Sickle cell case study answers

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Sickle cell case study answers in 2021

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Sickle cell anemia case study high school

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Sickle cell anemia: case study pdf

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Hesi sickle cell case study

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Sickle cell disease by race

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What are the symptoms of sickle cell disease?

Per her mother, N.S. did not experience vomiting, diarrhea, upper respiratory symptoms, respiratory distress, change in urination, neurologic abnormalities, or behavioral changes associated with her current illness.

What are the risks of sickle cell anemia?

Sickle cell disease, or sickle cell anemia, can increase risk of complications including: stroke, pulmonary hypertension, organ damage, blindness, vascular damage, gallstones, etc. For the purposes of this case study, AP will need to be monitored specifically for pulmonary, vascular, and neurological complications.

How is sickle cell anemia diagnosed in blood test?

Sickle cell anemia is diagnosed through blood test, testing for hemoglobin S (the defective form of hemoglobin descriptive of the disease), the presence of other abnormal hemoglobin variants, evaluating status and number of erythrocytes, and/or determination of one of more altered hemoglobin gene copies.

How did n.s.get sickle cell disease?

In the ED, it was recommended N.S. be admitted for painful sickle cell crisis. Past Medical History: N.S. was born full term via spontaneous vaginal delivery, weight 7lbs 8oz. She did show evidence of neonatal jaundice, which was successfully treated with phototherapy.

Last Update: Oct 2021

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Tonee

19.10.2021 09:26

B: sickle-shaped erythrocytes drive decreased organ perfusion. Sickle cell disease-specific communications protocol whenever possible to promote rapid, actual, and safe anodyne management and resolve of vasoocclusive crises in children and adults.

Zelmarie

27.10.2021 00:33

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19.10.2021 12:12

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18.10.2021 08:02

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