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Reduced-dose prasugrel monotherapy without aspirin after PCI with the SYNERGY stent in East Asian patients presenting with chronic coronary syndromes or non-ST-elevation acute coronary syndromes: rationale and design of the ASET Japan pilot study.
Masuda, Shinichiro; Muramatsu, Takashi; Ishibashi, Yuki; Kozuma, Ken; Tanabe, Kengo; Nakatani, Shimpei; Kogame, Norihiro; Nakamura, Masato; Asano, Taku; Okamura, Takayuki; Miyazaki, Yosuke; Tateishi, Hiroki; Ozaki, Yukio; Nakazawa, Gaku; Morino, Yoshihiro; Katagiri, Yuki; Garg, Scot; Hara, Hironori; Ono, Masafumi; Kawashima, Hideyuki; Lemos, Pedro A; Serruys, Patrick W; Onuma, Yoshinobu.
Afiliação
  • Masuda S; Department of Cardiology, National University of Ireland Galway (NUIG), Galway, Ireland.
  • Muramatsu T; Department of Cardiology, Fujita Health University Hospital, Toyoake, Japan.
  • Ishibashi Y; Division of Cardiology, Department of Internal Medicine, St. Marianna University School of Medicine, Kanagawa, Japan.
  • Kozuma K; Department of Cardiology, Teikyo University Hospital, Tokyo, Japan.
  • Tanabe K; Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.
  • Nakatani S; Department of Cardiology, JCHO Hoshigaoka Medical Center, Osaka, Japan.
  • Kogame N; Division of Cardiovascular Medicine, Toho University Ohashi Medical Center, Tokyo, Japan.
  • Nakamura M; Division of Cardiovascular Medicine, Toho University Ohashi Medical Center, Tokyo, Japan.
  • Asano T; Department of Cardiology, St. Luke's International Hospital, Tokyo, Japan.
  • Okamura T; Division of Cardiology, Department of Clinical Science and Medicine, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Miyazaki Y; Division of Cardiology, Department of Clinical Science and Medicine, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Tateishi H; Division of Cardiology, Department of Clinical Science and Medicine, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Ozaki Y; Department of Cardiology, Shibata Hospital, Aichi, Japan.
  • Nakazawa G; Department of Cardiology, Fujita Health University Okazaki Medical Center, Aichi, Japan.
  • Morino Y; Department of Cardiology, Kindai University Faculty of Medicine, Osaka, Japan.
  • Katagiri Y; Department of Cardiology, Iwate Medical University Hospital, Iwate, Japan.
  • Garg S; Department of Cardiology, Sapporo Higashi Tokushukai Hospital, Hokkaido, Japan.
  • Hara H; Department of Cardiology, Royal Blackburn Hospital, Blackburn, UK.
  • Ono M; Department of Cardiology, National University of Ireland Galway (NUIG), Galway, Ireland.
  • Kawashima H; Department of Cardiology, National University of Ireland Galway (NUIG), Galway, Ireland.
  • Lemos PA; Department of Cardiology, National University of Ireland Galway (NUIG), Galway, Ireland.
  • Serruys PW; Department of Cardiology, Teikyo University Hospital, Tokyo, Japan.
  • Onuma Y; Heart Institute (InCor), University of São Paulo, São Paulo, Brazil.
AsiaIntervention ; 9(1): 39-48, 2023 Mar.
Article em En | MEDLINE | ID: mdl-36936091
The Acetyl Salicylic Elimination Trial (ASET) Japan pilot study is a multicentre, single-arm, open-label, proof-of-concept study with a stopping rule based on the occurrence of definite stent thrombosis. This study aims to demonstrate the feasibility and safety of low-dose prasugrel monotherapy following percutaneous coronary intervention (PCI) in Japanese patients presenting with chronic coronary syndromes (CCS) or non-ST-elevation acute coronary syndromes (NSTE-ACS). Four hundred patients with a SYNTAX score <23 requiring PCI due to CCS or NSTE-ACS will be screened and considered eligible for the study. The enrolment is planned in two phases: 1) 200 patients presenting with CCS, followed by 2) 200 patients presenting with NSTE-ACS. After optimal PCI with implantation of a SYNERGY (Boston Scientific) stent, patients will be enrolled and loaded with prasugrel 20 mg, followed by a maintenance dose of prasugrel 3.75 mg once daily without aspirin continued for 3 months in Phase 1 (CCS patients), and for 12 months in Phase 2 (NSTE-ACS patients). After these follow-up periods, prasugrel will be replaced by standard antiplatelet therapy according to local practice. The primary endpoint is a composite of cardiac death, target vessel myocardial infarction, or definite stent thrombosis after the index procedure. The primary bleeding endpoint is any Bleeding Academic Research Consortium type 3 or 5 bleeding occurring within 3 months of the index PCI for CCS patients, or 12 months for NSTE-ACS patients. The ASET Japan study is designed to demonstrate the feasibility and safety of reduced-dose prasugrel monotherapy after PCI in East Asian patients with acute and chronic coronary syndromes.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article