Management of bleeding associated with direct oral anticoagulants: update on reversal strategies

被引:2
作者
Enriquez, Andres [1 ,2 ]
Baranchuk, Adrian [2 ]
Corbalan, Ramon [3 ]
机构
[1] Hosp Guillermo Grant Benavente, Dept Cardiol, Concepcion, Chile
[2] Queens Univ, Div Cardiol, Kingston, ON, Canada
[3] Hosp Clin Pontificia Univ Catolica Chile, Div Enfermedades Cardiovasc, Santiago, Chile
关键词
Anticoagulants; Hemorrhage; Risk Factors; VITAMIN-K ANTAGONISTS; FACTOR XA INHIBITORS; ATRIAL-FIBRILLATION; ANDEXANET ALPHA; LABORATORY MEASUREMENT; DABIGATRAN; WARFARIN; RIVAROXABAN; APIXABAN; PHARMACOKINETICS;
D O I
10.4067/S0034-98872019000100073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Direct oral anticoagulants (DOACs), including the direct thrombin inhibitor dabigatran and the direct factor Xa inhibitors rivaroxaban, apixaban and edoxaban have at least comparable efficacy as vitamin K antagonists along with a better safety profile, reflected by a lower incidence of intracranial hemorrhage. Specific reversal agents have been developed in recent years. Namely, idarucizumab, a specific antidote for dabigatran, is currently approved in most countries. Andexanet, which reverses factor Xa inhibitors, has been recently approved by the FDA, and ciraparantag, a universal antidote targeted to reverse all DOACs, is still under investigation. In this review we provide an update on the pharmacology of DOACs, the risk of hemorrhagic complications associated with their use, the measurement of their anticoagulant effect and the reversal strategies in case of DOAC-associated bleeding.
引用
收藏
页码:73 / 82
页数:10
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