Division of Cardiology/Electrophysiology, Johns Hopkins University, Baltimore, Maryland.
Division of Cardiothoracic Surgery, Heart and Vascular Institute, Cleveland Clinic, Cleveland, Ohio.
Heart Rhythm. 2015 Mar;12(3):517-523. doi: 10.1016/j.hrthm.2014.11.013. Epub 2014 Nov 13.
A minority of patients undergoing cardiac resynchronization therapy (CRT) use a surgically placed epicardial left ventricular (SPELV) pacing lead. Previous studies of outcomes in patients receiving such leads have been limited to small cohorts with limited follow-up.
We sought to compare outcomes between patients receiving SPELV pacing leads and patients with traditional percutaneously placed left ventricular (LV) leads.
We extracted clinical data on consecutive patients undergoing the new implantation of a cardiac resynchronization device. Long-term survival and response (defined as an improvement in LV ejection fraction of ≥5%) were compared between the 2 groups.
Between September 3, 2003, and August 6, 2007, 725 patients met inclusion criteria, of whom 96 (13.2%) had an SPELV pacing lead. Over a mean follow-up of 5.1 ± 2.5 years, there were 310 deaths, 17 heart transplants, and 15 left ventricular assist device placements (342 total end points). In univariate analysis, there was no difference in outcomes between patients with an SPELV pacing lead and patients with a percutaneously placed LV lead both early at 6 months (log rank, P = .53) and over a mean follow-up of 5.1 years (log rank, P = .58). In multivariate analysis, survival free of left ventricular assist device or heart transplant was similar in patients regardless of lead placement status (P = .89). From a subcohort of 455 patients, 297 patients (65.3%) met criteria for response. In multivariate analysis, there was no difference in the rate of response based on lead placement modality.
Patients undergoing epicardial LV lead placement using a surgical approach have outcomes and rates of reverse ventricular remodeling similar to those in patients undergoing LV lead placement using a percutaneous approach.
少数接受心脏再同步治疗(CRT)的患者使用经外科植入的心外膜左心室(SPELV)起搏导线。此前,对接受此类导线的患者的预后进行的研究仅限于随访时间有限的小队列。
我们比较了接受 SPELV 起搏导线和传统经皮左心室(LV)导线患者的预后。
我们提取了连续接受心脏再同步装置新植入的患者的临床数据。比较两组患者的长期生存和反应(定义为 LV 射血分数改善≥5%)。
2003 年 9 月 3 日至 2007 年 8 月 6 日,725 例患者符合纳入标准,其中 96 例(13.2%)使用 SPELV 起搏导线。平均随访 5.1±2.5 年后,共发生 310 例死亡、17 例心脏移植和 15 例左心室辅助装置置入(342 例总终点)。在单变量分析中,SPELV 起搏导线组和经皮 LV 导线组患者的预后在 6 个月时(对数秩检验,P=.53)和平均随访 5.1 年时(对数秩检验,P=.58)均无差异。多变量分析显示,无论导线放置状态如何,患者的左心室辅助装置或心脏移植生存率均相似(P=.89)。在 455 例亚组患者中,297 例(65.3%)符合反应标准。多变量分析显示,基于导线放置方式,反应率无差异。
采用外科方法进行心外膜 LV 导线放置的患者与采用经皮方法进行 LV 导线放置的患者的预后和逆室重构率相似。