An aspirin-free strategy for percutaneous coronary intervention in patients with diabetes: a pre-specified subgroup analysis of the STOPDAPT-3 trial.

And percutaneous coronary intervention Antiplatelet therapy Coronary stent Diabetes

Journal

European heart journal. Cardiovascular pharmacotherapy
ISSN: 2055-6845
Titre abrégé: Eur Heart J Cardiovasc Pharmacother
Pays: England
ID NLM: 101669491

Informations de publication

Date de publication:
23 Oct 2024
Historique:
medline: 24 10 2024
pubmed: 24 10 2024
entrez: 24 10 2024
Statut: aheadofprint

Résumé

Safety of aspirin-free strategy immediately after percutaneous coronary intervention (PCI) for cardiovascular events in patients with diabetes was unknown. We conducted the prespecified subgroup analysis on diabetes in the STOPDAPT-3 trial, which randomly compared prasugrel (3.75 mg/day) monotherapy (2984 patients) to dual antiplatelet therapy (DAPT) with prasugrel and aspirin (2982 patients) in patients with acute coronary syndrome or high bleeding risk. The co-primary endpoints were major bleeding events (Bleeding Academic Research Consortium 3 or 5) and cardiovascular events (a composite of cardiovascular death, myocardial infarction, definite stent thrombosis, or stroke) at 1 month. Of 5966 study patients, there were 2715 patients (45.5%) with diabetes. Patients with diabetes more often had chronic coronary syndrome, heart failure or cardiogenic shock, and comorbidities than those without. Patients with diabetes compared to those without had higher incidences of major bleeding and cardiovascular events. Regardless of diabetes, the effect of no-aspirin relative to DAPT was not different for the co-primary bleeding (diabetes: 5.05% versus 5.47%; HR, 0.92; 95%CI, 0.66-1.28 and non-diabetes: 3.99% versus 4.07%; HR, 0.98; 95%CI, 0.69-1.38; P for interaction = 0.81) and cardiovascular (diabetes: 5.54% versus 5.15%; HR, 1.08; 95%CI, 0.78-1.49 and non-diabetes: 2.95% versus 2.47%; HR, 1.20; 95%CI, 0.79-1.82; P for interaction = 0.70) endpoints. The incidences of subacute definite or probable stent thrombosis and any coronary revascularization were higher in the no-aspirin group than in the DAPT group regardless of diabetes. The effects of an aspirin-free prasugrel monotherapy (3.75 mg/day) relative to DAPT for major bleeding and cardiovascular events were not different regardless of diabetes. Clinical trial registration: ShorT and OPtimal duration of Dual AntiPlatelet Therapy after everolimus-eluting cobalt-chromium stent-3 [STOPDAPT-3]; NCT04609111.

Identifiants

pubmed: 39444052
pii: 7833553
doi: 10.1093/ehjcvp/pvae075
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04609111']

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.

Auteurs

Ko Yamamoto (K)

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

Masahiro Natsuaki (M)

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

Hirotoshi Watanabe (H)

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

Takeshi Morimoto (T)

Department of Data Science, Hyogo Medical University, Nishinomiya, Japan.

Yuki Obayashi (Y)

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

Ryusuke Nishikawa (R)

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

Kenji Ando (K)

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

Satoru Suwa (S)

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

Tsuyoshi Isawa (T)

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

Hiroyuki Takenaka (H)

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

Tetsuya Ishikawa (T)

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

Yuji Ikari (Y)

Department of Cardiology, Tokai University Hospital, Isehara, Japan.

Tairo Kurita (T)

Department of Cardiology, Mie University Hospital, Tsu, Japan.

Kazuaki Kaitani (K)

Department of Cardiology, Japanese Red Cross Otsu Hospital, Otsu, Japan.

Atsuhiko Sugimoto (A)

Department of Cardiology, Sagamihara Kyodo Hospital, Sagamihara, Japan.

Nobuhiko Ogata (N)

Department of Cardiology, Ageo Central General Hospital, Ageo, Japan.

Akihiro Ikuta (A)

Department of Cardiology, Kurashiki Central Hospital, Kurashiki, Japan.

Katsushi Hashimoto (K)

Department of Cardiovascular Medicine, Minamino Cardiovascular Hospital, Hachioji, Japan.

Yuki Ishibashi (Y)

Department of Cardiology, St. Marianna University Hospital, Kawasaki, Japan.

Kazunori Masuda (K)

Department of Cardiovascular Medicine, Uji-Tokushukai Medical Center, Uji, Japan.

Tomonori Miyabe (T)

Department of Cardiology, Tokyo Metropolitan Tama Medical Center, Fuchu, Japan.

Koh Ono (K)

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

Takeshi Kimura (T)

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

Classifications MeSH