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Front Cardiovasc Med. 2022;9:991293.

Net clinical benefit of antithrombotic therapy for atrial fibrillation patients with stable coronary artery disease.

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제1저자 이소령, 정진형 · 교신저자 최의근

소속 (6)
  1. Department of Internal Medicine, Seoul National University Hospital, Seoul, South Korea.
  2. Department of Medical Statistics, College of Medicine, Catholic University of Korea, Seoul, South Korea.
  3. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea.
  4. Department of Statistics and Actuarial Science, Soongsil University, Seoul, South Korea.
  5. Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Chest and Heart Hospital, Liverpool, United Kingdom.
  6. Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Abstract

OBJECTIVES To compare the net clinical benefit of oral anticoagulant (OAC) monotherapy to OAC plus single antiplatelet therapy (SAPT) in patients with atrial fibrillation (AF) and stable coronary artery disease (CAD) at 1- and 3-year after percutaneous coronary intervention (PCI).

BACKGROUND It has not been studied whether the net clinical benefit of the antithrombotic treatment options differs depending on the elapsed time from the index PCI.

METHODS Using the Korean nationwide claims database, we included AF patients who underwent PCI from 2009 to 2019 and constructed two cohorts: 1- and 3-year after PCI. In each cohort, the baseline characteristics of two groups were balanced using propensity score weighting. Ischemic stroke, myocardial infarction, major bleeding, and composite clinical outcomes were analyzed.

RESULTS Among patients with 1-year after PCI, OAC monotherapy (n = 678), and OAC plus SAPT (n = 3,159) showed comparable results for all clinical outcomes. In patients with 3-year after PCI, OAC monotherapy (n = 1,038) and OAC plus SAPT (n = 2,128) showed comparable results for ischemic stroke and myocardial infarction, but OAC monotherapy was associated with a lower risk of composite clinical outcomes (HR 0.762, 95% CI 0.607-0.950), mainly driven by the reduction of major bleeding risk (HR 0.498, 95% CI 0.345-0.701).

CONCLUSION Oral anticoagulant monotherapy may be a comparable choice for patients with AF and stable CAD compared to OAC plus SAPT. In patients with stable CAD more than 3-year after index PCI, OAC monotherapy would be a better choice, being associated with less major bleeding and a positive net clinical benefit.

Copyright © 2022 Lee, Jung, Choi, Lee, Kwon, Park, Kang, Han, Park, Oh and Lip.

Keywords

antiplatelet agentantithrombotic therapyatrial fibrillationcoronary artery diseaseoral anticoagulant

Figures

FIGURE 1
FIGURE 1 Study design and patient enrollment flow. (A) Cohort 1: patients with AF who underwent PCI, 1-year after index PCI. (B) Cohort 2: patients with AF who underwent PCI, 3-year after index PCI. AF, atrial fibrillation; OAC, oral anticoagulant; PCI, percutaneous coronary intervention; SAPT, single antiplatelet agent.
FIGURE 2
FIGURE 2 Weighted cumulative incidence curves for ischemic stroke/myocardial infarction, major bleeding, and composite clinical outcome: OAC plus SAPT vs. OAC monotherapy. (A) Cohort 1: patients with AF who underwent PCI, 1-year after index PCI. (B) Cohort 2: patients with AF who underwent PCI, 3-year after index PCI. HR, hazard ratio; OAC, oral anticoagulant; SAPT, single antiplatelet agent.
FIGURE 3
FIGURE 3 Hazard ratios of ischemic stroke, myocardial infarction, major bleeding, and composite clinical outcome: OAC plus SAPT vs. OAC monotherapy. (A) Cohort 1: patients with AF who underwent PCI, 1-year after index PCI. (B) Cohort 2: patients with AF who underwent PCI, 3-year after index PCI. IR, 100 person-years. CI, confidence interval; HR, hazard ratio; IR, incidence rate; IPTW, inverse probability of treatment weighting; OAC, oral anticoagulant; SAPT, single antiplatelet agent.
FIGURE 4
FIGURE 4 Hazard ratios of ischemic stroke, myocardial infarction, major bleeding, and composite clinical outcome: OAC plus SAPT vs. OAC monotherapy. AF, atrial fibrillation; CI, confidence interval; HR, hazard ratio; IPTW, inverse probability of treatment weighting; MI, myocardial infarction; OAC, oral anticoagulant; PCI, percutaneous coronary intervention; SAPT, single antiplatelet agent.

그림 출처: PubMed Central 공개 논문 (PMC9441665)

Conflict of interest statement

E-KC: research grants or speaking fees from Abbott, Bayer, BMS/Pfizer, Biosense Webster, Chong Kun Dang, Daewoong Pharmaceutical Co., Daiichi-Sankyo, DeepQure, Dreamtech Co., Ltd., Jeil Pharmaceutical Co. Ltd., Medtronic, Samjinpharm, Seers Technology, and Skylabs. GL: consultant and speaker for BMS/Pfizer, Boehringer Ingelheim, and Daiichi-Sankyo. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

그 밖의 정보
출판 형태
Journal Article
저널
Frontiers in cardiovascular medicine · ISSN 2297-055X
전자 출판
2022-08-22
참고문헌
26편