Cardiology Division, Heart Research Follow-up Program, University of Rochester Medical Center, Rochester, NY, USA.
Eur Heart J. 2011 Jul;32(13):1622-30. doi: 10.1093/eurheartj/ehq407. Epub 2010 Nov 12.
There are no data regarding the differential response to cardiac resynchronization therapy with defibrillator (CRT-D) by the aetiology of cardiomyopathy in mildly symptomatic patients. We evaluated the outcome of patients enrolled in MADIT-CRT by ischaemic and non-ischaemic aetiology of cardiomyopathy (ICM and non-ICM, respectively).
The clinical response to CRT-D was assessed among ICM (n = 1046) and non-ICM (n = 774) patients enrolled in MADIT-CRT during an average follow-up of 2.4 years, and echocardiographic response was assessed at 1 year. Cardiac resynchronization therapy with defibrillator vs. ICD therapy was associated with respective 34% (P = 0.001) and 44% (P = 0.002) reductions in the risk of heart failure or death among ICM and non-ICM patients (P for interaction = 0.455). In the ICM group, CRT-D was associated with mean (±SD) 29 ± 14% and 18 ± 10% reductions in left ventricular end-systolic volume (LVESV) and left ventricular end-diastolic volume (LVEDV), respectively. In the non-ICM group, CRT-D was associated with significantly greater volume reductions compared with the ICM group [37 ± 16% and 24 ± 12% reductions in LVESV and LVEDV, respectively (P < 0.001 for all)]. Risk subsets in the ICM group that showed a favourable clinical response to CRT-D included patients with QRS ≥150 ms, systolic blood pressure <115 mmHg, and left bundle branch block (LBBB), whereas in the non-ICM group females, patients with diabetes mellitus, and LBBB, displayed a favourable clinical response.
Mildly symptomatic ICM and non-ICM patients show significant differences in the echocardiographic response to CRT-D and in the clinical benefit within risk subsets suggesting that risk assessment for CRT-D in this population should be aetiology-specific.
在轻度症状患者中,针对心肌病的病因,心脏再同步治疗除颤器(CRT-D)的反应尚无数据。我们评估了心肌病的缺血性和非缺血性病因(分别为 ICM 和非 ICM)患者入组 MADIT-CRT 的结果。
在平均随访 2.4 年期间,评估了 MADIT-CRT 中 ICM(n = 1046)和非 ICM(n = 774)患者 CRT-D 的临床反应,并在 1 年时评估了超声心动图反应。与 ICD 治疗相比,CRT-D 治疗分别使 ICM 和非 ICM 患者心力衰竭或死亡的风险降低了 34%(P = 0.001)和 44%(P = 0.002)(P 交互作用= 0.455)。在 ICM 组中,CRT-D 分别使左心室收缩末期容积(LVESV)和左心室舒张末期容积(LVEDV)平均(±SD)减少 29 ± 14%和 18 ± 10%。在非 ICM 组中,与 ICM 组相比,CRT-D 显著降低了左心室收缩末期容积(LVESV)和左心室舒张末期容积(LVEDV)的容积[分别减少 37 ± 16%和 24 ± 12%(P < 0.001 )]。在 ICM 组中,对 CRT-D 有良好临床反应的风险亚组包括 QRS 波≥150 ms、收缩压<115 mmHg 和左束支传导阻滞(LBBB)的患者,而非 ICM 组中,女性、患有糖尿病和 LBBB 的患者对 CRT-D 有良好的临床反应。
轻度症状性 ICM 和非 ICM 患者对 CRT-D 的超声心动图反应以及风险亚组的临床获益存在显著差异,这表明该人群中 CRT-D 的风险评估应该是病因特异性的。