Efficacy and safety of conduction system pacing in heart failure patients with non-left bundle branch block morphology: a systematic review and meta-analysis

传导系统起搏治疗非左束支传导阻滞形态的心力衰竭患者的疗效和安全性:系统评价和荟萃分析

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Abstract

BACKGROUND: Conduction system pacing, including His bundle pacing and left bundle branch area pacing, has emerged as a physiological alternative to biventricular pacing (BiVP) for cardiac resynchronisation therapy (CRT). BiVP benefits patients with left bundle branch block (LBBB), but outcomes in non-LBBB morphologies are inconsistent. We synthesised the evidence for CSP in heart failure patients with non-LBBB conduction patterns. METHODS: We performed a systematic review and meta-analysis (PROSPERO CRD420251015905) of 21 studies (11 with quantitative data; n = 480). Comparative outcomes (CSP vs. BiVP) and baseline vs. follow-up CSP changes were pooled. Primary endpoints were left ventricular ejection fraction (LVEF), left ventricular end-diastolic diameter (LVEDD), New York Heart Association (NYHA) class, and QRS duration. Secondary endpoints included heart failure hospitalisation and all-cause mortality. RESULTS: In head-to-head analyses (198 patients; 99 per arm), CSP conferred a mean + 5.83% LVEF benefit (95% CI 3.06-8.60; p < 0.0001; I(2) = 0%), reduced LVEDD by 3.87 mm (95% CI 2.53-5.21; p < 0.001), improved NYHA class by -0.30 (95% CI -0.46 to -0.13; p = 0.0004), and narrowed QRS (SMD -0.91; 95% CI -1.18 to -0.64; p < 0.00001). CSP also halved HF hospitalisation risk (RR 0.44; 95% CI 0.24-0.81; p = 0.008; I(2) = 0%). In single-arm baseline and follow-up analyses (480 patients), CSP yielded a mean + 8.91% LVEF, -2.95 mm LVEDD, SMD -1.37 NYHA, and SMD -1.21 QRS (p < 0.0001). CONCLUSION: In non-LBBB heart failure, CSP delivers substantial improvements in ventricular systolic function, reverse remodelling, symptoms, and electrical synchrony versus BiVP, with reduced HF hospitalisation. These findings position CSP as a promising BiVP strategy for a traditionally non-responder subgroup and warrant confirmation in large, randomised trials.

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