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Technique and Patient Selection Criteria of Right Anterior Mini-Thoracotomy for Minimal Access Aortic Valve Replacement
Published on: March 26, 2018
Rivaroxaban in patients undergoing surgical mitral valve repair
Feridoun Noohi1,2, Parham Sadeghipour2,3, Sirous Kordrostami1
1Heart Valve Diseases Research Center, Rajaie Cardiovascular, Medical, and Research Center, Iran University of Medical Sciences, Vali-Asr Ave, 1995614331, Tehran, Iran.
Abstract:
In patients undergoing mitral valve repair (MVre), a 3-month course of anticoagulation is currently recommended. The role of the non-vitamin K antagonist oral anticoagulants has here been scarcely studied. In the present mixed cohort study, the safety and efficacy of rivaroxaban (prospective analysis) were compared with those of warfarin (retrospective analysis) in patients undergoing MVre. Anticoagulation therapy was continued for at least 3 months, and the patients were followed for 1 year following surgery. The present study recruited 736 patients undergoing MVre with or without concomitant coronary artery bypass or surgical repair on the other valves. Concomitant valvular replacement and severe chronic kidney diseases were the most important exclusion criteria. The final analysis was conducted on 153 patients treated with rivaroxaban and 144 patients treated with warfarin. Dissimilarities in baseline characteristics necessitated propensity score matching, in which 104 patients in each group were compared. No major bleeding or cerebrovascular accident occurred during the 1-year follow-up. Clinically relevant non-major bleeding was reported in 2 patients in the rivaroxaban group and 4 patients in the warfarin group, a difference non-statistically significant before and after propensity score matching (P = 0.371 and P = 0.407, respectively). The type of anticoagulation did not predict the 1-year outcome (HR 2.165, 95% CI 0.376 to 12.460; P = 0.387). In this mixed cohort study, rivaroxaban was both safe and efficient in patients with MVre. Such preliminary results should prompt larger randomized controlled trials.
Insights
Rivaroxaban demonstrated safety and efficacy comparable to warfarin for anticoagulation after mitral valve repair (MVre). This study suggests rivaroxaban as a viable option, warranting further investigation in larger trials.
Area of Science:
- Cardiology
- Pharmacology
- Surgical Innovation
Background:
- Current guidelines recommend 3-month anticoagulation post-mitral valve repair (MVre).
- Non-vitamin K antagonist oral anticoagulants (NOACs) role in MVre anticoagulation is understudied.
- Warfarin is a traditional anticoagulant, while rivaroxaban is a NOAC.
Purpose of the Study:
- To compare the safety and efficacy of rivaroxaban versus warfarin for anticoagulation in patients undergoing MVre.
- To evaluate clinical outcomes including bleeding events and cerebrovascular accidents over a 1-year follow-up period.
Main Methods:
- A mixed cohort study comparing prospective rivaroxaban data with retrospective warfarin data.
- 736 patients undergoing MVre were initially recruited; 153 treated with rivaroxaban and 144 with warfarin were analyzed.
- Propensity score matching was used to compare 104 patients in each group due to baseline dissimilarities.
Main Results:
- No major bleeding or cerebrovascular accidents occurred in either group during the 1-year follow-up.
- Clinically relevant non-major bleeding was infrequent and not significantly different between rivaroxaban (2 patients) and warfarin (4 patients) groups (P=0.407 post-matching).
- Anticoagulant type did not significantly predict 1-year outcomes (HR 2.165, P=0.387).
Conclusions:
- Rivaroxaban is a safe and effective anticoagulant option for patients undergoing mitral valve repair (MVre).
- These findings support the use of rivaroxaban in this patient population.
- Larger randomized controlled trials are recommended to confirm these preliminary results.
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