达比加群
医学
伊达鲁珠单抗
凝血酶原复合物浓缩物
抗凝剂
重症监护医学
围手术期
依杜沙班
华法林
直接凝血酶抑制剂的发现与发展
药效学
拜瑞妥
加药
凝血酶原复合物
临床试验
药理学
鱼精蛋白硫酸盐
麻醉
证据质量
肝素
凝血酶原时间
作者
Bianca Rocca,Hugo Ten Cate
标识
DOI:10.1056/nejmra2506021
摘要
The global rise in anticoagulant use has increased the number of major bleeding events that warrant timely and effective pharmacologic reversal. Reversal strategies should be informed by the pharmacodynamic and pharmacokinetic features of the anticoagulant and antidote, regulatory indications, quality of evidence, patient-specific factors, and availability of treatment options. Protamine sulfate neutralizes unfractionated heparin, whereas no specific antidotes exist for low-molecular-weight heparins or fondaparinux. Four-factor prothrombin complex concentrates effectively reverse vitamin K antagonists. Idarucizumab specifically reverses dabigatran, although delayed dabigatran rebound can occur. Andexanet alfa targets direct oral factor Xa inhibitors, but uncertainties regarding the efficacy-safety balance, monitoring, rebound, perioperative use, and cost have prompted off-label use of four-factor prothrombin complex concentrates, for which stronger evidence is needed. Key challenges remain, including determination of appropriate dosing, standardization and validation of laboratory monitoring, mitigation of thrombotic risk, and development of guidelines for perioperative treatment. Emerging agents aim to broaden targets and improve safety. Building high-quality evidence remains essential to advancing global, patient-centered anticoagulant and hemostatic care.
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