Cruz Roberto de Oliveira, Mota Mariza Aparecida, Conti Fabiana Mendes, Pereira Ricardo Antônio d'Almeida, Kutner Jose Mauro, Aravechia Maria Giselda, Castilho Lilian
Hospital Israelita Albert Einstein - HIAE, São Paulo, SP, BR.
Universidade Estadual de Campinas - UNICAMP, Campinas, SP, BR.
Einstein (Sao Paulo). 2011 Jun;9(2):173-8. doi: 10.1590/S1679-45082011AO1777.
To determine the incidence and the rate of red blood cell alloimmunization in polytransfused patients.
A polytransfused patient was defined as having received at least 6 units of red cell concentrates during a 3-month period. The records of all patients (n = 12,904) who had received red blood cell units were examined retrospectively by searching the computer database at Hospital Israelita Albert Einstein in São Paulo, Brazil, over a 6-year period, between 2003 and 2009.
During this time, 77,049 red cell concentrate transfusions were performed in 12,904 patients. There were 3,044 polytransfused patients, 227 of whom (7.5%) presented with irregular erythrocyte antibodies. The prevalence of alloantibody specificity was: Anti-E>anti-D>anti-K>anti-C>anti-Dia>anti-c>anti-Jka>anti-S in 227 polytransfused patients. We found combinations of alloantibodies in 79 patients (34.8%), and the most common specificities were against the Rh and/or Kell systems. These antibodies show clinical significance, as they can cause delayed hemolytic transfusion reactions and perinatal hemolytic disease. About 20% of the patients showed an IgG autoantibody isolated or combined with alloantibodies. Interestingly, a high incidence of antibodies against low frequency antigens was detected in this study, mainly anti-Dia.
Polytransfused patients have a high probability of developing alloantibodies whether alone or combined with autoantibodies and antibodies against low frequency antigens. Transfusion of red blood cells with a phenotype-compatible with RH (C, E, c), K, Fya, and Jka antigens is recommended for polytransfused patients in order to prevent alloimmunization and hemolytic transfusion reactions.
确定多次输血患者红细胞同种免疫的发生率和速率。
多次输血患者定义为在3个月内接受至少6单位红细胞浓缩物的患者。通过检索巴西圣保罗以色列人阿尔伯特·爱因斯坦医院的计算机数据库,对2003年至2009年6年间接受红细胞单位的所有患者(n = 12,904)的记录进行回顾性检查。
在此期间,12,904名患者共进行了77,049次红细胞浓缩物输血。有3,044名多次输血患者,其中227名(7.5%)出现不规则红细胞抗体。227名多次输血患者中同种抗体特异性的流行情况为:抗-E>抗-D>抗-K>抗-C>抗-Dia>抗-c>抗-Jka>抗-S。我们在79名患者(34.8%)中发现了同种抗体组合,最常见的特异性是针对Rh和/或Kell系统。这些抗体具有临床意义,因为它们可引起迟发性溶血性输血反应和围产期溶血性疾病。约20%的患者出现单独或与同种抗体联合的IgG自身抗体。有趣的是,本研究中检测到针对低频抗原的抗体发生率较高,主要是抗-Dia。
多次输血患者单独或与自身抗体及针对低频抗原的抗体联合出现同种抗体的可能性很高。建议为多次输血患者输注与RH(C、E、c)、K、Fya和Jka抗原表型相容的红细胞,以预防同种免疫和溶血性输血反应。