医学
传统PCI
冠状动脉疾病
经皮冠状动脉介入治疗
内科学
血运重建
左主干冠状动脉疾病
死亡率
心脏病学
随机对照试验
子群分析
外科
心肌梗塞
置信区间
作者
Masafumi Ono,Hideyuki Kawashima,Hironori Hara,Massimo Mancone,Michael J. Mack,David R. Holmes,Marie‐Claude Morice,A. Pieter Kappetein,Daniel J.F.M. Thuijs,Thilo Noack,Friedrich W. Mohr,Piroze Davierwala,Yoshinobu Onuma,Patrick W. Serruys
标识
DOI:10.1016/j.ijcard.2021.08.013
摘要
BACKGROUND: The significant interaction between major infection and 5-year mortality after percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG) for complex coronary artery disease (CAD) was observed previously. However, the very long-term outcomes beyond 5 years remains unclear. METHODS AND RESULTS: This is a subgroup analysis of the SYNTAX Extended Survival (SYNTAXES) trial, which is the extended follow-up of the randomized SYNTAX trial comparing PCI versus CABG in patients with three-vessel disease (3VD) or left-main CAD (LMCAD). Out of 1517 patients enrolled in the SYNTAX trial with available survival status from 5 to 10 years, 140 patients had experienced major infections and survived at 5 years (major infection group). From 5 to 10 years, the mortality of major infection group was 19.8% whereas the mortality of no major infection group was 15.1% (p = 0.157). After the adjustment of other clinical factors, the risk of mortality from 5 to 10 years did not significantly differ between major infection and no major infection groups (HR: 1.10; 95% CI: 0.62-1.96; p = 0.740). When stratified by the presence or absence of periprocedural major infections, defined as a major infection within 60 days after index procedure, there was also no significant difference in 10-year mortality between two groups (30.8% vs. 24.5%; p = 0.057). CONCLUSIONS: Despite the initial association between major infections and 5 years mortality, postprocedural major infection was not evident in the 10 years follow-up, suggesting that the impact of major infection on mortality subsided over time beyond 5 years. TRIAL REGISTRATION: SYNTAXES ClinicalTrials.gov reference: NCT03417050 SYNTAX ClinicalTrials.gov reference: NCT00114972.
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