Anesthetic management of a patient with sickle β+ thalassemia

Sickle cell disease is a congenital condition and its most common clinical manifestation is anemia due to chronic hemolysis. Persistent and accelerated hemolysis associated with multiple transfusions is a recognized risk factor for the development of cholelithiasis. The occurrence of gallstones is o...

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Bibliographic Details
Main Authors: Saswata Bharati, Subhabrata Das, Prasenjit Majee, Subrata Mandal
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2011-01-01
Series:Saudi Journal of Anaesthesia
Subjects:
Online Access:http://www.saudija.org/article.asp?issn=1658-354X;year=2011;volume=5;issue=1;spage=98;epage=100;aulast=Bharati