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温抗体型自身免疫性溶血性贫血中的红细胞输注

Red blood cell transfusion in warm-type autoimmune haemolytic anaemia.

作者信息

Salama A, Berghöfer H, Mueller-Eckhardt C

机构信息

Institute for Clinical Immunology and Transfusion Medicine, Justus Liebig University, Giessen, Germany.

出版信息

Lancet. 1992;340(8834-8835):1515-7. doi: 10.1016/0140-6736(92)92766-9.

Abstract

Blood transfusions are regarded as hazardous in patients with warm-type autoimmune haemolytic anaemia (AIHA) because of potential intensification of haemolysis and a presumed high incidence of alloimmunisation. We have retrospectively analysed data of 79 multitransfused patients (74 adults, 5 children) with detectable warm autoantibodies and transitory or persisting haemolytic anaemia. All patients had received blood transfusions on at least two occasions. Patients were reexamined at least twice within the first 6 months of transfusion (duration of follow-up 6 months-12 years). 53 patients had received blood transfusions because of decompensated AIHA, all of whom presented with detectable autoantibodies against red blood cells. None of these patients had transfusion-related alloimmunisation or a definite increase in haemolysis, even when the transfused red cells were serologically incompatible because of free serum autoantibodies. The other 26 patients had no signs of AIHA at presentation (negative direct and indirect antiglobulin test), but received blood transfusions for anaemia due to various other causes. 23 of these 26 patients went on to develop alloantibodies as well as autoantibodies upon transfusion, and 3 patients developed autoantibodies alone. Our findings do not support the generally accepted notion that transfusion therapy should be avoided in AIHA patients. Rather, they indicate that the incidence of alloimmunisation as well as adverse haemolytic transfusion reactions are less common in AIHA patients than in other multitransfused patients.

摘要

由于存在溶血加剧的可能性以及假定的高同种免疫发生率,输血在温抗体型自身免疫性溶血性贫血(AIHA)患者中被视为具有危险性。我们回顾性分析了79例多次输血患者(74例成人,5例儿童)的数据,这些患者可检测到温自身抗体,并伴有短暂性或持续性溶血性贫血。所有患者均至少接受过两次输血。在输血后的前6个月内对患者至少进行了两次复查(随访时间为6个月至12年)。53例患者因失代偿性AIHA接受输血,所有这些患者均呈现出可检测到的抗红细胞自身抗体。这些患者中没有一例发生输血相关的同种免疫或溶血明显增加,即使输注的红细胞因游离血清自身抗体在血清学上不匹配。另外26例患者在就诊时没有AIHA迹象(直接和间接抗球蛋白试验均为阴性),但因各种其他原因导致贫血而接受输血。这26例患者中有23例在输血后继而产生了同种抗体以及自身抗体,3例仅产生了自身抗体。我们的研究结果不支持普遍接受的观点,即AIHA患者应避免输血治疗。相反,它们表明AIHA患者中同种免疫以及不良溶血性输血反应的发生率比其他多次输血患者更低。

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