Unresolved issues in the use of direct acting oral anticoagulants

被引:0
|
作者
Chan, Noel [1 ,2 ]
Hirsh, Jack [1 ]
机构
[1] McMaster Univ, Dept Med, Hamilton, ON, Canada
[2] McMaster Univ, Populat Hlth Res Inst, Dept Med, DBCVRI, 20 Copeland Ave, Hamilton, ON L8L 2X2, Canada
关键词
Direct oral anticoagulants; vitamin K antagonists; factor XIa inhibitors; mechanical heart valve; antiphospholipid syndrome; valvular atrial fibrillation; DOAC drug level; ACUTE VENOUS THROMBOEMBOLISM; ATRIAL-FIBRILLATION; ANTITHROMBOTIC THERAPY; ACTIVATED PLATELETS; CHEST GUIDELINE; FACTOR XIA; DABIGATRAN; REVERSAL; RIVAROXABAN; WARFARIN;
D O I
10.1080/14779072.2023.2271388
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionCurrently approved direct oral anticoagulants (DOACs) target thrombin or coagulation factor Xa. Administered in fixed doses without routine laboratory monitoring, DOACs have simplified the approach to oral anticoagulation, when previously the choice was limited to vitamin K antagonists (VKAs).Area coveredWe discuss a) unresolved issues related to optimal use of DOACs and b) new developments including the potential for FXIa inhibitors to be effective and safer anticoagulants.Expert opinionBy simplifying oral anticoagulation, DOACs have facilitated the uptake of anticoagulation. The DOACs are approved for stroke prevention in atrial fibrillation and for the prevention and treatment of venous thromboembolism, and their indications are expanding to include the prevention of atherothrombosis. DOACs have now replaced vitamin K antagonists (VKAs) for most indications, but not all. DOACs are inferior to VKAs for patients with mechanical heart valves, left ventricular assist device, rheumatic atrial fibrillation, and those with antiphospholipid syndrome, and their safety and efficacy are uncertain in some populations (e.g. advanced renal and liver disease). Impediments to use include concerns for bleeding and cost. The newly developed FXIa and FXIIa inhibitors have the potential to be safer than current anticoagulants, but phase 3 trials are needed to confirm their clinical efficacy and safety.
引用
收藏
页码:913 / 921
页数:9
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