{"title":"Mid-Term Cardiac Outcomes in Prosthetic Valve Surgery and HF Patients Across EF After CSP.","authors":"Peng Li, Xiao-Xiao Jiang, Yi-Heng Yang, Wan-Xuan Ding, Ying Chen, Tian-Zhu Li, Xiao-Lei Yang, Yun-Long Xia, Ying-Xue Dong","doi":"10.1111/pace.15213","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Clinical outcomes of conduction system pacing (CSP) in patients with prosthetic valve surgery (PVS) and heart failure (HF) remain unclear. This study evaluated the feasibility, safety, and clinical impact of CSP in this population.</p><p><strong>Methods: </strong>Consecutive patients with atrioventricular block post-PVS and HF history undergoing CSP from January 2018 to December 2022 were enrolled. Exclusions included prior pacemaker implantation, biventricular pacing, or ventricular pacing <40%. Outcomes were assessed by left ventricular ejection fraction (LVEF) categories: reduced (HFrEF, LVEF ≤40%), mildly reduced (HFmrEF, 41%-49%), and preserved (HFpEF, ≥50%).</p><p><strong>Results: </strong>CSP succeeded in 90/96 patients (93.75%): 34 HFrEF (37.78%), 11 HFmrEF (12.22%), and 45 HFpEF (50.00%). All cohorts showed improved left ventricular end-diastolic diameter (LVEDD) (HFrEF: 56.35 ± 10.01 vs. 60.76 ± 8.36 mm, p < 0.001; HFmrEF: 52.54 ± 5.01 vs. 56.73 ± 4.10 mm, p = 0.017; HFpEF: 48.07 ± 4.22 vs. 48.80 ± 3.99 mm, p = 0.035). The HFrEF cohort demonstrated significant improvements in LVEF (44.15 ± 12.23% vs. 31.26 ± 5.98%, p < 0.001), left atrial diameter (50.12 ± 13.91 vs. 54.00 ± 17.14 mm, p = 0.006), and New York Heart Association class (2.63 ± 0.85 vs. 3.13 ± 0.78, p = 0.002). No deterioration occurred in HFmrEF/HFpEF. Complete LVEF/LVEDD normalization was achieved in 26.47% of HFrEF patients (9/34), with absence of rheumatic heart disease (RHD) as an independent predictor (HR = 8.851, 95% CI 1.336-58.646, p = 0.024). Over 25.49 ± 9.4 months, no cardiac perforation, thrombosis, pacemaker-induced cardiomyopathy (PICM), or infections occurred.</p><p><strong>Conclusions: </strong>CSP is feasible and safe, promoting cardiac reverse remodeling and mitigating PICM risk in PVS patients with HF across LVEF categories. Over 25% of HFrEF patients achieved complete normalization, predicted by non-RHD etiology.</p>","PeriodicalId":520740,"journal":{"name":"Pacing and clinical electrophysiology : PACE","volume":" ","pages":"691-699"},"PeriodicalIF":1.3000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pacing and clinical electrophysiology : PACE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/pace.15213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/4 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Clinical outcomes of conduction system pacing (CSP) in patients with prosthetic valve surgery (PVS) and heart failure (HF) remain unclear. This study evaluated the feasibility, safety, and clinical impact of CSP in this population.
Methods: Consecutive patients with atrioventricular block post-PVS and HF history undergoing CSP from January 2018 to December 2022 were enrolled. Exclusions included prior pacemaker implantation, biventricular pacing, or ventricular pacing <40%. Outcomes were assessed by left ventricular ejection fraction (LVEF) categories: reduced (HFrEF, LVEF ≤40%), mildly reduced (HFmrEF, 41%-49%), and preserved (HFpEF, ≥50%).
Results: CSP succeeded in 90/96 patients (93.75%): 34 HFrEF (37.78%), 11 HFmrEF (12.22%), and 45 HFpEF (50.00%). All cohorts showed improved left ventricular end-diastolic diameter (LVEDD) (HFrEF: 56.35 ± 10.01 vs. 60.76 ± 8.36 mm, p < 0.001; HFmrEF: 52.54 ± 5.01 vs. 56.73 ± 4.10 mm, p = 0.017; HFpEF: 48.07 ± 4.22 vs. 48.80 ± 3.99 mm, p = 0.035). The HFrEF cohort demonstrated significant improvements in LVEF (44.15 ± 12.23% vs. 31.26 ± 5.98%, p < 0.001), left atrial diameter (50.12 ± 13.91 vs. 54.00 ± 17.14 mm, p = 0.006), and New York Heart Association class (2.63 ± 0.85 vs. 3.13 ± 0.78, p = 0.002). No deterioration occurred in HFmrEF/HFpEF. Complete LVEF/LVEDD normalization was achieved in 26.47% of HFrEF patients (9/34), with absence of rheumatic heart disease (RHD) as an independent predictor (HR = 8.851, 95% CI 1.336-58.646, p = 0.024). Over 25.49 ± 9.4 months, no cardiac perforation, thrombosis, pacemaker-induced cardiomyopathy (PICM), or infections occurred.
Conclusions: CSP is feasible and safe, promoting cardiac reverse remodeling and mitigating PICM risk in PVS patients with HF across LVEF categories. Over 25% of HFrEF patients achieved complete normalization, predicted by non-RHD etiology.
目的:传导系统起搏(CSP)在人工瓣膜手术(PVS)合并心力衰竭(HF)患者中的临床效果尚不清楚。本研究评估了CSP在该人群中的可行性、安全性和临床影响。方法:纳入2018年1月至2022年12月连续接受pvs后房室传导阻滞和HF病史的患者。结果:96例患者中有90例(93.75%)CSP成功:34例HFrEF(37.78%), 11例HFmrEF(12.22%), 45例HFpEF(50.00%)。所有队列均显示左室舒张末期内径(LVEDD)改善(HFrEF: 56.35±10.01 vs 60.76±8.36 mm, p)。结论:CSP在不同LVEF类型的PVS合并HF患者中是可行且安全的,可促进心脏反向重构并减轻PICM风险。根据非rhd病因预测,超过25%的HFrEF患者达到完全正常化。