Higuchi Koji, Manne Mahesh, Tchou Patrick, Baranowski Bryan, Bhargava Mandeep, Callahan Thomas, Chung Mina, Dresing Thomas, Hussein Ayman, Kanj Mohamed, Mayuga Kenneth, Nakhla Shady, Saliba Walid, Rickard John, Wazni Oussama, Santangeli Pasquale, Sroubek Jakub, Varma Niraj
Cardiac Electrophysiology and Pacing Section, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
Department of Hospital Medicine, Cleveland Clinic, Cleveland, Ohio.
Heart Rhythm. 2025 Feb;22(2):339-348. doi: 10.1016/j.hrthm.2024.07.106. Epub 2024 Jul 29.
The risk of ventricular arrhythmias (VAs) after cardiac resynchronization therapy (CRT) has been associated with ischemic disease/scar, sex, and possibly left ventricular mass (LVM).
The purpose of this study was to evaluate sex differences and baseline/postimplant change in LVM on VA risk after CRT implantation in patients with nonischemic cardiomyopathy and left bundle branch block.
In patients meeting the criteria, baseline and follow-up echocardiographic images were obtained for LVM assessment. VA events were reported from device diagnostics and therapies. VA risk was stratified by receiver operating characteristic (Youden index cutoff point) for baseline LVM and baseline/postimplant change in LVM. Multivariate Cox regression model was also used for VA risk stratification.
One hundred eighteen patients (71 female patients [60.2%]; mean age 60.5 ± 11.3 years; left ventricular ejection fraction 19.2% ± 7.0%; QRS duration 165.6 ± 20 ms; LVM 313.9 ± 108.8 g) were enrolled and followed up for a median of 90 months (interquartile range 44-158 months). Thirty-five patients (29.6%) received appropriate shocks or antitachycardia pacing at a median of 73.5 months (interquartile range 25-130 months) postimplantation. Males had a higher VA incidence (male patients 18 of 47 [38.3%] vs female patients 17 of 71 [23.9%]; P = .02). Baseline LVM > 308.9 g separated patients with higher VA risk (P = .001). Less than a 20% decrease in LVM increased VA risk (P < .001). Baseline LVM was the only baseline characteristic predicting VA events in the Cox regression model (hazard ratio 1.01; 95% confidence interval 1.001-1.009; log-rank, P = .003). Sex differences in VA risk were eliminated by the baseline LVM parameters.
VA risk after CRT implantation in nonischemic cardiomyopathy was associated with baseline LV > 308.9 g and a decrease in LVM ≤ 20%, without sex differences.
心脏再同步治疗(CRT)后室性心律失常(VA)的风险与缺血性疾病/瘢痕、性别以及可能的左心室质量(LVM)有关。
本研究的目的是评估非缺血性心肌病和左束支传导阻滞患者在CRT植入后LVM的性别差异以及基线/植入后变化对VA风险的影响。
在符合标准的患者中,获取基线和随访超声心动图图像以评估LVM。通过设备诊断和治疗报告VA事件。根据基线LVM和LVM的基线/植入后变化,采用受试者操作特征(约登指数截断点)对VA风险进行分层。多变量Cox回归模型也用于VA风险分层。
共纳入118例患者(71例女性患者[60.2%];平均年龄60.5±11.3岁;左心室射血分数19.2%±7.0%;QRS时限165.6±20 ms;LVM 313.9±108.8 g),中位随访时间为90个月(四分位间距44 - 158个月)。35例患者(29.6%)在植入后中位73.5个月(四分位间距25 - 130个月)接受了适当的电击或抗心动过速起搏。男性的VA发生率较高(47例男性患者中有18例[38.3%],71例女性患者中有17例[23.9%];P = 0.02)。基线LVM>308.9 g可区分VA风险较高的患者(P = 0.001)。LVM下降少于20%会增加VA风险(P < 0.001)。在Cox回归模型中,基线LVM是预测VA事件的唯一基线特征(风险比1.01;95%置信区间1.001 - 1.009;对数秩,P = 0.003)。基线LVM参数消除了VA风险的性别差异。
非缺血性心肌病患者CRT植入后的VA风险与基线左心室>308.9 g和LVM下降≤20%有关,无性别差异。