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An Aspirin-Free Strategy for Immediate Treatment Following Complex Percutaneous Coronary Intervention.
Yamamoto, Ko; Natsuaki, Masahiro; Watanabe, Hirotoshi; Morimoto, Takeshi; Obayashi, Yuki; Nishikawa, Ryusuke; Ando, Kenji; Suwa, Satoru; Isawa, Tsuyoshi; Takenaka, Hiroyuki; Ishikawa, Tetsuya; Tamura, Toshihiro; Kawahatsu, Kando; Hayashi, Fujio; Akao, Masaharu; Serikawa, Takeshi; Mori, Hiroyoshi; Kawamura, Takayuki; Hagikura, Arata; Shibata, Naoki; Ono, Koh; Kimura, Takeshi.
Affiliation
  • Yamamoto K; Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
  • Natsuaki M; Department of Cardiovascular Medicine, Saga University, Saga, Japan.
  • Watanabe H; Department of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.
  • Morimoto T; Department of Clinical Epidemiology, Hyogo College of Medicine, Nishinomiya, Japan.
  • Obayashi Y; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Nishikawa R; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Ando K; Department of Cardiology, Kokura Memorial Hospital, Kitakyushu, Japan.
  • Suwa S; Department of Cardiology, Juntendo University Shizuoka Hospital, Izunokuni, Japan.
  • Isawa T; Department of Cardiology, Sendai Kousei Hospital, Sendai, Japan.
  • Takenaka H; Department of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan.
  • Ishikawa T; Department of Cardiology, Dokkyo Medical University Saitama Medical Center, Koshigaya, Japan.
  • Tamura T; Department of Cardiology, Tenri Hospital, Tenri, Japan.
  • Kawahatsu K; Department of Cardiology, Teine Keijinkai Hospital, Teine, Japan.
  • Hayashi F; Department of Cardiovascular Center, Japanese Red Cross Osaka Hospital, Osaka Japan.
  • Akao M; Department of Cardiology, Kyoto Medical Center, Kyoto, Japan.
  • Serikawa T; Department of Cardiology, Fukuoka Wajiro Hospital, Fukuoka, Japan.
  • Mori H; Showa University Fujigaoka Hospital, Yokohama, Japan.
  • Kawamura T; Department of Cardiology, Kindai University Faculty of Medicine, Osakasayama, Japan.
  • Hagikura A; Division of Cardiology, Tsukazaki Hospital, Himeji, Japan.
  • Shibata N; Ogaki Municipal Hospital, Ogaki, Japan.
  • Ono K; Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
  • Kimura T; Department of Cardiology, Hirakata Kohsai Hospital, Hirakata, Japan. Electronic address: taketaka@kuhp.kyoto-u.ac.jp.
JACC Cardiovasc Interv ; 17(9): 1119-1130, 2024 May 13.
Article in En | MEDLINE | ID: mdl-38749592
ABSTRACT

BACKGROUND:

There was no study evaluating the effects of an aspirin-free strategy in patients undergoing complex percutaneous coronary intervention (PCI).

OBJECTIVES:

The authors aimed to evaluate the efficacy and safety of an aspirin-free strategy in patients undergoing complex PCI.

METHODS:

We conducted the prespecified subgroup analysis based on complex PCI in the STOPDAPT-3 (ShorT and OPtimal duration of Dual AntiPlatelet Therapy after everolimus-eluting cobalt-chromium stent-3), which randomly compared low-dose prasugrel (3.75 mg/d) monotherapy to dual antiplatelet therapy (DAPT) with low-dose prasugrel and aspirin in patients with acute coronary syndrome or high bleeding risk. Complex PCI was defined as any of the following 6 criteria 3 vessels treated, ≥3 stents implanted, ≥3 lesions treated, bifurcation with 2 stents implanted, total stent length >60 mm, or a target of chronic total occlusion. The coprimary 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 ischemic stroke) at 1 month.

RESULTS:

Of the 5,966 study patients, there were 1,230 patients (20.6%) with complex PCI. Regardless of complex PCI, the effects of no aspirin relative to DAPT were not significant for the coprimary bleeding (complex PCI 5.30% vs 3.70%; HR 1.44; 95% CI 0.84-2.47; P = 0.18 and noncomplex PCI 4.26% vs 4.97%; HR 0.85; 95% CI 0.65-1.11; P = 0.24; P for interaction = 0.08) and cardiovascular (complex PCI 5.78% vs 5.93%; HR 0.98; 95% CI 0.62-1.55; P = 0.92 and noncomplex PCI 3.70% vs 3.10%; HR 1.20; 95% CI 0.88-1.63; P = 0.25; P for interaction = 0.48) endpoints without significant interactions.

CONCLUSIONS:

The effects of the aspirin-free strategy relative to standard DAPT for the cardiovascular and major bleeding events were not different regardless of complex PCI. (ShorT and OPtimal duration of Dual AntiPlatelet Therapy after everolimus-eluting cobalt-chromium stent-3 [STOPDAPT-3]; NCT04609111).
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prosthesis Design / Coronary Artery Disease / Drug Administration Schedule / Platelet Aggregation Inhibitors / Aspirin / Drug-Eluting Stents / Percutaneous Coronary Intervention / Everolimus / Prasugrel Hydrochloride / Dual Anti-Platelet Therapy Language: En Journal: JACC Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2024 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prosthesis Design / Coronary Artery Disease / Drug Administration Schedule / Platelet Aggregation Inhibitors / Aspirin / Drug-Eluting Stents / Percutaneous Coronary Intervention / Everolimus / Prasugrel Hydrochloride / Dual Anti-Platelet Therapy Language: En Journal: JACC Cardiovasc Interv Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2024 Document type: Article Affiliation country: Japón