Latest advances in the reversal strategies for direct oral anticoagulants

被引:2
|
作者
Escal, Jean [1 ,5 ]
Lanoiselee, Julien [2 ]
Poenou, Geraldine [3 ]
Zufferey, Paul [2 ]
Laporte, Silvy [3 ]
Mismetti, Patrick [4 ]
Delavenne, Xavier [1 ]
机构
[1] Jean Monnet Univ, St Etienne Univ Hosp, Pharmacol & Toxicol Lab, INSERM,SAINBIOSE U1059,, St Etienne, France
[2] St Etienne Univ Hosp, Dept Anesthesia & Intens Care, St Etienne, France
[3] Jean Monnet Univ, St Etienne Univ Hosp, Innovat & Pharmacol Clin Res Unit, INSERM,,SAINBIOSE U1059, St Etienne, France
[4] Jean Monnet Univ St Etienne, St Etienne Univ Hosp, Vasc & Therapeut Med Dept, INSERM,SAINBIOSE U1059, St Etienne, France
[5] Univ Jean Monnet St Etienne, CHU St Etienne, INSERM, SAINBIOSE U1059,Lab Pharmacol & Toxicol, F-42023 St Etienne, France
关键词
andexanet alfa; antidotes; ciraparantag; direct oral anticoagulants; idarucizumab; ACTIVATED-CHARCOAL; ANDEXANET ALPHA; PHARMACOKINETICS; DABIGATRAN; SAFETY; PHARMACODYNAMICS; CIRAPARANTAG; TOLERABILITY; IDARUCIZUMAB; METAANALYSIS;
D O I
10.1111/fcp.12992
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundSince the late 2000s, Europe has granted approval for various thrombotic risk-related uses of direct oral anticoagulants (DOACs). Unlike traditional anticoagulants, DOACs do not necessitate routine coagulation monitoring. Nevertheless, clinical practice often encounters bleeding events associated with these medications, making the need for effective reversal strategies evident.ObjectivesThe study aims to take stock of current reversal strategies for DOACs, with a particular emphasis on the latest compounds that have been developed or are currently under development.MethodsFor obtaining information regarding the ongoing reversal strategies and the compounds under development, we referred to ClinicalTrials website, PubMed, and Google Scholar.ResultsIn 2024, two specific antidotes to DOACs have already received approval when reversal of anticoagulation is needed owing to life-threatening or uncontrolled bleeding: idarucizumab that reverses the effects of dabigatran, and andexanet alfa, designed to counteract activated factor X inhibitors such as apixaban and rivaroxaban. Furthermore, ciraparantag, a potential universal reversal agent, is currently in advanced stages of clinical development. Concerns remain regarding the safety of specific reversal agents, especially concerning the risk of thrombosis. Additionally, the cost of these antidotes remains high. Consequently, nonspecific strategies to counteract anticoagulant medications, including activated charcoal, hemodialysis, and concentrates of coagulation factors, still have utility.ConclusionWith the validation of specific and nonspecific antidotes, DOACs could supplant traditional oral anticoagulants. This progress represents a significant advancement in anticoagulation therapy. However, ongoing research is crucial to address remaining safety concerns of the specific reversion agents of DOACs in clinical practice.
引用
收藏
页码:674 / 684
页数:11
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