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Red cell alloimmunization in sickle-cell anaemia patients / Bashawri, L.A.M.

Tác giả : Bashawri, L.A.M.

Năm xuất bản : 2007

Chủ đề : 1. Anemia, Sickle Cell. 2. Blood Transfusion. 3. Erythrocytes. 4. Isoantibodies.

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1181-1189 This study in King Fahd Hospital of the University, Saudi Arabia, assessed the frequency of alloimmunization to red cell antigens in sickle-cell anaemia patients over 1996-2004 in order to evaluate the risk of alloimmunization and identify the most common alloantibodies. A retrospective analysis of the transfusion history and medical records of 350 patients aged 2 to 75 years who had received at least 1 transfusion found that 48 patients had developed alloantibodies [13.7%]. The most common alloantibodies detected were: anti-E alone [18.8%], nonspecific [12.5%], inconclusive [12.5%], anti-K [10.4%] and anti-c 3 [6.3%]. Some patients had 1 alloantibody, while others more than 1 and even multiple antibodies. Nine patients had a persistent positive direct antiglobulin test
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https://iris.who.int/handle/10665/117364

 

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Sách, tuyển tập

Platelet aggregation and physiological anticoagulants in sickle-cell disease / Bashawri, L.A.M.;Al Mulhim, A.A.;Ahmed, M.A.;Bahnassi, A.A.

Tác giả : Bashawri, L.A.M.;Al Mulhim, A.A.;Ahmed, M.A.;Bahnassi, A.A.

Năm xuất bản : 2007