Ischemic/bleeding event after short dual-antiplatelet therapy in patients with high bleeding risk: Sub-analysis of the MODEL U-SES study.


Journal

Journal of cardiology
ISSN: 1876-4738
Titre abrégé: J Cardiol
Pays: Netherlands
ID NLM: 8804703

Informations de publication

Date de publication:
08 2021
Historique:
received: 16 12 2020
revised: 14 02 2021
accepted: 16 03 2021
pubmed: 21 4 2021
medline: 25 11 2021
entrez: 20 4 2021
Statut: ppublish

Résumé

This analysis aimed to evaluate the clinical impact of high bleeding risk (HBR) on adverse events after percutaneous coronary intervention (PCI). We retrospectively analyzed 1695 patients in the MODEL U-SES study, which was a multicenter, open-label, prospective observational study evaluating safety of 3-month dual antiplatelet therapy (DAPT) after Ultimaster stent (Terumo Corporation, Tokyo, Japan) implantation at 65 sites in Japan. Patients were divided into 2 groups (HBR/Non-HBR) according to modified Academic Research Consortium-HBR criteria. Ischemic/thrombotic event (cardiovascular death, myocardial infarction, ischemic stroke, and stent thrombosis) and bleeding event (Bleeding Academic Research Consortium 3 or 5) at 1 year were evaluated. Of 1695 patients, 840 patients were categorized as HBR and 855 patients were Non-HBR. One-year follow-up was completed in 95.3%. During 1-year follow-up, ischemic/thrombotic events were observed in 31 cases (1.8%) and bleeding events occurred in 21 cases (1.2%). Presence of HBR was significantly associated with higher incidence of ischemic/thrombotic events as compared to Non-HBR (adjusted hazard ratio, 0.16; 95% confidence interval, 0.05 to 0.50), whereas the incidence of bleeding events did not reach statistical significance between HBR and Non-HBR. In comparison of monotherapy after DAPT, P2Y In contemporary PCI practice, nearly half of patients had HBR and presence of HBR significantly increased risk of ischemic/thrombotic events. Both aspirin and P2Y

Sections du résumé

BACKGROUND
This analysis aimed to evaluate the clinical impact of high bleeding risk (HBR) on adverse events after percutaneous coronary intervention (PCI).
METHODS
We retrospectively analyzed 1695 patients in the MODEL U-SES study, which was a multicenter, open-label, prospective observational study evaluating safety of 3-month dual antiplatelet therapy (DAPT) after Ultimaster stent (Terumo Corporation, Tokyo, Japan) implantation at 65 sites in Japan. Patients were divided into 2 groups (HBR/Non-HBR) according to modified Academic Research Consortium-HBR criteria. Ischemic/thrombotic event (cardiovascular death, myocardial infarction, ischemic stroke, and stent thrombosis) and bleeding event (Bleeding Academic Research Consortium 3 or 5) at 1 year were evaluated.
RESULTS
Of 1695 patients, 840 patients were categorized as HBR and 855 patients were Non-HBR. One-year follow-up was completed in 95.3%. During 1-year follow-up, ischemic/thrombotic events were observed in 31 cases (1.8%) and bleeding events occurred in 21 cases (1.2%). Presence of HBR was significantly associated with higher incidence of ischemic/thrombotic events as compared to Non-HBR (adjusted hazard ratio, 0.16; 95% confidence interval, 0.05 to 0.50), whereas the incidence of bleeding events did not reach statistical significance between HBR and Non-HBR. In comparison of monotherapy after DAPT, P2Y
CONCLUSION
In contemporary PCI practice, nearly half of patients had HBR and presence of HBR significantly increased risk of ischemic/thrombotic events. Both aspirin and P2Y

Identifiants

pubmed: 33875313
pii: S0914-5087(21)00089-7
doi: 10.1016/j.jjcc.2021.03.015
pii:
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107-113

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Hirofumi Hioki (H)

Division of Cardiology, Teikyo University Hospital, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

Ken Kozuma (K)

Division of Cardiology, Teikyo University Hospital, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan. Electronic address: kozumak@med.teikyo-u.ac.jp.

Yoshihisa Kinoshita (Y)

Department of Cardiology, Toyohashi Heart Center, Toyohashi, Japan.

Mamoru Nanasato (M)

Department of Cardiology, Sakakibara Heart Institute, Fuchu, Japan.

Yoshiaki Ito (Y)

Department of Cardiology, Saiseikai Yokohamashi Tobu Hospital, Yokohama, Japan.

Junichi Yamaguchi (J)

Department of Cardiology, Tokyo Women's Medical University, Tokyo, Japan.

Nobuo Shiode (N)

Department of Cardiology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.

Kiyoshi Hibi (K)

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

Kengo Tanabe (K)

Division of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.

Junya Ako (J)

Department of Cardiology, Kitazato University Hospital, Sagamihara, Japan.

Yoshihiro Morino (Y)

Department of Cardiology, Iwate Medical University Hospital, Morioka, Japan.

Atsushi Hirohata (A)

Department of Cardiology, Sakakibara Heart Institute of Okayama, Okayama, Japan.

Shinjo Sonoda (S)

Department of Cardiology, Hospital of the University of Occupational and Environmental Health, Kitakyushu, Japan.

Yoshihisa Nakagawa (Y)

Department of Cardiology, Shiga University of Medical Science Hospital, Otsu, Japan.

Hisayuki Okada (H)

Department of Cardiology, Seirei Hamamatsu General Hospital, Shizuoka, Japan.

Takuo Nakagami (T)

Department of Cardiology, Omihachiman Community Medical Center, Omihachiman, Japan.

Itaru Takamisawa (I)

Department of Cardiology, Sakakibara Heart Institute, Fuchu, Japan.

Kenji Ando (K)

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

Mitsuru Abe (M)

Department of Cardiology, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.

Yuji Ikari (Y)

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

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH