Aprotinin: 1 year on

被引:8
作者
Dietrich, Wulf [1 ,2 ]
机构
[1] Univ Munich, Div Hemostasis & Transfus Med, Inst Res Cardiac Anesthesia & Working Grp Periope, Dept Anesthesiol, D-81377 Munich, Germany
[2] Univ Munich, Dept Transfus Med, Inst Res Cardiac Anesthesia & Working Grp Periope, D-81377 Munich, Germany
关键词
aprotinin; blood loss; dialysis; hypersensitivity; renal; safety; side effect; transfusion; BYPASS GRAFT-SURGERY; CARDIAC-SURGERY; ANTIFIBRINOLYTIC AGENTS; CARDIOPULMONARY BYPASS; ANAPHYLACTIC REACTIONS; CLINICAL-OUTCOMES; BLOOD-TRANSFUSION; RENAL DYSFUNCTION; DOSE APROTININ; RISK;
D O I
10.1097/ACO.0b013e32831c833f
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Purpose of review The nonspecific protease inhibitor aprotinin has been used successfully to reduce bleeding in cardiac surgery. Recent investigations have questioned its safety, and aprotinin has finally been withdrawn from marketing after a large prospective study demonstrated a trend toward higher mortality. Recent findings The initial studies of Karkouti and Mangano provoked a considerable number of large-scale investigations focusing on the safety issues of aprotinin. These studies were of retrospective nature and used sophisticated statistical methods to overcome a possible selection bias. Recently, aprotinin was predominantly used in patients with a higher risk of bleeding, which hampers a retrospective comparison with patients without the drug. This review summarizes the diverging results of these studies. Summary It remains a matter of speculation whether the quality and results of published data justify the withdrawal of aprotinin; however, one has to accept that this drug is no longer available. It is clear from the aprotinin story that there are no effective instruments to control the safety and clinical efficacy of a drug after its regulatory approval. This highlights the urgent need for independent clinical safety studies after the formal registration of a drug.
引用
收藏
页码:121 / 127
页数:7
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