Literature DB >> 12518188

Principles of blood transfusion in sickle cell anemia.

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.

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Year:  2002        PMID: 12518188

Source DB:  PubMed          Journal:  Saudi Med J        ISSN: 0379-5284            Impact factor:   1.484


  3 in total

1.  Blood Transfusion Frequency and Indications in Yemeni Children with Sickle Cell Disease.

Authors:  Abdul-Wahab M Al-Saqladi; Dikra M Maddi; Aida H Al-Sadeeq
Journal:  Anemia       Date:  2020-08-24

Review 2.  Management of sickle cell disease: a review for physician education in Nigeria (sub-saharan Africa).

Authors:  Ademola Samson Adewoyin
Journal:  Anemia       Date:  2015-01-18

Review 3.  Hypertransfusion therapy in sickle cell disease in Nigeria.

Authors:  Ademola Samson Adewoyin; Jude Chike Obieche
Journal:  Adv Hematol       Date:  2014-08-07
  3 in total

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