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Published on: February 26, 2013
Revolutionizing anticoagulation: DOAC versus VKA in atrial fibrillation with early post-bioprosthetic valves
Lizhu Han1, Yin Wang1, Hulin Wang1
1Department of Pharmacy, Personalized Drug Research and Therapy Key Laboratory of Sichuan Province, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Insights
Direct oral anticoagulants (DOACs) are as effective and safe as vitamin K antagonists (VKAs) in patients within 3 months of biological heart valve surgery. This finding suggests DOACs may be a viable alternative for early postoperative anticoagulation in atrial fibrillation patients.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Direct oral anticoagulants (DOACs) are standard for non-valvular atrial fibrillation.
- Recent guidelines suggest DOACs for atrial fibrillation patients ≥3 months post-bioprosthetic valve replacement.
- Efficacy and safety of DOACs within 3 months of biological valve surgery remain uncertain.
Purpose of the Study:
- To systematically review literature on DOACs versus vitamin K antagonists (VKAs) in atrial fibrillation patients early after biological valve surgery.
- To evaluate the efficacy and safety of DOACs in this specific patient cohort.
Main Methods:
- Systematic literature search of PubMed, Embase, Web of Science, and Cochrane Library up to August 15, 2025.
- Included randomized controlled trials (RCTs) comparing DOACs with VKAs.
- Assessed outcomes: all-cause death, stroke/thromboembolic events, bleeding events, and cardiovascular death.
Main Results:
- Six RCTs involving 2725 patients (1386 DOACs, 1339 VKAs) were analyzed.
- No significant differences found between DOACs and VKAs for all-cause death, stroke/thromboembolic events, or major bleeding.
- Secondary analysis also revealed no significant difference in cardiovascular death.
Conclusions:
- DOACs demonstrate comparable efficacy and safety to VKAs in the early postoperative period after biological valve replacement or repair.
- DOACs may serve as an alternative to VKAs for anticoagulation in this patient group.
Background:
Direct oral anticoagulants (DOACs) are extensively employed in patients with non-valvular atrial fibrillation and have recently been recommended for atrial fibrillation patients ≥3 months after bioprosthetic valve replacement. However, the efficacy and safety of DOACs in patients with atrial fibrillation within the first 3 months after biological valve replacement or repair remain unclear. This study systematically reviewed the literature to evaluate DOACs in this cohort.
Methods:
PubMed, Embase, Web of Science, and Cochrane Library were searched up to 15 August 2025, for randomized controlled trials (RCTs) comparing DOACs with vitamin K antagonists (VKAs) in atrial fibrillation patients within 3 months of biological valve surgery. Outcomes included all-cause death, stroke/thromboembolic events, bleeding events, and cardiovascular death.
Results:
Six RCTs with 2725 patients were included (1386 DOACs; 1339 VKAs). Primary analyses showed no significant differences between the groups in all-cause death [relative risk (RR) = 0.930; 95% confidence interval (CI), 0.729-1.186; P = 0.560], stroke/thromboembolic events (RR = 0.724, 95% CI: 0.495-1.059 P = 0.096), or major bleeding (RR = 1.042; 95% CI, 0.563-1.930; P = 0.895). The secondary analysis also showed no significant difference in cardiovascular death (RR = 1.127, 95% CI: 0.814-1.559, P = 0.472).
Conclusion:
DOACs demonstrated comparable efficacy and safety to VKAs in the early postoperative period after biological valve replacement or repair, suggesting that they may serve as an alternative to VKAs.
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