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Sickle Cell Disease Case Study · Would you please write one page on health History Includes (Comprehensively presents key/relevant Information accurately and in sufficient detail: person’s age, gen

Sickle Cell Disease Case Study

·    Would you please write one page on health History Includes (Comprehensively presents key/relevant Information accurately and in sufficient detail: person’s age, gender, ethnicity, past and current medical history, chief complaint, and history of present illness on admission. 

Information presented in a clear, organized, and professional manner)

. Second Paragraph on Laboratory and Diagnostic testing include(Comprehensively presents key/relevant Information accurately and in sufficient detail: description of the ordered/completed diagnostic tests, pertinent results (normal and abnormal ranges), and rationales for each diagnostic test.

·  Information presented in a clear, organized, and professional manner

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Introduction:
Sickle Cell Disease is a genetic disorder that affects the shape and function of red blood cells. As a medical professor, it is essential to conduct a comprehensive health history and laboratory and diagnostic testing for patients with sickle cell disease to provide accurate medical care. This assignment aims to present a detailed health history and laboratory and diagnostic testing for a patient with sickle cell disease.

Health History:
The patient is a 26-year-old African American male who presents with a history of sickle cell disease. The patient reports a history of frequent pain crises, which have been managed with pain medications in the past. He has a history of hospital admissions for sickle cell crises, with the most recent admission four months ago. The patient also reports a history of stroke and pneumonia. He denies any history of drug abuse or tobacco use. Furthermore, the patient reports a history of allergies to penicillin and sulfa drugs.

Laboratory and Diagnostic Testing:
The patient has undergone a complete blood count (CBC), which shows a decreased hemoglobin level of 8.7 g/dL (normal range: 13.5-17.5 g/dL) and an increased reticulocyte count of 11% (normal range: 0.5-2.5%). The peripheral smear shows sickle cells and target cells. The patient has also undergone a chest x-ray, which shows evidence of acute chest syndrome. The patient has been started on intravenous antibiotics and blood transfusion therapy.

In summary, a comprehensive health history and laboratory and diagnostic testing are essential for the accurate diagnosis and management of sickle cell disease. It is also crucial to present the information in a clear, organized, and professional manner.

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