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心脏再同步治疗除颤器和心脏再同步治疗起搏器植入后第一年的 Lead 并发症、器械感染和临床结局。

Lead complications, device infections, and clinical outcomes in the first year after implantation of cardiac resynchronization therapy-defibrillator and cardiac resynchronization therapy-pacemaker.

机构信息

Friedrich-Ebert Hospital, Medical Clinic, Friesenstr. 11, D 24531 Neumünster, Germany.

出版信息

Europace. 2013 Jan;15(1):71-6. doi: 10.1093/europace/eus247. Epub 2012 Aug 26.

DOI:10.1093/europace/eus247
PMID:22927665
Abstract

AIMS

The decision to implant a cardiac resynchronization therapy (CRT) system with (defibrillator, CRT-D) or without (pacemaker, CRT-P) cardioverter defibrillator should weigh its benefits and risks. This study examined the (i) incidence of loss of capture and infectious complications and (ii) 1-year clinical outcomes of 402 CRT-D and CRT-P recipients enrolled in the MASCOT study.

METHODS AND RESULTS

The indications for CRT-D or CRT-P were posed by the implanting physicians. All (i) losses of atrial and right and left ventricular capture, (ii) system-related infections, and (iii) clinical outcomes, including hospitalizations for worsening heart failure (HF) and deaths from all causes, were recorded up to 1 year of follow-up. Cardiac resynchronization therapy-defibrillator was implanted in 228 (57%) and CRT-P in 174 (43%) patients. The incidence of loss of capture was greater in CRT-D with 21 patients (9.2%) than in CRT-P with 6 patient (3.5%) recipients (P = 0.01), while the infection rates were 1.3% (3 patients) and 1.2% (2 patients), respectively (ns). In the CRT-D group, 42 of 228 patients (18.4%) died or were hospitalized for HF, compared with 38 of 174 patients (21.8%) in the CRT-P group (ns). In the CRT-D group, 23 patients (10.1%) were hospitalized for worsening HF and 20 (8.8%) patients died, vs. 22 (12.6%) and 19 (10.9%) patients, respectively, in the CRT-P group (ns for both comparisons).

CONCLUSIONS

Cardiac resynchronization therapy-defibrillator was implanted in 57% of candidates for CRT. Within 1 year after device implant, the incidence of loss of capture at any lead was nearly three-fold greater among CRT-D than among CRT-P recipients. System-related infections were infrequent and clinical outcomes were similar in both groups.

摘要

目的

决定植入心脏再同步治疗(CRT)系统(带除颤器,CRT-D)或不带除颤器(起搏器,CRT-P)应权衡其益处和风险。本研究检查了 MASCOT 研究中 402 例 CRT-D 和 CRT-P 受者的(i)丧失捕获和感染性并发症的发生率和(ii)1 年临床结局。

方法和结果

CRT-D 或 CRT-P 的适应证由植入医生提出。所有(i)心房和右、左心室捕获丧失,(ii)系统相关感染,和(iii)临床结局,包括因心力衰竭(HF)恶化而住院和因任何原因导致的死亡,均在 1 年随访时记录。228 例(57%)患者植入 CRT-D,174 例(43%)患者植入 CRT-P。CRT-D 组 21 例(9.2%)患者出现失夺获,而 CRT-P 组 6 例(3.5%)患者出现失夺获(P = 0.01),感染率分别为 1.3%(3 例)和 1.2%(2 例)(无统计学差异)。在 CRT-D 组中,228 例患者中有 42 例(18.4%)死亡或因 HF 住院,而在 CRT-P 组中,174 例患者中有 38 例(21.8%)(无统计学差异)。在 CRT-D 组中,23 例(10.1%)因 HF 恶化住院,20 例(8.8%)患者死亡,而在 CRT-P 组中,22 例(12.6%)和 19 例(10.9%)患者分别住院(两种比较均无统计学差异)。

结论

57%的 CRT 候选者植入了 CRT-D。在装置植入后 1 年内,CRT-D 组丧失任何部位捕获的发生率几乎是 CRT-P 组的三倍。系统相关感染较少,两组临床结局相似。

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