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首页> 外文期刊>The Lancet >Implant-based multiparameter telemonitoring of patients with heart failure (IN-TIME): A randomised controlled trial
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Implant-based multiparameter telemonitoring of patients with heart failure (IN-TIME): A randomised controlled trial

机译:心力衰竭患者基于植入物的多参数远程监控(IN-TIME):一项随机对照试验

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Background An increasing number of patients with heart failure receive implantable cardioverter-defibrillators (ICDs) or cardiac resynchronisation defibrillators (CRT-Ds) with telemonitoring function. Early detection of worsening heart failure, or upstream factors predisposing to worsening heart failure, by implant-based telemonitoring might enable pre-emptive intervention and improve outcomes, but the evidence is weak. We investigated this possibility in IN-TIME, a clinical trial. Methods We did this randomised, controlled trial at 36 tertiary clinical centres and hospitals in Australia, Europe, and Israel. We enrolled patients with chronic heart failure, NYHA class II-III symptoms, ejection fraction of no more than 35%, optimal drug treatment, no permanent atrial fibrillation, and a recent dual-chamber ICD or CRT-D implantation. After a 1 month run-in phase, patients were randomly assigned (1:1) to either automatic, daily, implant-based, multiparameter telemonitoring in addition to standard care or standard care without telemonitoring. Investigators were not masked to treatment allocation. Patients were masked to allocation unless they were contacted because of telemonitoring findings. Follow-up was 1 year. The primary outcome measure was a composite clinical score combining all-cause death, overnight hospital admission for heart failure, change in NYHA class, and change in patient global self-assessment, for the intention-to-treat population. The trial is registered with ClinicalTrials.gov, number NCT00538356. Findings We enrolled 716 patients, of whom 664 were randomly assigned (333 to telemonitoring, 331 to control). Mean age was 65·5 years and mean ejection fraction was 26%. 285 (43%) of patients had NYHA functional class II and 378 (57%) had NYHA class III. Most patients received CRT-Ds (390; 58·7%). At 1 year, 63 (18·9%) of 333 patients in the telemonitoring group versus 90 (27·2%) of 331 in the control group (p=0·013) had worsened composite score (odds ratio 0·63, 95% CI 0·43-0·90). Ten versus 27 patients died during follow-up. Interpretation Automatic, daily, implant-based, multiparameter telemonitoring can significantly improve clinical outcomes for patients with heart failure. Such telemonitoring is feasible and should be used in clinical practice. Funding Biotronik SE & Co. KG.
机译:背景技术越来越多的心力衰竭患者接受具有远程监护功能的植入式心脏复律除颤器(ICD)或心脏再同步除颤器(CRT-Ds)。通过基于植入物的远程监测,早期发现恶化的心力衰竭或上游因素可能导致恶化的心力衰竭,这可能会导致先发制人的干预并改善预后,但证据不足。我们在临床试验IN-TIME中研究了这种可能性。方法我们在澳大利亚,欧洲和以色列的36家三级临床中心和医院进行了这项随机对照试验。我们招募了患有慢性心力衰竭,NYHA II-III级症状,射血分数不超过35%,最佳药物治疗,无永久性心房颤动以及近期植入双腔ICD或CRT-D的患者。经过1个月的磨合阶段后,除标准护理或无远程护理的标准护理外,将患者随机分配(1:1)进行自动,每日,基于植入物的多参数远程监控。研究人员并未隐瞒治疗分配。除非因远程监控的结果而联系他们,否则患者将被屏蔽分配。随访时间为1年。主要结局指标是综合临床评分,综合针对意向治疗人群的全因死亡,因心力衰竭入院过夜,NYHA等级变更以及患者总体自我评估的变更。该试验已在ClinicalTrials.gov上注册,编号为NCT00538356。研究结果我们招募了716例患者,其中664例被随机分配(333例进行远程监护,331例进行对照)。平均年龄为65·5岁,平均射血分数为26%。 285名患者(43%)具有NYHA功能II级,而378名患者(57%)具有NYHA III级功能。大多数患者接受了CRT-Ds治疗(390; 58·7%)。 1年时,远程监控组333例患者中有63例(18·9%),而对照组331例中有90例(27·2%)(p = 0·013)的综合评分恶化(赔率为0·63, 95%CI 0·43-0·90)。随访期间有10例患者与27例患者死亡。解释自动的,每天的,基于植入物的多参数远程监护可以显着改善心力衰竭患者的临床结局。这种远程监视是可行的,应在临床实践中使用。资助Biotronik SE&Co. KG。

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