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Clopidogrel Monotherapy After 1-Month Dual Antiplatelet Therapy in Percutaneous Coronary Intervention: From the STOPDAPT-2 Total Cohort.
Obayashi, Yuki; Watanabe, Hirotoshi; Morimoto, Takeshi; Yamamoto, Ko; Natsuaki, Masahiro; Domei, Takenori; Yamaji, Kyohei; Suwa, Satoru; Isawa, Tsuyoshi; Watanabe, Hiroki; Yoshida, Ruka; Sakamoto, Hiroki; Akao, Masaharu; Hata, Yoshiki; Morishima, Itsuro; Tokuyama, Hideo; Yagi, Masahiro; Suzuki, Hiroshi; Wakabayashi, Kohei; Suematsu, Nobuhiro; Inada, Tsukasa; Tamura, Toshihiro; Okayama, Hideki; Abe, Mitsuru; Kawai, Kazuya; Nakao, Koichi; Ando, Kenji; Tanabe, Kengo; Ikari, Yuji; Morino, Yoshihiro; Kadota, Kazushige; Furukawa, Yutaka; Nakagawa, Yoshihisa; Kimura, Takeshi.
Affiliation
  • Obayashi Y; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Japan (Y.O., H. Watanabe, K. Yamamoto, K. Yamaji).
  • Watanabe H; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Japan (Y.O., H. Watanabe, K. Yamamoto, K. Yamaji).
  • Morimoto T; Department of Clinical Epidemiology, Hyogo College of Medicine, Nishinomiya, Japan (T.M.).
  • Yamamoto K; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Japan (Y.O., H. Watanabe, K. Yamamoto, K. Yamaji).
  • Natsuaki M; Department of Cardiovascular Medicine, Saga University, Japan (M.N.).
  • Domei T; Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan (T.D., K.A.).
  • Yamaji K; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Japan (Y.O., H. Watanabe, K. Yamamoto, K. Yamaji).
  • Suwa S; Department of Cardiology, Juntendo University Shizuoka Hospital, Izunokuni, Japan (S.S.).
  • Isawa T; Department of Cardiology, Sendai Kousei Hospital, Japan (T. Isawa).
  • Watanabe H; Department of Cardiology, Japanese Red Cross Wakayama Medical Center, Japan (H. Watanabe).
  • Yoshida R; Department of Cardiology, Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital, Japan (R.Y.).
  • Sakamoto H; Department of Cardiology, Shizuoka General Hospital, Japan (H. Sakamoto).
  • Akao M; Department of Cardiology, National Hospital Organization Kyoto Medical Center, Japan (M. Akao, M. Abe).
  • Hata Y; Department of Cardiology, Minamino Cardiovascular Hospital, Hachioji, Japan (Y.H.).
  • Morishima I; Department of Cardiology, Ogaki Municipal Hospital, Japan (I.M.).
  • Tokuyama H; Department of Cardiology, Kawaguchi Cardiovascular and Respiratory Hospital, Japan (H.T.).
  • Yagi M; Department of Cardiology, Sendai Cardiovascular Center, Japan (M.Y.).
  • Suzuki H; Department of Cardiology, Showa University Fujigaoka Hospital, Yokohama, Japan (H. Suzuki).
  • Wakabayashi K; Department of Cardiology, Showa University Koto Toyosu Hospital, Tokyo, Japan (K.W.).
  • Suematsu N; Division of Cardiology, Saiseikai Fukuoka General Hospital, Japan (N.S.).
  • Inada T; Division of Cardiology, Cardiovascular Center, Osaka Red Cross Hospital, Japan (T. Inada).
  • Tamura T; Department of Cardiology, Tenri Hospital, Japan (T.T.).
  • Okayama H; Department of Cardiology, Ehime Prefectural Central Hospital, Matsuyama, Japan (H.O.).
  • Abe M; Department of Cardiology, National Hospital Organization Kyoto Medical Center, Japan (M. Akao, M. Abe).
  • Kawai K; Department of Cardiology, Chikamori Hospital, Kochi, Japan (K. Kawai).
  • Nakao K; Division of Cardiology, Saiseikai Kumamoto Hospital Cardiovascular Center, Japan (K.N.).
  • Ando K; Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan (T.D., K.A.).
  • Tanabe K; Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan (K.T.).
  • Ikari Y; Department of Cardiology, Tokai University Hospital, Isehara, Japan (Y.I.).
  • Morino Y; Department of Cardiology, Iwate Medical University Hospital, Morioka, Japan (Y.M.).
  • Kadota K; Department of Cardiology, Kurashiki Central Hospital, Japan (K. Kadota).
  • Furukawa Y; Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Japan (Y.F.).
  • Nakagawa Y; Department of Cardiovascular Medicine, Shiga University of Medical Science, Otsu, Japan (Y.N.).
  • Kimura T; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Japan (Y.O., H. Watanabe, K. Yamamoto, K. Yamaji).
Circ Cardiovasc Interv ; 15(8): e012004, 2022 08.
Article in En | MEDLINE | ID: mdl-35912647
BACKGROUND: The benefit of clopidogrel monotherapy after 1-month dual antiplatelet therapy (DAPT) compared with 12-month DAPT with aspirin and clopidogrel was demonstrated in the STOPDAPT-2 (Short and Optimal Duration of Dual Antiplatelet Therapy After Everolimus-Eluting Cobalt-Chromium Stent-2), but not in the STOPDAPT-2 acute coronary syndrome (ACS); however, both trials were underpowered based on the actual event rates. METHODS: We obtained the prespecified pooled population of 5997 patients as the STOPDAPT-2 total cohort (STOPDAPT-2: N=3009/STOPDAPT-2 ACS: N=2988; ACS: N=4136/chronic coronary syndrome [CCS]: N=1861), comprising 2993 patients assigned to 1-month DAPT followed by clopidogrel monotherapy, and 3004 patients assigned to 12-month DAPT with aspirin and clopidogrel after percutaneous coronary intervention. The primary end point was the composite of cardiovascular (cardiovascular death, myocardial infarction, definite stent thrombosis, or any stroke) or bleeding (Thrombolysis in Myocardial Infarction major/minor) end points at 1 year. RESULTS: One-month DAPT was noninferior to 12-month DAPT for the primary end point (2.84% versus 3.04%; hazard ratio [HR], 0.94 [95% CI, 0.70-1.27]; Pnoninferiority=0.001; Psuperiority=0.68). There was no significant risk-difference for the cardiovascular end point between the 1- and 12-month DAPT groups (2.40% versus 1.97%; HR, 1.24 [95% CI, 0.88-1.75]; Pnoninferiority=0.14; Psuperiority=0.23). There was a lower risk of the bleeding end point with 1-month DAPT relative to 12-month DAPT (0.50% versus 1.31%; HR, 0.38 [95% CI, 0.21-0.70]; Psuperiority=0.002). One-month DAPT relative to 12-month DAPT was associated with a lower risk for major bleeding regardless of ACS or CCS (ACS: HR, 0.46 [95% CI, 0.23-0.94]; P=0.03, and CCS: HR, 0.26 [95% CI, 0.09-0.79]; P=0.02; Pinteraction=0.40), while it was associated with a numerical increase in cardiovascular events in ACS patients, but not in CCS patients, although not statistically significant and without interaction (ACS: HR, 1.50 [95% CI, 0.99-2.27]; P=0.053, and CCS: HR, 0.74 [95% CI, 0.38-1.45]; P=0.39; Pinteraction=0.08). CONCLUSIONS: Clopidogrel monotherapy after 1-month DAPT compared with 12-month DAPT with aspirin and clopidogrel had a benefit in reducing major bleeding events without being associated with increase in cardiovascular events. REGISTRATION: URL: https://www. CLINICALTRIALS: gov; Unique identifiers: NCT02619760, NCT03462498.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Platelet Aggregation Inhibitors / Percutaneous Coronary Intervention / Clopidogrel Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Circ Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2022 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Platelet Aggregation Inhibitors / Percutaneous Coronary Intervention / Clopidogrel Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Circ Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2022 Document type: Article Country of publication: United States