Jul 13, 2017 Others

What are resulting maladaptive responses for patients with these disorders?

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Maladaptive Responses to Immune Disorders

INSTRUCTIONS:

Maladaptive responses to disorders are compensatory mechanisms that ultimately have adverse health effects for patients. For instance, a patient’s allergic reaction to peanuts might lead to anaphylactic shock, or a patient struggling with depression might develop a substance abuse problem. To properly diagnose and treat patients, advanced practice nurses must understand both the pathophysiology of disorders and potential maladaptive responses that some disorders cause.

Consider immune disorders such as HIV, psoriasis, inflammatory bowel disease, and systemic lupus E. What are resulting maladaptive responses for patients with these disorders?





Select two of the following immune disorders: HIV, psoriasis, inflammatory bowel disease, or systemic lupus E (SLE).

Identify the pathophysiology of each disorder you selected. Consider the compensatory mechanisms that the disorders trigger. Then compare the resulting maladaptive and physiological responses of the two disorders.

Select one of the following factors: genetics, gender, ethnicity, age, or behavior. Reflect on how the factor might impact your selected immune disorders.

Post on or before Day 3 a brief description of the pathophysiology of your selected immune disorders. Explain how the maladaptive and physiological responses of the two disorders differ. Finally, explain how the factor you selected might impact the pathophysiology of each disorder.



Huether, S. E., & McCance, K. L. (2012). Understanding pathophysiology (Laureate custom ed.). St. Louis, MO: Mosby.

McPhee, S. J., & Hammer, G. D. (2012). Pathophysiology of disease: An introduction to clinical medicine (Laureate Education, Inc., custom ed.). New York, NY: McGraw-Hill Medical.

CONTENT:

Maladaptive Responses to Immune Disorders Name Institution Maladaptive Responses to Immune Disorders Pathophysiology of HIV and Psoriasis Psoriasis affects almost 2-3% of the global population and manifests as erythematous, indurated, rough plaques over the skin at times with involvement of the nails and joints. The disease is distinguished by exaggerated and messed up epidermal cell proliferation and keratinization. Though great steps have been made in the comprehension of the disease, the link of events that leads to this abnormal keratinization has not yet been explicated (Barker, 2012). A host of abnormalities witnessed in psoriasis such as am

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