| Recognize the clinical presentation and pathophysiology of common acute complications of sickle cell disease, including vaso-occlusive crises, acute chest syndrome, stroke, and splenic sequestration. |
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| Apply evidence-based strategies for the evaluation and management of acute sickle cell disease complications in both inpatient and emergency care settings. |
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| Identify indications for blood transfusion, exchange transfusion, and escalation of care in patients with severe or life-threatening sickle cell disease complications. |
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| Implement multidisciplinary approaches and preventive strategies to reduce morbidity, mortality, and recurrent hospitalizations among patients with sickle cell disease. |
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