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Episode 68 of 73

#68 Advances in Management of Sickle Cell Disease

Duration: 31:19
pain is the most common and devastating symptom of Sickle Cell Disease. Despite the slow and elusive developement of therapeutic intervention in Sickle cell disease that would halt the vasocclusive crisis and the related pain, last few decades have brought about good progress with successful hemopoe
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pain is the most common and devastating symptom of Sickle Cell Disease. Despite the slow and elusive developement of therapeutic intervention in Sickle cell disease that would halt the vasocclusive crisis and the related pain, last few decades have brought about good progress with successful hemopoetic stem cell transplant as well as several therapeutic agents targeting various aspect of teh pathophysiliogy of SCD.   In this episode, I review the 4 major targets in the pathophysiology of SCD and approved therapeutic interventions and agents as well as those that are further along clinical trial with very promising results.   Takeaways in This Episode What prompted me to do this update How this episode is different from and how it complements the earlier published episode about sickle cell disease The challenges presented by sickle cell disease The major presentation and impact of sickle cell disease 4 main therapeutic targets with advances and ongoing trials Newer FDA approved agents in management of vasocclusive crisis and pain The success and challenges of stem cell transplant for SCD   Links Pedia Pain Focus Episode #12. Master Your Sickle Cell Pain Care Skills Pedia Pain Focus Episode #62. Metaphors for Better Pediatric Pain Management  Pedia Pain Focus Episode #21. How to Counsel your Patients on Off-Label Medication Use Proactive Pain Solutions Physicians Academy Proactive Pain Solutions
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