Kennedy LeAnne D, Case L Douglas, Hurd David D, Cruz Julia M, Pomper Gregory J
Department of Pharmacy, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA.
Transfusion. 2008 Nov;48(11):2285-91. doi: 10.1111/j.1537-2995.2008.01858.x. Epub 2008 Jul 30.
Acetaminophen and diphenhydramine are commonly used as pretransfusion medications to prevent transfusion reactions. The purpose of this study was to prospectively compare the risk of transfusion reactions in hematology/oncology patients who receive acetaminophen with diphenhydramine or placebo before transfusion.
A randomized, double-blind, placebo-controlled transfusion reaction study of 315 eligible patients was performed. Inclusion criteria were patients aged 18 to 65 years admitted to the leukemia or bone marrow transplant (BMT) services. Patients were excluded if they had a known allergy to either acetaminophen or diphenhydramine or had a documented history of a febrile or allergic transfusion reaction. All blood products were administered using a leukofilter. Study medications were given 30 minutes before transfusions and no other acetaminophen or diphenhydramine was given within 4 hours of administration of the study medications. Patients were monitored for the development of reaction symptoms within 4 hours after the transfusion.
A total of 154 active drug patients were compared to 161 placebo patients. There was no significant difference in the overall risk of transfusion reactions between the two groups. However, analysis of specific reaction types revealed a significant decrease in the risk of febrile reactions when pretransfusion medication is used in addition to bedside leukoreduction.
Pretransfusion medication of leukemia or BMT patients without a history of transfusion reaction does not decrease the overall risk of transfusion reactions. However, pretransfusion medication may decrease the risk of febrile nonhemolytic transfusion reactions to leukoreduced blood products.
对乙酰氨基酚和苯海拉明通常用作输血前用药以预防输血反应。本研究的目的是前瞻性比较血液学/肿瘤学患者在输血前接受对乙酰氨基酚与苯海拉明或安慰剂时发生输血反应的风险。
对315例符合条件的患者进行了一项随机、双盲、安慰剂对照的输血反应研究。纳入标准为年龄在18至65岁之间、入住白血病或骨髓移植(BMT)科室的患者。如果患者已知对对乙酰氨基酚或苯海拉明过敏或有发热或过敏输血反应的记录病史,则被排除。所有血液制品均使用白细胞滤器输注。研究药物在输血前30分钟给予,在给予研究药物后4小时内不给予其他对乙酰氨基酚或苯海拉明。在输血后4小时内对患者进行反应症状发展的监测。
共比较了154例使用活性药物的患者和161例使用安慰剂的患者。两组之间输血反应的总体风险没有显著差异。然而,对特定反应类型的分析显示,除床边白细胞去除外,使用输血前用药时发热反应的风险显著降低。
对于无输血反应史的白血病或BMT患者,输血前用药不会降低输血反应的总体风险。然而,输血前用药可能会降低对白细胞去除的血液制品发生发热性非溶血性输血反应的风险。