Meta-analysis of Antithrombotic Therapy in Patients With Atrial Fibrillation Undergoing Percutaneous Coronary Intervention.

Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York. Electronic address: Toshiki.Kuno@mountsinai.org. Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York. Department of Cardiovascular Surgery, Shizuoka Medical Center, Shizuoka, Japan. Center for Interventional Vascular Therapy, New York-Presbyterian Hospital/Columbia University Medical Center, New York. Department of Cardiology, Japanese Red Cross Ashikaga Hospital, Ashikaga, Japan. Division of Cardiovascular Medicine, Section of Heart Failure and Transplantation, University of Iowa, Iowa. Department of Cardiology, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York. Division of Cardiovascular Medicine, New York University School of Medicine, New York.

The American journal of cardiology. 2020;(4):521-527
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Abstract

For patients with atrial fibrillation (AF) who undergo percutaneous coronary intervention (PCI), antithrombotic therapy including oral anticoagulants and antiplatelets are indicated. The optimal combination is not known. We investigated the efficacy and safety of different antithrombotic strategies in patients with AF undergoing PCI. PUBMED and EMBASE were searched through September 2019 for randomized trials investigating the efficacy and safety of different antithrombotic strategies in patients with AF who underwent PCI and/or acute coronary syndrome. Nine antithrombotic strategies were compared including combinations of vitamin K antagonist (VKA) with dual antiplatelet therapy (DAPT) or P2Y12 inhibitor, combinations of direct oral anticoagulants (DOAC) (apixaban, dabigatran, rivaroxaban, and edoxaban) with DAPT or P2Y12 inhibitor (clopidogrel, prasugrel, and ticagrelor). The primary safety outcome was trial defined primary bleeding outcome. The primary efficacy outcome was trial defined major adverse cardiovascular events. Our search identified 5 eligible trials that enrolled a total of 11,532 patients and compared 9 treatment strategies. VKA + DAPT significantly increased bleeding when compared with most combinations (for example, vs VKA + P2Y12 inhibitor: odds ratio 2.11; 95% confidence interval [1.76 to 2.52], p <0.001). Of all the combinations, apixaban + P2Y12 inhibitor showed the lowest bleeding risk (for example, vs VKA + P2Y12 inhibitor: odds ratio 0.63; 95% confidence interval [0.51 to 0.78], p <0.001) and was ranked the best treatment. There were no significant differences in ischemic outcome of major adverse cardiovascular events between various antithrombotic regimens. In conclusion, in patients with AF undergoing PCI, apixaban + P2Y12 inhibitors were associated with lowest bleeding compared with other regimens including other DOACs + P2Y12 inhibitors with no increase in ischemic outcomes.

Methodological quality

Publication Type : Meta-Analysis

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