The role of interventricular conduction delay to predict clinical response with cardiac resynchronization therapy

医学 心脏再同步化治疗 心脏病学 内科学 危险系数 置信区间 心力衰竭 心室 窦性心律 临床终点 接收机工作特性 随机对照试验 心房颤动 射血分数
作者
Michael R. Gold,Yinghong Yu,Nicholas Wold,John Day
出处
期刊:Heart Rhythm [Elsevier]
卷期号:14 (12): 1748-1755 被引量:37
标识
DOI:10.1016/j.hrthm.2017.10.016
摘要

Pacing at sites with late electrical activation or greater interventricular delay is associated with improvement in measures of cardiac resynchronization therapy (CRT) response, primarily reverse remodeling. However, little is known about whether such lead positions improve heart failure (HF) clinical outcomes.The purpose of this study was to assess the association between interventricular electrical delay and HF clinical outcomes.The Pacing Evaluation-Atrial SUpport Study was a multicenter randomized trial of patients undergoing CRT-defibrillator implantation. Interventricular delay was measured as the unpaced right ventricle-left ventricle (RV-LV) interval in sinus rhythm. The HF clinical composite score was the primary end point. In addition, the time to first HF hospitalization or death was measured and events were adjudicated by a blinded core laboratory. The cohort was divided at the median RV-LV interval into short (<67 ms) and long (≥67 ms) subgroups. In addition, receiver operating characteristic curves were constructed to identify the optimal cutoff of the RV-LV interval and spline analysis was performed to assess RV-LV interval as a continuous variable.A total of 1342 patients were included in this study. The clinical composite score at 1 year differed between groups, with more patients improving and fewer patients worsening in the long RV-LV group (P = .014). The time to first HF hospitalization or mortality also differed with a lower risk of an event in the long RV-LV group (hazard ratio 0.62; P = .002). Multivariate analysis showed that RV-LV time (hazard ratio 0.71; P = .038) and sex were independent predictors of this outcome.Baseline interventricular delay is a strong independent predictor of clinical response to CRT.
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