Asfour M, Narvios Aida, Lichtiger Benjamin
Department of Pathology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
MedGenMed. 2004 Jul 13;6(3):22.
Transfusion-dependent bone marrow transplant recipients are routinely transfused with ABO group and RhD-compatible blood components. However, because of the scarcity of RhD-negative blood components, particularly platelets, a policy was developed to transfuse RhD-positive blood components to RhD-negative patients during periods of shortage.
We reviewed the records of 78 RhD-negative patients with hematologic malignancies who received RhD-negative bone marrow and/or peripheral blood stem cells, from June 1995 to August 2000. The patients transfused with RhD-incompatible blood components were screened periodically for evidence of the development of red blood cell (RBC) alloimmunization.
Three of 78 patients (4%) developed anti-D antibodies after receiving RhD-incompatible platelet transfusions. One of the patients developed evidence of anti-RhD antibodies after receiving 42 units of RhD-positive random donor platelets; the second patient developed such evidence after receiving 6 apheresis platelets and 2 infusions of intravenous immunoglobulin G (positive for anti-RhD). The third patient received 206 RhD-positive random donor platelets and 5 apheresis units. All patients were discharged from the hospital. The overall immunization rate was 4%. Six patients received Rh-incompatible packed RBCs and showed no evidence of neither anti-RhD nor any other anti-RBC antibodies. All 78 patients had received RhD-incompatible platelets throughout their engraftment period.
Transfusion of RhD-positive blood components to Rh-negative patients with hematologic cancers, who have received RhD-negative bone marrow and/or peripheral blood stem cells, are at low risk of developing RhD antibodies. These findings allow for a flexible strategy of blood component therapy support for this special patient population during periods of shortage.
依赖输血的骨髓移植受者通常输注 ABO 血型和 RhD 相容的血液成分。然而,由于 RhD 阴性血液成分,尤其是血小板稀缺,因此制定了一项政策,即在短缺期间向 RhD 阴性患者输注 RhD 阳性血液成分。
我们回顾了 1995 年 6 月至 2000 年 8 月期间 78 例接受 RhD 阴性骨髓和/或外周血干细胞移植的 RhD 阴性血液系统恶性肿瘤患者的记录。定期筛查输注 RhD 不相容血液成分的患者是否出现红细胞(RBC)同种免疫的证据。
78 例患者中有 3 例(4%)在接受 RhD 不相容的血小板输注后产生了抗 D 抗体。其中 1 例患者在接受 42 单位 RhD 阳性随机供体血小板后出现抗 RhD 抗体证据;第 2 例患者在接受 6 次单采血小板和 2 次静脉注射免疫球蛋白 G(抗 RhD 阳性)后出现此类证据。第 3 例患者接受了 206 单位 RhD 阳性随机供体血小板和 5 个单采单位。所有患者均已出院。总体免疫率为 4%。6 例患者接受了 Rh 不相容的浓缩红细胞,未显示抗 RhD 或任何其他抗 RBC 抗体的证据。所有 78 例患者在植入期均接受了 RhD 不相容的血小板。
对于接受 RhD 阴性骨髓和/或外周血干细胞移植的 Rh 阴性血液系统癌症患者,输注 RhD 阳性血液成分产生 RhD 抗体的风险较低。这些发现为这一特殊患者群体在短缺期间的血液成分治疗支持提供了一种灵活的策略。