Long-term bleeding events post-percutaneous coronary intervention in patients with malignancy with and without anticoagulant therapy.

IF 3.1 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Yasuhiro Otsuka, Masanobu Ishii, So Ikebe, Tatsuya Tokai, Taishi Nakamura, Kenichi Tsujita, Naoyuki Akashi, Hideo Fujita, Yasuhiro Nakano, Tetsuya Matoba, Takahide Kohro, Yusuke Oba, Tomoyuki Kabutoya, Kazuomi Kario, Yasushi Imai, Arihiro Kiyosue, Yoshiko Mizuno, Kotaro Nochioka, Masaharu Nakayama, Takamasa Iwai, Yoshihiro Miyamoto, Hisahiko Sato, Ryozo Nagai
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引用次数: 0

Abstract

The prevalence of malignancies in patients undergoing percutaneous coronary intervention (PCI) is increasing with aging. Active malignancy is a significant contributor to high bleeding risk. For cancer patients requiring oral anticoagulant (OAC) therapy, the choice between direct oral anticoagulants (DOAC) and warfarin is critical. The aim of this study was to investigate long-term bleeding events in patients with malignancy undergoing PCI. The CLIDAS (Clinical Deep Data Accumulation System) multicenter database includes data from seven tertiary medical hospitals in Japan. This retrospective analysis included 6451 patients who underwent PCI between April 2013 and March 2019 and completed 3-year follow-up. The patients were divided into two groups; No malignancy (n = 5787) and Malignancy group (n = 664). Malignancy was defined by a history of cancer treatment. These groups were further subcategorized based on OAC therapy; (1) No malignancy without OAC (n = 5134), (2) No malignancy with DOAC (n = 261), (3) No malignancy with warfarin (n = 392), (4) Malignancy without OAC (n = 589), (5) Malignancy with DOAC (n = 38), and (6) Malignancy with warfarin (n = 37). The primary outcome was the incidence of bleeding events, defined according to the Global Use of Streptokinase and t-PA for Occluded Coronary Arteries classification of moderate and severe bleeding. The secondary outcomes were major adverse cardiac events (MACE) and net adverse clinical events (NACE). Multivariable Cox regression analysis showed that the malignancy with warfarin group had a significantly higher risk of bleeding events compared to the malignancy without OAC group (hazard ratio [HR], 3.64; 95% confidence interval [CI], 1.38-9.61, p value = 0.009). No significant differences were observed for MACE (HR, 1.39; 95% CI 0.59-3.25, p value = 0.454) or NACE (HR, 1.62; 95% CI, 0.80-3.29; p value = 0.184). Malignancy patients receiving warfarin were associated with a higher risk of bleeding events. DOACs may represent a preferable alternative to warfarin with regard to bleeding risk in patients with malignancy undergoing PCI.

恶性肿瘤患者经皮冠状动脉介入治疗后的长期出血事件。
在接受经皮冠状动脉介入治疗(PCI)的患者中,恶性肿瘤的患病率随着年龄的增长而增加。活动性恶性肿瘤是高出血风险的重要因素。对于需要口服抗凝剂(OAC)治疗的癌症患者,直接口服抗凝剂(DOAC)和华法林之间的选择至关重要。本研究的目的是调查恶性肿瘤患者接受PCI的长期出血事件。CLIDAS(临床深度数据积累系统)多中心数据库包括来自日本七家三级医院的数据。该回顾性分析包括2013年4月至2019年3月期间接受PCI治疗的6451例患者,并完成了为期3年的随访。患者分为两组;无恶性肿瘤(n = 5787)和恶性肿瘤组(n = 664)。恶性肿瘤是由癌症治疗史来定义的。这些组根据OAC治疗进一步细分;(1)无OAC恶性肿瘤(n = 5134),(2)无DOAC恶性肿瘤(n = 261),(3)无华法林恶性肿瘤(n = 392),(4)无OAC恶性肿瘤(n = 589), (5) DOAC恶性肿瘤(n = 38),(6)华法林恶性肿瘤(n = 37)。主要结局是出血事件的发生率,根据全球使用链激酶和t-PA治疗冠状动脉闭塞的中度和重度出血分类来定义。次要结局是主要不良心脏事件(MACE)和净不良临床事件(NACE)。多变量Cox回归分析显示,合并华法林的恶性肿瘤发生出血事件的风险明显高于未合并OAC的恶性肿瘤组(风险比[HR], 3.64;95%可信区间[CI], 1.38 ~ 9.61, p值= 0.009)。MACE无显著差异(HR, 1.39;95% CI 0.59-3.25, p值= 0.454)或NACE (HR, 1.62;95% ci, 0.80-3.29;P值= 0.184)。接受华法林治疗的恶性肿瘤患者发生出血事件的风险较高。对于接受PCI治疗的恶性肿瘤患者,DOACs可能是华法林出血风险的更好选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cardiovascular Intervention and Therapeutics
Cardiovascular Intervention and Therapeutics CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
6.30
自引率
12.50%
发文量
68
期刊介绍: Cardiovascular Intervention and Therapeutics (CVIT) is an international journal covering the field of cardiovascular disease and includes cardiac (coronary and noncoronary) and peripheral interventions and therapeutics. Articles are subject to peer review and complete editorial evaluation prior to any decision regarding acceptability. CVIT is an official journal of The Japanese Association of Cardiovascular Intervention and Therapeutics.
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