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Mitral Valve Replacement in a Patient with Sickle Cell Disease Using Perioperative Exchange Transfusion

Sickle cell disease is a genetic hemoglobinopathy in which a significant number of red blood cells carry hemoglobin-S as opposed to normal red blood cells that contain hemoglobin-A. Under certain conditions such as hypoxia, acidosis, and hypothermia, the red blood cells containing hemoglobin-S will...

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Bibliografiske detaljer
Udgivet i:J Extra Corpor Technol
Main Authors: Chabot, David, Sutton, Robin
Format: Artigo
Sprog:Inglês
Udgivet: American Society of ExtraCorporeal Technology 2008
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4680718/
https://ncbi.nlm.nih.gov/pubmed/19192758
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