Sickle cell disease is more than just a blood disorder—it’s a lifelong condition that demands fast, compassionate, and informed nursing care. In this episode, Dr. Morgan Taylor, DNP, CPNP, CCRN, breaks down the pathophysiology of sickle cell disease, explains why vaso-occlusive crises are so painful and dangerous, and walks you through a real-life emergency case involving a teen with acute chest syndrome.
Learn how to prioritize pain control, hydration, and oxygenation—and why those three interventions can make or break outcomes. Plus, we’ll tackle the stigma clients often face and explore the long-term role of hydroxyurea in preventing future crises. As always, Dr. Morgan Taylor wraps up with a high-yield NCLEX-style question and breakdown.
Topics discussed in this episode:
What causes sickled red blood cells and why they block oxygen delivery
Recognizing and managing vaso-occlusive crisis
A real ED case of a 16-year-old with acute chest syndrome
Pain management strategies and the importance of PCA pumps
Fluids and oxygen: two lifesaving interventions in sickle cell crisis
The long-term role of hydroxyurea in sickle cell care
Breaking down a test question on priority nursing interventions
This episode is packed with high-yield insights to help you recognize emergencies, challenge bias, and advocate fiercely for clients with sickle cell anemia. Tune in now to sharpen your clinical instincts and boost your NCLEX prep!
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