cause disease. However, under certain circumstances they can produce an infectious reaction known as an opportunistic infection. This is when the normally ‘normal bacteria/fungi’ become infectious secondary to a breakdown in the normal body defenses or in an immunocompromised individual (Heuther, 2020).

    Module 2 CF Discussion Post
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    Candice Russell posted Jan 27, 2021 2:26 PM

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    Cystic Fibrosis (CF) is an autosomal recessive inherited disease that results from defective epithelial chloride (Cl) ion transport. CF is described as a “multiorgan disease, affecting the lungs, digestive tract, and reproductive organs” (Brashers, 2020, p. 708). CF is caused by mutations, or errors, in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CFTR functions as a channel on the cell surface, allowing movement of chloride in and out of the cell. Proper functioning of the CFTR protein, allows for normal balance of Cl and fluid at the cell surface. Mutation of the CFTR gene results in abnormal expression of cystic fibrosis transmembrane conductance regulator (CFTCR) protein (Brashers, 2020, p. 709).In a review of inflammatory mechanism in airway diseases, Aghasafari et al. (2019) stated “Mutations in CFTR influence the lung epithelial innate immune function that leads to exaggerated and ineffective airway inflammation that fails to abolish pulmonary pathogens cystic fibrosis Essays.” Many resources emphasized the importance of understanding the airway environment and its structure, in order to understand CF respiratory symptoms. Surette (2014) stated upper airways, particularly the oral cavity, represent the most diverse microbiome site in the body (Stearns et al., 2011, as cited by Surette 2014). The mutation of the CFTR gene, which results in reducing airway surface fluids, compromises normal airway function. Surette (2014) states altered airway milieu results in a thick mucus secretion that impairs mucociliary clearance, “consequently the lower airways become colonized by bacteria” (p.61). Bhagirath et al. (2016) state CF patients present with abnormalities in the size and shape of the trachea, imaging of children displayed early structural defects. Pulmonary imaging of airways in infants and young children, with CF, displayed thicker walls, with higher dilation (Bhagirath et al., 2016). Bhagirath et al. (2016) further state these airways make “excellent reservoir for chronic and relapsing lower respiratory tract infections.Neutrophils, a type of white blood cell (WBC), has many functions, one being, protecting against infections. Neutrophils are considered the first line of defense when protecting us from infection. Margaroli and Tirouvanziam (2016) state “Neutrophils are generally considered to be rigid, pre-programmed effector leukocytes, in the case of CF, neutrophiles, “show complex properties that come in stark contrast with rigid pre-programmed phenotype.” Margaroli and Tirouvanziam (2016) described CF lungs to be a “hostile environment”, the presence of bacterial toxins may induce rapid necrosis of incoming neutrophils. Laval et al. (2016) documented “absence or dysfunction of CFTR in neutrophils impairs bacterial killing” (Painter et al., 2006; Bonfield et al., 2012, Ng et al., 2014; as cited by Laval et al., 2016).                                   Rossi, GA, Morelli, P, Galietta, LJ, Colin, AA. Airway microenvironment alterations and pathogen growth in cystic fibrosis. 
    Pediatric Pulmonology
    . 2019; 54: 497– 506. 
    https://doi-org.wilkes.idm.oclc.org/10.1002/ppul.24246
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    Surette MG. The cystic fibrosis lung microbiome. Ann Am Thorac Soc. 2014 Jan;11 Suppl 1:S61-5. doi: 10.1513/AnnalsATS.201306-159MG. PMID: 24437409.

    Margaroli, C., Tirouvanziam, R. Neutrophil plasticity enables the development of pathological microenvironments: implications for cystic fibrosis airway disease. 
    Mol Cell Pediatr
     
    3, 
    38 (2016). 
    https://doi.org/10.1186/s40348-016-0066-2

    Laval, J., Ralhan, A., & Hartl, D. (2016). Neutrophils in cystic fibrosis, 
    Biological Chemistry
    , 
    397
    (6), 485-496. doi: 
    https://doi.org/10.1515/hsz-2015-0271

    Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology / Sue E. Huether, Kathryn L. McCance ; section editor, Valentina L. Brashers
     (7th ed.). Elsevier.

    Bhagirath, A. Y., Li, Y., Somayajula, D., Dadashi, M., Badr, S., & Duan, K. (2016). Cystic fibrosis lung environment and Pseudomonas aeruginosa infection.
     BMC Pulmonary Medicine, 16
    http://dx.doi.org.wilkes.idm.oclc.org/10.1186/s12890-016-0339-5

    Aghasafari, P., George, U. & Pidaparti, R. A review of inflammatory mechanism in airway diseases. 
    Inflamm. Res.
     
    68, 
    59–74 (2019). 
    https://doi-org.wilkes.idm.oclc.org/10.1007/s00011-018-1191-2

    Reference:

                Rossi et al. (2019) in a review of airway microenvironment in CF, it was stated that a combination of factors, including impaired mucociliary clearance, and dysregulation of defense function, bacterial infection follows.

    Aghasafari et al. (2018) stated “inflammatory mechanisms employ a group of pattern recognition receptors (PRPs) to recognize molecular patterns expressed by invading pathogens” (p. 59). Toll-like receptors (TLRs), which is a type of PRP, are found on membrane surfaces. TLRs recognize molecular patterns shared by pathogens and activate inflammatory cells to start the resolution process cystic fibrosis Essays. Many factors affect the inflammatory response including tissue microenvironment and disease (Aghasafari et al., 2018). In CF there is an excessive inflammatory response, which plays a significant role in lung damage.

    Deficiency in the CFTR gene leads to thick and viscose mucus that clogs small airways, contributing to the development of persistent lung inflammation, which increases the risk of lung infections (Aghasafari et al., 2019). In a journal article discussing CF and infection, Bhagirath et al. (2016) stated “the dominant chronic inflammation is generated by the failure of microbial clearance and the creation of a toxic pro-inflammatory local microenvironment, which damages the lung and the innate immunity, further facilitating infections” (p. 3).

    CFTCR protein is an activated Cl channel present on the surface of many epithelial cells. These cells include the lining of the airways, bile ducts, the pancreas, sweat ducts, paranasal sinuses, and vas deferens. Improper functioning of the CFTCR protein inhibits the appropriate transport of Cl and fluid across epithelial membranes. Thick, dehydrated mucus secretions are the outcome of inadequate CFTCR protein functioning.

    Melissa CF
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    Tallona Boddy posted Jan 25, 2021 9:41 AM

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    The airway’s microenvironment in a patient such as, Melissa who does have a diagnosis of cystic fibrosis is most likely not a healthy microenvironment, unfortunately (as mentioned in the discussion prompt).  Melissa’s diagnosis of cystic fibrosis means that she does have a defective system of transport of her chloride ions in her epithelial cells (Huether et al., 2020, p.54). Our chloride ions form from a negatively charged part of salt, chloride is one of our essential electrolytes needed to help regulate fluids in and out of cells (
    Chloride ion,
     2021). When the chloride transport is not functioning correctly, imbalances take place.  For this scenario it is essentially (in the simplest terms) a salt/water ratio imbalance.  Melissa has thick, sticky mucus which is typically (for a patient that does not have cystic fibrosis) thin and more like a lubricant.  Melissa’s lungs have become clogged with this thick sticky mucus, essentially helping the bacteria become trapped in the lungs where they can colonize and thrive creating a biofilm (
    Infections
    n.d.) cystic fibrosis Essays.   Cystic Fibrosis Foundation. 
    Infections
    . Cystic Fibrosis Foundation. https://www.cff.org/Research/Research-Into-the-Disease/Research-into-CF-Complications/Infections/.U.S. National Library of Medicine. (2021, January 23). 
    Chloride ion
    . National Center for Biotechnology Information. PubChem Compound Database. https://pubchem.ncbi.nlm.nih.gov/compound/Chloride-ion.less1 UnreadUnread9 ViewsViews

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    January 27 at 1:12 PM
     by Cassie Fritzinger

    Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7
    th
     ed.).  Elsevier.

    References

    Week 2 discussion by Aina Oluwo
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    Aina Oluwo posted Jan 26, 2021 11:54 PM

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    According to Brown et al. (2017), Cystic fibrosis (CF) affects a great number of Caucasians both in the United States and across the world. It also occurs in about 1 out of 3,500 births per year in whites and northern Europeans. This life-threatening genetic autosomal recessive disorder causes severe respiratory discomfort by allowing a buildup of thick, viscous mucus secretions particularly in the pulmonary system thus eliciting a response in its patient with severe fatigue, coughing and shortness of breath. To the untrained eye, this can be mis-diagnosed as asthma and patients can sometimes be prescribed inhaler medication that sometimes work to clear airways but more often, this is only a temporary fix as the pathophysiology behind CF calls for more than inhalers to elicit open airway response.According to Brown et al. (2017) these pathogens cause an overwhelming inflammatory response which can be assessed in Melissa’s clinical presentation temperature of 101F, RR-28, increased coughing & SOB, productive green sputum. Ultimately, chronic infection and this repetitive inflammatory response can lead to airway destruction.Referencesfibrosis lung environment and Pseudomonas aeruginosa infection.
     BMC Pulmonary
    Brown, S. D., White, R., & Tobin, P. (2017). Keep them breathing: Cystic fibrosis
    Academy of Physician Assistants
    , 
    30
    (5), 23–27.Heuther, S., McCance, K., and Brashers, V.  (2020).  
    Understanding
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    Pathophysiology
     (7
    th
     ed.).  Elsevier.

    https://doi.org/10.1097/01.JAA.0000515540.36581.92

    pathophysiology, diagnosis, and treatment. 
    JAAPA: official journal of the American

    Medicine, 16
    http://dx.doi.org.wilkes.idm.oclc.org/10.1186/s12890-016-0339-5

    Bhagirath, A. Y., Li, Y., Somayajula, D., Dadashi, M., Badr, S., & Duan, K. (2016). Cystic

    Understanding the pathogenesis of the disease is key to management and prevention. In people with cystic fibrosis, these excess secretion of mucus and chronic bacterial infection result in a special type of chronic obstructive pulmonary disease that can further leave the airways become badly damaged and scarred. One of the ways to manage this disease is the application of pulmonary therapies such as chest percussions to loosen up mucus and administration of mucus liquefying solutions aerosolized dornase alfa (Huether et al, 2020).

     The pathophysiology of CF is caused by a mutation in the CF transmembrane conductance regulator (CFTR) gene. The CFTR protein produced by this gene regulates the movement of chloride and sodium ions across epithelial cell membranes thus a defect in this transport chain elicits a salt imbalance (Huether et al., 2020). This imbalance results in the secretions of thick mucus throughout the body causing obstructions to systems such as pulmonary and digestive. In a healthy person, the respiratory system have mucins which is secreted by goblet and submucosal glands. Bhagirath et al. (2016) further explained the unfolding of the mucins by bicarbonates makes them slippery to trap microorganisms and remove them from epithelial surfaces. Thus in a CF patient, the thick mucus in the respiratory tract hampers the bacterial mucociliary clearance and allows for microbial colonization with pathogens such as Staph aureus or Pseudomonas aeruginosa to mention a few (Bhagirath et al., 2016)  .

    Amandeep Kaur
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    Amandeep Kaur posted Jan 26, 2021 5:37 PM

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    Melissa is subject to a genetic disorder that renders her vulnerable to many respiratory infections, such as what she is experiencing right now. The pathophysiology for this disorder stems from her genetic makeup. Cystic Fibrosis is an autosomal recessive condition, this indicates that two copies of the defected gene must be present for the individual to present with the condition (
    Kelsey et al., 2019
    ). The mutation lies within the CFTR gene, found on the long arm of Chromosome 7, and spans 230kb with 27 coding exons. There have been over 2000 mutations that have identified, 127 of them disease-causing (
    Bhagirath et al., 2016)
    . The mutation leads to the improper formation of the CFTR protein, which can regulate many ions including, sodium, potassium, chloride, and sodium bicarbonate. This protein is expressed in many organs; kidneys, pancreas, intestine, heart, vans deferens, and the lungs.
     
    Kelsey, R., Manderson Koivula, F. N., McClenaghan, N. H., & Kelly, C. (2019). Cystic fibrosis-related diabetes: Pathophysiology and therapeutic challenges. 
    Clinical Medicine Insights: Endocrinology & Diabetes
    , 
    12
    , N.PAG.Bhagirath, A. Y., Li, Y., Somayajula, D., Dadashi, M., Badr, S., & Duan, K. (2016). Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. 
    BMC pulmonary medicine
    , 
    16
    (1), 174 cystic fibrosis Essays.

    References

    The most lethal defective pathway is the CFTR-dependent water-secreting in the epithelial tissue of the lungs (
    Bhagirath et al., 2016)
    . CTFR protein dysfunction caused there to be a hindrance to inadequate water section to the cell’s surface. This is due to the inability of CTFR protein to secrete chloride and bicarbonate, since these ions cannot be secreted water will not follow suit. This leads to the accumulation of thick sticky mucus in the respiratory tract. This will trap the infection causing microbials and there will be ineffective clearance in the lungs. Some of the most commonly found pathogens in cystic fibrosis are 
    Pseudomonas aeruginosa
    , 
    Staphylococcus aureus
    , 
    Haemophilus influenzae,
     and 
    Burkholderia cepacia
     complex. 
    The toxic environment will prime for there to be chronic respiratory infections, which will damage the lungs and innate immunity. Chronic use of antibiotic therapies to combat these infections can transpire resistant variant strains of pathogens, which can lead to death cystic fibrosis Essays.

  • The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays

    The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays

    Module 1: Discussion 2

    Must post first.

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    Mr. B is a 70-year-old man who developed sub sternal chest pains radiating down his left arm while at home. He was taken to the ER via ambulance. His breathing was labored, pulses rapid and weak, and his skin was cold and clammy.An ECG was done which revealed significant “Q” waves in most leads. Troponin level was elevated. Arterial blood was draw with the following results:

    Ph 7.22

    PCO2 30 mm

    Hg pO2 70 mm

    Hg O2 sat 88%

    HCO3 22 meq/liter

    Aside from the obvious diagnosis of MI, what is Mr. B’s acid base status and what caused this disturbance?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than text). Refer to grading rubric for online discussion The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays.

     
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    Sheryl Dixon posted Jan 20, 2021 11:39 PM

    Mr. B’s acid base status would suggest respiratory acidosis .Looking at his arterial blood result the PH is low and his HCO3 is elevated. Respiratory acidosis can be chronic and acute due to his age and the body distribution of body fluid. “Respiratory acidosis occurs when the alveolar hypoventilation, causing Hypercapnia which is excessive carbon dioxide in the blood” Huether, McCance & Brashers (2010).     With physiological aging regulation of the PH depends on the kidney and lung and these two organs is deceased with physiological aging (Nabata T, et al, 1992) The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays.  According to Epstein &Singh (2011) treatment for respiratory acidosis may include invasive or noninvasive ventilator support and specific medical therapies directed at the underlying pathophysiologyEpstein SK, Singh N. Respiratory acidosis. Respir Care. 2001 Apr; 46 (4):366-83. PMID: 11262556.Nabata T, et al. Abnormalities in acid –base balance in the elderly. Nihon Rinsho.1992 Sep; 50(9) 2249-53. Japanese .PMID1434020 less0 UnreadUnread

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    View profile card for Beth Certain

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    January 24 at 11:48 PM
     by Beth Certain

    Huether, S.E., McCance, K.L., & Brashers, V.L. (2010).Understanding Pathophysiology (7th ed.).Elsevier

                                                                          References

        Working in a long-term care the elderly diagnosis are somewhat overlooked by just checking the labs, I believe some doctors treat the lab and not the person, some don’t take into consideration the body composition. A lot of times in the elderly the acid base is overlooked because there is not a different scale for pediatrician, adult versus the elderly so the PH remained the same despite which age group The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays.

    Discussion Board 1

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    Hilary Szpara posted Jan 20, 2021 5:08 PM

    I believe that Mr. B’s acid base status is metabolic acidosis with respiratory compensation in the form of hyperventilation. When determining his acid base status, I looked at his levels of certain arterial blood gases (ABGs). To determine acidosis or alkalosis, I looked at what his arterial pH was, 7.22. With the normal range for pH being 7.35-7.45, Mr. B appears to be in acidosis. However, when I continued to analyze the numbers, noting that his PCO2 was 30 mmHg and HC03 was 22, I was somewhat confused. Since HCO3 is within normal limits of 22-26 mEq/L (Verma & Roach, 2010), it became harder for me to determine acid base status, since HCO3 is what helps determine whether or not it is a metabolic event. However, after continuing my research, I was able to find multiple sources that discussed the correlation between myocardial infarction (MI) and metabolic acidosis. I was able to find that during an MI, due to decrease in cardiac output and arterial hypoxemia, tissue hypoxia occurs, which leads to a rise in lactic acid and metabolic acidosis (Gandhi & Akholkar, 2015). The levels of lactic acid rise due to the decrease in systemic blood flow caused by the MI (Weil & Tang, 2011).Gandhi, A. A., & Akholkar, P. J. (2015). Metabolic acidosis in acute myocardial infarction. 
    International Journal of Advancement in Medicine, 2
    (3), 260-263. 
    http://dx.doi.org/10.18203/2349-3933.ijam20150556
      Huether, S.E., McCance, K.L., Brashers, V.L. (2020). 
    Understanding Pathophysiology
    . Elsevier. less0 UnreadUnread

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    January 24 at 11:20 PM
     by Gisselle Mustiga

    Weil, M.H., Tang, W. (2011). Clinical correlates of arterial lactate levels in STEMI patients. 
    Critical Care, 15
    (1), 113. 
    http://doi.org/10.1186/cc9383

    Verma, A. K., & Roach, P. (2010). The interpretation of arterial blood gases. 
    Australian Prescriber
    , 
    33
    (4), 124-129.

    However, Mr. B’s situation is not just that simple because his PCO2 level is low, which at first glance would be characteristic of alkalosis (Huether, McCance, & Brashers, 2020). Since in the description of Mr. B’s symptoms it was noted that he is having labored breathing, he could be compensating for the metabolic acidosis by hyperventilating in an attempt to blow off CO2 and raise his arterial pH.

    Mr. B

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    Lois Chappell posted Jan 22, 2021 6:19 AM

         Understanding clinical presentations due to changes at the cellular level will enable you to skillfully care for your patients in diverse practice settings.  In evaluating Mr. B’s acid base balance, we see that Mr. B is in metabolic acidosis with compensation.  Metabolic acidosis can occur rapidly in the case of lactic acidosis or slowly in the case of renal failure, diabetic ketoacidosis, or starvation (Heuther, McCance and Brashers, 2020).  To understand specific types of acidosis, we can look at the anion gap.  Goldberger, AL. Goldberger ZD, Shvilkin, AS.  (2017).  
    Goldberger’s Clinical Electrocardiography: A Simplified Approach 
    (9
    th
     ed).   Elsevier.  less0 UnreadUnread

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    January 24 at 7:41 PM
    by Sheryl Dixon The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays

    Heuther, S., McCance, K., and Brashers, V.  (2020).  
    Understanding Pathophysiology
     (7
    th
     ed.).  Elsevier.

    References

                    This week’s case study is one we see often in acute care but imagine if this patient entered your family practice.  Would you look at him and be able to triage him appropriately?  What are the signs and symptoms of a cardiac event, what if chest pain was not present?  Please follow an algorithm, like the one on page 128 of your text to determine acid base status.

         In our case study, we are told Mr. B is having a myocardial infarct (MI); the cause of his acid base disturbance is most likely lactic acidosis from tissue hypoxia due to arterial occlusion from a blood clot.  His hyperventilation is a compensatory response to rising acidosis; the body’s intrinsic balancing act is to blow off acid through an increased respiratory rate.  The q wave in his ECG seen in “most leads” may be an indication of a previous myocardial infarction (MI), but we need more information about the q wave presentation including which leads the q wave is present, and the height and width of the q wave in order to make a diagnosis (Goldberger, 2017).  Treatment for Mr. B will initially be aimed at saving myocardial tissue and quickly reversing acidosis before decompensation and organ damage occurs The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays.

    Arterial Blood Gas interpretation in the MI Client.
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    Caroline Otto posted Jan 20, 2021 10:10 PM

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    Metabolic Acidosis with compensated Respiratory alkalosisMyocardial ischemia undoubtedly causing lactic acidosis secondary to poor myocardial perfusion from the myocardial infarction which induces metabolic acidosis.A Ph balance less than 7.40 indicates an increase in hydrogen ions, and the Ph reflects the metabolic environment which is protected by buffers which work to maintain the Ph level inside the cells.Mr. B’s Ph is low, and his HCO3 is low indicating metabolic, however Mr. B also has a low PaCO2 indicating respiratory compensation for his metabolic acidosis.Castro, D., & Keenaghan, M. (2020). Arterial Blood Gas. In StatPearls. StatPearls Publishing.Mechanic OJ, Grossman SA. Acute Myocardial Infarction. [Updated 2020 Nov 20]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK459269/less3 UnreadUnread20 ViewsViews

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    View profile card for Eleany Yasein

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     by Eleany Yasein

    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). Understanding Pathophysiology 7
    th
     ed. Elsevier Mosby.

    References

    In this situation the lungs attempt to compensate by increasing ventilation which causes alkalosis.

    A state of cell injury creates an abruption in the physiologic functioning inside the homeostatic cell environment disturbing the acid-base balance.

    Coronary artery disease in the individual may cause a thrombus to form which will occlude a coronary artery. This phenomenon causes a state of hypoxia which will lead to

    Dennies Jones
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    Dennies Jones posted Jan 20, 2021 1:22 PM

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             Mr. B was experiencing Metabolic acidosis due to the lab values. According to Gandhi & Alkholkar (2015), Metabolic acidosis occurs in the primeval stages of acute myocardial infarction. Gandhi & Alkholkar (2015) also said that the “combination of a fall in cardiac output and arterial hypoxemia leads to tissue hypoxia, metabolic acidosis, and fall in-plasma bicarbonate due to rise in lactic acid. Metabolic acidosis is compensated by hyperventilation” (p.260). In Mr. B’s case, he was having labored breathing to compensate for the blood’s low PH level.   Gandhi, A.A. & Akholkar, P.J. (2015). Metabolic acidosis in acute myocardial infarction. 
    International Journal of Advances in Medicine 2
    (3), 260-263. Doi: 
    http://dx.doi.org/10.18203/2349-3933.ijam20150556
    Huether, S.E. (2020. Fluid and electrolytes, acid and base. In S.E. Huether & K.L. McCance (Eds.), 
    Understanding Pathophysiology
     (114-133). St. Louis, MO: Elsevier Mosby.less1 UnreadUnread2 ViewsViews

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    View profile card for Melissa Morgan

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    January 24 at 4:24 PM
     by Melissa Morgan

    Howarth, A. T. (1970). Acid-Base Changes and Hypoxia following Myocardial Infarction. 
    Annals of Clinical Biochemistry: International Journal of Laboratory Medicine,
     
    7
    (2), 38-40 The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. doi:10.1177/000456327000700204

    References

           Since the blood PH is low and the PCO2 is also low, it is understood that the acidosis was not caused by any respiratory factors but by metabolic processes within the body. According to Huether et al. (2020), an instance of primary metabolic acidosis is an individual experiencing DKA (diabetic ketoacidosis acidosis) from lack of insulin secretion or administration. Mr. B may have issues where he lacks insulin, or he cannot metabolize glucose. Mr. B’s body metabolizes store fat and, as a result, creating acid as a byproduct. According to A.T Howarth (1970), metabolic acidosis appears to be due to the increase of lactic acid. The lungs attempt to compensate by Kussmaul respiration.

    Aina Oluwo’s discussion 2
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    Aina Oluwo posted Jan 19, 2021 11:14 PM

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    Better ormore2 UnreadUnread14 ViewsViews

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    View profile card for Dennies Jones

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    Worse? 
    Cellular Physiology and Biochemistry
    , 51:949-960. /doi:10.1159/000495397

    Pang, B., Zhao, F., Zhou, Y., He, B., Huang, W., Zhang, F., . . . Jiang, Y. (2018). Systematic

    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding 

     References

    Module I: Discussion Post #2
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    Gisselle Mustiga posted Jan 20, 2021 8:38 PM

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    Huether et al. (2020) affirm that pathophysiology is essential in grasping disease mechanisms and examining how a modification to one’s body structure may impact their functionality and reveal the signs and symptoms of an ailment. Mr B’s case is an example of a patient that could have multiple diagnoses despite similarities in the disease indications. Mr B likely has respiratory acidosis in which the blood ends up acidic since not all the carbon dioxide is eliminated from the lungs. The condition occurs due to various reasons such as the diseases in one’s airways, pulmonary fibrosis, scoliosis, incompatible medications, obesity, and obstructive sleep apnea among others. In Mr B’s case, the remaining CO2 caused a reduction in the pH. levels of the body fluids and thus the acidity. The patient has metabolic acidosis due to the pH level of 7.22 and the bicarbonate level of at 22 mEq/liter The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. The former may be normal but the difference between the HCO3 and the PCO2 levels makes the illness to be respiratory due to elimination of normalcy. The oxygen reduction also results in the patient being hypoxemic as blood will not be sufficiently supplying oxygen to the body tissues.
    References
         Pathophysiology 7
    th
     ed. 
     Elsevier Mosby.Surat, P. (2018, August 24). 
    PH in the Human Body
    . https://www.news-medical.net/health/pH-in-the-HumanBodyless1 UnreadUnread15 ViewsViews

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    View profile card for Candice Russell

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    January 22 at 4:52 PM
     by Candice Russell

    Schück, O., & Matoušovic, K. (2015). Relation between pH and the strong ion difference (SID) in body fluids. 
    Biomedical Papers
    , 
    149
    (1), 69-73.

    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding  

    His situation was likely linked to his myocardial infarction that caused the labored breathing, weak yet rapid pulses, and the chest pains. In a normal setting, the body fluid’s pH levels should be about 7.35 to 7.45, the pCO2 should be between 35-45, and the HCO3 should be at about 22-26 (P, 2018). Again, the Hg PO2 ought to be at 80-100mm and the oxygen pressure at 90-100%. Evaluating these components is critical in maintaining the acid-base status of body fluids (Schück & Matoušovic, 2015). Mr B should treat his condition by opting for bronchodilator drugs to curb the effects of the obstruction in his airways. Secondly, he should consider a breathing machine or a Continuous Positive Airway Pressure (CPAP) therapy. Also, he should have an adequate oxygen supply especially when there is a reduction of the oxygen levels in his blood.

    Mr. B’s acid base status
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    Tallona Boddy posted Jan 20, 2021 6:03 PM

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    As stated in the discussion prompt, Mr. B appears to be experiencing a myocardial infarction, also known outside of the medical community as a heart attack.less1 UnreadUnread9 ViewsViews

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    View profile card for Jazmin Jerez-Rivera

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    Mayo Clinic (n.d) states that when experiencing a myocardial infarction patients can experience labored breathing, just like Mr. B.  The labored breathing is most likely due to poor perfusion and hypoexmia.  The body’s decreased ability to adequately perfuse and get the adequate amount of oxygen into the blood stream can consequently cause acid to build up, causing metabolic acidosis (Huether et al, 2020).  Metabolic acidosis when defined in its most simplest form is, the build up of acid in a person’s body fluids (Medline Plus, 2021).  Mr. B’s arterial blood gas shows a pH of 7.22, this is considered acidic and lower than the expected range. Mr. B’s PCO2 was 30 mm, this is also below an acceptable standard, and considered to be acidic. When a patient’s pH and PCO2 falls below the acceptable range they are then considered to have an acid-base imbalance, specifically metabolic acidosis.

    Fritzinger- NSG 530 Discussion Wk. 1
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    Cassie Fritzinger posted Jan 19, 2021 6:49 PM

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    Acute myocardial infarction (MI) produces tissue hypoxia resulting in an acid base imbalance secondary to the decrease in cardiac output and arterial hypoxemia (Gandhi & Akholkar, 2015). Mr. B, a 70-year-old gentleman experiencing a sudden MI displays this imbalance given his arterial blood gas (ABG) of pH: 7.22, pCO2: 30mm, and HCO3: 22 mew/L. This ABG shows the patient is in an uncompensated metabolic acidosis. The patient also presented with significant “Q” waves in most leads. According to MacAlpin (2006), a ‘Q’ wave abnormality has an indication of cardiac disease or coronary heart disease with MI and generally this is the chronic stage of an MI. It is also found that Q waves are associated with ventricular hypertrophy. When this patient experiences an MI there is a hypoxic injury to cardiac tissue. The body responds within minutes when there is a mitochondrial compromise. Then there is an insufficient production of Adenosine Triphosphate (ATP) which results in a loss of contractility of the heart, further decreasing the cardiac output. This loss of contractility is a result of the rapid decrease in mitochondrial phosphitylation. When this occurs, anaerobic metabolism generates ATP from glycogen. However, when the glycogen is depleted even anaerobic metabolism ceases as well (Heuther, McCance, & Brashers, 2020)Metabolic Acidosis can be severe, specifically in those with profound cardiogenic shock secondary to an MI (Gandhi & Akholkar, 2015). Gandhi & Akholkar (2015), also found that there was a link between the patient experiencing an MI’s admitting pH level and their mortality rate. They found that those with a pH <7.35 were statistical more likely to die. Similarly they found that these patients who had a HCO3 level of <22 were also more likely to develop ventricular dysrhythmias and more likely to die (Gandhi & Akholkar, 2015). Since acidosis has been shown to have an increased mortality rate, Lazzeri, Valente, Chiostri, Picariello, & Gensini (2010), suggest the use of the anion gap to show more subtle changes in the degree of acidosis to assist with predicting patient outcomes.. References Heuther, S. E., McCance, K. L., & Brashers, V. L. (2020). Understanding Pathophysiology (7th ed.). Elsevier.MacAlpin, R. N. (2006, July). Significance of abnormal Q waves in the electrocardiograms of adults less than 40 years old.  Annals of Noninvasive Electrocardiology , 11(3), 203-210. less1 UnreadUnread12 ViewsViews 12 1 1 RepliesReplies 1 View profile card for Steven Bartos Last post  January 22 at 3:14 AM  by Steven Bartos Lazzeri, C., Valente, S., Chiostri, M., Picariello, C., & Gensini, G. (2010) The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. Acid-base imbalance in uncomplicated ST-elevation myocardial infarction: the clinical role of tissue acidosis.  Internal and Emergency Medicine , 5, 61-66. 10.1007/s11739-009-0338-0 Gandhi, A., & Akholkar, P. (2015). Metabolic acidosis in acute myocardial infarction.  International Journal of Advances in Medicine , 2(3), 260-263. http://dx.doi.org/10.18203/2349-3933.ijam20150556 So, in short review of the case study, Mr. B. developed the chest & left arm pain secondary to the referred pain from his MI. His breathing became labored secondary to two reactions. First the decreased cardiac output increased the oxygen demand of all tissues thus his body began to compensate with increased respirations. Furthermore the labored breathing was also a result of the body’s compensation for the acidosis trying to blow off excess HCO3 (an acid). Mr. B.’s pulses were weak from his decreased cardiac output most likely from the decreased contractility of his heart from the decreased ATP production secondary to hypoxia. The decreased cardiac output further more caused his skin to become cool and clammy from decreased peripheral circulation and most likely hypotension. A failure of the sodium (Na+) potassium (K+) pump and Na+ Calcium (Ca+) exchange occurs with this prolonged hypoxia and resulting mechanisms. This causes Na+ and Ca+ into the cells causing it to swell and K+ out of the cells into the extracellular fluid. Without the sodium/potassium pump, there is free movement of sodium and water. Because of the shifting of electrolytes, the patient enters metabolic acidosis. The treatment for this process is to correct the hypoxia. Without fixing the hypoxia a process known as vacuolation and eventually cell death will occur. Decreased protein synthesis and calcium accumulate within the cell, the cell membrane becomes dysfunctional and the influx of calcium in the cells triggers a pro apoptotic protein causing cell apoptosis (Heuther, S.E., McCance, K.L. & Brashers, V.L., 2020). Module 1: Discussion 2 Subscribe Candice Russell posted Jan 21, 2021 11:34 PM Contains unread posts Arterial blood gas (ABG) measurements are collected for the assessment of ventilation, oxygenation, and the acid-base status of the body. The levels of pH, oxygen (O2), carbon dioxide (CO2), and bicarbonate (HCO3) are measured in arterial blood. Interpretation of ABG results allows for assessment of acid-base imbalances. “Slight changes in the amounts of hydrogen and changes in pH can significantly alter biologic processes in cells and tissues” (Brenneman & Huether, 2020, p. 123). Ranges for normal and abnormal lab values can vary based on where the measurements were conducted The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. Pompey & Abraham-Settles (2019) provide their interpretation of normal ABG values, “four values are used in ABG analysis: pH, PaCO2, HCO3, and PaO2” (p.53). Normal ABG values:  pH: 7.35-7.45, PaCO2: 35-35 mm Hg, HCO3: 22-26 mEq/L, PaO2: 80-100 mm HG.Elevation of PaCO2 with decreased pH, indicates respiratory acidosis. PaCO2 decrease with elevated pH, indicates respiratory alkalosis. HCO3 values are normal with respiratory imbalances. Elevated levels of HCO3 along with increased pH, indicates metabolic alkalosis. Decreased HCO3 along with decreased pH, indicates metabolic acidosis. Hypoxemia may be present if PaCO2 Level is decreased during a metabolic disturbance.The patient’s presentation can provide some background into acid-base imbalance. His cardiac and respiratory distress, signal signs of metabolic acidosis, in form of rapid pulse rate and labored breathing. Hypoxia noted as evidence by the patients’ presentation, as well as, decreased PaCO2 level.I feel the cause of metabolic acidosis is possibly due to ketoacidosis or lactic acidosis. In the case of normal anion gap, unable to be assessed due to unknown values, the possible cause could be gastrointestinal related or renal related. I also thought of mixed acid-base imbalance, respiratory alkalosis. Respiratory alkalosis secondary to metabolic acidosis, in response to hyperventilation, which is seen lactic acidosis  Huether, S. E., McCance, K. L., & Brashers, V. L. (2020).  Understanding pathophysiology / Sue E. Huether, Kathryn L. McCance ; section editor, Valentina L. Brashers (7th ed.). Elsevier.less0 UnreadUnread The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays 2 ViewsViews 2 0 0 RepliesReplies 0 Pompey, J. & Abraham-Settles, B. (2019). Clarifying the Confusion of Arterial Blood Gas Analysis. AJN, American Journal of Nursing, 119(3), 52–56. doi: 10.1097/01.NAJ.0000554035.74335.59. References  To find the cause of metabolic acidosis, anion gap needs to be determined. Anion gap is resulted by finding the sum of chloride (Cl) and HCO, which is then subtracted from cation sodium (Na). In this patients’case the Na and Cl are unknown. Normal values for Na 140, Cl 103, known value of HCO3 22. Using the anion gap formula 140 Na – [103 Cl+ 22 HCO3}is approximately 15, suggesting elevated anion gap, with normal values of approximately 10-12 mEq/L. Elevated anion gap in metabolic acidosis is indicative of possible ketoacidosis, lactic acidosis, ingestion of certain substances and renal disorders   ORDER A PLAGIARISM FREE PAPER NOW After assessing the provided lab values, I determined the acid-base imbalance to be metabolic acidosis, demonstrated by abnormal lab values of 7.22 for pH and 30 mm Hg for PCO2. It is noted that the HCO3 value remains in normal range, this is where things became confusing. According to Brenneman & Huether, (2020), when pH is low and PaCO2 is “normal or low, acidosis is not caused by respiratory factors. Instead, it is caused by metabolic processes within the body” (p. 128). However metabolic acidosis is said to be present with decreased pH and decreased HCO3. Our textbook appears to display decreased levels of HCO3 as less than 22 mEq/L, so for our purposes the patient’s lab values for HCO3 appear normal The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. PaO2 produces information relating to the person’s oxygenation status, however it does not assist in determining acid-base status. The measurement of blood pH, PaCO2 and bicarbonate level simultaneously, provides information on the acid-base status. Blood pH below normal values indicates acidity and values above normal indicate alkalinity.  The measurements of PaCO2 and HCO3 tells us the source of the imbalance, respiratory issue or metabolic issue. Abnormalities in PaCO2 signals a respiratory problem, as abnormal values in HCO3 indicate a metabolic problem. Amandeep Kaur Subscribe Amandeep Kaur posted Jan 20, 2021 5:39 PM Contains unread posts In this case study, Mr. B’s acid-base status is metabolic acidosis, which is partially compensated. Compensation is the body’s attempt to correct the pH levels by manipulating the carbon dioxide or the bicarbonate levels. Full compensation is when the pH is returned to the normal range. It is partially compensated because Mr. B is lowering his CO2 levels by hyperventilating, also known as Kussmaul respirations (Pompey & Abraham-Settles, 2019). Kussmaul respirations are deep and fast so they expel large amounts of CO2 from the body. Along with decreased CO2 levels hyperventilating can cause an O2 deficit and hypoxia.References  Pompey, J., & Abraham-Settles, B. (2019). Clarifying the confusion of arterial blood gas analysis: Is it compensation or combination?  AJN American Journal of Nursing ,                     119 (3), 52–56.less1 UnreadUnread15 ViewsViews 15 The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays 1 1 RepliesReplies 1 View profile card for Tallona Boddy Last post  January 21 at 11:12 PM  by Tallona Boddy Lazzeri, C., Valente, S., Chiostri, M., & Gensini, G. F. (2015). Clinical significance of lactate in acute cardiac patients.  World journal of cardiology ,  7 (8), 483–489. This disturbance in acid-base is caused by an increase in lactic acid. The heart is in a state of stress since an occlusion is causing an increase in cardiac pressure and a decrease in cardiac output. In times of stress, lactic acid acts as fuel to the heart as it can account for accelerated glycolysis (Lazzeri et al., 2015). This creates energy for the heart to effectively perfuse vital organs during the MI. Discussion 2 – Acid base status and disturbance cause Subscribe Jennifer Bryant posted Jan 20, 2021 10:43 PM Contains unread posts What is the acid-base status?What caused this disturbance?ReferencesMeng-Yu Wua,b Giou-Teng Yianga,b Wan-Ting Liaoc,d Andy Po-Yi Tsaie Yeung-Leung Chengf Pei-Wen Chengg,h Chia-Ying Lii,j Chia-Jung Lik (2018). Cellular Physiology and Biochemistry. Karger, 2018;46:1650-1667. Doi.org/10.1159/000less1 UnreadUnread18 ViewsViews 18 1 1 RepliesReplies 1 View profile card for Eleany Yasein Last post  January 21 at 10:23 PM  by Eleany Yasein Pompey, J. & Abraham-Settles, B. (2019). Clarifying the Confusion of Arterial Blood Gas Analysis. AJN, American Journal of Nursing, 119(3), 52–56. doi: 10.1097/01.NAJ.0000554035.74335.59. Several physiological mechanisms during a myocardial infarction leading to hypoxia and hypoperfusion.  Poor perfusion and decreased cardiac output causes ATP production to decrease and induce anaerobic metabolism.  Metabolic acidosis occurs from the retention of lactic acid. Dysfunction of the sodium-potassium pumps causes retention of sodium in the cells and potassium out of the cells (Meng-Yu et al, 2018) The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. Arterial blood gas values are used to assess ventilation, oxygenation and the acid-base status of a patient. When the pH is less than the normal value of 7.35, the indication is acidosis. (Pompey & Abraham-Settles 2019). PCO2 of 30 is lower than the normal range of 35-45 mmHg, HCO3 of 22 is on the low normal range of 22-26 mEq/L. This interpretation is compensated metabolic acidosis (Pompey & Abraham-Settles 2019). The respiratory system is compensating for the metabolic problem by labored breathing. Eleany Yasein, Module 1 Subscribe Eleany Yasein posted Jan 20, 2021 12:03 AM Contains unread posts          Based on Mr. B’s acid base status, he’s having metabolic acidosis. Disruption in the balance of plasma acidity is known as metabolic acidosis (Burger & Schaller, 2020). During metabolic acidosis, the level of pH and bicarbonate decreases (Matyukhin, Patschan, Ritter, & Patschan, 2020). A pH range that’s <7.35 is an indication of Acidemia. Alongside that, pCO2 level of <40mm, and HCO3 value of <24 mEq/L, show signs of metabolic acidosis (Burger & Schaller, 2020). Mr. B’s lab results have a low level of pH, pCO2, and HCO3. Some of the causes of metabolic acidosis can include: uncontrolled diabetes mellitus, hypoxia, sepsis, and GI related complications (Matyukhin et al., 2020). Mr B’s signs and symptoms indicate that he is having hypoxia, his O2 saturation in his blood is low. Additionally, loss of bicarbonate, and diabetic ketoacidosis, are some of the causes of metabolic acidosis (Burger & Schaller, 2020). Moreover, the results of metabolic acidosis can lead to acute kidney failure (Matyukhin et al., 2020). Some of the treatments for metabolic acidosis are, fluid therapy, administration of medications (such as vasopressors), renal replacement therapy, and management of sepsis (if/when needed) (Matyukhin et al., 2020).  Burger, M., & Schaller, D. J. (2020, November 20). Metabolic Acidosis. Retrieved January 20, 2021, Retrieved from  https://www.ncbi.nlm.nih.gov/books/NBK482146/ less1 UnreadUnread13 ViewsViews 13 The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays 1 1 RepliesReplies 1 View profile card for Amandeep Kaur Last post  January 21 at 6:12 PM  by Amandeep Kaur Matyukhin, I., Patschan, S., Ritter, O., & Patschan, D. (July 14, 2020). Etiology and Management of Acute Metabolic Acidosis: An Update.  Kidney & Blood Pressure Research,   45 (4), 523-531. doi:10.1159/000507813 Discussion 2 Subscribe Melissa Morgan posted Jan 20, 2021 11:03 PM Contains unread posts Mr. B’s acid base status is currently metabolic acidosis caused by poor perfusion and hypoxemia. “Tissue ischemia/reperfusion injury, hypoxia, and free radicals all contribute to acidosis” (Lin, et al., 2016). This condition can be caused by changes to the cardiovascular system, and manifestations include Kussmaul respirations, and an overall feeling of lethargy (Huether, McCance & Brashers, 2020). Metabolic acidosis can happen quickly, or it can develop over time. Metabolic acidosis is a result of the blood being too acidic (pH less than 7.40), and not enough bicarbonate HCO3 <22 (Huether, McCance & Brashers, 2020). Mr. B also has abnormal levels of CO2 and decreased oxygenation. The body reacts to this change by breathing deep and rapid, which is called hyperventilation; this is an attempt to expel excess carbon dioxide. Berend further comments on this change by stating “In the presence of an acid–base disorder that alters pH, physiological processes occur that tend to restore pH to normal. These changes are considered compensatory. For instance, a metabolic acidosis causes immediate hyperventilation, and a new steady-state Paco 2  is reached within hours” (2018). Treatment of this condition is based on what caused the disturbance and correcting it. Since we know that Mr. B is experiencing a myocardial infarction, treatment of metabolic acidosis would focus on treating this MI. In evaluating the cause of the acid base disturbance, the serum anion gap should also be assessed. The specific type of acidosis can be determined by the anion gap and can also help determine the cause of it (Huether, McCance & Brashers, 2020).Berend, K. (2018). Diagnostic Use of Base Excess in Acid-Base Disorders.  New England Journal of Medicine ,  378 (15), 1419–1428. https://doi-org.wilkes.idm.oclc.org/10.1056/NEJMra1711860Lin, Y.-R., Li, C.-J., Syu, S.-H., Wen, C.-H., Buddhakosai, W., Wu, H.-P., Chen, C. H., Lu, H.-E., & Chen, W.-L. (2016). Early Administration of Glutamine Protects Cardiomyocytes from Post-Cardiac Arrest Acidosis.  BioMed Research International ,  2016 , 1–8. https://doi-org.wilkes.idm.oclc.org/10.1155/2016/2106342less0 UnreadUnread 3 Views Views The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays 3 0 0 RepliesReplies 0 Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). Understanding pathophysiology (7 th  ed.). Saint Louis, MO: Elsevier Mosby References Discussion 2 Subscribe Jazmin Jerez-Rivera posted Jan 20, 2021 6:53 PM Contains unread posts After analyzing Mr B’s case his acid base status is metabolic acidosis with partial compensation. His myocardial infarction has decreased his cardiac output leading to his diminished oxygenation (Gandhi & Akholkar, 2015). This hypoxemic state leads to lactic acidosis in the body which can cause metabolic acidosis.  Decreased blood flow to the heart can also lead to myocardial ischemia which will produce some of the clinical manifestations like chest pain that radiates to the neck and arm. The body compensates cardiac ischemia by releasing angiotensin II which triggers vasoconstriction, fluid retention, and coronary spasm in the body (Huether, McCance & Brashers, 2020, p. 608). During ischemic injury, some cardiac cells may die so enzymes like CPK-MB and troponin will be released and later detected in the blood analysis. According to Koivula et. al., “Q waves are the hallmark of myocardial necrosis, but they may also represent reperfusion” (2019).  Unfortunately, when normal blood flow is restored to the damaged area of the heart this reperfusion can aggravate the injury further also leading to Q waves. Luckily, the heart will undergo some wound repair, but it will not contract like before.Gandhi A. A., & Akholkar P. J. Metabolic acidosis in acute myocardial infarction. International Journal of Advances in Medicine 2015; 2:260-3. DOI:  http://dx.doi.org/10.18203/2349-3933.ijam20150556 Koivula, K, Nikus, K, Viikilä, J, Lilleberg, J., Huhtala, H., Birnbaum, Y., Eskola, M. (2019). Comparison of the prognostic role of Q waves and inverted T waves in the presenting ECG of STEMI patients.  Annals of Noninvasive Elecrtrocardiology,  24, e12585.  https://doi.org/10.1111/anec.12585 less0 Unread Unread The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays 1 ViewsViews 1 0 0 RepliesReplies 0 Huether, S. E., McCance, K. L., Brashers, V. L. (2020). Understanding Pathophysiology (7 Ed.).  Elsevier.                                                             References Module 1, Discussion 2 Subscribe Beth Certain posted Jan 20, 2021 5:46 PM Contains unread posts Module 1, Discussion 2Mr. B has had an MI, which has caused his acid-base status to be unbalanced.Ph 7.22Hg pO2 70 mmHCO3 22 meq/literAnalyzing the five Arterial Blood Gas (ABG) components mentioned above will help to determine what may have caused this disturbance. Pietrangelo (2017) explains the blood requires the right balance of compounds of acid and basic (alkaline) in order for it to function properly. This is known as acid-base balance. The organs working to maintain acid-base balance are the lungs and the kidneys. Vital organs can be significantly impacted when the acid-base balance is even slightly out of the normal range. The first component of the ABG is the pH. Mr. B’s pH is 7.22 – normal values are 7.35 -7.45. A low pH indicates Mr. B has too much acid in his blood, causing acidemia. Mr. B’s pC02 value is 30 (normal values are 35-45). Decreased pC02 can be caused by hyperventilation (Rienecke, 2017). Mr. B’s breathing is labored, and he is having chest pain. Labored breathing and pain can cause low pC02. Mr. B has a p02 value of 70, the normal range is 75-100. This value shows how much oxygen is in the blood. Interestingly enough, Huether et al (2020) the p02 value has nothing to do with the acid-base balance. It provides information on the person’s oxygenation level. Mr. B’s HC03 value is 22, which is on the low side of normal. HC03 is the bicarbonate level in the blood and is the main component that regulates the pH. High or low HC03 is an indicator of how much the kidneys are compensating. Because the value is still within normal limits, there is not much renal compensation at this point. It could take days for the kidneys to show stress. Mr. B’s final lab value is the 02 saturation of 88%. Due to the acid-base imbalance, he is not getting enough oxygen and should be placed on oxygen The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. Because Mr. B was having an acute MI, this could result in a buildup of lactic acid, which can result from tissue ischemia (Burger & Schaller, 2020), contributing to metabolic acidosis.Burger, M., & Schaller, D. J. (2020).  Stat Pearls . Treasure Island.Huether, S. E., McCance, K. L., & Brashers V. L. (2019). Understanding pathophysiologyRienecke, K., (December, 2018).  The Effects of pC02 on Respiration . Retrieved January 20, 2021, from  https://healthfully.com/the-effects-of-pco2-on-respiration-6654236.html less0 UnreadUnread 1 ViewsViews 1 0 0 RepliesReplies 0  (7th Ed.). Elsevier Inc.   https://www.ncbi.nlm.nih.gov/books References I believe Mr. B. is in compensated metabolic acidosis. Hg O2 sat 88% PCO2 30 mm The labs were as follows: Beth Certain Module 1 Subscribe Steven Bartos posted Jan 20, 2021 5:10 PM Contains unread posts When there’s an acid base imbalance, this may be the result of either a respiratory or a metabolic system process. The respiratory system can quickly balance pH levels by simply increasing or decreasing respiratory rates. Hyperventilation, or labored breathing, in particular causes a decrease in carbon dioxide as a form of respiratory compensation (Pompey & Abraham-Settles, 2019). This is evident in this scenario as his Mr B’s pH level is acidic at 7.22, and PCO2 (carbon dioxide level) is low at 30mm. Mr B’s respiratory system is trying to balance the pH by breathing out the CO2. In this case, he is likely experiencing metabolic acidosis.ReferencesPompey, J., & Abraham-Settles, B. (2019) The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays. Clarifying the confusing of arterial blood analysis: Is it compensation or combination.  American Journal of Nursing ,  119 (3), 52-56. http://dx.doi.org/ 10.1097/01.NAJ.0000554035.74335.59 Ghandhi, A.A., & Akholkar, P.J. (2015). Metabolic acidosis in acute myocardial infarction.  International Journal of Advances in Medicine ,  2 (3), 260-263.  http://dx.doi.org/10.18203/2349-3933.ijam20150556 Research by Gandhi and Akholkar (2015) describes what may have caused the pH disturbance. During a myocardial infarction, cardiac output is decreased and arterial hypoxia (low blood oxygenation concentration) occurs which results in tissue hypoxia, metabolic acidosis, and decreased bicarbonate levels due to a rise in lactic acid. This falls in line with the scenario, as his pO2 is 70mm and his O2 sat is 88%, indicating hypoxemia; however, in this scenario his HCO3 (bicarbonate) levels are normal at 22 meq/liter. Hypoxia is likely what caused the rise in acidic levels The Cell, Inflammation, Repair, Regeneration, and Fibrosis discussion essays.

  • NSG-550-IKF – Diagnostic Reasoning for NPs announcements

    NSG-550-IKF – Diagnostic Reasoning for NPs announcements

    Hello Class,

    We have reached the final week of the class. This week we will be wrapping up with miscellaneous diagnostic tests and studies.

    During your review of the Module 12 materials, please pay attention to the following key concepts: Culture/Sensitivity, Minimum Inhibitory Concentration (MIC), Therapeutic Drug Monitoring, Testing for Alcoholism, Skin Biopsy, & Blood Smears.

    The content from this week will be included on Quiz #3 which will open on Fri., November 19, 2021 at 7AM ET and will close on Mon., November 22, 2021 at 11:59PM ET.

    Also, I kindly ask that you please take the time to fill out the course evaluation as it helps the department update the course from year to year. It also helps me to understand how I can better help my students in upcoming semesters NSG-550-IKF – Diagnostic Reasoning for NPs announcements.

    As always do not hesitate to reach out with any questions or concerns!

    Sincerely,

    Prof. Kane

    Module XI

    Nov 8, 2021 12:01 AM

    –

    Hello Everyone,

    Module 11 will focus on hematologic and cancer studies. The majority of the content will focus on the following: different types of anemia and ways to diagnose them; clotting factors; and select cancer markers.

    Throughout your review of the Module XI content, please pay attention to the following key concepts: serum iron, serum ferritin, complete blood count with differential, mean inhibitory concentration, d-Dimer, prothrombin time (PT), internationalized normal ratio (INR), activated partial thromboplastin time (aPTT), & serum tumor markers.

    Thank you all for your hard work on your clinical notes! I will be working diligently over the next 2 weeks to grade them and release the grades to all of you.

    Please see the below file, which is a review of the key concepts for Modules XI and XII.

    Modules 11 & 12 Concepts Review

    As always, please do not hesitate to reach out to me!

    Sincerely,

    Prof. Kane

    Quiz 2 Review
     (dismissed)

    Nov 2, 2021 9:00 PM

    –

    Class,

    The Quiz 2 average for your section was 85.19%.

    Please take some time to listen to the Quiz 2 review below. It will be available until Fri., 11/5/21 at 11:59PM ET.

    Please reach out with any questions you may have NSG-550-IKF – Diagnostic Reasoning for NPs announcements.

    Module X

    Nov 1, 2021 9:03 AM

    –

    Module X and Clinical Note

    Module X will focus on Reproductive Studies, primarily the female reproductive system. These include hormone levels, imaging studies, and specialized testing like the DEXA scan and colposcopy.

    During your review of the Module X content, please pay particular attention to the following key concepts: Papanicolaou test with Bethesda System for reporting results, Mammogram, Breast Ultrasound, Pregnancy testing (HCG), Fetal Biophysical Profile, Chlamydia and Gonorrhea testing, Fetal Non-Stress Test, Colposcopy, Progesterone lab test, Estrogen lab test, Prolactin lab test.

    Please see the Reproductive (Module X) Review that I have posted under Module X Content and that is linked here: Module X- Reproductive Review

    Please remember that your clinical note is due by Sunday, November 7, 2020 at 11:59 PM ET. You must submit the note through Turn It In. Remember that your similarity score should be <25% and should be appropriately cited per APA guidelines. I understand that some of the clinical note formatting may appear as “similar” and therefore I will take that into consideration when reviewing the clinical notes and the Turn It In scores. Please include a title page and a reference list. There is no need to include an abstract. If you have any questions, please do not hesitate to reach out to me NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Have a great week, Prof. Kane Module IX  (dismissed) Oct 25, 2021 12:01 AM – Hello Class, Module IX will focus on diagnostic studies of the nervous system. Several diagnostic studies will be reviewed this week including but not limited to: EEG, lumbar puncture, carotid duplex, CT scans, MRI. These studies are helpful in diagnosing disorders of the brain, spinal cord, and peripheral nerves. During your review of the Neurologic content please pay special attention to the following key concepts: MRI of the brain, MRA, EEG, lumbar puncture, CT of the brain, CT with myelogram, Nerve conduction studies, blood testing to rule in/rule out dementia, and Spinal x-rays. Please remember that your clinical note is due by the end of Module X – I posted an announcement and a video earlier in the week with the requirements/expectations for the clinical note. Please also see the below link on a review of key concepts for Module IX NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Module IX, Nervous System Review Clinical Note  (dismissed) Oct 18, 2021 8:26 PM – Class, Please remember that your clinical note is due by the end of Module X (due by Sunday, November 7, 2020 at 11:59 PM ET). You must submit the note through Turn It In. Remember that your similarity score should be <25% and should be appropriately cited per APA guidelines. There is no need to include an abstract, but it should include a title page and reference page(s) per APA format. I have linked the detailed instructions and sample format for the clinical note to this post. I have also posted a video below regarding the expectations of the clinical note. If you have any questions, please do not hesitate to reach out to me.Clinical Note Guidelines Quiz #2  (dismissed) Oct 17, 2021 8:07 PM – Hello Class, I hope you enjoyed your break from discussions during Week 7 of the course. There is an assigned discussion post this week on the GI content (Week #8).Please remember that Quiz #2 will open Friday, October 22, 2021 at 7AM ET and will close on Monday, October 25, 2021 at 11:59PM ET. The material for Quiz #2 will include information from the Pulmonary, Cardiovascular, and Gastrointestinal/Hepatic Modules NSG-550-IKF – Diagnostic Reasoning for NPs announcements. We are over halfway through this course! Keep pressing forward! Please reach out if you have any questions. Best, Prof. Kane Modules VII and VIII  (dismissed) Oct 11, 2021 12:01 AM – Module VI Wrap-Up During Module VI the class was asked to discuss a case study of a 56-year old male with hypertension. Hypertension is a growing concern worldwide. Please see the article below on the unique role of nurses and nurse practitioners in the diagnosis, treatment, and prevention of hypertension both in the United States and across the globe. Expanding the Role of Nurses to Improve Hypertension Care Modules VII & VIII This week we will start our review of the gastrointestinal and hepatobiliary systems. We will spend two weeks on this content as there are many diagnostic studies to review. We will review lab tests (i.e. liver function tests, pancreatic enzymes, etc.). We will go over several different types of imaging studies (x-ray, ultrasound), nuclear studies, endoscopic studies, stool testing, fluid analysis, and miscellaneous testing. Please be sure to take the time to review all of the studies listed in these modules, as many will appear on Quiz #2 NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Please see the following Review of Key Concepts: Modules VII and VIII- GI Review During your review of the Gastrointestinal/Hepatobiliary content please pay special attention to the following key concepts: CT of abdomen/pelvis, stool testing (C. Diff, ova/parasite, occult blood), amylase, lipase, Comprehensive metabolic panel (CMP), liver function tests, ERCP, colonoscopy, flexible sigmoidoscopy, upper endoscopy, barium swallow x-ray, and testing for H. Pylori. Please note: There is  NO DISCUSSION POST for Week 7  of the course. The discussion post is  DUE DURING WEEK 8  of the course . Early posts will NOT be accepted or graded. Please continue to work on APA formatting for your discussion posts as it is part of the discussion post rubric, and will also be necessary for the upcoming clinical note that is due during Week 10 of the course. Thanks, Prof. Kane Discussion Posts  (dismissed) Oct 5, 2021 9:13 PM – I have just finished grading your Module IV discussions and will be moving onto the Module V posts. Moving forward please take note of the following: – WebMD is NOT a peer reviewed source, and therefore continued use of this source will result in greater point deductions. While WebMD is a website that provides a lot of useful information,  it is not a peer reviewed/scholarly source. – Posts must be a minimum of 150 words (of narrative text). Citations in the reference list do NOT count toward the 150 word minimum. Initial posts must be posted by Wednesday of the academic week at 11:59PM ET and replies must be posted by Sunday of the academic week by 11:59PM ET NSG-550-IKF – Diagnostic Reasoning for NPs announcements. – Continued APA errors moving forward will result in greater point reductions. Please take the feedback I have provided and use it to improve your APA formatting. Incorrect APA formatting puts writers/students at risk of plagiarism.  If you submitted your Module VI post (cardiovascular) and believe you made APA errors, you can edit and post a reply with your corrected references.  If you would like additional help on APA formatting, refer to the APA manual or please email me and I would be happy to copy your post into a Word Document to provide detailed corrections for you. Thanks, Prof. Kane Module VI  (dismissed) Oct 4, 2021 12:01 AM – As we end Module V, please be sure to see my discussion post on the Module V discussion board. There is an excellent reference that will be helpful as you prepare for your next quiz! Module VI will address important diagnostic studies to assess and evaluate the cardiovascular system. We will explore diagnostic studies to diagnose conditions such as: deep vein thromboses, peripheral arterial disease, myocardial infarction, dyslipidemia, heart failure, abdominal aortic aneurysm, and hypertension NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Throughout your review of the Module VI content, please pay attention to the following key concepts: Measurement of blood pressure (criteria for diagnosis of hypertension), Holter Monitor, Lipid Profile, Venous Doppler (Duplex), Arterial Doppler, Ankle/Brachial Index, Tests to diagnose acute myocardial infarction (Creatinine kinase, troponins, electrocardiography [EKG]), Echocardiogram, Cardiac stress test, Natriuretic Peptides. Please see the below link with additional information for this module: Module VI, Cardiovascular Review Quiz 1 Review  (dismissed) Sep 28, 2021 9:10 PM – Hello Class, Below you will find an audio recording of the Quiz 1 Review. Your class average was 90.69% – Well done! The quiz review will only be available until Sun., 10/3/2021 at 11:59PM. After this date, you will not be able to listen to the recording. Thanks, Prof. Kane Module V  (dismissed) Sep 27, 2021 12:01 AM – I am continuing to work on grading your Diabetes discussion posts. Thank you for your patience as I try to provide you with a lot of feedback in the first few weeks. I should have them all graded by Tuesday of this week NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Module V Module V will introduce diagnostic tests that help us to examine the pulmonary/respiratory system. Endoscopic testing, chest x-ray, testing for tuberculosis, and testing for sleep apnea are just some of the concepts that will be reviewed this week. This week’s case study will focus on the diagnosis and management of COPD. Always remember that a thorough H&P is vital in the care of any patient! Throughout your review of the Module V Materials, please pay attention to the following key concepts: Pulmonary Function Tests/Spirometry, Polysomnography, Screening and Testing for Tuberculosis, Bronchoscopy, Pleural Tap, Diagnosis of Influenza, Diagnosis and Management of Pulmonary Emboli, Pleural Tap, Ventilation/Perfusion Scan, CT Scan, Chest X-ray. Later this week I will also post an exam review. Please watch for the link to the exam review in the “Announcements.” Please see the below link with a review of some of the highlights of the Module V content.   ORDER A PLAGIARISM FREE PAPER NOW Module V- Pulmonary Disorders Module IV  (dismissed) Sep 20, 2021 12:01 AM – Module III Wrap-up As we finish up Module III, if you haven’t already, be sure to look at the thyroid disorder handout and my discussion thread on the Module III discussion post. These are some things that you should review as you prepare for Quiz #1. Diabetes mellitus is a complex disorder that requires prompt diagnosis and appropriate management to minimize the risk of complications NSG-550-IKF – Diagnostic Reasoning for NPs announcements.   Module IV   During Module IV diagnostic studies related to the skeletal and immunologic systems will be reviewed. We will discuss laboratory studies related to immunologic and rheumatology conditions. Imaging studies as they relate to the skeletal system will also be reviewed.   Throughout your review of the Module 4 materials, please pay attention to the following key concepts: Bone X-rays, Bone Densitometry/Density (DEXA) Scans, Vitamin D and Calcium Levels, Tests Used to Diagnose/Monitor Rheumatoid Arthritis (Antinuclear Antibody, Rheumatoid Factor, Erythrocyte Sedimentation Rate), HIV Testing, and Arthroscopy. The materials from this module WILL BE INCLUDED on Quiz #1. Please remember that Quiz #1 will open on Fri., Sept. 24, 2021 at 7AM ET and will close on Mon., Sept. 27, 2021 at 11:59PM ET. Please remember to use the RPNow Software to take the quiz. The quiz study guide is available under the “Course Resources” section. I also recommend you go back through my weekly announcements and review the “Key Concepts” that I have identified for each module. Please do not hesitate to reach out to me with any questions or concerns. Discussion Grades and APA Formatting  (dismissed) Sep 19, 2021 9:08 PM – Hello Class, Grades for the Module II Discussion Post have been entered into the “Grades” section of the course. This week I was lenient with grading especially in regard to APA, grammatical, spelling, and typographical errors. I took the time to provide a great deal of feedback on errors in the posts (please see the attached word documents in the feedback section of your grades). Please take the time to read the comments. It is my expectation that you will correct these errors moving forward and improve as the course goes on. I will be deducting more points moving forward if these errors persist. It is expected that your discussion posts are written at a scholarly, graduate level. They should be grammatically correct and be free of typographical errors. APA formatting is important to the nursing profession and our contribution to research. APA formatting also protects you from plagiarism, if sources are not appropriately credited in your work, there is always the risk of plagiarism. Please remember we are using the APA 7 th Edition Manual NSG-550-IKF – Diagnostic Reasoning for NPs announcements.Some reminders include: -Discussion posts are required to be 150 words at a minimum. -You must use peer-reviewed scholarly references that were written in the last 5-7 years. -Please avoid the overuse of direct quotations. The majority of your posts should include paraphrases of peer-reviewed works to display your understanding of the sources. -Please review capitalization and italics guidelines for article and journal titles in the reference list (p. 317 of APA Manual 7th ed.). -Please review correct in text citations of works by multiple authors which has changed in APA 7 th  edition(p. 266 of APA Manual 7th ed.). -Please review reference list citations of 2 works by the same author with the same date (p. 267 of APA Manual 7th ed.). -Please review that periodical/journal names and volume numbers should italicized (p. 317 of APA Manual 7th edition). -Per APA 7 th  edition, no longer use “doi:” or “retrieved from”, instead just use a hyperlink or web address (p. 317 and p. 351 of APA Manual 7 th  ed.). -Please review proper protocols for abbreviations (must define each abbreviation in text). Do not use abbreviations in reference list NSG-550-IKF – Diagnostic Reasoning for NPs announcements. For any further questions or concerns, please do not hesitate to reach out to me. You will also find helpful information regarding APA 7 th  edition formatting at:  Owl at Purdue N550 Quizzes  (dismissed) Sep 15, 2021 12:01 AM – Review guides for the upcoming 3 quizzes can be found in the “Quiz Study Guides” folder of the course. Please remember these are guides to help you focus your studies and are not all-encompassing of what will be included on the quizzes. Each quiz typically consists of 25-30 questions, and the questions are typically a mix of multiple choice and true/false questions. I recommend you review the content listed on the study guide, the key concepts that I post at the beginning of each module in the “Announcements” section, and you read my discussion posts and comments/questions to students on the discussion boards in preparation for the quizzes. The questions you will find on the quizzes will be similar to questions you may see on your boards. They are higher-level, critical thinking questions. Although it is NOT required, it may be helpful to invest in an exam-review book to practice these types of questions. You will make good use of a review book, especially if you are in the Adult-Gerontology or Family NP programs. Quizzes will open on Fridays at 7:00AM ET and will close on Mondays at 11:59PM ET. Please remember your first quiz will open on Fri., 9/24/2021 at 7AM and will close on Mon., 9/27/2021 at 11:59PM ET. I recommend that you do not wait until the last minute to take the quiz in case there are software glitches. Please also remember that you must utilize ProctorNow (RPNow) software for the quizzes. The practice quiz is still open. It is not a graded quiz, but I recommend you take the practice quiz to test the software with your computer NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Module III  (dismissed) Sep 13, 2021 12:01 AM – Module II Wrap-up During Module II we reviewed urologic studies. In regard to the discussion post, please remember that a CT scan is considered the gold standard of imaging for kidney, bladder, and ureteral stones. I will work on grading your discussion posts this week. I will try to copy your initial posts/replies into Word documents so that I can make corrections as indicated so that you have thorough feedback. Please review the feedback, it is expected that you will continue to improve upon your mistakes every week. While grading will be lenient on the first few discussions, if improvement is not noted more points will be deducted as the course goes on. Module III Module III of the course will focus on diagnostic studies used to diagnose conditions dealing with the endocrine system. This is one of my favorite weeks of this course because I have practiced in outpatient endocrinology for the last 6 years! This week you will learn about diagnostic studies pertaining to diabetes mellitus, thyroid disorders, adrenal disorders, and parathyroid disorders. I will also post a handout on thyroid disorders in the “Course Resources” section. I think you will find it helpful as you prepare for your exam NSG-550-IKF – Diagnostic Reasoning for NPs announcements. Throughout your review of the Module 3 materials, please pay attention to the following key concepts: Thyroid Nodule Diagnosis/Imaging and Biopsy, Interpretation of Thyroid Function Tests, Tests used to Diagnose and Monitor Diabetes Mellitus (i.e., Hemoglobin A1C, Fasting Blood Glucose, Oral Glucose Tolerance Tests), Pertinence of Microalbuminuria in the Management of Diabetes Mellitus, Serum Hormone Levels (i.e, cortisol, ACTH, Parathyroid Hormone, Insulin and C-Peptide levels). I look forward to reading your discussion posts this week! As always please reach out to me with any questions you may have. Prof. Kane Thyroid Disorders Handout Module II  (dismissed) Sep 6, 2021 12:01 AM – During Module 2 of the course we will be learning about diagnostic testing for the urinary and renal systems. The content for this week will include ultrasound, radiologic, laboratory, and microscopic studies for the diagnosis of urinary and renal disorders. Although diagnostic testing is important in ascertaining a diagnosis, never forget to utilize your history taking and physical assessment skills in practice! Throughout your review of the Module 2 materials, please pay attention to the following key concepts: Testing to Diagnose and Manage Chronic Kidney Disease (CKD), Imaging Studies Specific to the Kidneys and Bladder, Diagnosis and Management of Kidney Stones, Diagnosis and Management of Urinary Tract Infections, Interpretation of Urinalysis and Urine Culture/Sensitivity, Urine Toxicology Testing, Prostate Specific Antigen (PSA), and Serum Carbon Dioxide (bicarbonate) Level NSG-550-IKF – Diagnostic Reasoning for NPs announcements. This week you will complete your first graded discussion post. If you have not done so already, please review the grading rubric and requirements for discussion posts (found in the course resources section and my introductory video). A minimum of 150 words per post, APA formatting according to APA 7 th  edition, 2 peer-reviewed references from the last 5-7 years (other than your text book), and scholarly writing mechanics are required for all discussion posts moving forward. Please remember discussions posted prior to Monday at 12:01AM ET will NOT be accepted or graded. You must post your initial post by Wednesday at 11:59PM ET and you must reply to another student/faculty member by Sunday at 11:59PM ET. I look forward to reading your responses! If you have any questions, please feel free to reach out to me via email. Sincerely, Prof. Kane Module I – Wrapping Up  (dismissed) Sep 4, 2021 10:13 PM – Class, As Module I comes to a close, please be sure to look at my discussion post on the Module I discussion board, which summarizes some of the key concepts of this week! Enjoy your holiday weekend, Prof. Kane Module I  (dismissed) Aug 30, 2021 12:01 AM – Hello Class, Module 1 will provide you with an introduction to the course and will also lay the foundation for diagnostic reasoning. Diagnostic reasoning is a vital tool that nurse practitioners utilize daily in clinical practice! There is a discussion post this week which asks each of you to introduce yourself to the rest of the class NSG-550-IKF – Diagnostic Reasoning for NPs announcements. APA format is not required for the post this week. Although the discussion post this week is NOT graded, I ask that you please review all of the Module 1 content as some of these concepts may appear on Exam #1. Throughout your review of the Module 1 materials, please pay attention to the following key concepts: Clinical Reasoning, Sensitivity & Specificity, American College of Radiology (ACR) Appropriateness Criteria, ACR Practice Guidelines for Communication of Diagnostic Imaging Findings, and Examples of Various Diagnostic Studies (i.e. ultrasound, microscopic studies, radiologic studies). As always if you have any questions or concerns, please do not hesitate to reach out to me. Sincerely, Prof. Kane Welcome to Nursing 550  (dismissed) Aug 23, 2021 11:10 AM – Hello Everyone, Welcome to Nursing 550. My name is Julieann Kane and I am so excited to serve as your instructor/facilitator for N550. I am currently a family nurse practitioner working full time in a busy endocrinology practice in Kingston, PA. I have been working in endocrinology for the last 6 years. I have earned my board certification in Advanced Diabetes Management. I have been teaching as an adjunct faculty member in the graduate nursing programs at Wilkes University for the last several semesters. I am currently enrolled in the DNP program at Wilkes University. I reside in Dunmore, PA with my husband, our 5-month old daughter, and our 3 dogs. In my spare time I serve as the secretary for the local Nurse Practitioners of NEPA professional group. I look forward to working with each and every one of you, and I am confident it will be a great semester! NSG-550-IKF – Diagnostic Reasoning for NPs announcements Please take a moment to view the below video link in which I review the course syllabus and the requirements for the course. If you have any questions, please do not hesitate to reach out to me via email (preferably through the “Live” email system) NSG-550-IKF – Diagnostic Reasoning for NPs announcements.

  • sickle cell disease essay

    sickle cell disease essay

    Module 9: Discussion

     

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    A 38-year-old African-American woman was admitted for arthroscopic knee surgery. Her hematocrit was 25%, blood pressure was 140/94 mm Hg, and pulse was 112 beats/minute. She had a history of joint and bone pain, jaundice, and abdominal pain.

    Due to the presenting symptoms (joint and bone pain, abdominal pain, and jaundice) a diagnosis of Sickle Cell Disease was considered.

    Provide a brief discussion of the pathophysiology of sickle cell disease and discuss the clinical manifestations and the etiology associated with each manifestation of this disease.

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

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    Thank you for a thorough post Gisselle.

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    Sickle Cell Disease
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    Tallona Boddy posted Mar 16, 2021 1:37 PM

    Contains unread posts

    Sickle cell disease, specifically, is an inherited blood disorder, by both parents. In the U.S., sickle cell disease is part of the newborn screening, via a blood test and can be diagnosed at any time during a person’s lifespan (Centers for Disease, 2020) sickle cell disease essay.  Diagnosis of sickle cell disease is completed through blood tests, the hemoglobin electrophoresis, high performance liquid chromatography (HPLC) and deoxyribonucleic acid (DNA) test, (St. Jude Research, n.d.).  A patient may present to their provider with any of the above mentioned symptoms, as well as, other symptoms such as fever, severe unexplained episodes of pain, pale skin or eyes, or signs and symptoms of a stroke.  The etiology for these manifestations is again due to the shape of the sickle cell.  A fever is due to a damaged spleen from the sickle cells, causing increased infections.  Pale skin or eyes is due to the anemia and poor oxygenation, the sickle cells blocking and sticking to one another in smaller vessels.  Signs and symptoms of a stroke are due to a potential blood clot caused by the sticky red blood cells sticky to one another and occluding a larger vessel (Mayo Clinic, 2020). Centers for Disease Control and Prevention. (14 December, 2020). 
    Sickle cell disease
    . 
    https://www.cdc.gov/ncbddd/sicklecell/index.html
    Mayo Clinic. (30 January, 2020). 
    Sickle cell anemia
    . 
    https://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/symptoms-causes/syc-20355876
    St. Jude Children’s Research Hospital. (n.d.). 
    Diagnostic screening for sickle cell disease
    . 
    https://www.stjude.org/treatment/disease/sickle-cell-disease/diagnosing-sickle-cell.html
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    March 22 at 12:25 AM
     by Gisselle Mustiga

     

     

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    Sickle cell disease affects a person’s red blood cells, typically, red blood cells are round, sickle cell red blood cells are crescent (moon) shaped and sticky.  The crescent shaped red blood cells have difficulty moving through a person’s blood vessels, compared to traditional round, non-sticky red blood cells.  The crescent shaped red blood cells tend to get stuck in small blood vessels and stick to one another.  Due to the sticky, crescent shape of the red blood cells the patient can experience a number of symptoms sickle cell disease essay. Anemia is often present due to the sickle cells breaking easier and dying within 10-20 days, not meeting the average 120 day lifespan of a red blood cell.  Pain, hand/foot swelling and vision problems are common symptoms due to the sickle cells sticky nature and crescent shape, building up and blocking blood flow in the body (Mayo Clinic, 2020).

    Module 9, Eleany Yasein
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    Eleany Yasein posted Mar 17, 2021 9:09 PM

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    Sickle cell disease is autosomal recessive, genetic disorder that affects multisystem in the body (Sedrak & Kondomudi, 2021). It mostly affects African Americans, about 1 in 12 African Americans carry the mutation. This disorder is caused due to a mutation on chromosome 11, there is an amino acid substitution (glutamic acid is changed to Valine) in position 6. This mutation causes the Hemoglobin molecule to change and alter the erythrocyte shape. There is adhesion of the erythrocytes and formation of heterocellular aggregation, leading to vessel occlusion and hypoxia. Moreover, Hemoglobin binds to nitric oxide and releases oxygen, which causes the erythrocytes to sickle. There is an increased HbS (sickled HbA) formation and activation of inflammatory mediators and free radicals are released, which causes reperfusion injury. Furthermore, there is an increase nitric oxide binding, neutrophil adhesiveness, platelet activation and hypercoagulability (Sedrak & Kondomudi, 2021).ReferencesSundd, P., Gladwin, T. M., & Novelli, M. E. (2018 October 17). Pathophysiology of Sickle Cell Disease. 
    Annual Review Pathology, 14, 263-292. 
    doi: 
    10.1146/annurev-pathmechdis-012418-012838
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    View profile card for Aina Oluwo

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    March 21 at 10:13 PM
     by Aina Oluwo

    Sedrak, A., & Kondamudi, N. (2021, January 22). Sickle Cell Disease. 
    StatPerarls
    . 
    https://www.ncbi.nlm.nih.gov/books/NBK482384/

    Patients with sickle cell disease will present with different rage of clinical manifestations depending on the body system affected and the severity (Sedrak & Kondomudi, 2021). Vaso-occlusive crisis is the most common presentation seen. Microvascular occlusion leads to ischemia, which leads to tissue damage and triggers inflammation process. This activates nociceptors and cause pain. Patient complain of pain in different part of their body, including their bones, back, chest and abdomen. Patients can also present with acute chest syndrome, which is caused due to the hypoxia and release of inflammatory mediators. Symptoms include, fever, cough, chest pain, which can lead to respiration failure (Sedrak & Kondomudi, 2021). Moreover, Sickle cell disease causes intravascular and extravascular hemolysis causing chronic anemia (Sundd et al., 2018). This causes increase in cardiac output, ventricular dilation and cause vascular injury. The endothelial dysfunction and vascular injury cause multiorgan failure. Patients can present with renal dysfunction, hypertension, cerebrovascular accidents, and pulmonary hypertension (Sundd et al., 2018).

    Module 9: The Hematologic System – SCD
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    Gisselle Mustiga posted Mar 16, 2021 2:11 PM

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    Sickle cell anemia results from mutation of the b globin gene. It should be noted that the red blood cells containing the abnormal b alleles undergo polymerization and become rigid when exposed to deoxygenated environments. These rigid red blood cells are often susceptible and liable to hemolysis and also have increased densities. Their weights affect the endothelial walls’ blood flow and integrity (Inusa et al., 2019). Hemolysis results in complex activities and events, including the consumption and dysregulation of nitric oxide. It also causes endothelial dysfunction, leading to severe complications, including stroke, priapism, leg ulceration and pulmonary hypertension. Compared to the red blood cell with a half-life of 120 days, sickle RBCs can only exist for a maximum of 20 days due to hemolysis (Huether et al. 2020). Distortion of the normal discoid RBCs into sickle cell results from the formation of long fibers of deoxyhemoglobin S.ReferencesInusa, B. P., Hsu, L. L., Kohli, N., Patel, A., Ominu-Evbota, K., Anie, K. A., & Atoyebi, W. (2019). Sickle cell disease—genetics, pathophysiology, clinical presentation and treatment. 
    International Journal of Neonatal Screening
    , 
    5
    (2), 20. 
    https://www.mdpi.com/2409-515X/5/2/20/pdf
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    View profile card for Steven Bartos

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    March 21 at 10:00 PM
     by Steven Bartos

    Nickel, R. S., & Hsu, L. L. (2016). Clinical manifestations of sickle cell anaemia: infants and children. In 
    Sickle Cell Anemia
     (pp. 213-229). Springer, Cham. 
    http://ndl.ethernet.edu.et/bitstream/123456789/42788/1/pdf.237#page=223

    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding Pathophysiology 7
    th
     ed
    . Elsevier Mosby sickle cell disease essay.

    The first clinical manifestation of sickle cell anemia is the vaso-occlusive crisis which occurs due to obstruction of microcirculation resulting in ischemic injuries and pain to the organs. This is associated with increased emergency department visits and hospitalization among patients with SCD. The pain can affect any body part, including soft tissues, joints, abdomen and bones (Nickel & Hsu, 2016). The other manifestation associated with the pain is infarctions and auto-splenectomy that affects the spleen resulting in failures and life-threatening infections. Papillary necrosis is a renal manifestation that results in isosthenuria. The other manifestation is the aplastic crisis which is caused by infection with Parvovirus B-19, causing fifth disease, mild rash, and fever.  Splenic sequestration is characterized by rapid enlargement of the spleen and increased reticulocyte counts. Sickle cell disease can also cause progressive injury to the liver with significant fibrosis, often cirrhosis, and decreased liver function by adulthood. Asymptomatic patients commonly have hepatomegaly and elevated liver enzyme levels. Other manifestations include acute chest syndrome and hand-foot syndrome.

    Sickle Cell Anemia
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    Lois Chappell posted Mar 21, 2021 9:39 PM

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         Sickle cell disease an autosomal recessive genetic disorder belonging to a is a group of inherited red blood cell disorders affecting millions of people worldwide (Sundd, Gladwin,& Novelli, 2019).  Sickle cell anemia is the most common form of the disease, and accounts for 70% of African Americans who have sickle cell disease (Sundd, Gladwin, & Novelli, 2019).  In sickle cell disease, red blood cells that are normally round become hard and sticky and form a “c” shape, causing them to get stuck during normal blood flow.  Along with endothelial interactions, systemic inflammation, oxidant stress, and  activation of the coagulation system, these cellular alterations can cause the  predominant symptoms of sickle cell disease including stroke, acute chest syndrome and infection (Centers  for Disease Control, 2021).     Center for Disease Control and Prevention (2021).  Sickle Cell Disease.  Retrieved from     Field, J., Vichinsky, E., Tyrnauer, J.  (2021).  Acute chest syndrome in adults with sickle cell disease.  Retrieved from     Ochocinski, D.,  Dalal, M., Black, L. Vandy, C., Lew, J., Sullivan,  K., and Kissoon, N.  (2020).  Life-threatening infectious
    https://doi.org/10.3389/fped.2020.00038
    .292. https://doi.org/10.1146/annurev-pathmechdis-012418-012838 sickle cell disease essay.           less0 UnreadUnread

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         Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
    , 
    14
    , 263–

    complications in sickle cell disease: a concise narrative review.  
    Frontiers in Pediatrics
    , 
    8.
       Retrieved from

    https://www.uptodate.com/contents/acute-chest-syndrome-in-adults-with-sickle-cell-disease.

    https://www.cdc.gov/ncbddd/sicklecell/index.html.

         In sickle cell disease, strokes can occur as a result of red blood cells getting stuck in a vessel, reducing blood flow to the brain (Centers for Disease Control, 2021).  Acute chest syndrome can be caused by infection, asthma, or hypoventilation or as the result of  fat emboli, bone marrow necrosis or both (Up to Date, 2021).  Infection in sickle cell disease is due to impaired splenic clearance of bacteria (Ochocinski, Dalal, Black, Vandy, Lew, Sullivan, and Kissoon, 2020).

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    Hilary Szpara posted Mar 17, 2021 12:09 PM

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    Sickle cell disease is a broad term that describes a group of conditions which arise from the inheritance of hemoglobin S (HbS) (Houwing et al., 2019). There are different variations of the gene mutation and people can also have the sickle cell trait or be a sickle cell carrier (Houwing et al., 2019). Sickle cell disease is an inherited disease that is autosomal recessive and is caused by single mutation in the B-globin gene (Houwing et al., 2019). There are four major pathobiological processes which drive the disease; including vaso-occlusion, hemolysis-mediated endothelial dysfunction, sterile inflammation, and hemoglobin S polymerization (Sundd et al., 2019).  With hemoglobin S polymerization, the hemoglobin S polymers grow rapidly and form long fibers which increase cellular rigidity and distort the cell membrane, leading to the sickling of the cell, dehydration, energetic failure and stress, and premature hemolysis (Sundd et al., 2019) sickle cell disease essay. Vaso-occlusion leading to ischemia is responsible for the vaso-occlusive crises. Chronic hemolysis and sickle shape increases the plasma viscosity and contributes to the impaired flow of blood through capillaries (Sundd et al., 2019). Endothelial dysfunction occurs due to the chronic hemolysis, which results in anemia. The anemia exerts extra stress on the cardiovascular system by increasing cardiac output, ventricular chamber dilation, and ventricular wall stress (Sundd et al., 2019). Vaso-occlusion contribute to the ischemia-reperfusion injury, along with the release of erythrocyte damage-associated molecular patterns (eDAMPs), which are products of hemolysis, contribute to the process of sterile inflammation (Sundd et al., 2019). There are also a variety of complications that can arise due to sickle cell disease, including increased risk of infection, cerebrovascular accidents, acute chest syndrome, acute kidney injury, hepatobiliary complications, splenic complications, priapism, as well as a long list of chronic complications (Houwing et al., 2019).  Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
    , 
    14
    , 263–292. https://doi.org/10.1146/annurev-pathmechdis-012418-012838less1 UnreadUnread4 ViewsViews

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    View profile card for Candice Russell

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    March 21 at 8:16 PM
     by Candice Russell

    Houwing, M. E., De Pagter, P. J., Van Beers, E. J., Biemond, B. J., Rettenbacher, E., Rijneveld, A. W., Schols, E. M., Philipsen, J. N. J., Tamminga, R. Y. J., Fijn van Draat, K., Nur, E., Cnossen, M. H. (2019). Sickle cell disease: Clinical presentation and management of a global health challenge. 
    Blood Reviews, 37.

    Sickle Cell Disease
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    Jennifer Bryant posted Mar 16, 2021 3:54 PM

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    Sickle cell disease is a collection of inherited blood disorders that affects approximately 100,000 people in the United States and millions worldwide. Sickle cell disease is caused by the inheritance of abnormal beta-globin alleles carrying the sickle mutation on the HBB gene (Ware et al., 2017).Acute splenic sequestration crisis results from the trapping of red blood cells in the spleen of a person with sickle cell disease. The pooling and destruction of blood cells within the spleen results in decreased circulating blood volume, potentially leading to hypovolemic shock, cardiovascular collapse, and even death (Esterson et al, 2021).             Hyperhemolytic crisis is a rare and dangerous complication of sickle cell disease where the hemoglobin level drops rapidly. This can quickly lead to organ failure and death (Srinivasan & Gourishankar, 2019).Darbari, DS, Sheehan, VA, Ballas, SK. (2020) The vaso‐occlusive pain crisis in sickle cell246. 
    https://doi-org.wilkes.idm.oclc.org/10.1111/ejh.13430
    sectional imaging appearance of an uncommon diagnosis, 
    Clinical Imaging
     69 369-373Minhas, P. S., Virdi, J. K., & Patel, R. (2017). Double whammy- acute splenic sequestration
    Community Hospital Internal Medicine Perspectives, 7
    (3), 194-195.Srinivasan, A & Gourishankar A. (2019) “A Differential Approach to an Uncommon Case ofhttps://doi.org/10.1177/2333794X19848674.(2018). Vaso-occlusive crisis in sickle cell disease: Current paradigm on paindoi:http://dx.doi.org.wilkes.idm.oclc.org/10.2147/JPR.S185582disease sickle cell disease essay.
     The Lancet, 390
    (10091), 311-323.less2 UnreadUnread5 ViewsViews

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    View profile card for Dennies Jones

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    March 21 at 7:33 PM
     by Dennies Jones

    doi:http://dx.doi.org.wilkes.idm.oclc.org/10.1016/S0140-6736(17)30193-9

    Ware, R. E., de Montalembert, M., Tshilolo, L., & Abboud, M. R. (2017). Sickle cell

    management.
     Journal of Pain Research, 11
    , 3141-3150.

    Uwaezuoke, S. N., Ayuk, A. C., Ndu, I. K., Eneh, C. I., Mbanefo, N. R., & Ezenwosu, O. U.

    Acute Anemia in a Child With Sickle Cell Disease.” 
    Global Pediatric Health 

    doi:http://dx.doi.org.wilkes.idm.oclc.org/10.1080/20009666.2017.1340729

    crisis in patient with aplastic crisis due to acute parvovirus infection.
     Journal of

    https://doi.org/10.1016/j.clinimag.2020.10.016.

    Esterson, Y.B., Sheth, S., Kawamoto, S. (2021) Splenic sequestration in the adult: cross

    disease: Definition, pathophysiology, and management. 
    Eur J Haematol
    . 105: 237-

    References

                Transient aplastic crisis usually occurs in older children or adults with sickle cell disease commonly due to acute human parvovirus B19 infection and is characterized by reticulocytopenia and mild neutropenia/thrombocytopenia (Minhas et al, 2017).

                Vaso-occlusive crisis or acute painful crisis constitutes the major morbidity in sickle cell disease (Uwaezuoke et al, 2018). Sickled erythrocytes cause vaso-occlusion together with many other cellular and plasma factors and abnormal endothelial interactions, leading to a broad range of acute and chronic clinical complications caused by repeated ischemia and inflammation (Ware et al., 2017).

    Sickle cell
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    Aina Oluwo posted Mar 17, 2021 10:23 PM

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    According to literature, Sickle cell disease (SCD) is an autosomal recessive disorder of a gene mutation that affects about 1 in 500 African American children and 1 in 36,000 Hispanic American children. (Borhade & Kondamudi, 2021). SCD based on its pathology results in symptoms ranging from anemia to sickle cell crisis (SCC) with often manifests as ”acute pain crisis’’ and will often require hospitalization. The term “sickle cell crisis” is used to describe several acute conditions such as the vaso-occlusive crisis (acute painful crisis), aplastic crisis, splenic sequestration crisis, hyper hemolytic crisis, hepatic crisis, dactylitis, and acute chest syndrome. (Borhade & Kondamudi, 2021) sickle cell disease essay.In our case study, our 38 y/o patient presented with low hematocrit and associated joint and bone pain as well as findings consistent with jaundice and abdominal pain.  The diagnosis of sickle cell disease was considered based on this presentation however it is essential to note that a diagnosis of sickle cell disease cannot be made by the findings of low hematocrit only but rather a combination of all her symptoms as well as genotype assessment. Individuals will have at least one sickle hemoglobin (HbS) allele, which is an abnormal allele for the β-globin gene (Adams-graves & Bronte-Jordan, 2016). The disease can be misdiagnosed or incorrectly self-reported by patients and this is where the providing physician must assess the patient’s presenting physical symptoms as well as a complete detailed history of past medical presentations and subsequently obtain genotype testing for sickle cell disease confirmation. Normal red blood cells are round and flexible and move easily through blood vessels however in sickle cell disease, abnormal hemoglobin causes red blood cells to become sickle shaped and rigid and this allows the cells to easily become lodged in smaller blood vessels, depriving tissues of oxygen and triggering painful episodes (Tanabe et al 2019). Once these cells begin to occlude vessels, this triggers painful events leading to hemolysis, anemia in varying organs and most notably, the spleen. Splenic injury greatly increases the risk of death from infection at a young age sickle cell disease essay.The pathophysiology of sickle cell disease is characterized by a single amino acid substitution in the β-globin chain leads to polymerization of mutant hemoglobin S, impairing erythrocyte rheology and survival. Clinically, erythrocyte abnormalities in SCD manifest in hemolytic anemia and cycles of microvascular vaso-occlusion leading to end-organ ischemia-reperfusion injury and infarction. (Sundd et al 2019). With continued progression of the disease the risk for multiorgan injury as well as severe clinical presentations are often seen and an interplay between multiple disciplines are essential in combating and providing appropriate medical management to limit recurrence of acute crisis and frequent ED visits and hospitalizations.

    Adams-Graves, P., & Bronte-Jordan, L. (2016). Recent treatment guidelines for managing adult patients
    of Hematology, 9
    (6), 541. 
    https://doi.org/10.1080/17474086.2016.1180242
    https://www.ncbi.nlm.nih.gov/books/NBK526064/
    Complications of Sickle Cell Disease. 
    The American journal of nursing
    , 
    119
    (6), 26–35.

    Sundd, P., Gladwin, M., & Novelli, E. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of
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    View profile card for Jazmin Jerez-Rivera

    Last post 
    March 20 at 11:34 AM
     by Jazmin Jerez-Rivera

    pathology,
     14, 263–292. 
    https://doi.org/10.1146/annurev-pathmechdis-012418-012838

    https://doi.org/10.1097/01.NAJ.0000559779.40570.2c

    Tanabe, P., Spratling, R., Smith, D., Grissom, P., & Hulihan, M. (2019). CE: Understanding the

    Borhade, M., & Kondamudi, N. (2021). 
    Sickle cell Crisis
    . Statpearls.

    with sickle cell disease: Challenges in access to care, social issues, and adherence.
     Expert Review

     References

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    Steven Bartos posted Mar 17, 2021 8:07 PM

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    Sickle cell disease (SCD) is a group of autosomal recessive disorders where a mutation in the B-globin gene produces mutated hemoglobin molecules that causes the erythrocytes to form a sickle shape (Gladwin, 2016). The sickling is a result of decreased oxygenation and pH, and dehydration sickle cell disease essay. Acute infections, temperature changes, and high altitude can increase sickling, as this affects oxygenation. Sickle cells’ irregular shape block the blood vessels, causing a thickening of the blood and decreased circulation, resulting in vascular injury and dysfunction of the spleen, bones, and liver. SCD has a higher prevalence among black people and African countries (Huether et al., 2017). The disease can manifest in the form of various disorders, with the most common being to the cardiovascular, hepatobiliary, renal, and musculoskeletal joint systems.The hepatobiliary system is defined as liver dysfunction and hyperbilirubinemia as a result of intrahepatic sickling, subsequently causing ischemia, pooling of blood in the liver and spleen, and cholestasis. Pancreatitis, peptic ulcer disease, as well acute and chronic liver failure are common manifestations. Abdominal pain and jaundice are common symptoms related to these disorders (Shah, et al., 2017).Musculoskeletal issues are common in patients with SCD, with its etiology stemming from the vaso-occlusion of postcapillary venules, resulting in bone infarction and inflammation. Steroid induced vaso-occlusive disease may also present itself when patients are being treated for rheumatic conditions as well, as this type of steroid therapy can cause painful vaso-occlusive episodes. Osteomyelitis, intramedullary marrow hyperplasia, osteonecrosis, restricted bone growth, inflammatory arthritis, and gout are also common musculoskeletal manifestations of SCD (Hughes et al., 2016).Airy, M., & Garabed, E. (2017). The kidney in sickle hemoglobinopathies. 
    Clinical Nephrology, 87
    (2), 55 – 68. 
    http://dx.doi.org.wilkes.idm.oclc.org/10.5414/CN108991
    Hughes, M., Akram, Q., Rees, D.C., & Jones, A.K.P. (2016). Haemoglobinopathies and the rheumatologist. 
    Rheumatology, 55
    (12), 2109 – 2118. 
    https://doi.org/10.1093/rheumatology/kew042
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    View profile card for Tallona Boddy

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    March 20 at 12:43 AM
     by Tallona Boddy

    Shah, R., Taborda, C., & Chawla, S. (2017). Acute and chronic hepatobiliary manifestations of sickle cell disease: A review. 
    World Journal of Gastrointestinal Pathophysiology, 8
    (3), 108 – 116. 
    https://dx.doi.org/10.4291%2Fwjgp.v8.i3.108

    Gladwin, M.T. (2016). Cardiovascular complications and risk of death in sickle-cell disease. 
    The Lancet, 387
    (10037), 2565 – 2574. 
    http://dx.doi.org.wilkes.idm.oclc.org/10.1136/bcr-2020-236743

    References

    Kidney problems develops as a result of the sickling process obstructing the glomerulus, tubule, and medulla of the kidney. Albuminuria and the inability to concentrate urine are warning signs of renal failure due to SCD. Chronic kidney disease accounts for approximately 14 – 18% of mortality in SCD (Airy & Eknoyan, 2017) sickle cell disease essay.

    Cardiovascular issues develop as a result of repeated vaso-occlusive episodes, which lead to cardiac ischemia. However, chronic hemolytic anemia, whereby red blood cells die faster than they are made, is the major cause of cardiovascular morbidity and mortality in patients with SCD. Chronic red blood cell transfusions and associated secondary iron overload is another factor that causes heart damage. Pulmonary hypertension, chronic thromboembolic pulmonary hypertension, systolic and diastolic heart dysfunction, and ischemic heart disease are found in patients with sickle cell. An elevated pulse and high blood pressure may be typical vital signs given these manifestations (Gladwin, 2016) sickle cell disease essay.

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    Joanne Hogan posted Mar 16, 2021 11:07 AM

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    Sickle cell is one of the most common life threatening inherited disorders in the world, most commonly affecting people of African, Arab, and Indian ancestry (Inusa et al., 2019). The gene frequency is more prominent in Western Africa with the likelihood being 25-30% (Inusa et al., 2019).Clinical manifestation of sickle cell can be mild but hemolytic anemia generally causes jaundice, pallor, and fatigue (Huether et al., 2020). Vasospasm and vasoocclusion cause severe pain that may last days to weeks (Huether et al., 2020). Leg ulceration, priapism, stroke, and pulmonary hypertension can occur due to hemolysis and tissue ischemia (Inusa et al., 2019). In children under the age of 5, sequestering occurs and large amounts of blood pools in the liver and spleen which can cause death if not noticed (Huether et al., 2020). Aplastic crisis can occur due to the rapid cell cycle of the red blood cells in sickle cell patients and hyperhemolytic crisis may occur due to certain infections or drugs (Huther et al., 2020). Infection is more common in sickle cell patients and can trigger a sickle cell crisis (Inusa et al., 2019). Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7th ed.). Elsevier.Piccin, A., Murphy, C., Eakins, E., Rondinelli, M., Daves, M., Vecchiato, C., Wolf, D., Mc Mahon, C., & Smith, O. P. (2019). Insight into the complex pathophysiology of sickle cell anaemia and possible treatment. 
    European Journal of Haematology
    , 
    102
    (4), 319–330. 
    https://doi.org/10.1111/ejh.13212
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    View profile card for Melissa Morgan

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    March 19 at 5:02 PM
     by Melissa Morgan

    Inusa, B., Hsu, L., Kohli, N., Patel, A., Ominu-Evbota, K., Anie, K., & Atoyebi, W. (2019). Sickle cell disease—genetics, pathophysiology, clinical presentation and treatment. 
    International Journal of Neonatal Screening
    , 
    5
    (2), 20. https://doi.org/10.3390/ijns5020020

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    References

    Sickle cell anemia is an autosomal recessive disease and is caused by abnormal hemoglobin production due to a mutation in the inherited β -globin gene (Piccin et al., 2019). In this mutation, the hydrophobic amino acid valine is substituted with the hydrophilic glutamic amino acid in the β- globin chain (Inusa et al., 2019). This mutation results in hemoglobin called hemoglobin- S that is poorly soluble when deoxygenated and highly unstable (Piccin et al., 2019). Red blood cells are dehydrated which causes low potassium levels and altering of the cell membrane, giving red blood cells their sickle shape (Piccin et al., 2019). Sickling causes clogged vessels and increases blood viscosity (Huether et al., 2020). The sickling of cells is usually not permanent, and cells can regain their normal shape after they are reoxygenated and rehydrated (Huether et al., 2020).

    Dennies Jones
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    Dennies Jones posted Mar 17, 2021 9:37 PM

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     with a hematocrit of 25%, elevated blood pressure and pulse, BP 140/94, and P 112. The patient has a history of joint and bone pain, jaundice, and abdominal pain. Due to symptoms, she was diagnosed with sickle cell disease.  According to Harding et al. (2020),”Sickle cell disease (SCD) is a group of inherited, autosomal recessive disorders characterized by an abnormal form of hemoglobin in the RBC. Because this is a genetic disorder, SCD is usually found during routine neonatal screening” (p. 33838).         According to (Bender M.A 2021), “The clinical manifestation of Sickle cell disease is characterized by intermittent vaso-occlusive events and chronic hemolytic anemia. Vaso-occlusive events result in tissue ischemia leading to acute and chronic pain and organ damage that can affect any organ system, including the bones, spleen, liver, brain, lungs, kidneys, and joints. Dactylitis (pain and/or swelling of the hands or feet) is often the earliest manifestation of SCD” (p. 10). Baba, I., Lewis, H., Neeraj, K., Patel, A., Ominu-Evbota, K., Kofi, A., & Wale, A. (2019). Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment. Neonatal Screening. doi:doi:10.3390/ijns5020020 less1 UnreadUnread4 ViewsViews

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    View profile card for Sheryl Dixon

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     by Sheryl Dixon

    Harding, Mariann M., Kwong, Jeffrey, Roberts, Dottie, Hagler, Debra, Reinisch, Courtney. Lewis’s Medical-Surgical Nursing E-Book (Kindle Locations 33838-33840). Elsevier Health Sciences. Kindle Edition.

    Bender, M. A. (2021). Sickle Cell Disease. In M. P. Adam (Eds.) et. al., GeneReviews®. University of Washington, Seattle.

    Reference:

              SCD is one of the most common inherited disorders. It predominantly affects people of color. Early screening is essential for the survival of newborns. Among the common causes of death is the absence of early diagnosis followed by education and preventive therapies such as penicillin prophylaxis and chronic surveillance include infections, severe anemia, and multi-organ failure (Baba et al., 2019).

             Baba et al. (2019) explained the pathophysiology of sickle cell as “red blood cells (RBCs) that contain HbS or HbS in combination with other abnormal β alleles when exposed to deoxygenated environment undergo polymerization and become rigid. The rigid RBCs are liable to hemolysis. Due to increased density, it may affect blood flow and endothelial vessel wall integrity” (p.5)—the dense, rigid RBCs lead to vaso-occlusion tissue ischemia, infarction as well as hemolysis.

             A 38-year-old African American was admitted for knee surgery. The patient presented

    Sickle Cell
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    Jazmin Jerez-Rivera posted Mar 17, 2021 9:23 PM

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    Sickle cell disease (SCD) is an autosomal recessive disorder which produces hemoglobin S inside erythrocytes. The mutation occurs when glutamic acid is substituted with valine causing a mutation in the hemoglobin tetramer HbS (Sundd et. al., 2019). Erythrocytes gain their sickle shape under conditions of low oxygen and dehydration in the body. Protein strands form inside the red blood cell (RBC) causing it to stretch taking on a crescent shape (NHLBI, 2020). Clinical manifestations vary depending on the severity of the disease. Early symptoms include jaundice, fatigue and dactylitis (painful swelling of hands and feet) (NHLBI, 2020). According to Huether et. al (2020) there are four major types of crises associated with this disease. A vasocclusive crises is caused by impaired blood flow through microcirculation. The plasma becomes thickened due to the increased hemolysis of RBC. This along with the changed shape increases adhesion of erythrocytes in the vessels blocking blood flow and causing pain for the individual (Sundd et. al., 2019). Sequestration occurs in children, where the liver and spleen become pooled with blood. Mortality is high if not treated in a timely manner (Huether et. al., 2020). Aplastic crisis is severe anemia that occurs due to a delay in erythropoiesis. It is usually caused by a parvovirus infection (NHLBI, 2020). Hyperhemolytic crisis can be caused by infections, medications or a reaction to a blood transfusion (Huether et. al., 2020). Huether, S. E., McCance, K. L., Brashers, V. L. (2020). Understanding Pathophysiology (7 Ed.).  Elsevier.Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
    , 
    14
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    View profile card for Amandeep Kaur

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    March 18 at 11:33 PM
     by Amandeep Kaur

    National Heart, Lung, and Blood Institute, (2020). Sickle Cell Disease. Retrieved from https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease Sickle cell disease essay

    References

    Module 9
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    Sheryl Dixon posted Mar 17, 2021 10:43 PM

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    Sickle cell diseases (SCD) is a group of inherited red blood cell disorders. Healthy red blood cells are round, and they move through small blood vessels to carry oxygen to all parts of the body. In someone who has SCD, the red blood cells become hard and sticky and look like a C-shaped farm tool called a “sickle”. The sickle cells die early, which causes a constant shortage of red blood cells. Also, when they travel through small blood vessels, they get stuck and clog the blood flow. This can cause pain and other serious problems such infection, acute chest syndrome and stroke (CDC,2020).Hemoglobin Sβ0 thalassemiaHemoglobin SCHemoglobin SEIn all types of sickle cell disease, at least one of the two abnormal genes cause a person’s body to make hemoglobin S. When a person has two hemoglobin S genes (hemoglobin SS), the disease is called sickle cell anemia. This is the most common and often most severe type of sickle cell disease. Hemoglobin SC disease and hemoglobin Sβ thalassemia are two other common types of sickle cell disease. Hemoglobin SD and hemoglobin SE are much less common(nhlibi.2020). CDC, (2020).
     What is Sickle cell disease
    . Retrieved from 
    https://www.cdc.gov/ncbddd/sicklecell/facts.html
    Nhlbi, (2020).
     Sickle Cell Disease. Also known as Sickle Cell Anemia, Hemoglobin S or SS disease, Sickling disorder due to hemoglobin S.
      Retrieved from https://www.nhlbi.nih.gov/health-topics/sickle-cell-diseaseless1 UnreadUnread6 ViewsViews

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    View profile card for Caroline Otto

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    March 18 at 10:31 PM
     by Caroline Otto

    Ihtc, (2020). 
    Sickle Cell Disease Inheritance Patterns and Trait.
     Retrieved from https://www.ihtc.org/sickle-cell-causes

                                                                                                        References

    As this sickle cell disease inheritance each parent has one hemoglobin A gene and one hemoglobin S gene, meaning each child of these parents has: a 25% chance of inheriting two normal genes (the child does not have sickle cell trait or disease).a 50% chance of inheriting one hemoglobin A gene and one hemoglobin S gene (the child has sickle cell trait).25% percent chance of inheriting two hemoglobin S genes (the child has sickle cell disease) (ihtc.2020).

    Hemoglobin SS

    Hemoglobin SD

    Hemoglobin Sβ+ thalassemia

    People who have sickle cell disease have abnormal hemoglobin, called hemoglobin S or sickle hemoglobin, in their red blood cells. Hemoglobin is a protein in red blood cells that carries oxygen throughout the body. People who have sickle cell disease inherit two abnormal hemoglobin genes, one from each parent. The types of sickle cell disease include the following:

    Sickle Cell Disease
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    Caroline Otto posted Mar 18, 2021 10:19 PM

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    Most of the patients I have encountered in my practice seek medical treatment for pain. They have pain in their joints, hip, or spine. This is because of the abnormal B-globin chain of Hb S polymers realigning and forming their sickle shape under periods of decreased oxygenation and dehydration, and they essentially clump in the joints causing acute pain. My patients usually report stress, a recent illness or heat exhaustion and causes. The other reason I see patients in my practice is because they will get called by their PCP and told to come to the ER because their hemoglobin is low. (They had gone to the Doctor for a check up and had labs drawn).PathophysiologyA Homozygous form is sickle cell anemia, and this type is the most severe, and it occurs when the patient has inherited two copies of Hb S (Lonergan, Cline, & Abbondanzo, 2020).The heterozygous carrier state rarely has clinical manifestations. All forms of sickle cell disease are lifelong conditions. It is most common among persons with ancestry from sub-Saharan Africa, although it may be present among individuals with ancestry from Mediterranean countries, the Arabian Peninsula, parts of India, and Spanish-speaking areas of South America, however these are less common.Clinical Manifestations and EtiologyThere are four types of acute crises that these patients experience.

    Vasoocclusive crisis (thrombotic crisis) sickling in the microcirculation. Vasospasm occurs due to the bunched up sickled cells that cause obstruction of the blood vessel. If not treated and reversed, infarction and thrombosis will occur. This type is very painful and may last for days and even up to weeks with the average duration of being 4-6 days. This type is unpredictable, and chronic vasoocclusion eventually results in end-stage renal disease sickle cell disease essay.

    Sequestration crisis: Typically, only seen in children less than five years of age. The spleen and liver are largely affected here due to large amounts of blood pooling. The risk of mortality is high and approximately half of children who experience sequestration crises will have recurrent episodes.

    Aplastic crisis: Profound anemia is caused by lowered erythropoiesis despite an increased need for new erythrocytes. In this condition the current life cycle is only 10-20 days, and the compensatory response in the bone marrow is compromised, and if the patient suffers a viral infection aplastic crisis develops and this crisis may last from 7 to 10 days.

    Hyperhemolytic crisis: this is rare, and it occurs in association with certain drugs or infections, and it may occur in the form of an acute or chronic reaction following a blood transfusion.

    References:Lonergan, G. J., Cline, D. B., & Abbondanzo, S. L. (2020). Sickle cell anemia. Radiographics : a review publication of the Radiological Society of North America, Inc, 21(4), 971–994. https://doi.org/10.1148/radiographics.21.4.g01jl23971more0 UnreadUnread

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    Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. Annual review of pathology, 14, 263–292. https://doi.org/10.1146/annurev-pathmechdis-012418-012838

    Huether, S. E., McCance, K.L. & Brashers, V.L. (2020). Understanding Pathophysiology 7th ed. Elsevier Mosby

    General manifestations of Sickle Cell Disease include Pallor, fatigue, jaundice, and irritability in children, also pain.

    In the US, Sickle cell anemia is most common in black people with a reported incidence of around 1:365 live births.  Interesting to note; however, its prevalence in African countries, such as Nigeria and the Democratic Republic of Congo, may be as high as 30%, and it is believed that the sickle cell trait may provide protection against lethal forms of malaria, thereby resulting in a genetic advantage for carrier who reside in regions of the world that are endemic for malaria, such as sub-Saharan Africa.

    Sickle cell-thalassemia and sickle cell-Hb C disease are compound heterozygous forms in which the child inherits Hb S from one parent and another type of abnormal hemoglobin from the other parent. A sickle cell trait occurs when the child inherits Hb S from one parent and normal hemoglobin (Hb A) from the other.

    This a group of autosomal recessive disorders characterized by the production of hemoglobin S within the erythrocytes. Hemoglobin S- Hb S; sickle hemoglobin; is formed because of a genetic mutation in which one amino acid (valine) replaces another (glutamic acid). When there is an increase in Oxygen demand, and dehydration, Hb S stretches and elongates giving rise to its formidable shape of the “sickle”. These sickled cells die early resulting in hemolytic anemia (Huether, page 551).

    Incidentally, Sickle cell patients are the ones who have had the lowest Hemoglobin’s I have ever cared for. The lowest hemoglobin I ever took care of was a 4, and because they have had multiple blood transfusions, typing and cross matching takes forever in these patients because of their Antibodies.

    Module 9 Discussion
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    Melissa Morgan posted Mar 17, 2021 8:19 PM

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    Pathophysiology. 
    Sickle cell disease (SCD) is an autosomal recessive disorder that makes the hemoglobin S sickle shaped under conditions of decreased oxygenation and dehydration (Huether, et al., 2020). The three most common sickle cell disease are sickle cell anemia, sickle cell-thalassemia disease, and sickle cell-Hb C disease sickle cell disease essay. Sickle cell anemia is the most severe out of the three and results when someone inherits two copies of Hb S, a homozygous form (Huether, et al., 2020). “Sickle cell-thalassemia and sickle cell-Hb C disease are compound heterozygous forms in which the child inherits Hb S from one parent and another type of abnormal hemoglobin from the other parent” (Huether, et al., 2020, p. 551). People who inherit Hb S from just one parent and not the other do not develop the disease and rarely show clinical manifestations (Huether, et al., 2020). Sickle cell anemia is most common in black people in the United States. According to Sundd et al., about 176,000 people die from SCD each year due to complications (2019).Aplastic crisis is presented with profound anemia that is caused by lowered erythropoiesis “despite an increased need for new erythrocytes” (Huether, et al., 2020, p. 554). This type of crisis can last 7-10 days, and usually is a result of a viral infection that has compromised the body’s ability to make new red blood cells after premature hemolysis (Huether, et al., 2020). The fourth type of crisis is hyperhemolytic crisis and may be a result of certain drugs or infections, acute or chronic reaction following a blood transfusion; this type of crisis is not usually seen in patients (Huether, et al., 2020). Many patients will initially seek medical help for a sickle cell crisis in an acute setting, however, “this initial event is the primary risk factor for potentially life-threatening complications” (Novelli & Gladwin, 2016, p. 1).Huether, S., McCance, K., and Brashers, V. (2020).  
    Understanding Pathophysiology
     (7
    th
     ed.).  ElsevierSundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
    , 
    14
    , 263–292. https://doi.org/10.1146/annurev-pathmechdis-012418-012838less0 UnreadUnread

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    Novelli, E. M., & Gladwin, M. T. (2016). Crises in Sickle Cell Disease. 
    Chest
    , 
    149
    (4), 1082–1093. https://doi.org/10.1016/j.chest.2015.12.016

    References

     Clinical manifestations. 
    Signs and symptoms of sickle cell disease can vary, because some patients have mild symptoms and others suffer from repeated vasoocclusive crises (Huether, et al., 2020). Clinical manifestations include pallor, fatigue, jaundice, and irritability (Huether, et al., 2020). This disease has four types of acute crises. Vasoocclusive crisis (thrombotic crisis) begins in the microcirculation and obstructs blood flow, which causes a vasospasm through the vessels (Huether, et al., 2020). This type of crisis is extremely painful with an average duration of 4-6 days, can last for weeks, and include complications like stroke, and end-stage renal disease (Huether, et al., 2020). Thrombosis and infarction of local tissue will occur if blood flow is not restored. The frequency of this crisis is variable and unpredictable. In Sequestration crisis is usually seen in children less than 5 years of age. The spleen and liver become saturated with blood, and because the spleen can hold one-fifth of the body’s blood supply at one time, the mortality rate is high if the patient is not treated (Huether, et al., 2020) sickle cell disease essay. About 50% of children will have recurrent episodes.

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    Candice Russell posted Mar 16, 2021 9:14 PM

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                “Sickle Cell Disease (SCD) is a group of autosomal recessive disorders characterized by the production of hemoglobin S within erythrocytes” (Linder and McCance, 2020, p. 551). About 100,000 people in the United States and millions worldwide are affected by this inherited disorder. There are many forms of SCD, the most prevalent are sickle cell anemia, sickle cell-thalassemia, and sickle cell Hb C disease. Allali et al. (2020) stated “Although the genetic and molecular bases have long been characterized, the pathophysiology remains incompletely elucidated and therapeutic options are limited” (para. 1). In documenting the pathophysiology of SCD, evidence continues to point to innate immune cells playing a significant role in promoting inflammation, adhesion, and pain in SCD (Allali et al., 2020, para. 1) Sundd et al. (2019) stated the pathophysiology of SCD “is considered to be a vicious cycle of four major processes” (para. 1). Sundd et al. (2019) described this cycle as (
    a
    ) hemoglobin S polymerization, (
    b
    ) impaired biorheology and increased adhesion-mediated vaso-occlusion, (
    c
    ) hemolysis-mediated endothelial dysfunction, and (
    d
    ) concerted activation of sterile inflammation (Toll-like receptor 4– and inflammasome-dependent innate immune pathways. The promotion of acute and chronic pain and end-stage-organ injury/failure in SCD are produced by the coordination of molecular, cellular, and biophysical processes (Sundd et al., 2019, para. 1). Linder and McCance (2020) detailed the pathophysiology of SCD, stating when oxygenated appropriately, soluble Hb S causes no issues. When the reduction of oxygen tension takes place, polymerization of abnormal beta-globin chain in Hb S produce abnormal fluid polymers (Linder and McCance, 2020, p. 553). Sickle shaped red blood cells (RBCs) form due to the flawed hemoglobin (Hb). Normal RBCs are smooth, disk-shaped, and flexible, moving through blood vessels with ease. Sickle shaped RBCs are stiff and sticky, making it difficult to move through blood vessels.            Splenic Sequestration Crisis: Reduction of oxygen tension due to decreased blood flow through the spleen and increased polymerization in Hb S, resulting in narrowing capillaries in the splenic vascular bed. Entrapment of affected blood cells and RBC polymerization leads to a cycle of hypoxia and reduced blood flow causing enlargement of the spleen (Inusa et al., 2019, para. 6.5). Pooling of blood within the liver and spleen results in shock and circulatory failure sickle cell disease essay. A rapid increase in spleen size can cause abdominal distension, sudden weakness, polydipsia, tachycardia, and tachypnea. Increased risk of mortality if this crisis is left untreated. Death can occur in 1-2 hours due to circulatory failure (Araujo, 2009, as cited by Inusa et al., 2019, para. 6.5)Hyperhemolytic Crisis: Certain drugs and infections may induce this unusual crisis (Linder and McCance, 2020, p. 555). Rapid reduction in Hb levels is a rare and dangerous complication of sickle cell disease, which can quickly lead to organ failure and death (Srinivasan & Gourishankar, 2019, para. 1). This crisis can be acute or chronic, usually preceded by a blood transfusion.Sickle cell anemia, the most severe form of SCD, occurs in 1 out of 365 African American people. Some symptoms associated with sickle cell anemia include episodic pain, swelling of hands and feet, joint and bone pain, neuropathic pain, jaundice, pallor, dizziness, fatigue, and abdominal pain. With this patient’s reported hx of symptoms, race, along with a decreased hematocrit level, it is appropriate to consider sickle cell anemia. This patient’s presentation of tachycardia may or may not be involved in sickle cell anemia, however, it is common for SCD patients to experience tachycardia. Allali, S., Maciel, T. T., Hermine, O., & de Montalembert, M. (2020). Innate immune cells, major protagonists of sickle cell disease pathophysiology. 
    Haematologica
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    (2), 273–283. https://doi.org/10.3324/haematol.2019.229989   less0 UnreadUnread

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    Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
    , 
    14
    , 263–292. https://doi.org/10.1146/annurev-pathmechdis-012418-012838

    Srinivasan, A., & Gourishankar, A. (2019). A Differential Approach to an Uncommon Case of Acute Anemia in a Child With Sickle Cell Disease. 
    Global pediatric health
    , 
    6
    , 2333794X19848674. https://doi.org/10.1177/2333794X19848674

    Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology / Sue E. Huether, Kathryn L. McCance ; section editor, Valentina L. Brashers
     (7th ed.). Elsevier.

    Reference:

    Clinical manifestations can vary in SCD, ranging from mild symptoms to repeated vasoocclusive crises.  The most common signs of SCD are associated with anemia and pain. Tiredness, fatigue, bone, and abdominal pain are present. Pain can be acute or chronic, damage to many parts of the body can occur. There is an increased risk of infections, which can be life-threatening, due to a damaged spleen. Damage to the lungs, known as acute chest syndrome, can occur due to infection or sickled cells. Other complications of SCD include stroke and priapism in males. Many other complications are noted in SCD, as it can affect many body systems and structures. SCD is present at birth, signs, and symptoms are usually not present until 6 months after birth sickle cell disease essay.

    Aplastic Crisis: In SCD erythrocyte lifespan is 10 to 20 days, leading to a significant reduction in Hb concentration. “Profound anemia is caused by lowered erythropoiesis despite increased need for new erythrocytes” (Linder and McCance, 2020, p. 554). Normal compensation of prematurely hemolyzed cells is compromised in SCD, occurring after a viral infection. “The most common cause of acquired bone marrow failure in SCD and other haemolytic disorders is caused by Parvovirus B19” (Minhas et al., 2017, as cited by Inusa et al., 2019, para. 6.3) Aplastic crisis typically last about 1 week.

                Vaso-Occlusive Crisis (Pain): Pain is considered a cardinal feature of SCD. Intense pain may be manifested in early infancy to adulthood. Pain accounts for most hospitalizations and has a significant impact on quality of life for individuals with SCD. Microcirculation of sickled RBCs obstructs blood flow through the vessels. Microvascular occlusion initiates the stimulation of nociceptive nerve fibers, causing pain. “The microcirculation is obstructed by sRBCs, thereby restricting the flow of blood” to the organ and this results in (i) ischaemia, (ii) oedema, (iii) pain, (iv) necrosis, and (v) organ damage” (De Montalembert, 2002, as cited by Inusa et al., 2019, para. 6.1). Pain is characterized as unpredictable, episodic, and spontaneous, it’s “described as one of the most excruciating forms of pain that affect human beings” (Inusa et al., 2019, para. 6.1).

    A. Kaur
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    Amandeep Kaur posted Mar 15, 2021 2:13 PM

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    Sickle cell disease is a chronic disorder of red blood cells (Vacca Jr.& Blank, 2017). It causes an abnormal production of hemoglobin, which is responsible for carrying oxygen. Due to the inability of the hemoglobin to carry oxygen pH becomes acidic. The RBS will also lose its normal round, pliable, biconcave shape. Intracellular changes cause the RBC to become deformed, rigid, and crescent-shaped. The RBC begins to adhere to different areas vessels of the body and can accumulate, causing increased blood viscosity. Manifestations include anemia due to cells easily breaking apart and dying (Sickle cell anemia, 2020). Individuals can also have episodes of pain, this is due to blocked blood flow through the tiny vessels of the chest, abdomen, and joints. Other symptoms include swelling of hands and feet, frequent infections, delayed growth or puberty, and issues with vision. These symptoms are consistent with the patient’s symptoms. This disease is an inherited disease, specifically, it is autosomal recessive (Sundd et al., 2019). This means both parents would need to at least be carriers of the disease for the children to have it. It is more prevelent among individuals of African American descent sickle cell disease essay.  References Sickle cell anemia. (2020, January 30). Retrieved March 15, 2021, from https://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/symptoms-causes/syc-20355876Sundd, P., Gladwin, M. T., & Novelli, E. M. (2019). Pathophysiology of Sickle Cell Disease. 
    Annual review of pathology
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    View profile card for Cassie Fritzinger

    Last post 
    March 16 at 10:59 AM
     by Cassie Fritzinger

    Vacca Jr., V. M., & Blank, L. (2017). Sickle cell disease: Where are we now? 
    Nursing
    , 
    47
    (4), 26–35.

    Fritzinger, Discussion wk 9
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    Cassie Fritzinger posted Mar 12, 2021 3:11 PM

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          Sickle Cell Disease (SCD) is an inherited disease which needs to be passed down from both parents. If there is only one genetic mutation the patient is considered to have ‘sickle cell trait’ and is generally healthy. The person with both genetic mutations will display the sickle cell phenotype. The incidence of SCD is approximately 100,000 Americans have SCD, and it is more often seen in Blank/African Americans with 1 in every 365 births having SCD and 1 in every 13 having the trait (NIH, 2020).      Symptoms often seen in patients with SCD include jaundice or sclera icterus from a significant amount of red cell hemolysis. The patient will also most likely experience fatigue from the significant anemia associated with SCD. SCD patients may also display painful swelling of their hands and feet from blood flow being blocked inside small bones in the hands and feet (NIH, 2020).  Triggers which can exacerbate a sickle cell crisis include extremes of temperature (or rapid change in temperature) dehydration, stress, & venous stasis such as that when hospitalized or bedbound (Espinoza, 2020).      Sickle cell disease patient’s can be often complex to treat. They will often require higher doses of pain medications than the non-SCD patient. Sickle cell pain crisis often last an average of 4-6 days or longer without proper treatment. For our patient of discussion, she was hospitalized for an arthroscopic knee surgery, she is already starting low with the hematocrit percentage of 25%, her blood pressure may be elevated due to pain or other physiologic reasons such as compensation for low blood volume. Further, her heart rate is also high noting the same cause potential. Abdominal pain would make one suspicious for concerns in the liver/spleen. While our discussion does not say if we are treating this patient pre-operatively or post-operatively, it would be important to optimize the patient’s pre/post op oxygenation, hydration, normothermia, positioning, and of course pre/postop anxiolytic use to decrease the chances of further crisis developing from these triggers sickle cell disease essay.

    Increase ambient temperature in the OR maintain thermoregulation with warm forced air blankets over the body wherever possible.

    500ml bolus of Lactated Ringers followed by 8ml/kg/hr maintenance

    Padding with warm blankets to decrease venous stasis and loss of thermoregulation through conduction.

    Preoxygenate and avoid a traumatic intubation to decrease any chance of hypoxic episode

    Administer Dexamethasone and Cefazolin for inflammation and decreased risk of infection/illness post operatively

    Administer anxiolytic medication as appropriate to help the patient relax prior to surgery

    Maintain adequate pain control

    Post op treatments would be similar to ensure the patient maintains adequate hydration, pain control, thermoregulation, and limits venous stasis. In 2019 the FDA approved Voxelotor a medication for SCD which prevents red blood cells from binding and changing to sickle shape. They will also decrease the destruction of blood cells decreasing the risk of anemia and improving overall blood flow to end organs. An IV medication Crizanlizumab-tmca can also be given with similar results (NIH, 2020). The common treatment of Hydroxyurea has shown to reduce and prevent sick cell complications by inhibiting DNA synthesis as well as providing an anti-inflammatory effect through decreased leukocyte production.           Espinoza, C. (2020). Perioperative Management for Sickle Cell Disease: Efficacy of Recommendations. International Student Journal of Nurse Anesthesia, 19(3), 46–49.NIH (2020). Sickle Cell Disease. National Heart, Lung, and Blood Institute. Retrieved March 12, 2021 from https://www.nhlbi.nih.gov/health-topics/sickle-cell-disease

    Zazzman, S. M., Zamora, F. J., & Roberts, J. D. (2019). Inpatient pain management in sickle cell disease. American Society of Health System Pharmacists. 76 (23) 1965-1971. 10.1093/ajhp/zxz228

    Heuther, S. E., McCance, K. L., & Brashers, V. L. (2020). Understanding Pathophysiology (7th ed.). Elsevier.

    References

          Inpatient management for the patient with SCD includes adequate pain management up to and including intravenous or parenteral patient-controlled analgesia (PCA). However it is important to transition the patient to oral products to ensure adequate pain control once discharged from the hospital. Zassman, Zamora, & Roberts (2019), provides a tier approach to transitioning the patient to oral agents. While there are multifactorial considerations in choosing agents to transition, it is important to do an appropriate 24-hour capture of the parenteral medication which is effective for patient pain control sickle cell disease essay. Next is to choose a short-acting oral agent (something they can be discharged home on) and convert the parenteral 24 total dose into a equivalent 24 hour oral medication dose. It would also be important to consider decreasing this dose by 25%-50% for incomplete cross-tolerance. This 24 hour dose should then be divided appropriately throughout the day dosing (Zassman, Zamora, & Roberts 2019).

    Espinoza (2020), recommends the following Pre/Intraoperative treatments

          Significant complications which can occur in SCD include sequestration crisis, aplastic crisis, and hyperhemolytic crisis.  Sequestration crisis (typically seen in children) is when the patient’s blood gets stuck within the liver & spleen. Because a large volume percentage of the patient’s blood can be held within the spleen there is not enough circulating blood placing the patient at significant risk of mortality if not recognized and treated early (Heuther, McCance, & Brasher, 2020). Aplastic crisis generally caused from parvovirus B19 (fifth disease) can cause bone marrow suppression of blood production leading to worsening/severe anemia (NIH, 2020). Hyperhemolytic crisis while rare is a condition of SCD when there is a significant amount of hemoglobin lysis/loss which can be caused from certain medications, infections and occasionally blood transfusion reactions. This creates a significant anemia which can lead to death from decreased organ perfusion (Heuther, McCance, & Brasher, 2020).

          Every state within the District of Columbia, United States and US territories require prenatal and newborn screening for SCD. For this reason parents are often aware of their child having SCD at a very young age and can manage their condition better (NIH, 2020). Our patient in discussion would most likely have known she had SCD by the age of 38, unless she was lucky enough to never have any sickle cell crisis and was not previously evaluated by a medical professional who may have suspected SCD. A sickle cell crisis is also known as a vasoocclusive crisis. This generally begins when sickle cell shaped red blood cell enter the host microcirculation subsequently causing vasospasm and blockage of the vessel. When this is not reversed it will lead to ischemia or infarction of the local tissue. The red blood cells take this sickle shape in SCD secondary to a genetic mutation when amino acids are altered. Under decreased oxygen and dehydration conditions the cell stretches and elongates assuming the sickle cell shape (Heuther, McCance, & Brasher, 2020) sickle cell disease essay.

  • Transcultural Nursing – Cultural Competence in the Health History and Physical Examination

    Transcultural Nursing – Cultural Competence in the Health History and Physical Examination

    Introduction

    As the dynamics of our world are continually changing and becoming more multicultural, healthcare providers are facing a challenge in providing cultural competent care to this multicultural population. Dr. Madeleine M. Leininger was the first to use the term “transcultural nursing” (TCN) in describing the blending of anthropology and nursing into a specialization in nursing. Anthropology is the scientific study of humans, past and present. Building on the physical, biological, social sciences and humanities, anthropologists use this knowledge to find solutions to human problems. Using the combined studies of nursing and anthropology, Dr. Leininger established TCN as a theory and evidence-based formal area of study and practice within nursing that focuses on people’s culturally based beliefs, attitudes, values, behaviors, and practices related to health, illness, healing and human caring (Leininger, 1991, 1995) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Learning objectives for the module
    :

    Upon completion of the module, students will be able to:

    Define transcultural nursing.

    Discuss the contributions of transcultural theories to the advancement of transcultural study and practice.

    Explore the national standards for culturally and linguistically appropriate services in healthcare.

    Compare individual advanced practice cultural competence and organizational cultural competence.

    Readings:

    Andrews & Boyle, J. Chapters 1,2

    Websites:

    The Model of Cultural Competence Through an Evolutionary Concept Analysis: 
    http://tcn.sagepub.com/content/15/2/93.full.pdf+html

    Communication Between Cultures: 

    Topic 1: Theories of Transcultural Nursing

    For over 50 years nurses have recognized the necessity to provide culturally specific care to a population that is increasingly becoming more racially and culturally diverse. Based on the knowledge that various races and cultures have different needs and requirements the need to develop culturally competent nursing care continues. In order to provide nurses with the foundations to be knowledgeable about the various cultures being seen in their practices transcultural models have been developed. Perhaps the most notable theorist, Dr.Madeline Leininger has provided the basic foundation for cultural competency in nursing practice. Other models by Purnell, and Giger and Davidhizer are also commonly used nursing cultural models Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Using any of these models allows nurses at all levels to gain knowledge and provide culturally competent care. Having a greater nursing knowledge of the culturally diverse needs of our patients is vital in improving the quality of healthcare.

    Topic 2: Culturally Competent Nursing Care

    In order for the nurse to begin the process of becoming a culturally competent provider, one must start with cultural self-assessment. Evaluation of their own unconscious biases, cultural stereotypes, prejudices, and tendencies to discriminate against those different than themselves will give them valuable insight. With increased study and education, these unconscious tendencies can be resolved. To aid in the educational process, the American Academy of Nursing (AAN) Expert Panel on Global Nursing and Health and Transcultural Nursing Society have developed guidelines for the practice of culturally competent nursing care. These include knowledge of cultures, education and training in culturally competent care, clinical reelection. Cross-cultural communication, culturally competent practice, cultural competence in health care systems and organizations, patient advocacy and empowerment, multicultural workforce, cross-cultural leadership, evidence-based practice and research. As universally accepted guidelines nurses worldwide have a framework for providing culturally competent care Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    A five step problem solving process is provide to assist nurses in delivering culturally competent care. This five step process consists of

    a constructively critical self-assessment

    mutual goal setting with the client and other members of the health care team

    development of a plan of care

    implementation of the care plan

    evaluation of the plan.

    Discuss It

     

     

    Module 2

    Discussion

    The culture of the deaf and hearing impaired is often overlooked because it is characterized as a nonethnic culture.  What cultural characteristics do deaf people have in common with other cultural groups? If your client is both deaf and identifies with another cultural group as well, how does this affect your ability to provide quality cultural care?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight.  Both responses should be a minimum of 150 words, scholarly written, APA formatted, and referenced.  A minimum of 2 references are required (other than your text) for both posts.  Refer to the Grading Rubric for Online Discussion in the Course Resource section.

    Module 2: Discussion

    Special Guidance on APA formatting in Discussion Posts

    APA formatting is required in discussion posts with the following two exceptions (due to limitations with the text editor in LIVE):  
    double line space and indent 1/2 inch from the left margin
    . Discussion posts will NOT be evaluated on those two formatting requirements he Health History and Physical Examination. All other APA formatting guidelines should be followed. For example, in-text citations must be formatted with the appropriate information and in the correct sequence (Author, year), reference list entries must include all appropriate information following  guidelines for capitalization, italics, and be in the correct sequence. Refer to the APA Publication Manual 7th ed. for each source type’s specific requirements. Please let your instructor know if you have any questions.

    Module 2: Discussion

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    The culture of the deaf and hard of hearing is often overlooked because it is characterized as a nonethnic culture.  What cultural characteristics do deaf people have in common with other cultural groups? If your client is both deaf and identifies with another cultural group as well, how does this affect your ability to provide quality cultural care?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight.  Both responses should be a minimum of 150 words, scholarly written, APA formatted, and referenced.  A minimum of 2 references are required (other than your text) for both posts.  Refer to the Grading Rubric for Online Discussion in the Course Resource section.

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    Understanding the nuances of the patients culture as well as understanding the communication techniques for the Deaf culture is vital for providing competent care and a responsibility of the health care provider.  Collaboration within our healthcare community may be key! Well done!

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    Module 2 Discussion
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    Jerrica Goins posted Sep 8, 2021 9:18 PM

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    Individuals who are involved in or affiliated with the Deaf culture do not view deaf or the use of signed language as a disability. Diversity within the Deaf community must be considered and awareness of factors such as racial background, hearing status, and communication mode fall under the broader identity of being deaf. Understanding Deaf culture and learning about ASL are essential to building rapport and strengthening the therapeutic alliance (Boness, 2016). However, not all Deaf persons identify within this community. When a client identifies with another cultural group it is imperative to have a basic understanding of the culture they identify with. View the patient as an individual and find out their cultural preferences. The approach to them receiving care and treatment may need to be altered, to provide culturally competent care. For instance, there may be a patient who is deaf and is a member of the LGBTQ community. The provider needs to understand the population’s history, unique health concerns, risks, and develop communication skills that avoid discrimination, and provide compassionate care. Health professionals should be aware that the LGBTQ population experiences higher rates of challenges due to discrimination, social pressures, sexual behaviors, and less healthcare access (Bass & Nagy, 2020).Bass, B., & Nagy, H. (2020). 
    Cultural Competence in the Care of LGBTQ Patients
    . PubMed; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK563176/less1 UnreadUnread2 ViewsViews

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    View profile card for Kadijatu Sesay

    Last post 
    September 12 at 9:30 PM
     by Kadijatu Sesay

    Boness, C. L. (2016). Treatment of Deaf Clients: Ethical Considerations for Professionals in Psychology. 
    Ethics & Behavior
    , 
    26
    (7), 562–585. https://doi.org/10.1080/10508422.2015.1084929

    References

    Module 2 DP – H. Stetson
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    Heather Stetson posted Sep 6, 2021 6:26 PM

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    Historically, those afflicted with deafness or hard of hearing have been labeled as persons suffering from a disability. However, labeling an individual with a disability indicates there is an issue with deafness or being hard of hearing that needs to be “fixed” (Mauldin & Fannon, 2021). Many people who are deaf or hard of hearing do not feel as if they are disabled, but rather as individuals with their own unique cultural identity (Higgins, 2016). Characteristics the deaf and hard of hearing people have with other cultures include a common communication style (language/dialect), identity, and a shared heritage (Andrews et al., 2020). According to Mauldin and Fannon (2021), “People who are deaf and use ASL to communicate belong to a linguistic minority group in the United States and have historically identified as capital-D Deaf; the convention has largely been to use lower case deaf to describe an audiological status and a capital-D to denote cultural membership in a signing community” (p.4). If the client is both deaf and also identifies with another cultural group this added layer simply means the practitioner will need to be that much more vigilant in providing culturally competent care. The five steps for providing culturally competent and congruent care include self-assessment, mutual goal setting, care planning, implementation of care plan, and evaluation of care (Andrews et al., 2020).  less1 UnreadUnread2 ViewsViews

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    View profile card for Idida Aleman Musial

    Last post 
    September 12 at 8:08 PM
     by Idida Aleman Musial

    Mauldin, L., & Fannon, T. (2021). They told me my name: Developing a deaf identity. 
    Symbolic Interaction, 44
    (2), 339-366. 
    https://doi.org/10.1002/symb.482

    Higgins, M., & Lieberman, A. M. (2016). Deaf students as a linguistic and cultural minority: Shifting perspectives and implications for teaching and learning. 
    Journal of Education (Boston, Mass.), 196
    (1), 9-18. 
    https://doi.org/10.1177/002205741619600103

    Andrews, M., Boyle, J. & Collins, J. (2020). 
    Transcultural concepts in nursing care
     (8th ed.). Wolters Kluwer.

    Kadijatu Sesay
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    Kadijatu Sesay posted Sep 8, 2021 10:50 PM

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    Deaf and hearing-impaired people face multi challenges that evolve around isolation, neglect, and deprivation of essential social services that affect their welfare and survival. They are often isolated in the community because they are presumed different from everyone else, (Mugeere et al., 2016). In every culture, one will find people who are deaf or hearing impaired. The cultural characteristic deaf people have in common with other cultural groups is that many deaf people are born to hearing parents. More so, deaf or hearing impaired can be found in any culture regardless of race, ethnicity, social-economic status, or education Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. Deaf people maintain intimate relationships using facial expressions, touch, sign language, eye contact which are like other cultural groups, (Mugeere et al., 2016). ReferencesMugeere, A., Atekyereza, P. R., Kirumira, E. K., & Hojer, S. (2016, May 26). 
    Deaf identities in a multicultural setting: The Ugandan context
    . African journal of disability. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5433488/
    . less1 UnreadUnread5 ViewsViews

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    View profile card for Jerrica Goins

    Last post 
    September 12 at 8:05 PM
     by Jerrica Goins

    Marschark, M., Zettler, I., & Dammeyer, J. (2017, July 1). 
    Social dominance orientation, language orientation, and deaf identity
    . Journal of deaf studies and deaf education. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881267/
    .

    If my client is both deaf and identifies with another cultural group, this will affect my ability to provide quality care in the sense that it might be difficult to communicate or provide an interpreter in the new culture since different cultures have different variations in their mode of communication and identity expression, (Marschark et al., 2017).

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    Gisselle Mustiga posted Sep 6, 2021 12:29 AM

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    The topic of whether deafness should be viewed as a culture or not is of debate. Deafness has always been seen as a physical impairment that is associated with cognitive and blindness disabilities. Recently, views of deafness as a culture have been raised, considering the condition as a trait and not disability. This is because deafness does not need to be corrected; it is not a pathology (Chovaz, 2016). The deaf and the hearing cultures have various common factors which influence communication with each other. One of them is that deaf people go to churches and attend school for the deaf, just like hearing people who also go to school and attend churches to attain education and religious purposes (Giger & Haddad, 2020). Moreover, both hearing and deaf people use the English language; the only difference is how they communicate it. 
    References
    Chovaz, C. J. (2016). The Differences in our similarities.
     
    The Journal of Deaf Studies and Deaf Education
    , 16(3). 416.  https://doi.org/10.1093/deafed/enr002 less1 UnreadUnread5 Views ViewsTranscultural Nursing – Cultural Competence in the Health History and Physical Examination

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    View profile card for Emilia Rodriguez

    Last post 
    September 12 at 4:17 PM
     by Emilia Rodriguez

    Giger, J. N., & Haddad, L. (2020). Transcultural nursing-e-book
    : Assessment and Intervention
    . Elsevier Health Sciences.

    Andrews, M., Boyle, J., & Collins, J.W. (2020). 
    Transcultural concepts in nursing care
     (8th ed.). Wolters Kluwer

    If my client is deaf and identifies themselves with a particular cultural group, this will significantly influence how I will give quality and holistic care. This is because all cultural preferences of the patients must be respected while providing care. Providing quality care to clients that are deaf raises essential ethical consideration in relation to competency, assessment, confidentiality, evaluation, and diagnosis (Andrews et al., 2020). The nurse must therefore consider the relevant ethic codes that are required in providing treatment that is ethical. This is because the nurse is responsible for ensuring that the patient or client is comfortable and satisfied with healthcare services. Thus, all healthcare services providers must maintain a professional relationship with the client while also offering care in line with their culture and beliefs (Andrews et al., 2020).

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    Julie Robichaud posted Sep 8, 2021 7:48 AM

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              The deaf and hearing impaired are considered a nonethnic culture, but can be linked to another culture and become a double minority such as a Russian patient who is also deaf (Andrews et al., 2020). Deaf patients have many of the same characteristics as other cultural groups which include, decreased comprehension due to a language barrier, decreased psychosocial well-being due to difficulty with social and interpersonal skills, economic dependence due to perceived disability, and decreased quality of life due to unnecessary limitations sometimes placed by healthcare providers (Andrews et al., 2020) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. Caring for a patient that is deaf or hearing impaired and also identifies with another cultural group, may require more help or interventions. All cultures, ethnic and nonethnic, have different needs that have to be taken into consideration. Cultural respect combines a body of knowledge, beliefs, and behaviors that are specific to ethnic, nonethnic, racial, religious, geographic, and social groups (NIH, 2017). Cultural respect ensures reduction in health disparities and improves access to quality and safe healthcare that is respectful and responsive to culturally diverse patients (NIH, 2017). Andrews, M.M., Boyle, J.S. & Collins, J.W. (2020). 
    Transcultural concepts in nursing care 
    (8th ed.). Wolters KluwerNational Institutes of Health. (2017, February 15). 
    Cultural respect. 
    https://www.nih.gov/institutes-nih/nih-office-director/office-communications-public-liason/clear-communication/cultural-respect
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    View profile card for Laura Riccardi

    Last post 
    September 11 at 1:07 PM
     by Laura Riccardi

    Ohta, G. (2015). National standards for culturally and linguistically appropriate services (CLAS) in health and health care. 
    Hawaii Journal of Medicine and Public Health, 74(7), 
    p.12.

    Barksdale, C.L., Rodick, W.H., Hopson, R., Kenyon, J., Green, K. & Jacobs, C.G. (2016). Literature review of the National CLAS Standards: Policy and practical implications in reducing health disparities Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. J
    ournal of Racial and Ethnic Health Disparities, 4(4). 
    https://doi.org/10.1007/s40615-016-0267-3

              The National CLAS Standards can be used to provide quality cultured care for patients with one diverse culture or those who belong to more than one cultural group. It is a great tool to improve cultural respect, competence, and healthcare service. The fifteen standards address governance, leadership, and workforce; communication and language assistance; and engagement, continuous improvement, and accountability (Ohta, 2015). There can be gaps in knowledge and communication between a provider and a patient who share the same race or ethnicity, which suggests that there is a need for a standard of care for appropriate cultural and linguistic competency training at least annually for all healthcare providers (Barksdale et al., 2016). This would improve culture competency, health services, and patient satisfaction.

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    Emilia Rodriguez posted Sep 8, 2021 11:19 PM

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    Deaf Culture
    Notably, deaf individuals typically identify with different cultures and cultural groups in addition to deaf culture. This is best exemplified by the case of deaf individuals with ethnic or racial minority backgrounds. Such intersections are consequential for the healthcare providers’ delivery of culturally competent care because of two principal reasons (Hill et al., 2020). Firstly, the overlap necessitates broadened comprehension of the sociocultural determinants of effective care delivery, given that such understanding must encompass both the sociocultural determinants of deafness and of the additional cultural dimensions and characteristics. For example, the provider must comprehend both the sociocultural aspects of deafness and of the Hispanic culture in the context of healthcare delivery when interacting with a deaf service user who also identifies with the Hispanic ethnic culture. Additionally, the overlap affects the ability to provide quality cultural care because it expands the domains of context-specific cultural competencies requisite for the effective case management.Englerth, K., Dennis, C., & Scott, S. (2020). Looking for the signs: OTs’ experiences with deaf culture. 
    American Journal of Occupational Therapy
    , 
    74
    (4_Supplement_1), 7411510311p1-7411510311p1. https://doi.org/10.5014/ajot.2020.74S1-PO7321Leigh, I. W., Andrews, J. F., Harris, R. L., & Ávila, T. G. (2020). 
    Deaf culture: Exploring deaf communities in the United States
    . Plural Publishing.less1 UnreadUnread1 ViewsViews

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    View profile card for Jeffrey Mahoney

    Last post 
    September 11 at 12:53 PM
     by Jeffrey Mahoney

    Hill, C., Deville, C., Alcorn, S., Kiess, A., Viswanathan, A., & Page, B. (2020). Assessing and providing culturally competent care in radiation oncology for deaf cancer patients. 
    Advances in radiation oncology
    , 
    5
    (3), 333–344. https://doi.org/10.1016/j.adro.2020.02.007

    References

    Deaf culture refers the set of values, social beliefs, shared community institutions, literary traditions, art, and other cultural aspects that both influence deafness and also utilize sign language as the primary mode of communication. While deaf culture is characterized by unique and distinctive components it also has several cultural characteristics in common with other cultural groups including hearing culture and other ethnic and non-ethnic cultures (Englerth et al., 2020). Three areas of similarity, in this regard, include the feeling of community, behavioral norms, and social structure. Regarding social structure, deaf culture like all ethnic cultural groups is for instance characterized by the existence of a leadership structure that is felt to embody the unique characteristics of the entire group (Leigh et al., 2020). Self-recognition and recognition by others is also a central feature of the feeling of community within deaf culture as it is in other cultural groups (Hill et al., 2020). Behavioral norms governing different aspects of life such as decision-making and consensus-building also characterize deaf culture as they do all other cultural groups Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

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    Frances Hall posted Sep 8, 2021 8:26 AM

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    Hearing loss is a major source of disability in adults, associated with serious communication and psychosocial problems and high health care costs, with economic implications at the societal and individual levels (Cunningham & Tucci, 2017). On a global level, hearing loss is the most prevalent disabling condition; however, lack of trained hearing health professionals and limited access to assistive technology restricts access to hearing health-care services (Ingram et al., 2016). The primary effect of adult hearing loss is impaired communication, which can adversely affect relationships with family and friends and create difficulties in the workplace. Untreated hearing loss in adults also has indirect health, psychosocial, and economic effects and leads to social isolation and a reduced quality of life (Cunningham & Tucci, 2017). I would think the inability to communicate weather it’s talking or speaking another language, and not having the ability to be understood correctly is something all cultural groups have in common. People with hearing loss described various negative emotions in response to hearing loss, including depression, sadness, desperation, frustration, shame, and embarrassment. These feelings were largely related to others’ reactions to their inability to hear (Ingram et al., 2016). ReferencesCunningham, L. L., & Tucci, D. L. (2017). Hearing loss in adults. 
    New England Journal of Medicine
    , 
    377
    (25), 2465–2473. 
    https://doi.org/10.1056/nejmra1616601
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    View profile card for Francesca Provencher

    Last post 
    September 11 at 12:31 PM
     by Francesca Provencher

    Ingram, M., Marrone, N., Sanchez, D., Sander, A., Navarro, C., de Zapien, J., Colina, S., & Harris, F. (2016). Addressing hearing health care disparities among older adults in a us-mexico border community. 
    Frontiers in Public Health
    , 
    4
    . 
    https://doi.org/10.3389/fpubh.2016.00169

    Brooks, L. A., Manias, E., & Bloomer, M. J. (2019). Culturally sensitive communication in healthcare: A concept analysis. 
    Collegian
    , 
    26
    (3), 383–391. 
    https://doi.org/10.1016/j.colegn.2018.09.007

     Three major uses of culturally sensitive communication were identified, including understanding one’s own culture, open and sensitive communication, and strategies to collaborate with the patient and family for optimal patient care (Brooks et al., 2019). Knowing that most of the stress of being deaf are the reactions people have toward them not being able to hear makes it so important for us as practitioners to be aware of this to provide compassionate care.

    Module 2:Discussion
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    Idida Aleman Musial posted Sep 8, 2021 9:00 PM

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     The Transcultural Interprofessional Practice (TIP) model by Andrews/Boyle is comprised five essential components in nursing care (Andrews & Boyle, 2019). Performing a self-assessment, collaborative goal setting with the family and the patient, developing, implementing and evaluating a plan of care are the five essential components of competent and culturally congruent nursing care. Implementing these aspects into clinical practice will improve the current nursing care culture. TIP promotes cultural congruent nursing care that is affordable, accessible, and based on evidence-based practice.      more2 UnreadUnread3 ViewsViews

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    View profile card for Donna Wrobel

    Last post 
    September 10 at 6:35 PM
     by Donna Wrobel

    Young, J., Jerolimov, D., & Ofner, S. (2021). Promoting nursing students’ transcultural self‐efficacy to care for burmese refugees using a set of educational strategies. Nursing Forum (Hillsdale), 56(2), 460-466. 
    https://doi.org/10.1111/nuf.12541

    Wehbe-Alamah, H., McFarland, M., Andrews, M., & Lograsso, S. (2021;2019;). An ethnohistory of the transcultural nursing scholars and their contributions to the field. Journal of Transcultural Nursing, 32(1), 50-58. 
    https://doi.org/10.1177/1043659619892671

    Andrews, M. M., & Boyle, J. S. (2019). The Andrews/Boyle transcultural interprofessional practice (TIP) model. Journal of Transcultural Nursing, 30(4), 323-330. 
    https://doi.org/10.1177/1043659619849475

    Andrews, M., Boyle, J., & Collins, J.W. (2020). Transcultural concepts in nursing care (p.47, 8th ed.). Wolters Kluwer

    Reference:

    Providing care to individuals with special needs can be challenging for nurses, especially when one is not prepared. According to Andrews and Boyle, a deaf individual might self-identify with nonethnic cultures. Communication becomes a challenge when providing care to an individual that also comes from a subculture (Wehbe-Alamah, et al. 2021;2019). In order to be prepared for these types of challenges, preparation should start in nursing school. Nursing instructors and nurses can also promote culturally congruent care for deaf patients by teaching nursing students the importance of competent care for all individuals. Therefore, nursing students will benefit from knowledge on transcultural care for individuals of different backgrounds (Young, et al. 2020) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Impaired communication places clients with special needs at a higher risk for health disparities and inequities. The inability to communicate needs to the healthcare provider can become a barrier. This is a one common element that a deaf, or hard of hearing, individual has in common with members of other cultural groups.

    Module 2 – Francesca Provencher
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    Francesca Provencher posted Sep 8, 2021 6:26 PM

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              Taking care of a deaf patient has similarities to taking care of a patient from a different culture. It is important that when taking care of a patient that cannot hear their healthcare providers have appropriate resources to communicate with them. Clear communication can be one of the most crucial tools when it comes to diagnosing, treating, and educating a patient. The literature states, communication barriers between healthcare providers and patients contribute to health disparities which is particularly true concerning communication between providers and deaf patients. This is caused due to lack of understanding of cultural and linguistic differences, ineffectiveness of various means of communication and level of health literacy within that population (Hommes et al., 2018). Sirch, L., Salvador, L., & Palese, A. (2017). Communication difficulties experienced by deaf male patients during their in-hospital stay: findings from a qualitative descriptive study. 
    Scandinavian Journal of Caring Sciences
    , 
    31
    (2), 368–377. 
    https://doi-org.wilkes.idm.oclc.org/10.1111/scs.12356
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    View profile card for James Neal

    Last post 
    September 10 at 6:19 PM
     by James Neal

    Hommes, R. E., Borash, A. I., Hartwig, K., & Degracia, D. (2018). American Sign Language Interpreters Perceptions of Barriers to Healthcare Communication in Deaf and Hard of Hearing Patients. 
    Journal of Community Health
    , 
    43
    (5), 956–961. 
    https://doi-org.wilkes.idm.oclc.org/10.1007/s10900-018-0511-3

              The research shows communicating strategies, include, sign language and oralism which have always been the two main methods of approach to language for deaf people (Sirch et al., 2017). Sign language is the normal form of communication for a deaf person and articulates the awareness and familiarities of their culture. According to the author “sign language is self-contained and has its own syntax, grammar, and semantics, which are different from spoken and written languages” (Sirch et al., 2017, p. 368). On our unit we utilize a variety of different tools to communicate with deaf patients, this includes interpreters that use American Sign Language (ASL) that come in person to the hospital along with an iPad that we can type ASL in and an interpreter comes on the screen. A deaf patient may also be proficient in lip reading so a provider would always have to make sure they were patient facing when providing information Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Module 2 Discussion – Jahenein Nagel

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    Jahenein Nagel posted Sep 6, 2021 6:58 PM

    Discrimination and prejudice remain uncomfortably common in the world. These attitudes are most obviously encountered between majority and minority groups with regard to religion, gender, race, ethnicity, and disability (Marschark et al., 2017). Prejudice and discrimination often involve one (majority) group seeking social dominance over another (minority) group (Marschark et al., 2017)         Clason (2019) asserts that practitioners must be aware of how factors such as racial background, hearing status, and communication mode fall under the broader identity of being Deaf. The following guidelines are important tips to remember when communicating with the Deaf: (a) acknowledge the fact that your first attempts to communicate will feel awkward and uncomfortable; (b) it is acceptable to use paper and pen; (c) take the time to communicate and connect; (d) understand that deaf people listen with their eyes so only speak when you have eye contact, even if they are using an interpreter; (e) use the beginning and ending of a conversation as an opportunity to make physical and visual contact with the deaf person, especially if they have been using an interpreter during your conversation and make eye contact; (f) Recognize that Deaf clients may benefit from a counseling approach that is visual, tactile, or expressive (Clason, 2019).Clason, D. (2019, December 24). 
    The importance of deaf culture
    . Healthy Hearing. 
    https://www.healthyhearing.com/report/52285-The-importance-of-deaf-culture
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    View profile card for Gisselle Mustiga

    Last post 
    September 10 at 6:19 PM
     by Gisselle Mustiga

    Marschark, M., Ettler, I., & Dammeyer, J. (2017, May 30). 
    Social dominance orientation, language orientation, and deaf identity
    . NCBI. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881267/#enx018C2

    References

    Some Deaf individuals view themselves not as disabled, but as a member of a linguistic-cultural minority identified, most centrally, by their use of sign language (Marschark et al., 2017). According to Marschark et al. (2017), Deaf cultural identity is not a function of hearing status alone, but includes internalization of values and beliefs with regard to affiliation with the deaf community, language modality, and social networks. Deaf culture is the set of social beliefs, behaviors, art, literary traditions, history, values, and shared institutions of communities that are influenced by 
    deafness
     and which use 
    sign languages
     as the main means of communication (Marschark et al., 2017). When used as a cultural label especially within the culture, the word 
    deaf
     is often written with a capital 
    D
    and referred to as “big D Deaf” in speech and sign (Clason, 2019) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. When used as a label for the 
    audiological
     condition, it is written with a lower case
     d 
    (Clason, 2019).

    Jeff Mahoney
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    Jeffrey Mahoney posted Sep 6, 2021 12:59 PM

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    According to Andrews et al. (2020), healthcare providers often group the culture of the deaf in with the disabled. However, from an emic perspective, the deaf often see themselves as well, whole, and non-impaired – identifying with a linguistic minority versus a culture of disability (Andrews et al., 2020).With the knowledge that a patient may identify with the culture of the deaf and another cultural group, it may be helpful to assess which other cultural group to determine the level of acculturation that person has experienced. Those that identify with the culture of the deaf on average have a sixth grade reading level proficiency, further supporting the need for an interpreter for health education (Sirch et al., 2017; Hubbard et al., 2018). Similarly, the health literacy of the Deaf is 6.9 times more likely to be inadequate – suggestive of meager education rather than intelligence (Hubbard et al., 2018). What other ways have you discovered to provide culturally competent care to this group?ReferencesHubbard, L. J., D’Andrea, E., & Carman, L. A. (2018). Promoting best practice for perinatal care of deaf women.
     Nursing for Women’s Health, 22
    (2), 126-136. https://doi.org/10.1016/j.nwh.2018.02.002 less1 UnreadUnread2 ViewsViews

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    View profile card for Karimah Moss

    Last post 
    September 10 at 12:40 PM
     by Karimah Moss

    Sirch, L., Salvador, L., & Palese, A. (2017). Communication difficulties experienced by deaf male patients during their in‐hospital stay: Findings from a qualitative descriptive study.
     Scandinavian Journal of Caring Sciences, 31
    (2), 368-377. https://doi.org/10.1111/scs.12356

    Andrews, M., Boyle, J., & Collins, J.W. (2020). 
    Transcultural concepts in nursing care
     (8th ed.). Wolters Kluwer.

    .

                 From this emic viewpoint, the culture of the deaf relate more so to patients that speak a foreign language. As such, a culturally competent nurse must first learning the patient’s perspective on their status (Hubbard et al., 2018). The nurse should be asking the following question: Does the patient identify with Deaf culture, or did they simply develop deafness later in life? The nurse would also benefit from learning which form of sign language that person is fluent in such as American sign language or Italian Sign Language (Hubbard et al., 2018).

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    Evelyn Anderson posted Sep 8, 2021 10:16 PM

    Contains unread posts Transcultural Nursing – Cultural Competence in the Health History and Physical Examination

    One cultural characteristic that the deaf have in common with cultural groups is the language they use. Language can be a defining aspect of an individual’s culture. According to Krasniqi
     
    (2019), language and culture are supportive to each other in many situations, and they reflect many different aspects of the culture. They complement each other through words, attitudes, gestures and behavior (Krasniqi, 2019). Deaf communities consider themselves a linguistic minority using sign language as their identified form of language (Higgins & Lieberman 2016). In addition to the language of sign they use, deaf people consider themselves part of a cultural group connected through experiences and cultural practices and traditions (Higgins & Lieberman, 2016). Cultural practices and traditions are also defining aspects of many cultures.    Higgins, M., & Lieberman, A. M. (2016). Deaf Students as a Linguistic and Cultural Minority: Shifting Perspectives and Implications for Teaching and Learning. 
    Journal of education (Boston, Mass.)
    , 
    196
    (1), 9–18. 
    https://doi.org/10.1177/002205741619600103
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    View profile card for Jahenein Nagel

    Last post 
    September 10 at 11:10 AM
     by Jahenein Nagel

    Ladha, T., Zubairi, M., Hunter, A., Audcent, T., & Johnstone, J. (2018). Cross-cultural communication: Tools for working with families and children. 
    Paediatrics & child health
    , 
    23
    (1), 66–69. https://doi.org/10.1093/pch/pxx126

    Krasniqi, K. (2019). The relationship between language and culture (case study Albanian language).
     
    Linguistics and Literature Studies 7(2): 71-74. 
    https://www.hrpub.org/download/20190330/LLS5-19312921.pdf

    References:

    If a client is deaf and identifies with another cultural group as well, then consideration for both cultures is identified and addressed thoughtfully. This can be difficult for the practitioner as they will need to address both cultures in a considerate and thoughtful way to provide the best treatment possible for the individual. It may require using multiple modalities such as hearing-impaired services and interpreter services. One tool that may help communicate cross culturally is the LEARN model Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. The LEARN model helps create mutual understanding between the patient and provider to promote best patient care (Ladha et al. 2018). Each letter provides a framework to follow: Listen- Assess the patients understanding of their health condition, causes and their treatments; Explain- your own perception of their condition, causes and treatments; Acknowledge-use respect when discussing your point of view and their own; Recommend-create and offer a treatment plan to both the patient and family; Negotiate-seek a treatment plan agreement with the patient and family that incorporates cultural relevant treatment from the patients cultural point of view (Ladha et al. 2018).

    Module Ⅱ
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    James Neal posted Sep 7, 2021 12:43 PM

    Contains unread posts

    What cultural characteristics do deaf people have in common with other cultural groups?
    Culture is comprised of shared values, traditions and norms, a common language, and identity. In anthropology, culture is noted to be learned, shared, and exists as an integrated whole, or a connected framework that members understand and operate within (Haviland, 2001). The Deaf community exhibits each of these criteria, qualifying it as a culture. 
    If your client is both deaf and identifies with another cultural group as well, how does this affect your ability to provide quality cultural care?
    References
    Lane, H. (2005). Ethnicity, ethics, and the deaf-world. 
    Journal of Deaf Studies and Deaf Education
    , 
    10
    (3), 291–310. 
    https://doi.org/10.1093/deafed/eni030
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    View profile card for Frances Hall

    Last post 
    September 9 at 1:40 PM
     by Frances Hall

    Haviland, W. A. (2001). 
    Cultural anthropology
     (10th ed.). Wadsworth Publishing.

    One has to be both knowledgable and aware of both cultural backgrounds; affiliation with one group does not preclude identification with the other. This makes that person’s overall cultural identity more complex, but as covered in last week’s module, we should ideally be approaching each individual as unique without simply assuming each person embodies every aspect of their larger cultural identities.

    In fact, Lane (2005) and others have argued that Deaf culture should indeed be characterized as an ethnic culture, making a case that its classification as a disability has caused harm to the community, and its reclassification as an ethnic culture would afford the deaf further legal protections and may erase the idea that those who are deaf or heard of hearing fail to meet an accepted physical ideal.

    The Deaf culture and community is something that exists separately from those who are simply hard of hearing or deaf, an audiological condition that is federally recognized as a disability. The Deaf culture does not see being deaf as a disability, but rather as a difference in human experience and as a component of cultural identity Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Week 2 Laura
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    Laura Riccardi posted Sep 6, 2021 7:25 PM

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    The deaf population can be defined as a subculture. A subculture refers to a group that has values and norms that are distinct from the majority within a wider society (Andrews et al., 2020). The deaf community is distinct due to their own way of communication through sign language and reading people’s mouth movements. They can have a normal fulling life in their own adaption to the world in general.Other examples of nonethnic cultures include the blind, sexual orientation,  and age-specific. Characteristics of the deaf, blind, and transgender population learn to live and communicate within their own environments. Elements in these populations are feeling comfortable around others like themselves who understand them. Also, communication is more freely understood between the group. Other attributes can include specific healthcare providers in their communities who will not judge them and be able to understand their needs.  Other characteristics can include loneliness and depression due to people not understanding them. Removing barriers to social participation and integration should be an objective to prevent social exclusion and loneliness which can include general attitudes, legislation, and social, cultural, or physical structures (Brunes et al., 2019). Andrews, M. M., Boyle, J. S., & Collins, J. W. (2020). 
    Transcultural concepts in nursing care
     (8th ed.). Wolters Kluwer.Brunes, A., B. Hansen, M., & Heir, T. (2019). Loneliness among adults with visual impairment: Prevalence, associated factors, and relationship to life satisfaction. 
    Health and Quality of Life Outcomes
    , 
    17
    (1). 
    https://doi.org/10.1186/s12955-019-1096-y
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    View profile card for Jennifer Johnson

    Last post 
    September 8 at 9:57 PM
     by Jennifer Johnson

    Bodenmann, P., Singy, P., Kasztura, M., Graells, M., Cantero, O., Morisod, K., Malebranche, M., Smith, P., Beyeler, S., Sebaï, T., & Grazioli, V. S. (2021). Developing and evaluating a capacity-building intervention for healthcare providers to improve communication skills and awareness of hard of hearing and d/deaf populations: Protocol for a participative action research-based study. 
    Frontiers in Public Health
    , 
    9
    . 
    https://doi.org/10.3389/fpubh.2021.615474

    References

    Examples of challenges with the deaf community include using complex medical terminology or drug prescription instructions, which are not understood by the patient, potentially leading to preventable adverse events (Bodenmann et al., 2021). Awareness from organizations is needed to be able to adapt to this population when seeking healthcare. If hospitals and facilities lack resources it can result in limited and negative consequences within this population Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    NSG 556 Module 2
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    Jennifer Johnson posted Sep 6, 2021 9:57 PM

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    A cultural characteristic that both deaf and hearing impaired people have in common with other racially and ethnically diverse groups is that they are both a minority group in this country, and around the world. According to the World Health Organization (WHO), about 432 million adults and 34 million children have disabling hearing loss (Andrews et al., 2020; WHO, 2021). However, according to Andrews et al. (2020), although deaf and hearing impaired people may be racially and/or ethnically a part of the majority, they may self-identify with nonethnic cultures. And still others may be considered a “double minority”; identifying both with a racial or ethnic minority 
    and 
    with the nonethnic culture of the deaf (Andrews et al., 2020; Nelson Schmitt & Leigh, 2015).It is interesting to note that until the APN knows how best to communicate with the patient, he/she must use their culturally competent non-verbal skills to create a supportive environment that will be the foundation of their therapeutic relationship. The experienced APN can do this simply with a kind gesture or a friendly and welcoming look in their eyes, rather than a rushed and exasperated expression on their face. And this is crucial, because research shows that non-verbal communication plays an important role in cultivating trust between racial/ethnically diverse patients and care providers; trust that is vital for positive health outcomes (Loire et al., 2017).

    Andrews, M., Boyle, J., & Collins, J.W. (2020). 
    Transcultural Concepts in Nursing Care (8th ed.). 
    Wolters Kluwer. Nelson Schmitt, S. S., & Leigh, I. W. (2015). Examining a sample of black deaf individuals on the deaf acculturation scale. 
    Journal of Deaf Studies and Deaf Education, 20
    (3), 283-295. doi:10.1093/deafed/env017less1 UnreadUnread4 Views Views Transcultural Nursing – Cultural Competence in the Health History and Physical Examination

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    View profile card for Krista Romig

    Last post 
    September 8 at 8:26 PM
     by Krista Romig

    World Health Organization. (2021, April 1). 
    Deafness and Hearing Loss.
     Retrieved September 6, 2021 from https://www.who.int/news-room/fact-sheets/detail/deafness-and-hearing- loss

    Lorié, Á., Reinero, D. A., Phillips, M., Zhang, L., & Riess, H. (2017). Culture and nonverbal expressions of empathy in clinical settings: A systematic review. 
    Patient Education and Counseling, 100
    (3), 411-424. doi.org/10.1016/j.pec.2016.09.018

    References

    The culturally competent advanced practice nurse (APN) knows how to be mindful of the needs not only of the hearing impaired patient, but of their racial and ethnic uniqueness as well. First and foremost, the APN must ascertain how the patient prefers to communicate. Do they use sign language, is an interpreter required, do they prefer written communication, or perhaps telecommunication devices for the deaf (TDD) (Andrews et al., 2020). Once the APN understands the best way to communicate with the patient, then the assessment, planning, and implementation of care can begin.

    Module 2
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    Emily Meeks posted Sep 7, 2021 6:24 PM

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     In the event an individual is a “double minority,” such as being deaf and also identifies with another cultural group, it is necessary to modify the care being provided to meet the needs of both cultures (Andrews et al., 2020, p. 47). Say the patient is deaf and speaks another language. A misconception is that sign language is universal, when in fact it is not, and greatly impacts the quality of care. In researching this topic, I found that there are up to 300 sign languages, and they can differ depending on geographic location and language of the community (Brooks, 2018). While it is impossible for an advanced practice nurse to know the beliefs of all cultural groups, it is necessary for one to withhold judgement or assumptions, and accommodate to the best of their abilities.Andrews, M., Boyle, J., & Collins, J. (2020). 
    Transcultural concepts in nursing care
    . (8
    th
     ed.)Brooks, R. (2018). 
    A guide to the different types of sign language around the world Transcultural Nursing – Cultural Competence in the Health History and Physical Examination
    . K International. 
    https://www.k-international.com/blog/different-types-of-sign-language-around-the-world/
    .
    https://www.nationaldeafcenter.org/sites/default/files/The%20Deaf%20Community-
    %20An%20Introduction.pdfless0 UnreadUnread

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    National Deaf Center (2019). 
    The deaf community: an introduction.

    Philadelphia, PA: Wolters Kluwer.

    References

    When discussing culture, one may immediately think of those from racially or ethnically diverse backgrounds. However, one must be able to identify that every group or subset of persons whom form a group of individuals, have a unique culture as well (Andrews et al., 2020). For example, the LGBTQ community, socioeconomic status, those with disabilities or are deaf, each encompass a nonethnic culture. The deaf culture is formed by way of language differences, shared-life experiences and struggles with adaptation (National Deaf Center, 2019). Characteristics the deaf culture have in common with other cultural groups could include language barriers, living in a community that doesn’t always accommodate diversity, biases, and social groups/ activities.

    Module 2
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    Karimah Moss posted Sep 7, 2021 10:46 AM

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    Module 2When healthcare professionals are not culturally competent and fail to recognize that a patient has cultural needs (deaf or ethnic culture), barriers are created leading to disparities. Like ethnic cultural groups, those that are part of the deaf cultural heritage are at risk for healthcare inequalities. Their access to information regarding health prevention, treatment, and care is significantly less than those who do not have hearing difficulties (Kuenburg et al., 2016). “Community perceptions of health such as diverse experiences and understanding of ill-health as well as language and communication barriers have been linked to challenging health care access in culturally and linguistically diverse populations” (Kuenburg et al., 2016, p. 1).
    References
    Kuenburg, A., Fellinger, P., & Fellinger, J. (2016) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. Health care access among deaf people. 
    Journal of Deaf Studies and Deaf Education
    , 
    21
    (1), 1–10. 
    https://doi.org/10.1093/deafed/env042
    Therivel, J., & Punwani, K. (2016, October 28). 
    Evidence-based care sheet: Clients who identify as deaf: Providing culturally competent care
     [PDF]. EBSCO Host. 
    https://www.ebscohost.com/assets-sample-content/SWRC-Culturally-Competent-Care-Clients-Who-Identify-as-Deaf-Care-Sheet.pdf
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    Pendergrass, K. M., Newman, S. D., Jones, E., & Jenkins, C. H. (2017). Deaf: A concept analysis from a cultural perspective using the Wilson method of concept analysis development. 
    Clinical Nursing Research
    , 
    28
    (1), 79–93. 
    https://doi.org/10.1177/1054773817719821

    Abou-Abdallah, M., & Lamyman, A. (2021). Exploring communication difficulties with deaf patients. 
    Clinical Medicine
    , 
    21
    (4), e380–e383. 
    https://doi.org/10.7861/clinmed.2021-0111

    Having a patient that is deaf and part of another cultural group, will impact how I provide culturally competent care. I would want to ensure that I utilize all available resources to effectively communicate and assess their deaf and ethnic cultural needs. On a few different occasions, I delivered care to a deaf patient. During each interaction, the patients declined the use of an interpreter and preferred to lip read. Now with COVID-19, this would be impossible, and I would need to utilize a clear face mask should I encounter this situation again. However, I would do my best to encourage the use of an interpreter to ensure that myself or the patient does not misunderstand anything important due to our communication or language differences (Abou-Abdallah & Lamyman, 2021). With the interpreter’s assistance, I will be able to assess the patient’s unique cultural needs and make certain that they are appropriately addressed and relayed to all other members of the team Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

    Individuals who utilize American Sign Language (ASL) as their primary method of communication, define the term “deaf” as a cultural heritage. The term “deaf” within the healthcare setting is usually defined as a pathological condition (Pendergrass et al., 2017). While the deaf and hearing-impaired community is a nonethnic culture, this community does have unique cultural characteristics as ethnic cultural groups do. It is equally important for healthcare professionals to demonstrate cultural competence when providing care to the deaf community as it is with ethnic cultural groups. Both groups have distinct health beliefs, attitudes towards healthcare and health professionals, cultural needs, values, and communication challenges (Therivel & Punwani, 2016). Ineffective communication can lead to lack of trust and medical errors which will negatively impact the patient’s health outcome (Abou-Abdallah & Lamyman, 2021).

    Module 2 Discussion
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    Donna Wrobel posted Sep 6, 2021 1:07 PM

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    Although many people do not characterize the deaf community as a unique culture, deaf individuals do view themselves as members of a distinct society based on their use of sign language as their primary language. According to Giger and Davidhizer’s theory, culture is determined by shared beliefs and experiences in the areas of communication, time, space, social organization, environmental control and biologic variations (Giger & Davidhizar, 2002). Characteristics specific to the deaf community are based on shared life experiences that are different from hearing individuals in a world that is designed for verbal communication (
    The Deaf Community: An Introduction
    , n.d.). Deaf culture is based on the notion that disability is a social and environmental construct rather than a medical condition based on a loss of physical function. Members of the community are accepted based on whether an individual chooses to self-identify as deaf, rather than a medical diagnosis (Sligar, 2019).Many people identify as members of more than one specific culture. For example, a patient may identify as a member of the Latino culture and a member of the LGBTQ community Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. It is the responsibility of the APRN to become educated regarding the needs and beliefs of their patients, regardless of which culture the patient identifies with. If a patient indicates that they belong to more than one culture, it is necessary for the APRN to question the patient regarding how this may affect their beliefs and goals regarding their care. This is no different if the patient belongs to the deaf community as well as another culture as the needs of the patient must always be taken into consideration.
    Definition of culture
    . (2021). Merriam-Webster.com. Retrieved September 5, 2021, from 
    https://www.merriam-webster.com/dictionary/culture
    Huang, S. (2017). The relationship between language and culture: Evidence from the deaf bi-bi community. 
    Perspectives of the ASHA Special Interest Groups
    , 
    2
    (14), 55–65. 
    https://doi.org/10.1044/persp2.sig14.55
    The deaf community: an introduction. (n.d.). National Deaf Center on Postsecondary Outcomes. 
    https://www.nationaldeafcenter.org/
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    Sligar, S. R. (2019, November). Deaf and hearing: Conducting cross-cultural research in a postsecondary setting. JADARA Journal of American Deafness and Rehabilitation Association. 
    https://nsuworks.nova.edu/jadara/vol40/iss1/3

    Giger, J., & Davidhizar, R. (2002). The giger and davidhizar transcultural assessment model. 
    Journal of Transcultural Nursing
    , 
    13
    (3), 185–188. 
    https://doi.org/10.1177/10459602013003004

    References

    In all cultures, the use of a common language helps to establish membership and identification as well as social support within the community and language and culture are usually tightly connected (Huang, 2017). The basis of deaf culture is the use of the common language of ASL (American Sign Language) but the community also maintains shared rules for behavior, traditions, beliefs and values much the same as other ethnic and racial cultures do. One such accepted behavior is to maintain eye contact while conversing, rather than looking away as hearing persons do (Sligar, 2019) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. These behaviors and beliefs are equivalent to the meaning of culture in the Merriam-Webster Dictionary in which the term is defined as the “customary beliefs, social forms, and material traits of a racial, religious, or social group as well as the shared attitudes, values, goals and practices that characterize an institution or organization” (
    Definition of Culture
    , 2021). Based on this definition, the deaf community makes up a distinct culture based on their shared beliefs and experiences that distinguish them from the hearing community.

    Romig- Module 2
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    Krista Romig posted Sep 6, 2021 12:29 AM

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    Deaf culture is often overlooked when considering culturally competent care as it is not a culture based on ethnicity. However, the deaf community has their own culture, which is based on deaf people being a cultural minority. Many people in the deaf community do not see their hearing loss as a disability, and rather embrace their differences just like many other cultural groups (Andrews et al., 2020).As healthcare providers, it is important to provide culturally competent care for to our patients. It has been found that deaf patients often have negative experiences within healthcare facilities, including limited ASL access and healthcare inequity. There are also many misconceptions about deaf patients (Greene & Scott, 2021). Since the deaf community often does not see themselves as disabled, it is important to determine what their goals are rather than push what we see as their goals onto them. As medical professionals, we tend to see anything out of the normal as something to fix, so it is typical to encourage hearing aids and cochlear implants on patients with hearing loss (Andrews et al., 2020). However, if the patient does not see their hearing loss as a disability and does not want it fixed, this can upset them.When providing care to patients of cultural minorities, the most important thing when providing quality cultural care is communication with the patient. It is important to ask questions to better understand the patients’ culture and goals of treatment. By being respectful and wanting to gain a better understanding of the patients’ culture, we can provide culturally competent care to all patients.Andrews, M., Boyle, J., & Collins, J. W. (2020). Transcultural concepts in nursing care (8th ed.). Wolters Kluwer.Hoffman, D. & Andrews, J. F. (2016). Why deaf culture matters in deaf education. 
    Journal of Deaf Studies and Deaf Education, 21
    (4), 426-427. 
    https://doi.org/10.1093/deafed/enw044

    Greene, S. J. & Scott, J. A. (2021) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination. Promoting cultural awareness, professionalism, and communication skills in medicine through anatomy: The Deaf culture session. 
    Clinical Anatomy, 34
    (6), 899-909. 
    https://doi-org.wilkes.idm.oclc.org/10.1002/ca.23752

    References

    Patients in the Deaf community can also belong to other cultural groups as well, such as being black or gay. It is important to not make assumptions about the patient based on their cultural groups, but instead to understand the challenges the patient has likely encountered.

    Many people believe that the only difference deaf people experience is how they communicate. However, the Deaf community has much more in common than just American Sign Language.  The deaf community recognizes the difficulties living in a hearing world and shares their experiences as deaf individuals (Hoffman & Andrews, 2016) Transcultural Nursing – Cultural Competence in the Health History and Physical Examination.

  • pelvic inflammatory disease discussion essays

    pelvic inflammatory disease discussion essays

    Ann is a 32-year-old married female who presents to her nurse practitioner reporting lower abdominal pain, cramping, slight fever, and dysuria of 3 days duration.

    History includes:

    LMP 2 weeks ago (regular)

    Reports oral contraceptive use

    Reports pain in lower abdomen with cramping and pain on urination for 3 days

    Denies any GI problems, reports regular bowel movements.

    Denies vaginal discharge

    Ann is married and in a monogamous relationship. Has one child age 2

    Reports no use of condoms/sexual intercourse 2-3 times per week

    Denies any history of STDs pelvic inflammatory disease discussion essays

    Physical Exam reveals:

    Temp 100. 6, P 80 BP 100/62 Wt. 125 Ht. 5’3’’

    HEENT WNL

    No CVA tenderness

    Pain in lower quadrants with light palpation. Positive inguinal lymphadenopathy

    External genitalia without lesions or discharge

    Pelvic exam reveals minimal cervical mucopus

    Bimanual exam reveals uterine and adnexal tenderness and cervical motion pain. Uterus anterior, midline, smooth, not enlarged

    1. Based on the above case the diagnosis is PID,  What is an appropriate CDC-recommended therapeutic regimen for this patient?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight. Both responses must be a minimum of 150 words, scholarly written, APA formatted, and referenced. A minimum of 2 references are required (other than your text). Refer to grading rubric for online discussion.

    Pelvic inflammatory disease (PID) comprises a spectrum of inflammatory disorders of the upper female genital tract (CDC, 2015). The diagnosis of PID should be made clinically in the absence of other obvious causes in an at-risk woman with unexplained pelvic pain and cervical motion, uterine, or adnexal tenderness (Curry et al, 2019). In this example, the patient’s bimanual exam meets CDC criteria for a likely PID diagnosis. No laboratory tests are needed to begin treatment (Huether et al, 2020). Although Ann is married and states she is in a monogamous relationship, one must consider one partner has had other sexual partners. Many women falsely believe they are in a monogamous relationship or that their partner does not harbor an STI; therefore, a low threshold for screening is warranted (Cuerry et al, 2019). Sexually transmitted organisms, especially 
    N. gonorrhoeae
     and 
    C. trachomatis
    , are implicated in many cases (CDC, 2015) pelvic inflammatory disease discussion essays. Both Ann and her husband should be tested for gonorrhea and chlamydia.
    Recommended Intramuscular/Oral Regimens per CDC Guidelines:
    The patient should be re-evaluated in 3 days to ensure antibiotic treatment is effective. Partners should also be treated to prevent recurrence. Curry, A., Williams, T., & Penny, M. L. (2019). Pelvic inflammatory disease: Diagnosis,Heuther, S., McCance, K., and Brashers, V.  (2020).  
    Understanding
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    View profile card for Steven Bartos

    Last post 
    March 13 at 12:17 PM
     by Steven Bartos

    Pathophysiology
     (7
    th
     ed).  Elsevier.

    management, and prevention.
     American Family Physician, 100
    (6), 357-364.

    Centers for Disease Control – 2015 Sexually Transmitted Diseases Treatment Guidelines

    References

    Ceftriaxone
     250 mg IM in a single dose

    PLUS

    Doxycycline
     100 mg orally twice a day for 14 days

    WITH* or WITHOUT

    Metronidazole
     500 mg orally twice a day for 14 days

    Presumptive treatment should be initiated based on the significant complications of PID. Intramuscular/oral therapy can be considered for women with mild-to-moderately severe acute PID.

    Module 8 Discussion Post – The Reproductive System
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    Gisselle Mustiga posted Mar 8, 2021 9:41 PM

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    Pelvic inflammatory disease is a condition and disorder that affects the female reproductive organs. This condition primarily occurs when sexually transmitted bacteria move from the vagina to other parts of the reproductive systems, including the uterus, fallopian tubes, and ovaries (Llata et al., 2015). PID is associated with morbidity and mortality among women and is also associated with infertility, pelvic pain, and ectopic pregnancy. Some of the significant signs and symptoms of this condition include pain during intercourse, generalized pain, abnormal virginal discharge, fever, and painful and frequent urination (Huether et al. 2020). It should be noted that the bacteria that cause this infection is acquired during unprotected sex pelvic inflammatory disease discussion essays. The CDC recommends that sexually active young women should be put under empiric treatment of PID if they show the above symptoms.
    References
    Huether, S. E., McCance, K. L. & Brashers, V. L. (2020). 
    Understanding Pathophysiology 7
    th
     ed
    . Elsevier Mosby.  less1 UnreadUnread3 ViewsViews

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    View profile card for Sheryl Dixon

    Last post 
    March 13 at 12:14 AM
     by Sheryl Dixon

    Llata, E., Bernstein, K. T., Kerani, R. P., Pathela, P., Schwebke, J. R., Schumacher, C., … & Weinstock, H. S. (2015). Management of Pelvic Inflammatory Disease in Selected US Sexually Transmitted Disease Clinics: Sexually Transmitted Disease Surveillance Network, January 2010–December 2011. 
    Sexually transmitted diseases
    , 
    42
    (8), 429. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6740322/

    CDC, (2020). 
    Pelvic Inflammatory Disease (PID): Detailed Fact Sheet
    . CDC. 
    https://www.cdc.gov/std/pid/stdfact-pid-detailed.htm

    According to CDC (2020), PID can be treated using different types of antibiotics such as Metronidazole. These drugs are broad spectrum and cover all the likely pathogens to causes the condition. Sexually transmitted organisms, especially 
    Neisseria

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    gonorrhoea
     and 
    Chlamydia trachomatis
     have been implicated in many cases; however microorganisms that comprise the vagina flora such as anaerobes, 
    Gardnerella vaginalis
    , 
    Haemophilus influenzae
    , entetric Gram-negative rods and 
    Streptococccus agalactiae
     also have been associated with PID. However, it should be noted that antibiotic treatment does not reverse the already-caused scarring. Therefore, it is advised that women should seek care immediately if they experience symptoms, especially pelvic pains. Prompt antibiotic treatment can reduce adverse effects of the condition, such as organ damage to the reproductive system. The provider should advise the patients to finish taking all the prescribed medications. Moreover, the women’s sexual partners should be treated even if they show no symptoms to avoid any chances of reinfection. Individuals can avoid contracting this condition by avoiding unsafe sexual practices and adopting temporary abstinence, especially during treatment.

    Pelvic Inflammatory Disease
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    Jazmin Jerez-Rivera posted Mar 8, 2021 9:34 PM

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    Pelvic inflammatory disease (PID) is caused by an underlying infection of the reproductive organs of the upper genital tract. It is a sexually transmitted infection that can go undiagnosed for some time before a show of symptoms. Ann presents with many symptoms that meet the diagnostic criteria for pelvic inflammatory disease. These consist of pain in the lower abdomen with cramping, dysuria, cervical motion pain, cervical mucopus, adnexal tenderness and cervical motion pain (Huether et. al., 2020) pelvic inflammatory disease discussion essays. The main pathogens are usually Neisseria gonorrhoeae and chlamydia trachomatis but can be caused by other organisms. The CDC recommends a broad-spectrum coverage that includes parenteral and oral regimens (CDC, 2015).  A study by Risser et. al. reveals treatment recommendations for outpatient therapy, “one dose of parenteral cephalosporin, followed by 2 weeks of oral doxycycline, with or without 2 weeks of metronidazole” (2017, p. 9). It is also important to remind women to abstain from sex until medication is completed, and symptoms are resolved (CDC, 2015). Partners should also be treated to prevent reinfection.Centers for Disease Control and Prevention. (2015). Pelvic Inflammatory Disease (PID). Retrieved from 
    https://www.cdc.gov/std/tg2015/pid.htm
    Risser, W. L., Risser, J. M., & Risser, A. L. (2017). Current perspectives in the USA on the diagnosis and treatment of pelvic inflammatory disease in adolescents. 
    Adolescent health, medicine and therapeutics
    , 
    8
    , 87–94. https://doi.org/10.2147/AHMT.S115535less2 UnreadUnread4 ViewsViews

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    View profile card for Dennies Jones

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    March 12 at 11:33 PM
     by Dennies Jones

    Huether, S. E., McCance, K. L., Brashers, V. L. (2020). Understanding Pathophysiology (7 Ed.).  Elsevier.

    References

    Module 8 PID
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    Joanne Hogan posted Mar 9, 2021 4:33 PM

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    Module 8Symptoms of PID are generally nonspecific and it is important to rule out pregnancy before making a diagnosis (Cueva et al., 2020). The most frequent manifestations of PID include vaginal discharge, pelvic discomfort, lower abdominal tenderness, fever, and cervical motion tenderness (Cueva et al., 2020). If left untreated, long term effects of inflammation can cause changes in the epithelial cells of the lining of the upper reproductive tract, causing necrosis or obstruction (Huether et al., 2020). Scarring an also occur which can increase the risk for ectopic pregnancy later on (Huether et al., 2020). Cueva, F., Caicedo, A., & Hidalgo, P. (2020). A need for standardization of the diagnosis and treatment of pelvic inflammatory disease: Pilot study in an outpatient clinic in quito, ecuador. 
    Infectious Diseases in Obstetrics and Gynecology
    , 
    2020
    , 1–6. 
    https://doi.org/10.1155/2020/5423080
    Vanthuyne, A., & Pittrof, R. (2016). Diagnosis and treatment of pelvic inflammatory disease. 
    Prescriber
    , 
    27
    (10), 47–50. 
    https://doi.org/10.1002/psb.1507
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    View profile card for Candice Russell

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    March 12 at 5:20 PM
     by Candice Russell

    Huether, S. E., McCance, K. L., & Brashers, V. L. (2020). 
    Understanding pathophysiology
     (7th ed.). Elsevier.

    References

    Treatment of pelvic inflammatory disease starts with prevention. Education should be provided to high-risk patients regarding safe sex practices. Also, patients should have access to pregnancy and STI testing (Vanthuyne & Pittrof, 2016). The goal of treatment in PID is to reduce inflammation and prevent long term effects (Cueva et al., 2020). Treatment often includes antibiotics and can usually be managed on an outpatient basis (Huether et al., 2020). The antibiotics prescribed are generally broad spectrum to isolate aerobic and anerobic bacteria in the genital tract (Vanthuyne & Pittrof, 2016). The most common antibiotic regimen is doxycycline with or without a combination of a cephalosporin or ceftriaxone (Huether et al., 2020). Metronidazole is often given in conjunction to provide coverage for anaerobic organisms and to assist with treatment of bacterial vaginosis which commonly occurs alongside PID (Vanthuyne & Pittrof, 2016). Antibiotics will be given twice a day for 2 weeks and it is important a follow up appointment is made within 5 days of treatment initiation to check for progress (Cueva et al., 2020).

    Pelvic inflammatory disease (PID) is an inflammatory process caused by an infection in sexually active females of reproductive age (Vanthuyne & Pittrof, 2016). PID results from the movement of micro-organisms from the lower to the upper genital tract (Vanthuyne & Pittrof, 2016). The most common causes of PID are sexually transmitted diseases, specifically gonorrhea and chlamydia (Huether et al., 2020). Anaerobic organisms can cause PID due to their ability to disrupt the pH level in the vagina, causing less protective mucus development which usually protects the cervix under normal conditions (Huether et al., 2020) pelvic inflammatory disease discussion essays. Risk factors for PID include having multiple sexual partners, young age (<25 years), history of STIs, and a prior history of PID (Vanthuyne & Pittrof, 2016). Module 8, Eleany Yasein Subscribe Eleany Yasein posted Mar 10, 2021 10:55 AM Contains unread posts Pelvic inflammatory disease (PID) is caused due to inflammation of the upper genital tract from an infection (Jennings & Krywko, 2020). This disorder affects women that are 15 to 25 years of age. It can spread to the uterus, fallopian tubes or ovaries, and cause infertility and ectopic pregnancy. Signs and symptoms of PID include lower abdominal or pelvic pain, dyspareunia, vaginal discharge, and vaginal bleeding. PID is caused by sexually transmitted bacteria. The most common bacteria are N. gonorrhoeae and C. trachomatis (Jennings & Krywko, 2020). Centers for Disease Control and Prevention. (2015, June 4).  Pelvic Inflammatory Disease (PID).  U.S. Department of Health and Human Services.  https://www.cdc.gov/std/tg2015/pid.htm Jennings, K. L., & Krywko, M. D. (2020, November 20).  Pelvic Inflammatory Disease . StatPearls. https://www.ncbi.nlm.nih.gov/books/NBK499959/ pelvic inflammatory disease discussion essays

  • Cultural Diversity in Health and Illness Discussion Essay

    Cultural Diversity in Health and Illness Discussion Essay

    Introduction

    Our nation has been a melting pot of cultures since its birth and this multiculturalism is increasing rapidly. This diversity is creating  a significant challenge for interactions at all levels of society particularly in healthcare. In order to meet this challenge,  advanced practice nurses we must first understand the concept of culture, as well as health and illness.

    Culture is defined by Dayer-Berenson, as “the shared values, traditions, norms, customs, arts, history, folklore, and institutions of a group of people who are unified by race, ethnicity, language, nationality, sexual orientation, and/or religion.”(2014). In order to help our patients connect with their healthcare providers it is vital as advanced practice nurses to provide culturally sensitive and competent care. This will help us identifiy healthcare disparities and their impact on current health care in the United States Cultural Diversity in Health and Illness Discussion Essay.

    Learning objectives for the module
    :

    At the end of this module, the student will be able to:

    Define health and illness

    Define diversity

    Identify ways to provide culturally competent care

    Describe the impact of diversity on healthcare disparities

    Readings:

    Andrews & Boyle, J. , Chapters 2, 3

    The Process of Cultural Competence in the Delivery of Healthcare Services by Campinha-Bacote (2002)
    http://journals.sagepub.com.ez
    proxy.wilkes.edu/doi/pdf/10.11
    77/10459602013003003

    Cultural Competence for Healthcare Providers 

    Websites:

    The Model of Cultural Competence through Evolutionary Concept Analysis by Suh (2004). 
    http://journals.sagepub.com.ez
    proxy.wilkes.edu/doi/pdf/10.11
    77/1043659603262488

    Communication Between Cultures: 

    Topic 1: Health and Illness

    The concepts of health and illness are not easily defined and are difficult to understand. The World Health organization (WHO) defines health as “a state of complete physical, mental, and social well-being and not merely the absence of disease.”  Other definitions include the state of being free from illness or injury, or a general condition of the body or mind in equilibrium. The many definitions of health make it difficult to grasp and understand it’s meaning. The definitions of illness are just as elusive. Is it the absence or opposite of health or is it better defined as a disease or condition?  No matter the definition we need to understand that the experience of being ill is also defined by the patient.   What health may mean to a 21 year old athlete versus a 60 year old diabetic will vary greatly. Therefore we find individuals defining health and illness according to their own definitions. We also must realize that culture greatly affects one’s definition of health and illness, therefore as advanced practice nurses in order to provide competent care we must understand health and illness from our client’s perspective Cultural Diversity in Health and Illness Discussion Essay.

     

    Topic 2: Cultural Diversity

    The United States is a multicultural nation made up of cultures from around the world. According to the US Census Bureau, Asian and mixed race people are the two fastest growing populations in the US. Although non-hispanic whiltes remain the largest group of Americans at 198 million, they are the only group with a higher death rate than birth rate. Hispanics follow  the non-hispanic whites at 57.5 million and blacks or African Americans at 46.8 million. With the increase in these diverse populations come issues which tremendously effect their health care. Language barriers and low incomes lead to lower access and availability of health care and therefore less favorable outcomes according to the Institute of Medicine (IOM) report (2003). This results in daily challenges for the nurse to identify the diverse needs of the patients and address them in order to provide quality health care. In order to combat these culturally driven healthcare disparities the advanced practice nurse must be prepared to meet the unique healthcare needs for all culturally diverse paients in their care Cultural Diversity in Health and Illness Discussion Essay.

     

    Module 3

    Discussion

    Based on the various definitions of health, define health and explain if you agree with one definition more than the other? Why?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight.  Both responses should be a minimum of 150 words, scholarly written, APA formatted, and referenced.  A minimum of 2 references are required (other than your text) for both posts.  Refer to the Grading Rubric for Online Discussion in the Course Resource section.

    Module 3: Discussion

    Special Guidance on APA formatting in Discussion Posts

    APA formatting is required in discussion posts with the following two exceptions (due to limitations with the text editor in LIVE):  
    double line space and indent 1/2 inch from the left margin
    . Discussion posts will NOT be evaluated on those two formatting requirements. All other APA formatting guidelines should be followed. For example, in-text citations must be formatted with the appropriate information and in the correct sequence (Author, year), reference list entries must include all appropriate information following  guidelines for capitalization, italics, and be in the correct sequence. Refer to the APA Publication Manual 7th ed. for each source type’s specific requirements. Please let your instructor know if you have any questions Cultural Diversity in Health and Illness Discussion Essay.

    Module 3: Discussion

    Must post first.

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    Based on the various definitions of health, define health and explain if you agree with one definition more than the other? Why?

    Post your initial response by Wednesday at midnight. Respond to one student by Sunday at midnight.  Both responses should be a minimum of 150 words, scholarly written, APA formatted, and referenced.  A minimum of 2 references are required (other than your text) for both posts.  Refer to the Grading Rubric for Online Discussion in the Course Resource section.

    Feedback

    100 / 100

    I think most of us agree that although the WHO definition has been widely accepted we define health differently today because we recognize the need for the individual to define what health means to them.  As an example, a Diabetic who maintains their BS at 140 or below may identify as being healthy.  Good points, thank you.

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    Module III
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    Evelyn Anderson posted Sep 17, 2021 8:03 AM

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    Health is a broad term that can have many definitions or viewpoints considering the context of which it is being used. Health can be seen as a physical and mental state of well-being with environmental and sociological elements that can play a role in a persons’ health. Also, consideration must be given for how each person views health and what it means to them. Defining health can have an impact on health care professionals and society in how it is socially developed and impacts policy development and implementation in the health care system (Leonardi, 2018) Cultural Diversity in Health and Illness Discussion Essay. The definition of health can impact a persons behavior and their ability to make decisions regarding their health (Leonardi, 2018).  Some scholars consider questions of health by asking if health is a complete state of well-being? or is health a resilience to disease and injury and recovery from a specific disease? (Oleribe et al. 2018). The World Health Organization (WHO) defines health as a complete state of mental, physical and social well-being (Leonardi, 2018). Scholars contend that it is near impossible for any one person to have complete mental, physical and social well-being (Leonardi, 2018). It doesn’t appear that any one definition of health is the complete answer and the determinants of health is all always changing. Health is a complex state of being with many contributing factors. References:Leonardi, F. (2018). The definition of health: Towards new perspectives. 
    International Journal of Health Services
    , 48 (4), 735-748. 
    https://doi.org/10.1177/0020731418782653
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    View profile card for Jerrica Goins

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    September 19 at 11:10 PM
     by Jerrica Goins

    Oleribe, O., Ukwedeh, O., Burstow, N., Gomaa, A., Sonderup, M., Cook, N., Waked, I., Spearman, W., & Taylor-Robinson, S. (2018). Health: Redefined
    . The Pan African Medical Journal, 30, 292-292
    . 
    https://doi.org/10.11604/pamj.2018.30.292.15436

    Module 3: Discussion
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    Gisselle Mustiga posted Sep 14, 2021 9:57 PM

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    Health is a notion that individuals create and relate to culture and social norms that should be defined congruently in natural design, objectives, and facts. The world health organization (WHO) proposes health as the absence of disease or illness and complete physical wellness. The concept of health is complex since when health is taken as a subjective aspect, it creates a notion for judgments and social norms that portray health definition. The former (health based on objectivity, subjectivity, and facts) is more realistic since it governs all aspects than the absence of illness or complete physical wellness (Campinha-Bacote, 2019). The latter is that individuals can have medical or lifestyle conditions and still lead healthy lives.From a patient’s perspective, health-related values involve cultural identity, ethnicity, moral and ethical views, individual preferences, and socioeconomic status (Andrew et al., 2020). Health care providers’ and patient’s values are linked through communication Cultural Diversity in Health and Illness Discussion Essay. Through communication, the nurses obtain subjective data from the patient, including the past and present state of health and cultural aspects which might interfere with the nurses’ ability to make health care decisions (Suh, 2004). Objective data are also taken to assess the patient’s strength and delve into their lifestyles to identify possible risk factors that make an individual susceptible to illnesses.Andrews, M. M., Boyle, J. S., Collins, J. W. (Eds.). (2020). 
    Transcultural concepts in nursing care
     (8th ed.). Philadelphia, PA: Wolters Kluwer Health.Suh, E. E. (2004). The model of cultural competence through an evolutionary concept analysis. 
    Journal of Transcultural Nursing
    , 
    15
    (2), 93-102.less1 UnreadUnread0 ViewsViews

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    View profile card for Idida Aleman Musial

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    September 19 at 10:40 PM
     by Idida Aleman Musial

    Campinha-Bacote, J. (2019). Cultural compatibility: A paradigm shift in the cultural competence versus cultural humility debate—Part I. 
    Online Journal of Issues in Nursing
    , 
    24
    (1).

    References

    Health professionals understand cultural competence and that individual’s health is not separate from social and environmental contexts. They attend to physical, social, and ecological contexts that affect health and understand the difference between health and health aspects. Andrews et al., 2020 transcultural interprofessional practices (TIP) constitute systematic, patient-centered, and logical scientific ways of availing safe, affordable, evidence-based practices for individuals from different diversities. The critical components of the TIP relate to the individual’s context regarding beliefs, attitudes, and health-related values Cultural Diversity in Health and Illness Discussion Essay.

    NSG 556: Module 3
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    Jennifer Johnson posted Sep 14, 2021 9:52 PM

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    Early definitions of health, as understood by the biomedical community, focused solely on the normal functioning of the body, and the absence of disease (Association of Faculties of Medicine of Canada, 2016). Currently however, a more recent definition of health from the World Health Organization, broadly encompasses an individual or community’s ability to “realize aspirations and satisfy needs, and to change or cope with the environment” (World Health Organization, 1984, p. 4). A flushing out of that definition reveals a strong emphasis on health promotion within it. I agree with and appreciate this aspect of health promotion within the definition because we cannot define health for our patients (McCartney et al., 2019). We can 
    promote
     health within our patients; we can educate them, provide treatments and offer recommendations, and we can even prescribe medications and testing to collect objective evidence. But we cannot 
    provide
     health for our patients. 

    Association of Faculties of Medicine of Canada. (2016, August 12). 
    Concepts of Health and Illness: Definitions of Health.
     AFMC Primer on Population Health: A virtual textbook on Public Health concepts for clinicians. https://phprimer.afmc.ca/en/part-i/chapter-1/ World Health Organization. Regional Office for Europe. (‎1984, September 13)‎. 
    Health promotion : a discussion document on the concept and principles : summary report of the Working Group on Concept and Principles of Health Promotion. 
    Copenhagen : WHO Regional Office for Europe. https://apps.who.int/iris/handle/10665/107835less2 UnreadUnread3 ViewsViews

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    View profile card for Gisselle Mustiga

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    September 19 at 10:02 PM
     by Gisselle Mustiga

     

    McCartney, G., Popham, F., McMaster, R., & Cumbers, A. (2019). Defining health and health inequalities. 
    Public Health, 172
    , 22-30. https://doi.org/10.1016/j.puhe.2019.03.023

    Resources

    What we can offer is an opportunity for our patients to achieve health within their own environment. Our patients’ understanding of health, well-being, illness or disease will vary based on their culture, background and environment (McCartney et al., 2019). The experiences of health between patients can vary as greatly as they differ from each other. For some, living with heart disease and diabetes may be such a challenge that their lives are turned upside down. For others, chronic illness can be easily managed and will not be such a hindrance to their experience of being healthy. Factors such as education, environment, socioeconomic status, cultural background and beliefs, genetic disposition, mental health, and access to care all play a significant and complex role in one’s understanding of health (McCartney et al., 2019). The advanced practice nurse must take these factors into account when assessing a patient’s experience of health Cultural Diversity in Health and Illness Discussion Essay.

    Module 3 Discussion
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    Jerrica Goins posted Sep 15, 2021 11:57 PM

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    The World Health Organization started defining health in 1948 as a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity (McCartney et al., 2019). Today, managing disease, not solely its absence, is a means to a healthy life. Many people have a chronic disease that are managed and are considered to be healthy because they have their disease under control. Modern concepts of health recognize health as more than the absence of disease, implying a maximum capacity of the individual for self-realization and self-fulfillment (Svalastog et al., 2017). The health of individuals is also linked to the environment in which they live and especially to their ability to adapt and integrate into their life context. I believe that this is a more universal definition of health because it uses an approach that can be individualized. Health is a resource to support an individual’s function and provides the means to lead a full life with meaning and purpose. Health is also a positive concept that emphasizes social and personal resources, as well as physical capabilities.References Svalastog, A. L., Donev, D., Jahren Kristoffersen, N., & Gajović, S. (2017). Concepts and definitions of health and health-related values in the knowledge landscapes of the digital society. 
    Croatian Medical Journal
    , 
    58
    (6), 431–435. https://doi.org/10.3325/cmj.2017.58.431less2 UnreadUnread3 ViewsViews

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    View profile card for Francesca Provencher

    Last post 
    September 19 at 8:09 PM
     by Francesca Provencher

    McCartney, G., Popham, F., McMaster, R., & Cumbers, A. (2019). Defining health and health inequalities. 
    Public Health
    , 
    172
    (172), 22–30. https://doi.org/10.1016/j.puhe.2019.03.023

    Module 3 Discussion – Jahenein Nagel
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    Jahenein Nagel posted Sep 13, 2021 4:24 PM

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    For many years the definition of health has remained unchanged as a narrow concept, encompassing physical wellbeing from a medical context (Oleribe et al., 2018). The World Health Organization (WHO) defines health as a “state of complete physical, mental and social well-being and not merely the absence of disease or infirmity” (Fallon & Karlawish, 2019, p. 1104). To some, “health is wealth” -given that in the absence of good health, an individual or society cannot attain its full potential (Oleribe et al., 2019).By adopting the social constructionism point of view, one can understand that health is not simply present in nature, waiting to be discovered by scientists, but rather is continuously created by individuals and groups who interact among themselves in different social contexts (Leonardi, 2018, p. 739). This implies that health cannot have a unique definition in isolation; instead, health embodies as many definitions as there are people who use it (Leonardi, 2018, p. 739). When considering the various definitions of health, this is the definition that I agree with. When health is perceived through this perspective, it is a never-ending system of events, within which an observer may select some of these events and construct a theoretical configuration of health, depending on its own theories, knowledge purposes, and operational targets: no one of these can be absolutely better than another, because each definition may only be more or less useful for pursuing specific knowledge and operational targets in the different scopes of application (Leonardi, 2018, p. 739). To sum it up, health is subjective, fluid, and ever changing. In my opinion, health cannot be summed up in one restrictive definition.Fallon, C. K., & Karlawish, J. (2019) Cultural Diversity in Health and Illness Discussion Essay. Is the WHO definition of health aging well? Frameworks for “health” after three score and ten. 
    American Journal of Public Health
    , 
    109
    (8), 1104-1106. 
    http://dx.doi.org.wilkes.idm.oclc.org/10.2105/AJPH.2019.305177
    Oleribe, O. O., Ukwedeh, O., Burstow, N. J., Gomaa, A. I., Sonderup, M. W., Cook, N., Waked, I., Spearman, W., & Taylor-Robinson, S. D. (2018, August 24). 
    Health: redefined
    . NCBI. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320447/
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    View profile card for Emilia Rodriguez

    Last post 
    September 18 at 10:43 PM
     by Emilia Rodriguez

    Leonardi, F. (2018). The definition of health: Towards new perspectives. 
    International Journal of Health Services
    , 
    48
    (4), 735-748. 
    https://doi-org.wilkes.idm.oclc.org/10.1177%2F0020731418782653

    References

    The definition of health has many implications for practice, policy, health services, and health promotion (Leonardi, 2018, 736). Furthermore, the definition affects health professionals, and in turn they strongly affect how health is socially constructed in modern societies (Leonardi, 2018, p. 736). Views of health have a strong impact on people’s health behaviors and this affects their ability to make appropriate health decisions (Leonardi, 2018, p, 736). To put it concisely, the definition of health is of paramount importance in all health fields.

    Discussion 3
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    Emilia Rodriguez posted Sep 15, 2021 3:12 PM

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    Definitions of Health
                
    According to Farre and Rapley (2017), the medical model definition of health emphasizes the absence of disease. Consequently, health is defined as the presence of normal or high functioning of the body and the absence of infirmity or disease. The medical model emphasizes the integrity of the physiological, anatomical, and psychological integrity of the body.
                
    According to Svalastog et al. (2017), the holistic model was championed by World Health Organization in 1947. The holistic model defines health as a state of complete mental, physical and social wellbeing and not just the absence of an illness or infirmity (Svalastog et al., 2017). The holistic model positively promoted the view of health, unlike the medical model. According to Svalastog et al. (2017), the holistic model had been viewed as having unmeasurable aspects and generally considered vague especially with the terms such as wellbeing. However, the holistic model can sum population or individual-based indicators of wellbeing to define health.
                
    According to Dalh et al. (2018), the wellness model of health definition was championed by World Health Organization as an imitative of health promotion Cultural Diversity in Health and Illness Discussion Essay. The wellness model presents health in a dynamic perspective emphasizing health as a process or a force. The wellness model defines health as the extent to which a group or individual’s ability to satisfy their needs, realize their aspiration and the environmental coping capability; health is a resource for day to day living, as well as social and personal wellbeing.
                
    I agree with the wellness model definition of health. The wellness model, unlike the other definitions, views health as a process of living rather than a state of wellbeing. Consequently, the wellness model emphasizes health promotion since the current health status is largely a sum of our past living conditions and lifestyle choices.Dahl, A. J., Peltier, J. W., & Milne, G. R. (2018). Development of a value co‐creation wellness model: The role of physicians and digital information seeking on health behaviors and health outcomes. 
    Journal of Consumer Affairs
    , 
    52
    (3), 562-594. https://doi.org/ 10.1111/joca.12176Svalastog, A. L., Donev, D., Kristoffersen, N. J., & Gajović, S. (2017). Concepts and definitions of health and health-related values in the knowledge landscapes of the digital society. 
    Croatian Medical Journal
    , 
    58
    (6), 431. https://doi.org/10.3325%2Fcmj.2017.58.431less1 UnreadUnread1 ViewsViews

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    View profile card for Kadijatu Sesay

    Last post 
    September 18 at 6:33 PM
     by Kadijatu Sesay

    Farre, A., & Rapley, T. (2017, December). The new old (and old new) medical model: Four decades navigating the biomedical and psychosocial understandings of health and illness. In 
    Healthcare
     (Vol. 5, No. 4, p. 88). Multidisciplinary Digital Publishing Institute. https://doi.org/10.3390/healthcare5040088

    References

    The Definition I Agree With

    The Wellness Model

    The Holistic Model

    The Medical Model

    Francesca Provencher- Module 3
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    Francesca Provencher posted Sep 13, 2021 8:16 PM

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              Throughout the reading its it obvious that there are many different definitions for the word health. One definition stated by the World Health Organization (WHO) states health is a “state of complete physical, mental, and social well-being, not merely the absence of disease or infirmity” (Leonardi, 2018, p. 735). Another definition of health found in the literature includes, having an absence of diseases or illnesses and defined by physical limitations (Leonardi, 2018). I agree with the WHO definition of health. It is important that we not only look at the physical ailments that an individuals may have but make mental and social ailments equally as important. Leonardi F. (2018). The Definition of Health: Towards New Perspectives Cultural Diversity in Health and Illness Discussion Essay. 
    International journal of health services : planning, administration, evaluation
    , 
    48
    (4), 735–748. 
    https://doi.org/10.1177/0020731418782653
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    View profile card for Jeffrey Mahoney

    Last post 
    September 18 at 11:56 AM
     by Jeffrey Mahoney

    Bradley, K., Goetz, T., & Viswanathan, S. (2018). Toward a Contemporary Definition of Health. 
    Military medicine
    , 
    183
    (suppl_3), 204–207. 
    https://doi.org/10.1093/milmed/usy213

    Being a mental health nurse and a future mental health nurse practitioner, I see how important mental health is. There are a variety of mental illnesses that if go untreated can cause physical ailments as well. The literature states, the new definition of health transforms the word from requiring the absence of disease to a state where a person has a full life. Health is not a fixed state of being, but a dynamic quality of living where body, mind, and spirit are utilized to make the most of each day (Bradley et al., 2018). I believe it is important to not only be in a disease free state but to feel that way too and have the capabilities of living a full life.

    Module Ⅲ
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    James Neal posted Sep 15, 2021 2:14 AM

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    There are significant differences in how health is defined in various cultures, and being cognizant of these differences can play a major role in determining how successful we’ll be both in meeting the goals of our patients, as well as their clinical outcomes Cultural Diversity in Health and Illness Discussion Essay. These types of examples are numerous. In a similar study, those from Asian cultures were much more dissatisfied with Western medical care they received because they ultimately attributed the cause of their initial illness to more supernatural occurrences (Armstrong & Swartzman, 1999). Even within ostensibly the same culture, there are variations in how individuals view health. As an example, some people view having their terminally ill, elderly relative as anything less than full code status to be an affront, whereas others resent that their relative is in the hospital receiving any treatment at all, believing that being at home and in nature is more healthful than the hospital environment. This should remind us, again, that we must be cautious about generalizing people’s health beliefs with those held by the culture we perceive them to be in. Armstrong, T. L., & Swartzman, L. C. (1999). Asian versus western differences in satisfaction with western medical care: The mediational effects of illness attributions. 
    Psychology & Health
    , 
    14
    (3), 403–416. 
    https://doi.org/10.1080/08870449908407337
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    View profile card for Jahenein Nagel

    Last post 
    September 18 at 10:39 AM
     by Jahenein Nagel

    Levesque, A., & Li, H. Z. (2014). The relationship between culture, health conceptions, and health practices. 
    Journal of Cross-Cultural Psychology
    , 
    45
    (4), 628–645. 
    https://doi.org/10.1177/0022022113519855

    References

    As a simple example of this principle, a study in health perception differences in Canada between those with French, English, or First Nation backgrounds found notable differences in how each group viewed health. While those from a European background were more similar, First Nation individuals were more likely to view health as extending beyond the scope of the individual and into the broader family and community (Levesque & Li, 2014). Perhaps without coincidence, First Nation individuals weighted traditional cultural remedies much more highly than other groups in the study (Levesque & Li, 2014). Notably, they did not consider an absence of pain in their definition of health, whereas most other cultures do (Levesque & Li, 2014).

    Week 3 Laura
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    Laura Riccardi posted Sep 13, 2021 6:44 PM

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    The World Health Organization (WHO) defines health as a complete state of physical, mental, and social well-being (
    Preamble to the Constitution of the World Health Organization
    , 1948). A contemporary definition of health could reach beyond this paradigm to recognize that we are all, to some extent, less than perfect, that we each have aspects that need care, and that we all are in some way infirm or even “diseased” (Bradley et al., 2018).  This modern definition is focussing not on disease but on a feeling of fullness in your life. I have to agree with the contemporary definition as if you don’t have complete well-being and fullness, a person may have an incomplete, lacking mental state. This could alternatively affect your health in the basic terms as mentioned by the WHO. Social support and interaction is an important part of feeling complete. As evidenced with the COVID pandemic, isolation led people to feel scared, nervous, and unsure regarding their future. This affected all cultures all over the world. One study found that the country of Scotland was locked down for 66 days and people were only allowed to leave to go to work (Ingram et al., 2021). The people in Scotland who lacked interpersonal contact led to cognitive decline and higher levels of negative moods(Ingram et al., 2021). Bradley, K. L., Goetz, T., & Viswanathan, S. (2018). Toward a contemporary definition of health. 
    Military Medicine
    , 
    183
    (suppl_3), 204–207. 
    https://doi.org/10.1093/milmed/usy213
    Preamble to the Constitution of the World Health Organization
    . (1948, April 7) Cultural Diversity in Health and Illness Discussion Essay. WHO. Retrieved September 10, 2021, from 
    http://www.who.int/about/definition/en/print.html
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    View profile card for Frances Hall

    Last post 
    September 17 at 11:25 AM
     by Frances Hall

    Ingram, J., Hand, C. J., & Maciejewski, G. (2021). Social isolation during covid ‐19 lockdown impairs cognitive function. 
    Applied Cognitive Psychology
    . 
    https://doi.org/10.1002/acp.3821

    References

    Romig- Module 3
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    Krista Romig posted Sep 13, 2021 5:19 PM

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    There are many different definitions for the term health and patients’ may have different understanding and priorities when it comes to their health. It is important to reflect on what our personal definition of health is and to assess the patients’ goals for their health. According to the World Health Organization health is “a state of complete physical, mental, and social well-being and not merely the absence of disease” (World Health Organization, n.d.). However, according to Merriam-Webster (n.d.), health is “the condition of being well or free from disease”.
    References
    World Health Organization. (n.d.) Cultural Diversity in Health and Illness Discussion Essay. 
    Constitution of the World Health Organization
    . World Health Organization.
     
    https://www.who.int/about/governance/constitution
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    View profile card for Jennifer Johnson

    Last post 
    September 16 at 7:40 PM
     by Jennifer Johnson

    Merriam-Webster. (n.d.). 
    Health
    . Merriam-Webster. 
    https://www.merriam-webster.com/dictionary/health

    I agree with the World Health Organization’s definition of health. I believe that health is based on more than just the absence of sickness. As a psychiatric nurse, I see many patients who are technically “healthy” and are not doing well. I believe in holistic care for patients and agree that they need to be well mentally and socially as well as physically.

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    Emily Meeks posted Sep 14, 2021 4:47 PM

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    After reading a number of definitions for the term health, it is in my opinion that the definition presented by the World Health Organization is no longer applicable today, given the prevalence of chronic illnesses and disabilities. We have learned from this weeks’ reading that the experience of being ill is determined by the patient. Health, to one individual, may not mean the same thing to another. Health is multidimensional, involving one’s physical, mental, and social sense of well-being, their ability to adapt and find balance. Definitions provided by Sartorius (2006), Huber et al. (2016), and Krahn et al. (2021) each incorporate these aspects.
    References
    Knottnerus, J. A. (2016). Towards a ‘patient-centered’ operationalization of the new dynamic concept of health: a mixed methods study. 
    BMJ Open
    , 6(1).Krahn, G., Robinson, A., Murray, A., & Havercamp, S. (2021). It’s time to reconsider how weSartorius, N. (2006). The meaning of health and its promotion. 
    Croatian Medical Journal,
    World Health Organization. (2006). 
    Constitution.
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    View profile card for James Neal

    Last post 
    September 16 at 4:44 PM
     by James Neal

    https://www.who.int/governance/eb/who_constitution_en.pdf

    47(4): 662-664. 
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2080455/

    define health: perspective from disability and chronic conditions. 
    Disability and Health Journal,
     14(4). 
    https://doi.org/10.1016/j.dhjo.2021.101129

    http://dx.doi.org/10.1136/bmjopen-2015-010091

    Huber, M., van Vliet, M., Giezenberg, M., Winkens, B., Heerkens, Y., Dagnelie, P.C., &

    Personally, I am more inclined to agree with Huber et al. (2016), as they go on to explain the new concept of health as an individual’s strength and self-management, rather than weakness. Describing that health is a dynamic state, with emphasis on a person being more than their illness and continue to have potential to be healthy (Huber et al., 2016). Reinforced by Krahn et al., health can occur even in the presence of limitations or disorders (2021). For example, a person with a mental health illness or controlled diabetes, living qualities lives, can still be considered healthy. Health is no longer “merely the absence of disease” (WHO, 2006, p. 1).

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    Donna Wrobel posted Sep 14, 2021 5:32 PM

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    The World Health Organization (WHO) defines health as “physical, mental and social well-being, not just the absence of disease” and a fundamental right of all human beings regardless of race, religion, political belief, economic or social status (
    Constitution
    , 2021). The Centers for Disease Control & Prevention (CDC) defines health similarly but narrows the definition to the absence of morbidity or mortality (
    Health Related Quality of Life
    , 2018). Finally, the Health Resources & Services Administration (HRSA) describes health status as the overall rate of disease incidence and prevalence and the morbidity, mortality or survival rates in a population (
    Glossary
    , 2020).In my opinion, health is more than just the absence of disease or disability but the level of well-being that allows the patient to meet or exceed their physical and mental abilities and goals. Because mental and physical health are related and can affect each other in both positive and negative ways, the definition of health must account for both. The concept of health has evolved from as far back as the ancient Greeks as a balance between the person and their environment to today where it is believed to be the capacity of the individual for realizing and fulfilling their own potential to function in their environment (Svalastog et al., 2017) Cultural Diversity in Health and Illness Discussion Essay. Health is a dynamic concept that changes over a person’s life and can be influenced by their own perception of their capacity as well as their practices and behaviors which affect these physical and mental abilities. 
    Constitution
    . (2021). World health organization. 
    https://www.who.int/about/governance/constitution
    Glossary. (2020, December). Health resources & services administration (HRSA). Retrieved September 11, 2021, from 
    https://bhw.hrsa.gov/glossary
    Leininger, M. (1999). What is transcultural nursing and culturally competent care? 
    Journal of Transcultural Nursing
    , 
    10
    (1), 9. less1 UnreadUnread2 ViewsViews

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    View profile card for Krista Romig

    Last post 
    September 16 at 12:53 AM
     by Krista Romig

    Svalastog, A., Donev, D., Jahren Kristoffersen, N., & Gajović, S. (2017). Concepts and definitions of health and health-related values in the knowledge landscapes of the digital society. Croatian Medical Journal, 58(6), 431–435. 
    https://doi.org/10.3325/cmj.2017.58.431

    Health related quality of life
    . (2018, October 31). Centers for disease control & prevention. 
    https://www.cdc.gov/hrqol/wellbeing.htm

    Evans, M. K. (2020). Health equity — are we finally on the edge of a new frontier? 
    New England Journal of Medicine
    , 
    383
    (11), 997–999. 
    https://doi.org/10.1056/nejmp2005944

    References

    Each of these organizations defines the concept of health a bit differently although they all describe it as the absence of disease Cultural Diversity in Health and Illness Discussion Essay. The definition of the World Health Organization, which includes the aspects of mental and social well-being comes closest to the definition of health that is taught in most nursing programs. Nursing is holistic in practice which focuses on the whole person, including their physical, mental and social health in order to assist the patient to maintain or regain their well-being (Leininger, 1999). As we learned in the previous module, the deaf community does not focus on their hearing deficit as a disability. If health was defined solely by the presence of disability or the absence of morbidity or mortality, then all deaf individuals would be deemed unhealthy, which is not the case.

    Module 3: Discussion
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    Idida Aleman Musial posted Sep 15, 2021 11:39 PM

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    Culture plays an important role in health and illness. I agree with the World Health Organization’s definition of health because it portrays the individual as a whole. Research defines health as “wellbeing” of the individual, mentally and physically (Barkham, et al. 2019). When health is disrupted, the equilibrium is affected. Individuals from different cultures have express pain, discomfort, or illness in general in a variety of ways. Age is another possible barrier when providing care. For example, the way that teenagers describe their symptoms can be challenging, however we should still treat them as individuals (Joseph & Fleary, 2021). Healthcare professionals have a big responsibility when providing care to a diverse public. Health disparities exists because of the lack of cultural sensitivity to individuals that are different from us. Researchers found health disparities with “Asian and Native American racial groups had stronger effects from racial discrimination than did blacks” (Carter, et al. 2019). There are many areas that require improvement when it comes to addressing health. For instance, when providing care to an obese individual, we have to be aware of our bias and judgment (Bąk-Sosnowska, et al. 2017;2016). We can make a difference in the way that healthcare is delivered by providing unbiased and free of judgment care Cultural Diversity in Health and Illness Discussion Essay. Reference:   less0 UnreadUnread

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    Carter, R. T., Johnson, V. E., Kirkinis, K., Roberson, K., Muchow, C., & Galgay, C. (2019). A meta-analytic review of racial discrimination: Relationships to health and culture. 
    Race and Social Problems
    , 11(1), 15-32. 
    https://doi.org/10.1007/s12552-018-9256-y

    Bąk-Sosnowska, M., & Skrzypulec-Plinta, V. (2017;2016;). Health behaviors, health definitions, sense of coherence, and general practitioners’ attitudes towards obesity and diagnosing obesity in patients. 
    Archives of Medical Science
    , 13(2), 433-440. 
    https://doi.org/10.5114/aoms.2016.58145

    Barkham, M., Broglia, E., Dufour, G., Fudge, M., Knowles, L., Percy, A., Turner, A., Williams, C., & the SCORE Consortium. (2019). Towards an evidence‐base for student wellbeing and mental health: Definitions, developmental transitions and data sets. 
    Counselling and Psychotherapy Research
    , 19(4), 351-357. 
    https://doi.org/10.1002/capr.12227

    Kadijatu Sesay
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    Kadijatu Sesay posted Sep 15, 2021 10:14 PM

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    Health can be defined in many ways. To some, health can be defined as eating well, exercising, and sleeping well. Others can define health as not being in the hospital or having chronic illnesses. The World Health Organization defines health as “Health is a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity.”Pasanen et al., (2021) also define health and well-being as the quality of life. The importance of well mental health and social well-being play a large role in impacting one’s perception of health. In my opinion, health is a combination of both definitions that I discussed. Health is a combination of well physical and mental health along with managing modifiable risk factors for poor health Cultural Diversity in Health and Illness Discussion Essay. Environmental factors also play a large role in shaping our health. Health is finding a state of well-being that includes taking care of oneself, maintaining optimal mental health, and controlling environmental risk factors. In patients with chronic medical conditions, health also means managing symptoms and maintaining an active physical lifestyle.    Rojas-Rueda, D., Morales-Zamora, E., Alsufyani, W.A., Herbst, C.H., Albalwi, S.M., Alsukait, R. & Alomran, M. (2021, January). Environmental risk factors and health: An umbrella review of meta-analysis. 
    International Journal of Environmental Resources and Public Health, 18
    (2). DOI: 
    10.3390/ijerph18020704
    World Health Organization. 2021. The constitution of the world health organization. 
    https://www.who.int/about/governance/constitution
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    Pasanen, T.P., Tamminen, N., Martelin, T., Mankinen, K. & Solin, P. (2021, July). Profiles of subjective health among people living alone: A latent class analysis. 
    BMC Public Health, 20
    (1), 1-12. 
    https://doi.org/10.1186/s12889-021-11396-2

    References:

    Rojas-Rueda et al., (2021) state that health is shaped by environmental, psychosocial, and physical surroundings as well as genetic predispositions. Rojas-Rueda et al., (2021) also report that chronic disease burdens are impacted by our environmental influences.

    Module 3
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    Karimah Moss posted Sep 13, 2021 12:01 PM

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    Module 3Others define health as the individual’s ability to function and participate. Health is exclusively based on the ability or inability to participate and function in society. This places emphasis only on physical health and other aspects such as pain or mental health are only important when they impact the ability to participate (McCartney et al., 2019).
    References
    McCartney, G., Popham, F., McMaster, R., & Cumbers, A. (2019). Defining health and health inequalities. 
    Public Health
    , 
    172
    , 22–30. 
    https://doi.org/10.1016/j.puhe.2019.03.023
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    View profile card for Donna Wrobel

    Last post 
    September 15 at 12:31 PM
     by Donna Wrobel

    Krahn, G. L., Robinson, A., Murray, A. J., Havercamp, S. M., & The Nisonger RRTC on Health and Function. (2021). It’s time to reconsider how we define health: Perspective from disability and chronic condition. 
    Disability and Health Journal
    , 
    14
    (4), 1–5. 
    https://doi.org/10.1016/j.dhjo.2021.101129

    An additional interpretation is that “health is the dynamic balance of physical, mental, social, and existential well-being in adapting to conditions of life and the environment Cultural Diversity in Health and Illness Discussion Essay. This definition incorporates environmental factors and recognizes health as fluid across the life span, with adaptation to life circumstance at its core” (Krahn et al., 2021, p. 4). Existential well-being refers to how the individual perceives their well-being in terms of spiritual integrity, satisfaction in life, comfort with death and illness, and purpose of life. With existential well-being, one has the freedom to live a life that is compatible with their values and religious practices without feeling discriminated against (Krahn et al., 2021). This is the definition I most agree with because it addresses essential areas of health that the other two definitions I discussed do not. It looks at all components of one’s life that can have an impact on overall well-being. When discussing health, it is important to view the individual as a whole, rather than seeing only one part of the person. I also love how this definition includes those with disabilities. It separates physical functional abilities from health and states that good health can occur even when limitations are present with a disability (Krahn et al., 2021).

    This week, I will be discussing the term health and its varying definitions. One definition of health is that it is as an ideal outcome. This interpretation places the individual into two distinct categories, healthy or unhealthy. According to this definition, healthy and unhealthy are determined by whether or not the person has achieved an overall state of well-being. However, this explanation of health does not take into account that people with certain medical conditions or disabilities, and the aging population may view themselves as being healthy (McCartney et al., 2019) Cultural Diversity in Health and Illness Discussion Essay.

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    Frances Hall posted Sep 15, 2021 12:32 AM

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    The modern understanding of health became official when the World Health Organization (WHO), at the time of its establishment in 1948, included the definition of health in its Constitution. This generally accepted definition states that “health is a state of complete physical, mental, and social well-being and not merely the absence of disease or infirmity”(Svalastog et al., 2017). Health is an amorphous word that lacks a single definition. To some, “health is wealth”, given that in the absence of good health, an individual or society cannot attain its full potential(Oleribe et al., 2018). We all understand that without health, we are not living a rewarding and full life.  Health is viewed a resource and a total, personal, situation-specific phenomenon. Absence of disease is not enough, the life situation as a whole must be taken into consideration (Svalastog et al., 2017). Now that is a definition I like, health is the total of all the aspects that make up our lives. Starting with the health of our family and welfare physically and mentally. To be able to live according to one personal values is also an important issue.  Everyone will have a different perception of health as it is a personal thing and as providers of healthcare we need to make sure our care plans are individualized for meet their needs. Oleribe, O., Ukwedeh, O., Burstow, N., Gomaa, A., Sonderup, M., Cook, N., Waked, I., Spearman, W., & Taylor-Robinson, S. (2018). Health: Redefined. 
    Pan African Medical Journal
    , 
    30
    . 
    https://doi.org/10.11604/pamj.2018.30.292.15436
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    Svalastog, A., Donev, D., Jahren Kristoffersen, N., & Gajović, S. (2017). Concepts and definitions of health and health-related values in the knowledge landscapes of the digital society. 
    Croatian Medical Journal
    , 
    58
    (6), 431–435. 
    https://doi.org/10.3325/cmj.2017.58.431

    References

    Discussion 3
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    Julie Robichaud posted Sep 13, 2021 10:04 AM

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              Health means something different to each individual and culture. In 1948, Mahalama Gandhi came up with the idea that health was more important than wealth, and that society could not prosper if its people were not healthy (Oleribe et al., 2018). Health has multiple dimensions that include situational, professional, societal, and cultural definitions (Oleribe et al., 2018). Unfortunately we presently live in an unhealthy society with terrorism, murder, and other social vices that make the world unhealthy (Oleribe et al., 2018). This suggests that health should not just refer to oneself, but also to society which could result in an enhanced community that is safe, fulfilling, and happy. A redefined health according to Oleribe et al (2018), is “a satisfactory and acceptable state of physical (biological), mental (intellectual), emotional (psychological), economic (financial), and social (societal) wellbeing.”McCartney, G., Popham, F., McMaster, R. & Cumbers, A (2019). Defining health and health inequalities. 
    ScienceDirect, 172,
     pp. 22-30. 
    https://doi.org/10.1016/j.puhe.2019.03.023
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    View profile card for Karimah Moss

    Last post 
    September 14 at 3:15 PM
     by Karimah Moss

    Oleribe, O.O., Ukwedeh, O., Burstow, H.J., Gomaa, A.I., Sonderup, M.W., Cook, N., Waked, I., Spearman, W. & Taylor-Robinson, S.D. (2018). 
    The Pan African Medical Journal, 30. 
    https://doi.org/10.11604/pamj.2018.30.292.15436

              I disagree with the WHO definition of health because there is no such thing as a “complete” physical, mental, and social well-being. This describes an absolute and impossible state to fulfill. I have always looked at things holistically, because looking at the “whole” picture is necessary, practical, and achieves a better outcome. I would define health as it pertains to myself, society, and I would include my family. I would include my family because they are as important to me as my health and well-being. The definition I relate to the most is one defined by J.M. Last, which defines health as a structural, functional, and emotional state compatible with effective life as an individual and member of society (McCartney et al., 2019).

    Module 3 DP-H. Stetson
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    Heather Stetson posted Sep 13, 2021 6:14 PM

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    Health can be defined differently depending on various factors such as an individual’s cultural background, socioeconomic status, and/or age. The commonly accepted definition of health was adopted in 1948 by the World Health Organization (n.d.) as “a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity” (para. 1). The creation of this definition was important during this time because it catalyzed the creation of national healthcare systems (Leonardi, 2018). However, in today’s medically complex world the WHO’s definition of health is viewed by some as outdated and unachievable for most people.              less0 UnreadUnread

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    World Health Organization [WHO]. (n.d.). 
    Constitution Cultural Diversity in Health and Illness Discussion Essay
    . Retrieved September 11, 2021, from 
    https://www.who.int/about/governance/constitution

    Leonardi, F. (2018). The definition of health: Towards new perspectives. 
    International Journal of Health Services, 48
    (4), 735-748. 
    https://doi.org/10.1177/0020731418782653

    Card, A. J. (2017). Moving beyond the WHO definition of health: A new perspective for an aging world and the emerging era of value‐based care. 
    World Medical and Health Policy, 9
    (1), 127-137. 
    https://doi.org/10.1002/wmh3.221

                This definition of health offered by Card (2017) aligns with the philosophy of treating patients from a holistic perspective. It considers that health does not occur on a continuum. It is more inclusive of socio-cultural considerations and does not indicate that for a person to be healthy they must have a complete absence of disease.

    The experience of physical and psychological well-being. Good health and poor health do not occur as a dichotomy, but as a continuum. The absence of disease or disability is neither sufficient nor necessary to produce a state of good health. (p. 131)

    According to Leonardi (2018), due to the advancements in modern medicine, people are living longer lives with more chronic illnesses. Additionally, most people do not experience a “complete” state of physical, mental, and social well-being on an absolute continuum. The WHO’s definition does not have a holistic approach for what health means for an individual. As a healthcare provider, I feel health should be viewed as a holistic endeavor. An alternate  definition of health proposed by Card (2017) states health is:

    Jeff Mahoney

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    Jeffrey Mahoney posted Sep 13, 2021 12:27 PM

    VanderWeele et al. (2019) proffer that the term health has evolved into two concepts – referring narrowly to the wholeness of the body (absence of disease) and broadly to wholeness of the complete person (a state in which all aspects of the person are good). The scholars support their definition by citing the etymology of the term health from Old English 
    hælþ 
    or “wholeness” (VanderWeele et al., 2019).I also recognize that definition of health can be difficult to define in patients who suffer from chronic disease. In this case, I believe that Margaret Newman’s theory of health as expanding consciousness is useful. Newman posits that if a patient with chronic illness recognizes how their patterns have led to disease, then the awareness of the pattern itself can be seen as health (Younas & Parveen, 2017).ReferencesYounas, A., & Parveen, S. (2017). Finding patterns of meaning: Margaret Newman’s theory of health as expanding consciousness.
     Creative Nursing, 23
    (4), 207-214. https://doi.org/10.1891/1078-4535.23.4.207

    VanderWeele, T. J., McNeely, E., & Koh, H. K. (2019). Flourishing as a definition of health—Reply.
     JAMA : The Journal of the American Medical Association, 322
    (10), 981-982. https://doi.org/10.1001/jama.2019.10355

    They contend that clinicians at the very least should be concerned with the narrow definition – and they worry that a broader view could lead to clinician burn-out (VanderWeele et al., 2019) Cultural Diversity in Health and Illness Discussion Essay. However, the scholars suggest that clinicians who are in certain specialties (eg, nursing, psychiatry, or family medicine) may benefit from adopting the broader view (VanderWeele et al., 2019). As I understand that health is shaped by cultural values and defined differently by the individual, I resonated most with their final notion. Patient-centered care produces cultural competent care when the clinician respects the core themes that patient values within their daily lives (VanderWeele et al., 2019) Cultural Diversity in Health and Illness Discussion Essay.