Cid Joan, Ortin Xavier, Elies Enric, Castellà Dolors, Panadés Marta, Martín-Vega Carmen
Center de Transfusió i Banc de Teixits, Hospital Joan XXIII, Tarragona, Spain.
Transfusion. 2002 Feb;42(2):173-6. doi: 10.1046/j.1537-2995.2002.00038.x.
Rh antigens are not present on the platelet surface. However, platelet concentrates may contain enough RBCs to elicit an anti-D response. Thus, D status must be considered in platelet transfusion. In immunosuppressed patients, frequencies of D alloimmunization of up to 19 percent have been previously reported.
Here a prospective study is reported in which 22 D- patients with hematologic disease received D+ platelet transfusions. Platelet concentrates were prepared from whole-blood donations according to the buffy coat method and were pooled before administration. The antibody screen test to detect anti-D was performed by LISS- IAT using the gel test.
Our series comprises 22 immunosuppressed D+ patients with a median age of 56 years (range, 23-79). The patients received 121 D-incompatible pooled platelet transfusions. The mean +/- SD of RBC content was 4.17 +/- 1.74 mL. None of the 22 patients developed detectable anti-D after a median follow-up of 8 weeks (range, 1-37).
The risk of D alloimmunization is low in patients with hematologic disease after D-incompatible platelet transfusions using platelet concentrates prepared by the buffy coat method.
Rh抗原不存在于血小板表面。然而,血小板浓缩物可能含有足够的红细胞以引发抗-D反应。因此,在血小板输注中必须考虑D血型状态。在免疫抑制患者中,先前报道的D同种免疫频率高达19%。
本文报道一项前瞻性研究,22例D阴性血液病患者接受了D阳性血小板输注。血小板浓缩物采用白膜层法从全血捐献中制备,并在输注前进行汇集。采用凝胶试验的LISS-IAT法进行检测抗-D的抗体筛查试验。
我们的研究系列包括22例免疫抑制的D阴性患者,中位年龄56岁(范围23 - 79岁)。这些患者接受了121次D血型不相容的汇集血小板输注。红细胞含量的平均值±标准差为4.17±1.74 mL。22例患者在中位随访8周(范围1 - 37周)后均未产生可检测到的抗-D。
对于血液病患者,使用白膜层法制备的血小板浓缩物进行D血型不相容的血小板输注后,D同种免疫的风险较低。