Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology-IRCCS Fondazione Policlinico San Matteo, Pavia, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Coronary Care Unit and Laboratory of Clinical and Experimental Cardiology-IRCCS Fondazione Policlinico San Matteo, Pavia, Italy; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Int J Cardiol. 2019 May 15;283:122-127. doi: 10.1016/j.ijcard.2018.12.068. Epub 2019 Jan 2.
Implantable cardioverter-defibrillator (ICD) is an effective therapy to reduce mortality in heart failure. When the ICD generator approaches the end of life, most of the patients undergo an elective generator replacement (GR) even if they no longer meet implantation criteria. Whether arrhythmic risk should be re-assessed at the time of GR is still an open question. The aim of our study was to assess, via a meta-analysis, the occurrence of appropriate ICD therapies after GR in patients stratified based on the presence/absence of ICD indication at the time of GR.
Via a systematic literature search for primary prevention studies (January 2000-Sectember 2018), 2976 studies were analyzed. 6 studies were lastly included. Patients were categorized into two groups: "with ICD indication" in case of LVEF≤35% at the time of GR and/or appropriate therapies during the first ICD life; "without ICD indication" in case of a LVEF>35% and no previous ICD therapies. Incidences of appropriate ICD therapies were computed as number of events per 100 person-year.
We included 478 pts. (65%) with and 255 patients (35%) without persistent ICD indication. The incidence of appropriate therapies was 12.3/100-person-year in patients with vs. 3.4 in patients without persistent ICD indication (2.98 fold higher risk of ICD therapies).
Patients who no longer meet ICD implantation criteria at the time of GR present a significantly lower risk of appropriate ICD therapies after GR. The results of this study underline the importance of an arrhythmic risk re-stratification at the time of GR.
植入式心脏复律除颤器(ICD)是降低心力衰竭患者死亡率的有效治疗方法。当 ICD 发生器接近使用寿命终点时,大多数患者即使不再符合植入标准,也会进行选择性发生器更换(GR)。在 GR 时是否应重新评估心律失常风险仍然是一个悬而未决的问题。我们的研究目的是通过荟萃分析评估根据 GR 时是否存在 ICD 适应证对患者进行分层后,GR 后 ICD 适当治疗的发生情况。
通过对原发性预防研究(2000 年 1 月至 2018 年 9 月)进行系统的文献检索,分析了 2976 项研究。最后纳入了 6 项研究。患者分为两组:GR 时 LVEF≤35%和/或有适当 ICD 治疗的患者为“有 ICD 适应证”;LVEF>35%且无先前 ICD 治疗的患者为“无 ICD 适应证”。适当 ICD 治疗的发生率以每 100 人年的事件数计算。
我们纳入了 478 例(65%)有持续 ICD 适应证和 255 例(35%)无持续 ICD 适应证的患者。有持续 ICD 适应证的患者中适当 ICD 治疗的发生率为 12.3/100 人年,无持续 ICD 适应证的患者中为 3.4/100 人年(有持续 ICD 适应证的患者发生 ICD 治疗的风险高 2.98 倍)。
在 GR 时不再符合 ICD 植入标准的患者在 GR 后发生适当 ICD 治疗的风险显著降低。这项研究的结果强调了在 GR 时进行心律失常风险再分层的重要性。