Department of Medicine University of Virginia Health System Charlottesville VA.
Center for Outcomes Research and Evaluation Yale-New Haven Hospital New Haven CT.
J Am Heart Assoc. 2022 Jul 5;11(13):e023743. doi: 10.1161/JAHA.121.023743. Epub 2022 Jun 29.
Background As patients derive variable benefit from generator changes (GCs) of implantable cardioverter-defibrillators (ICDs) with an original primary prevention (PP) indication, better predictors of outcomes are needed. Methods and Results In the National Cardiovascular Data Registry ICD Registry, patients undergoing GCs of initial non-cardiac resynchronization therapy PP ICDs in 2012 to 2016, predictors of post-GC survival and survival benefit versus control heart failure patients without ICDs were assessed. These included predicted annual mortality based on the Seattle Heart Failure Model, left ventricular ejection fraction (LVEF) >35%, and the probability that a patient's death would be arrhythmic (proportional risk of arrhythmic death [PRAD]). In 40 933 patients undergoing GCs of initial noncardiac resynchronization therapy PP ICDs (age 67.7±12.0 years, 24.5% women, 34.1% with LVEF >35%), Seattle Heart Failure Model-predicted annual mortality had the greatest effect size for decreased post-GC survival (<0.0001). Patients undergoing GCs of initial noncardiac resynchronization therapy PP ICDs with LVEF >35% had a lower Seattle Heart Failure Model-adjusted survival versus 23 472 control heart failure patients without ICDs (model interaction hazard ratio, 1.21 [95% CI, 1.11-1.31]). In patients undergoing GCs of initial noncardiac resynchonization therapy PP ICDs with LVEF ≤35%, the model indicated worse survival versus controls in the 21% of patients with a PRAD <43% and improved survival in the 10% with PRAD >65%. The association of the PRAD with survival benefit or harm was similar in patients with or without pre-GC ICD therapies. Conclusions Patients who received replacement of an ICD originally implanted for primary prevention and had at the time of GC either LVEF >35% alone or both LVEF ≤35% and PRAD <43% had worse survival versus controls without ICDs.
由于植入式心脏复律除颤器(ICD)的初始原发性预防(PP)患者接受器械更换(GC)后获益各不相同,因此需要更好的预测结果的指标。
在 2012 年至 2016 年期间,全国心血管数据注册 ICD 注册中心对接受初始非心脏再同步治疗 PP ICD 器械更换的患者进行了研究,评估了 GC 后生存和与未植入 ICD 的心力衰竭控制患者相比的生存获益的预测因素。这些因素包括基于西雅图心力衰竭模型预测的每年死亡率、左心室射血分数(LVEF)>35%,以及患者死亡是否为心律失常的概率(心律失常死亡的比例风险[PRAD])。在 40933 名接受初始非心脏再同步治疗 PP ICD 器械更换的患者中(年龄 67.7±12.0 岁,24.5%为女性,34.1%的 LVEF>35%),西雅图心力衰竭模型预测的每年死亡率对 GC 后生存的影响最大(<0.0001)。与 23472 名未植入 ICD 的心力衰竭控制患者相比,LVEF>35%的接受初始非心脏再同步治疗 PP ICD 器械更换的患者的西雅图心力衰竭模型调整后的生存率较低(模型交互风险比为 1.21[95%CI,1.11-1.31])。在 LVEF≤35%的接受初始非心脏再同步治疗 PP ICD 器械更换的患者中,模型显示,PRAD<43%的患者中有 21%的生存情况较对照组差,PRAD>65%的患者中有 10%的生存情况较好。PRAD 与生存获益或危害的关联在接受或未接受 GC 前 ICD 治疗的患者中相似。
在 GC 时 LVEF 单独>35%或 LVEF≤35%和 PRAD<43%的患者,与未植入 ICD 的对照组相比,接受最初用于原发性预防的 ICD 更换的患者的生存情况较差。