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首页> 外文期刊>The Lancet >5-year outcome of an interventional strategy in non-ST-elevation acute coronary syndrome: the British Heart Foundation RITA 3 randomised trial.
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5-year outcome of an interventional strategy in non-ST-elevation acute coronary syndrome: the British Heart Foundation RITA 3 randomised trial.

机译:非ST段抬高的急性冠脉综合征的干预策略的5年结果:英国心脏基金会RITA 3随机试验。

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BACKGROUND: The long-term outcome of an interventional strategy in patients with non-ST-elevation acute coronary syndrome is unknown. We tested whether an interventional strategy (routine angiography followed by revascularisation) was better than a conservative strategy (ischaemia-driven or symptom-driven angiography) over 5 years' follow-up. METHODS: In a multicentre randomised trial, 1810 patients (from 45 hospitals in England and Scotland, UK) with non-ST-elevation acute coronary syndrome were randomly assigned to receive an early intervention (n=895) or a conservative strategy (n=915) within 48 h of the index episode of cardiac pain. In each group, the aim was to provide the best medical treatment, and also to undertake coronary arteriography within 72 h in the interventional strategy with subsequent management guided by the angiographic findings. Analysis was by intention to treat and the primary outcome (composite of death or non-fatal myocardial infarction) had masked independent adjudication. RITA 3 has been assigned the International Standard Randomised Control Trial Number ISRCTN07752711. FINDINGS: At 1-year follow-up, rates of death or non-fatal myocardial infarction were similar. However, at a median of 5 years' follow-up (IQR 4.6-5.0), 142 (16.6%) patients with intervention treatment and 178 (20.0%) with conservative treatment died or had non-fatal myocardial infarction (odds ratio 0.78, 95% CI 0.61-0.99, p=0.044), with a similar benefit for cardiovascular death or myocardial infarction (0.74, 0.56-0.97, p=0.030). 234 (102 [12%] intervention, 132 [15%] conservative) patients died during follow-up (0.76, 0.58-1.00, p=0.054). The benefits of an intervention strategy were mainly seen in patients at high risk of death or myocardial infarction (p=0.004), and for the highest risk group, the odds ratio of death or non-fatal myocardial infarction was 0.44 (0.25-0.76). INTERPRETATION: In patients with non-ST-elevation acute coronary syndrome, a routine invasive strategy leads to long-term reduction in risk of death or non-fatal myocardial infarction, and this benefit is mainly in high-risk patients. The findings provide support for national and international guidelines in the need for more robust risk stratification in acute coronary syndrome.
机译:背景:对于非ST段抬高的急性冠脉综合征患者,干预策略的长期结果尚不清楚。我们测试了在五年的随访中,介入策略(常规血管造影,然后进行血管重建)是否优于保守策略(缺血性驱动或症状驱动的血管造影)。方法:在一项多中心随机试验中,将1810例非ST段抬高的急性冠脉综合征患者(来自英格兰和苏格兰的45家医院)随机分配接受早期干预(n = 895)或采取保守策略(n = 915)在心脏疼痛指​​数发作的48小时内。在每个组中,目的是提供最佳的治疗,并在介入策略的72小时内进行冠状动脉造影,并在血管造影结果的指导下进行后续治疗。分析是按治疗意向进行的,主要结局(死亡或非致命性心肌梗死的综合)掩盖了独立的裁决。 RITA 3已获得国际标准随机对照试验编号ISRCTN07752711。结果:在1年的随访中,死亡率或非致命性心肌梗死的发生率相似。但是,在5年的随访中位数(IQR 4.6-5.0)中,有142例(16.6%)接受干预治疗的患者和178例(20.0%)接受了保守治疗的患者死亡或患有非致命性心肌梗塞(几率0.78, 95%CI 0.61-0.99,p = 0.044),对心血管死亡或心肌梗死有相似的获益(0.74,0.56-0.97,p = 0.030)。 234例(102 [12%]干预,132 [15%]保守)患者在随访期间死亡(0.76,0.58-1.00,p = 0.054)。干预策略的益处主要见于具有高死亡或心肌梗塞风险的患者(p = 0.004),对于最高风险组,死亡或非致命性心肌梗塞的比值比为0.44(0.25-0.76) 。解释:对于非ST段抬高的急性冠状动脉综合征患者,常规的侵入性治疗可长期降低死亡或非致命性心肌梗塞的风险,这种益处主要发生在高危患者中。这些发现为国家和国际指南提供了支持,要求在急性冠脉综合征中进行更强有力的风险分层。

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