What are your recommendations for adult sickle cell patients who end up being admitted several times a year for pain crises despite hydroxyurea, crizanlizumab, voxelotor, etc?  

What can you recommend that might help keep them out of the hospital? Do you consider a program of exchange transfusions in this situation?



Answer from: at Academic Institution

Answer from: at Academic Institution
Comments
at Duke University
I would also look for other sources of chronic inf...
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