van Dijk B A, Hirasing R A, Overbeeke M A
TNO Preventie en Gezondheid, divisie Jeugd, Leiden, Amsterdam.
Ned Tijdschr Geneeskd. 1999 Jul 10;143(28):1465-9.
To inventory prevalence and morbidity of haemolytic disease of newborn caused by irregular anti-erythrocyte antibodies other than antirhesus-D.
Prospective registration study.
All paediatricians (n = 380) in general hospitals and contact persons (n = 79) in university hospitals were asked for monthly reports of clinical cases of haemolytic disease of newborn during 2 years (1996-1997).
Response was 97%. A total of 130 reports were received in two study years, 49 of which could not be confirmed as non-RhD-non-AB0 antagonism. In the group of which the transfusion history was known (n = 60), 29 pregnant women (48%) had received transfused blood at some time. Of the antibodies found, anti-c, anti-E and anti-K were the most frequent. The direct antiglobulin test was positive in 61 of the 81 cases, negative in 10 cases, while in 10 cases it was unknown or false-negative due to earlier intrauterine transfusions (in three neonates). The highest bilirubin levels recorded were 572, 559 and 520 mumol/l (all three with maternal anti-c antagonism). Therapeutic data were known concerning 80 of the 81 newborn: 21 (16%) received no treatment, 24 (29%) only phototherapy and the others--in addition to phototherapy if any--also blood transfusion, exchange transfusion or intrauterine transfusion, or a combination of these.
It was calculated that the actual prevalence of irregular anti-erythrocyte antibodies in Dutch pregnant women probably amounts to approximately 0.25%. This finding may possibly be confirmed since starting 1 July 1998 all pregnant women in the country are screened for the presence of these antibodies. It is recommended that girls and women in the reproductive age group should receive primary prevention of development of irregular anti-erythrocyte antibodies by application of a selective blood transfusion policy, taking into account the occurrence of the antigens c, E and K.
统计由抗D以外的不规则抗红细胞抗体引起的新生儿溶血病的患病率和发病率。
前瞻性登记研究。
要求综合医院的所有儿科医生(n = 380)和大学医院的联系人(n = 79)每月报告2年(1996 - 1997年)内新生儿溶血病的临床病例。
回复率为97%。在两个研究年度共收到130份报告,其中49份不能确认为非RhD - 非AB0血型不合。在已知输血史的组中(n = 60),29名孕妇(48%)曾在某个时候接受过输血。在所发现的抗体中,抗 - c、抗 - E和抗 - K最为常见。81例中61例直接抗球蛋白试验呈阳性,10例呈阴性,而在10例中(3例新生儿)由于早期宫内输血,结果未知或呈假阴性。记录到的最高胆红素水平分别为572、559和520 μmol/l(均为母亲抗 - c血型不合)。81例新生儿中有80例有治疗数据:21例(16%)未接受治疗,24例(29%)仅接受光疗,其他新生儿——如有光疗的话——还接受了输血、换血或宫内输血,或这些治疗的组合。
据计算,荷兰孕妇中不规则抗红细胞抗体的实际患病率可能约为0.25%。自1998年7月1日起,该国所有孕妇都接受这些抗体的筛查,这一发现可能会得到证实。建议育龄期女孩和妇女应通过应用选择性输血政策接受原发性预防,以防止不规则抗红细胞抗体的产生,同时考虑抗原c、E和K的出现情况。