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Description

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

 

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