Vijayaraman Pugazhendhi, Longacre Colleen, Kron Jordana, Subzposh Faiz, Zimmerman Patrick, Butler Kiah, Crossley George H, Ellenbogen Kenneth A
Geisinger Heart Institute, Wilkes-Barre, Pennsylvania.
Medtronic Inc, Mounds View, Minnesota.
Heart Rhythm. 2025 Mar;22(3):735-743. doi: 10.1016/j.hrthm.2024.08.052. Epub 2024 Sep 1.
Conduction system pacing (CSP) has emerged as an alternative therapy to traditional right ventricular (RV) pacing. However, most CSP studies reflect small cohorts or single-center experience.
This analysis compared CSP with dual-chamber (DC) RV pacing in a large, population-based cohort using data from the Micra Coverage with Evidence Development study.
Medicare administrative claims data were used to identify patients implanted with a DC RV pacemaker. Lead placement data from Medtronic's device registration system identified patients treated with CSP (n = 6197) using a 3830 catheter-delivered lead or DC RV (non-3830 lead, non-CSP placement; n = 16,989) at the same centers. CSP patients were stratified into left bundle branch area pacing (LBBAP; n = 4738) and His bundle pacing (HBP; n = 1459). Incident heart failure hospitalizations, all-cause mortality, complication rates, and reinterventions at 6 months were analyzed.
CSP patients with a 3830 catheter-delivered lead experienced significantly lower rates of incident heart failure hospitalization (hazard ratio [HR], 0.70; P = .02) and all-cause mortality at 6 months compared with DC RV patients (HR, 0.66; P < .0001). There was no difference in chronic complications (HR, 0.97; P = .62) or need for reintervention (HR, 0.95; P = .63) with CSP compared with DC RV, although LBBAP patients experienced significantly lower rates of complications (HR, 0.71; P = .001) compared with HBP.
DC pacemaker patients treated with CSP using a 3830 catheter-delivered lead experienced significant all-cause mortality and heart failure hospitalization benefits compared with DC RV pacing. LBBAP had lower complications compared with HBP. These real-world results align with findings in small clinical studies demonstrating the benefits of CSP.
传导系统起搏(CSP)已成为传统右心室(RV)起搏的替代疗法。然而,大多数CSP研究反映的是小样本队列或单中心经验。
本分析使用来自Micra覆盖范围与证据发展研究的数据,在一个大型的基于人群的队列中比较CSP与双腔(DC)RV起搏。
医疗保险行政索赔数据用于识别植入DC RV起搏器的患者。美敦力设备注册系统的导线放置数据识别出在同一中心接受CSP治疗的患者(n = 6197),使用3830导管输送导线或DC RV(非3830导线,非CSP放置;n = 16989)。CSP患者被分层为左束支区域起搏(LBBAP;n = 4738)和希氏束起搏(HBP;n = 1459)。分析了6个月时的心衰住院发生率、全因死亡率、并发症发生率和再次干预情况。
与DC RV患者相比,使用3830导管输送导线的CSP患者6个月时的心衰住院发生率(风险比[HR],0.70;P = 0.02)和全因死亡率显著更低(HR,0.66;P < 0.0001)。与DC RV相比,CSP的慢性并发症(HR,0.97;P = 0.62)或再次干预需求(HR,0.95;P = 0.63)没有差异,尽管LBBAP患者的并发症发生率显著低于HBP患者(HR,0.71;P = 0.001)。
与DC RV起搏相比,使用3830导管输送导线进行CSP治疗的DC起搏器患者在全因死亡率和心衰住院方面有显著获益。与HBP相比,LBBAP的并发症更少。这些真实世界的结果与小型临床研究中证明CSP益处的结果一致。