Integrated Heart Centre, Shaare Zedek Medical Centre, Hebrew University, Jerusalem, Israel.
Arrhythmia center, Sheba Medical Centre, Tel Aviv University, Tel Hashomer, Israel.
Europace. 2022 May 3;24(5):835-844. doi: 10.1093/europace/euab253.
To evaluate the benefit of speckle tracking radial strain imaging (STRSI)-guided left ventricular (LV) lead (LVL) positioning in cardiac resynchronization therapy (CRT) in patients (pts) with ischaemic cardiomyopathy with CRT indication.
We conducted a prospective randomized controlled trial. Patients were enrolled in nine centres with 2:1 randomization into two groups (guided vs. control). Patients underwent STRSI to identify the optimal LV position from six LV segments at midventricular level. Implantation via STRSI was attempted for recommended segment in the guided group only. Follow-up included echocardiography (6 months) and clinical evaluation (6 and 12 months). The primary endpoint was comparison % reduction in LV end-systolic volume at 6 months with baseline. Secondary endpoints included hospitalizations for heart failure and death, and improvement in additional echocardiographic measurements and quality of life score. A total of 172 patients (115 guided vs. 57 control) were enrolled. In the guided group, 60% of the implanted LV leads were adjudicated to be successfully located at the recommended segment, whereas in the control group 44% reached the best STRSI determined segment. There was no difference between the groups in any of the primary or secondary endpoints at 6 and 12 months.
Our findings suggest that echo-guided implantation of an LV lead using STRSI does not improve the clinical or echocardiographic response compared with conventional implantation.
评估斑点追踪径向应变成像(STRSI)指导左心室(LV)导联(LVL)定位在有 CRT 适应证的缺血性心肌病患者 CRT 中的获益。
我们进行了一项前瞻性随机对照试验。将患者按 2:1 的比例随机分为两组(有指导组和对照组)纳入 9 个中心。患者接受 STRSI 以从中间段的 6 个 LV 节段中识别最佳 LV 位置。仅在有指导组尝试通过 STRSI 植入建议节段。随访包括超声心动图(6 个月)和临床评估(6 个月和 12 个月)。主要终点是与基线相比,6 个月时 LV 收缩末期容积的百分比降低。次要终点包括心力衰竭和死亡住院,以及额外超声心动图测量和生活质量评分的改善。共纳入 172 例患者(115 例有指导组 vs. 57 例对照组)。在有指导组中,60%植入的 LVL 被判定成功位于建议节段,而对照组中 44%达到最佳 STRSI 确定的节段。在 6 个月和 12 个月时,两组在任何主要或次要终点上均无差异。
我们的研究结果表明,与传统植入相比,使用 STRSI 指导 LV 导联植入并未改善临床或超声心动图反应。