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ENDURALIFE-Powered Cardiac Resynchronisation Therapy Defibrillator Devices for Treating Heart Failure: A NICE Medical Technology Guidance

机译:ENDURALIFE驱动的心脏再同步治疗除颤器设备:NICE医疗技术指南

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摘要

ENDURALIFE™-powered cardiac resynchronisation therapy defibrillator (CRT-D) devices were the subject of an evaluation by the National Institute for Health and Care Excellence, through its Medical Technologies Evaluation Programme, for the treatment of heart failure. Boston Scientific (manufacturer) submitted a case for the adoption of the technology, claiming that it has a longer battery life resulting in a longer time to CRT-D replacement. Other claimed benefits were fewer complications associated with replacement procedures, fewer hospital admissions, less time spent in hospital and reduced demand on cardiology device implantation rooms. The submission was critiqued by Cedar, an external assessment centre. The submitted clinical evidence showed that ENDURALIFE-powered devices implanted during the period 2008–2010 were superior, in terms of longevity, to other devices at that time. Submitted economic evidence indicated that, because of a reduction in the need for replacement procedures, ENDURALIFE-powered devices were cost saving when compared to comparator devices. Cedar highlighted uncertainty of the applicability of the clinical evidence to devices marketed today. The Medical Technologies Advisory Committee noted that this was unavoidable due to the follow-up time required to study battery life. Clinical experts noted that increased battery life is an important patient benefit. However, centres use devices from multiple manufacturers to negate pressure on clinical services in the event of a major device recall. The clinical and economic evidence showed benefits to the patient, and further analysis requested by the committee suggested that ENDURALIFE-powered CRT-Ds may save between £2120 and £5627 per patient over 15 years through a reduction in the need for replacement procedures. ENDURALIFE-powered CRT-D devices received a positive recommendation in Medical Technologies Guidance 33.
机译:由国家卫生与医疗研究院通过其医疗技术评估计划,对由ENDURALIFE™驱动的心脏再同步治疗除颤器(CRT-D)设备进行了评估,以治疗心力衰竭。波士顿科学公司(制造商)提交了采用该技术的案例,声称该技术具有更长的电池寿命,从而导致更换CRT-D的时间更长。其他声称的好处是,与更换程序相关的并发症更少,住院次数更少,住院时间更少以及对心脏病设备植入室的需求减少了。外部评估中心Cedar对来文进行了批评。提交的临床证据表明,就寿命而言,在2008-2010年期间植入的ENDURALIFE驱动的器械优于当时的其他器械。提交的经济证据表明,由于减少了更换程序的需求,与比较器设备相比,ENDURALIFE驱动的设备节省了成本。 Cedar强调了临床证据在当今市场上销售的设备是否适用的不确定性。医疗技术咨询委员会指出,由于需要研究电池寿命的后续时间,因此这是不可避免的。临床专家指出,延长电池寿命是患者的一项重要利益。但是,在发生重大设备召回事件时,中心会使用来自多个制造商的设备来消除对临床服务的压力。临床和经济证据表明对患者有益,并且委员会要求的进一步分析表明,采用ENDURALIFE技术的CRT-D可以通过减少更换程序的需求,在15年内为每位患者节省2120至5627英镑。 ENDURALIFE驱动的CRT-D设备在《医疗技术指南33》中获得了积极推荐。

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