Aspirin versus Clopidogrel Monotherapy After Percutaneous Coronary Intervention: 1-Year Follow-up of the STOPDAPT-3 Trial.

29 coronary stent P2Y12 inhibitor antiplatelet therapy aspirin bleeding monotherapy percutaneous coronary intervention

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
31 Aug 2024
Historique:
received: 01 08 2024
revised: 17 08 2024
accepted: 28 08 2024
medline: 1 9 2024
pubmed: 1 9 2024
entrez: 31 8 2024
Statut: aheadofprint

Résumé

There was no previous trial comparing aspirin monotherapy with a P2Y12 inhibitor monotherapy following short dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) with drug-eluting stents (DES). In the STOPDAPT-3, patients with acute coronary syndrome (ACS) or high bleeding risk (HBR) were randomly assigned to either 1-month DAPT with aspirin and prasugrel followed by aspirin monotherapy (aspirin group) or 1-month prasugrel monotherapy followed by clopidogrel monotherapy (clopidogrel group). This secondary analysis compared aspirin monotherapy with clopidogrel monotherapy by the 30-day landmark analysis. The co-primary endpoints were the cardiovascular endpoint defined as a composite of cardiovascular death, myocardial infarction, definite stent thrombosis, or ischaemic stroke, and the bleeding endpoint defined as Bleeding Academic Research Consortium 3 or 5. Of 6002 assigned patients, 5833 patients (aspirin group: N = 2920 and clopidogrel group: N = 2913) were included in the 30-day landmark analysis. Median age was 73 (interquartile range 64-80) years, women 23.4%, ACS 74.6%, and HBR 54.1%. The assigned monotherapy was continued at 1 year in 87.5% and 87.2% in the aspirin and clopidogrel groups, respectively. The incidence rates beyond 30 days and up to 1 year were similar between the aspirin and clopidogrel groups for both cardiovascular endpoint (4.5 and 4.5 per 100 person-year, hazard ratio [HR] 1.00 [95% confidence interval (CI) 0.77-1.30], P = .97), and bleeding endpoint (2.0 and 1.9, HR 1.02 [95% CI 0.69-1.52], P = .92). Aspirin monotherapy compared to clopidogrel monotherapy was associated with similar cardiovascular and bleeding outcomes beyond 1 month and up to 1 year after PCI with DES.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
There was no previous trial comparing aspirin monotherapy with a P2Y12 inhibitor monotherapy following short dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) with drug-eluting stents (DES).
METHODS METHODS
In the STOPDAPT-3, patients with acute coronary syndrome (ACS) or high bleeding risk (HBR) were randomly assigned to either 1-month DAPT with aspirin and prasugrel followed by aspirin monotherapy (aspirin group) or 1-month prasugrel monotherapy followed by clopidogrel monotherapy (clopidogrel group). This secondary analysis compared aspirin monotherapy with clopidogrel monotherapy by the 30-day landmark analysis. The co-primary endpoints were the cardiovascular endpoint defined as a composite of cardiovascular death, myocardial infarction, definite stent thrombosis, or ischaemic stroke, and the bleeding endpoint defined as Bleeding Academic Research Consortium 3 or 5.
RESULTS RESULTS
Of 6002 assigned patients, 5833 patients (aspirin group: N = 2920 and clopidogrel group: N = 2913) were included in the 30-day landmark analysis. Median age was 73 (interquartile range 64-80) years, women 23.4%, ACS 74.6%, and HBR 54.1%. The assigned monotherapy was continued at 1 year in 87.5% and 87.2% in the aspirin and clopidogrel groups, respectively. The incidence rates beyond 30 days and up to 1 year were similar between the aspirin and clopidogrel groups for both cardiovascular endpoint (4.5 and 4.5 per 100 person-year, hazard ratio [HR] 1.00 [95% confidence interval (CI) 0.77-1.30], P = .97), and bleeding endpoint (2.0 and 1.9, HR 1.02 [95% CI 0.69-1.52], P = .92).
CONCLUSIONS CONCLUSIONS
Aspirin monotherapy compared to clopidogrel monotherapy was associated with similar cardiovascular and bleeding outcomes beyond 1 month and up to 1 year after PCI with DES.

Identifiants

pubmed: 39215959
pii: 7745594
doi: 10.1093/eurheartj/ehae617
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Hirotoshi Watanabe (H)

Division of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.

Masahiro Natsuaki (M)

Department of Cardiovascular Medicine, Saga University, Saga, Japan.

Takeshi Morimoto (T)

Department of Clinical Epidemiology, Hyogo Medical University, Nishinomiya, Japan.

Ko Yamamoto (K)

Department of Cardiology, Kokura Memorial Hospital, Kitakyusyu, Japan.

Yuki Obayashi (Y)

Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Ryusuke Nishikawa (R)

Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Tomoya Kimura (T)

Department of Clinical Epidemiology, Hyogo Medical University, Nishinomiya, Japan.
Department of Cardiology, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.

Kenji Ando (K)

Department of Cardiology, Kokura Memorial Hospital, Kitakyusyu, Japan.

Takenori Domei (T)

Department of Cardiology, Kokura Memorial Hospital, Kitakyusyu, Japan.

Satoru Suwa (S)

Department of Cardiology, Juntendo University Shizuoka Hospital, Izunokuni, Japan.

Manabu Ogita (M)

Department of Cardiology, Juntendo University Shizuoka Hospital, Izunokuni, Japan.

Tsuyoshi Isawa (T)

Department of Cardiology, Sendai Kousei Hospital, Sendai, Japan.

Hiroyuki Takenaka (H)

Division of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.

Takashi Yamamoto (T)

Division of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.

Tetsuya Ishikawa (T)

Department of Cardiology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Japan.

Itaru Hisauchi (I)

Department of Cardiology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Japan.

Kohei Wakabayashi (K)

Department of Cardiology, Showa University Koto Toyosu Hospital, Tokyo, Japan.

Yuko Onishi (Y)

Department of Cardiology, Hiratsuka Kyosai Hospital, Hiratsuka, Japan.

Kiyoshi Hibi (K)

Division of Cardiology, Yokohama City University Medical Center, Yokohama, Japan.

Kazuya Kawai (K)

Division of Cardiology, Chikamori Hospital, Kochi, Japan.

Ruka Yoshida (R)

Division of Cardiology, Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital, Nagoya, Japan.

Hiroshi Suzuki (H)

Division of Cardiology, Showa University Fujigaoka Hospital, Yokohama, Japan.

Gaku Nakazawa (G)

Department of Cardiology, Kindai University Faculty of Medicine, Osakasayama, Japan.

Takanori Kusuyama (T)

Division of Cardiology, Tsukazaki Hospital, Himeji, Japan.

Itsuro Morishima (I)

Department of Cardiology, Ogaki Municipal Hospital, Ogaki, Japan.

Koh Ono (K)

Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Takeshi Kimura (T)

Division of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.

Classifications MeSH