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タイトル: Details on the effect of very short dual antiplatelet therapy after drug-eluting stent implantation in patients with high bleeding risk: insight from the STOPDAPT-2 trial
著者: Watanabe, Hirotoshi
Domei, Takenori
Morimoto, Takeshi
Natsuaki, Masahiro
Shiomi, Hiroki  kyouindb  KAKEN_id
Toyota, Toshiaki
Ohya, Masanobu
Suwa, Satoru
Takagi, Kensuke
Nanasato, Mamoru
Hata, Yoshiki
Yagi, Masahiro
Suematsu, Nobuhiro
Yokomatsu, Takafumi
Takamisawa, Itaru
Doi, Masayuki
Noda, Toshiyuki
Okayama, Hideki
Seino, Yoshitane
Tada, Tomohisa
Sakamoto, Hiroki
Hibi, Kiyoshi
Abe, Mitsuru
Kawai, Kazuya
Nakao, Koichi
Ando, Kenji
Tanabe, Kengo
Ikari, Yuji
Hanaoka, Igarashi, Keiichi
Morino, Yoshihiro
Kozuma, Ken
Kadota, Kazushige
Furukawa, Yutaka
Nakagawa, Yoshihisa
Kimura, Takeshi
著者名の別形: 渡部, 宏俊
塩見, 紘樹
木村, 剛
キーワード: Antiplatelet therapy
Coronary stent
Bleeding
High bleeding risk
Percutaneous coronary intervention
発行日: Jan-2021
出版者: Springer Nature
誌名: Cardiovascular Intervention and Therapeutics
巻: 36
号: 1
開始ページ: 91
終了ページ: 103
抄録: Previously we briefly reported the effect of 1-month dual antiplatelet therapy (DAPT) for patients with high bleeding risk (HBR) receiving percutaneous coronary intervention (PCI) in the STOPDAPT-2 trial, but full analysis data have not been available. We conducted post hoc subgroup analysis regarding the effect of very short DAPT for HBR patients in STOPDAPT-2 trial. The primary endpoint was a 1-year composite of cardiovascular (cardiovascular death, myocardial infarction, definite stent thrombosis, or stroke) and bleeding (TIMI major/minor bleeding) outcomes. Major secondary endpoints were 1-year cardiovascular composite endpoint and bleeding endpoint. HBR was defined by the academic research consortium (ARC) HBR criteria. Among the 3009 study patients, 1054 (35.0%) were classified as HBR and 1955 (65.0%) were as non-HBR. There were no significant interactions between HBR/non-HBR subgroups and the assigned DAPT group on the primary endpoint (HBR; 3.48% vs. 5.98%, HR 0.57, 95% CI 0.32-1.03, and non-HBR; 1.81% vs. 2.36%, HR 0.78, 95% CI 0.42-1.45; P for interaction = 0.48), the major secondary cardiovascular endpoint (HBR; 3.07% vs. 4.03%, HR 0.77, 95% CI 0.40-1.48, and non-HBR; 1.41% vs. 1.61%, HR 0.89, 95% CI 0.43-1.84; P for interaction = 0.77), and the major secondary bleeding endpoint (HBR; 0.41% vs. 2.71%, HR 0.15, 95% CI 0.03-0.65, and non-HBR; 0.40% vs. 0.85%, HR 0.48, 95% CI 0.14-1.58; P for interaction = 0.22). In conclusion, the effects of 1-month DAPT for the primary and major secondary endpoints were consistent in HBR and non-HBR patients without any significant interactions. The benefit of 1-month DAPT in reducing major bleeding was numerically greater in HBR patients.Clinical trial registration Short and optimal duration of dual antiplatelet therapy after everolimus-eluting cobalt-chromium stent-2 [STOPDAPT-2]; NCT02619760.
著作権等: This is a post-peer-review, pre-copyedit version of an article published in Cardiovascular intervention and therapeutics. The final authenticated version is available online at: http://dx.doi.org/10.1007/s12928-020-00651-9.
この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
This is not the published version. Please cite only the published version.
URI: http://hdl.handle.net/2433/261812
DOI(出版社版): 10.1007/s12928-020-00651-9
PubMed ID: 32086787
出現コレクション:学術雑誌掲載論文等

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