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Alternative Imaging Modalities in Ischemic Heart Failure (AIMI-HF) IMAGE HF Project I-A: study protocol for a randomized controlled trial

机译:缺血性心力衰竭(AIMI-HF)的替代成像方式IMAGE HF项目I-A:一项随机对照试验的研究方案

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Background Ischemic heart disease (IHD) is the most common cause of heart failure (HF); however, the role of revascularization in these patients is still unclear. Consensus on proper use of cardiac imaging to help determine which candidates should be considered for revascularization has been hindered by the absence of clinical studies that objectively and prospectively compare the prognostic information of each test obtained using both standard and advanced imaging. Methods/Design This paper describes the design and methods to be used in the Alternative Imaging Modalities in Ischemic Heart Failure (AIMI-HF) multi-center trial. The primary objective is to compare the effect of HF imaging strategies on the composite clinical endpoint of cardiac death, myocardial infarction (MI), cardiac arrest and re-hospitalization for cardiac causes. In AIMI-HF, patients with HF of ischemic etiology (n?=?1,261) will follow HF imaging strategy algorithms according to the question(s) asked by the physicians (for example, Is there ischemia and/or viability?), in agreement with local practices. Patients will be randomized to either standard (SPECT, Single photon emission computed tomography) imaging modalities for ischemia and/or viability or advanced imaging modalities: cardiac magnetic resonance imaging (CMR) or positron emission tomography (PET). In addition, eligible and consenting patients who could not be randomized, but were allocated to standard or advanced imaging based on clinical decisions, will be included in a registry. Discussion AIMI-HF will be the largest randomized trial evaluating the role of standard and advanced imaging modalities in the management of ischemic cardiomyopathy and heart failure. This trial will complement the results of the Surgical Treatment for Ischemic Heart Failure (STICH) viability substudy and the PET and Recovery Following Revascularization (PARR-2) trial. The results will provide policy makers with data to support (or not) further investment in and wider dissemination of alternative ‘advanced’ imaging technologies. Trial registration NCT01288560
机译:背景缺血性心脏病(IHD)是心力衰竭(HF)的最常见原因。然而,血运重建在这些患者中的作用仍不清楚。缺乏临床研究客观地和前瞻性地比较使用标准成像和高级成像获得的每种检查的预后信息,阻碍了正确使用心脏成像以帮助确定应考虑进行血管重建的候选人的共识。方法/设计本文介绍了在缺血性心力衰竭的替代成像方式(AIMI-HF)多中心试验中使用的设计和方法。主要目的是比较HF成像策略对心脏死亡,心肌梗塞(MI),心脏骤停和因心脏原因而再次住院的复合临床终点的影响。在AIMI-HF中,患有缺血性病因的HF(n?=?1,261)的患者将根据医师提出的问题(例如,是否存在缺血和/或生存能力)遵循HF成像策略算法。与当地惯例达成协议。患者将被随机分为缺血性和/或生存力的标准(SPECT,单光子发射计算机断层扫描)成像模式或高级成像模式:心脏磁共振成像(CMR)或正电子发射断层扫描(PET)。此外,不能随机分组但根据临床决策被分配到标准或高级影像学的合格且同意的患者将包括在注册系统中。讨论AIMI-HF将是最大的随机研究,评估标准和先进的影像学方法在缺血性心肌病和心力衰竭治疗中的作用。该试验将补充缺血性心力衰竭手术治疗(STICH)生存力子研究,PET和血运重建后恢复(PARR-2)试验的结果。结果将为决策者提供数据,以支持(或不支持)对替代“先进”成像技术的进一步投资和更广泛的传播。试用注册NCT01288560

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