Percutaneous coronary angioplasty versus coronary artery bypass grafting in the treatment of unprotected left main stenosis: updated 5-year outcomes from the randomised, non-inferiority NOBLE trial

医学 传统PCI 经皮冠状动脉介入治疗 心肌梗塞 血管成形术 内科学 心脏病学 危险系数 临床终点 冠状动脉疾病 冲程(发动机) 人口 外科 随机对照试验 置信区间 工程类 环境卫生 机械工程
作者
Niels Ramsing Holm,Timo H. Mäkikallio,Mitchell Lindsay,Mark S. Spence,Andrejs Ērglis,Ian Menown,Thor Trovik,Thomas Kellerth,Gintaras Kalinauskas,Lone Juul Hune Mogensen,Per Hostrup Nielsen,Matti Niemelä,Jens Flensted Lassen,Keith G. Oldroyd,G Berg,Pēteris Stradiņš,Simon Walsh,Alastair Graham,Petter Cappelen Endresen,Ole Fröbert,Uday Trivedi,Vesa Anttila,David Hildick‐Smith,Leif Thuesen,Evald Høj Christiansen,Noble study investigators
出处
期刊:The Lancet [Elsevier]
卷期号:395 (10219): 191-199 被引量:283
标识
DOI:10.1016/s0140-6736(19)32972-1
摘要

Background Percutaneous coronary intervention (PCI) is increasingly used in revascularisation of patients with left main coronary artery disease in place of the standard treatment, coronary artery bypass grafting (CABG). The NOBLE trial aimed to evaluate whether PCI was non-inferior to CABG in the treatment of left main coronary artery disease and reported outcomes after a median follow-up of 3·1 years. We now report updated 5-year outcomes of the trial. Methods The prospective, randomised, open-label, non-inferiority NOBLE trial was done at 36 hospitals in nine northern European countries. Patients with left main coronary artery disease requiring revascularisation were enrolled and randomly assigned (1:1) to receive PCI or CABG. The primary endpoint was major adverse cardiac or cerebrovascular events (MACCE), a composite of all-cause mortality, non-procedural myocardial infarction, repeat revascularisation, and stroke. Non-inferiority of PCI to CABG was defined as the upper limit of the 95% CI of the hazard ratio (HR) not exceeding 1·35 after 275 MACCE had occurred. Secondary endpoints included all-cause mortality, non-procedural myocardial infarction, and repeat revascularisation. Outcomes were analysed in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT01496651. Findings Between Dec 9, 2008, and Jan 21, 2015, 1201 patients were enrolled and allocated to PCI (n=598) or CABG (n=603), with 17 subsequently lost to early follow-up. 592 patients in each group were included in this analysis. At a median of 4·9 years of follow-up, the predefined number of events was reached for adequate power to assess the primary endpoint. Kaplan-Meier 5-year estimates of MACCE were 28% (165 events) for PCI and 19% (110 events) for CABG (HR 1·58 [95% CI 1·24–2·01]); the HR exceeded the limit for non-inferiority of PCI compared to CABG. CABG was found to be superior to PCI for the primary composite endpoint (p=0·0002). All-cause mortality was estimated in 9% after PCI versus 9% after CABG (HR 1·08 [95% CI 0·74–1·59]; p=0·68); non-procedural myocardial infarction was estimated in 8% after PCI versus 3% after CABG (HR 2·99 [95% CI 1·66–5·39]; p=0·0002); and repeat revascularisation was estimated in 17% after PCI versus 10% after CABG (HR 1·73 [95% CI 1·25–2·40]; p=0·0009). Interpretation In revascularisation of left main coronary artery disease, PCI was associated with an inferior clinical outcome at 5 years compared with CABG. Mortality was similar after the two procedures but patients treated with PCI had higher rates of non-procedural myocardial infarction and repeat revascularisation. Funding Biosensors.
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