| Literature DB >> 12518188 |
Hussain H Al-Saeed1, Ahmed H Al-Salem.
Abstract
Sickle cell anemia (SCA) is one of the commonly inherited hemoglobinopathies in the Kingdom of Saudi Arabia. It is characterized by periods of remissions and exacerbations called crises as well as certain pathological phenomenon such as acute chest syndrome, priapism, hepatopathy, and cerebrovascular stroke. Blood transfusion (BT) as therapy and prophylaxis in SCA, although was advocated as early as the 1940's, there are still debates regarding its benefits and risks. This is a review of the value of BT in patients with SCA with emphasis on the risks and benefits as well as guidelines towards safe BT.Entities:
Mesh:
Year: 2002 PMID: 12518188
Source DB: PubMed Journal: Saudi Med J ISSN: 0379-5284 Impact factor: 1.484