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Current Trends in the Management of Sickle Cell Disease: REVIEW ARTICLE
Author(s) -
Abdelaziz Elamin
Publication year - 2008
Publication title -
sudan journal of medical sciences
Language(s) - English
Resource type - Journals
ISSN - 1858-5051
DOI - 10.4314/sjms.v2i2.38477
Subject(s) - medicine , disease , therapeutic modalities , intensive care medicine , modalities , intervention (counseling) , anemia , sickle cell anemia , treatment modality , review article , medical care , pediatrics , family medicine , pathology , psychiatry , physical therapy , surgery , social science , sociology
Sickle cell disease (SCD) is common in Sudan and in sub-Saharan Africa. It is also prevalent in the Arabian Gulf countries and in India. Despite the tremendous advances in diagnostic and therapeutic modalities, Children with sickle cell anemia continue to suffer from repetitive crisis and have frequent severe complications. These morbid events as well as mortality can be greatly reduced by specialized medical care that focuses on prevention and active intervention. This article reviews the most recent and evidence-based guidelines for preventive care and medical management of SCD and its most commonly encountered complications. Keywords : hemolytic crisis, children, pain management, bone marrow transplant Sudan Journal of Medical Sciences Vol. 2 (2) 2007: pp. 129-138

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