Permanent pacemaker reduction using temporary-permanent pacemaker as a 1-month bridge after transcatheter aortic valve replacement: a prospective, multicentre, single-arm, observational study.

High-degree atrioventricular block Pacemaker dependency Permanent pacemaker Temporary-permanent pacemaker Transcatheter aortic valve replacement

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 21 12 2023
revised: 28 03 2024
accepted: 03 04 2024
medline: 16 7 2024
pubmed: 16 7 2024
entrez: 16 7 2024
Statut: epublish

Résumé

The permanent pacemaker (PPM) implantation and pacemaker dependency rates after transcatheter aortic valve replacement (TAVR) are highly variable as some of the conduction disturbances are reversible. It remains poorly investigated how to optimise temporary pacing in these patients. This study aimed to explore the potential reduction in the PPM implantation rate using temporary-permanent pacemaker (TPPM) as a 1-month bridge. This is a prospective, multicentre, single-arm, observational study. Consecutive patients undergoing TAVR from March 1, 2022 to March 1, 2023 in 13 tertiary hospitals in China were screened. Patients who developed high-degree atrioventricular block, complete heart block, or first-degree atrioventricular block plus new onset left bundle branch block during the TAVR procedure or within 1 month after TAVR were included to receive TPPM. Patients with pre-existing PPM implantation or indications for PPM implantation before the TAVR procedure were excluded. Patients with TPPM were monitored to determine whether the conduction disturbances persisted or recovered. The primary endpoint was the rate of freedom from indications for PPM implantation 1 month after TAVR. This study is registered with ChiCTR, ChiCTR2200057931. Of 688 patients who have undergone TAVR, 71 developed conduction disturbance and met the inclusion criteria, 1 patient withdrew due to noncompliance, 70 patients received TPPM and completed follow-up. There were 41 (58.6%) men and 29 (41.4%) women in the study, with a mean age of 74.3 ± 7.3 years. At 1 month follow-up, 75.7% (53/70) of the patients with TPPM did not require PPM implantation. For 688 patients who have undergone TAVR, the rate of PPM implantation at 1 month was 2.47% (17/688, 95% CI 1.55%-3.92%), representing a significant reduction in self-comparison with the rate at 48 h after TPPM (2.47% vs. 8.28% [95% CI 6.45%-10.58%], P < 0.0001). Similar results were obtained in the subgroup analysis of patients with HAVB/CHB. Multivariate analysis revealed the baseline PR interval, difference between the membranous septum length and implantation depth, and timing of postprocedural conduction disturbance occurrence were independent predictors of freedom from indications for PPM implantation at 1 month after TAVR. Using TPPM as a 1-month bridge allows for a buffer period to distinguish whether conduction disturbances are reversible or persistent, resulting in a significant reduction in the PPM implantation rate after TAVR when compared with the current strategy. However, this is an observational study, the results need to be confirmed in a randomized trial. Beijing Science and Technology Plan 2022 from Beijing Municipal Science & Technology Commission.

Sections du résumé

Background UNASSIGNED
The permanent pacemaker (PPM) implantation and pacemaker dependency rates after transcatheter aortic valve replacement (TAVR) are highly variable as some of the conduction disturbances are reversible. It remains poorly investigated how to optimise temporary pacing in these patients. This study aimed to explore the potential reduction in the PPM implantation rate using temporary-permanent pacemaker (TPPM) as a 1-month bridge.
Methods UNASSIGNED
This is a prospective, multicentre, single-arm, observational study. Consecutive patients undergoing TAVR from March 1, 2022 to March 1, 2023 in 13 tertiary hospitals in China were screened. Patients who developed high-degree atrioventricular block, complete heart block, or first-degree atrioventricular block plus new onset left bundle branch block during the TAVR procedure or within 1 month after TAVR were included to receive TPPM. Patients with pre-existing PPM implantation or indications for PPM implantation before the TAVR procedure were excluded. Patients with TPPM were monitored to determine whether the conduction disturbances persisted or recovered. The primary endpoint was the rate of freedom from indications for PPM implantation 1 month after TAVR. This study is registered with ChiCTR, ChiCTR2200057931.
Findings UNASSIGNED
Of 688 patients who have undergone TAVR, 71 developed conduction disturbance and met the inclusion criteria, 1 patient withdrew due to noncompliance, 70 patients received TPPM and completed follow-up. There were 41 (58.6%) men and 29 (41.4%) women in the study, with a mean age of 74.3 ± 7.3 years. At 1 month follow-up, 75.7% (53/70) of the patients with TPPM did not require PPM implantation. For 688 patients who have undergone TAVR, the rate of PPM implantation at 1 month was 2.47% (17/688, 95% CI 1.55%-3.92%), representing a significant reduction in self-comparison with the rate at 48 h after TPPM (2.47% vs. 8.28% [95% CI 6.45%-10.58%], P < 0.0001). Similar results were obtained in the subgroup analysis of patients with HAVB/CHB. Multivariate analysis revealed the baseline PR interval, difference between the membranous septum length and implantation depth, and timing of postprocedural conduction disturbance occurrence were independent predictors of freedom from indications for PPM implantation at 1 month after TAVR.
Interpretation UNASSIGNED
Using TPPM as a 1-month bridge allows for a buffer period to distinguish whether conduction disturbances are reversible or persistent, resulting in a significant reduction in the PPM implantation rate after TAVR when compared with the current strategy. However, this is an observational study, the results need to be confirmed in a randomized trial.
Funding UNASSIGNED
Beijing Science and Technology Plan 2022 from Beijing Municipal Science & Technology Commission.

Identifiants

pubmed: 39010979
doi: 10.1016/j.eclinm.2024.102603
pii: S2589-5370(24)00182-2
pmc: PMC11247154
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102603

Informations de copyright

© 2024 The Author(s).

Déclaration de conflit d'intérêts

HJ received grants from Pi-Cardia for his institution, and received consulting fees from Edwards Lifesciences and Medtronic Inc. All other authors declare no competing interests.

Auteurs

Sanshuai Chang (S)

Interventional Center of Valvular Heart Disease, Beijing AnZhen Hospital, Capital Medical University, National Clinical Research Centre for Cardiovascular Diseases, Beijing, China.

Zhengming Jiang (Z)

Interventional Center of Valvular Heart Disease, Beijing AnZhen Hospital, Capital Medical University, National Clinical Research Centre for Cardiovascular Diseases, Beijing, China.

Xinmin Liu (X)

Interventional Center of Valvular Heart Disease, Beijing AnZhen Hospital, Capital Medical University, National Clinical Research Centre for Cardiovascular Diseases, Beijing, China.

Yida Tang (Y)

Department of Cardiology and Institute of Vascular Medicine, Peking University Third Hospital, Beijing, China.

Ming Bai (M)

Department of Cardiology, The First Hospital of Lanzhou University, Lanzhou, China.

Jizhe Xu (J)

Department of Cardiology, The First Hospital of Lanzhou University, Lanzhou, China.

Haiping Wang (H)

Department of Cardiology, Qingdao Fuwai Cardiovascular Hospital, Qingdao, China.

Yuguo Chen (Y)

Department of Emergency Medicine and Chest Pain Center, Qilu Hospital of Shandong University, Cheeloo College of Medicine Shandong University, Jinan, China.

Chuanbao Li (C)

Department of Emergency Medicine and Chest Pain Center, Qilu Hospital of Shandong University, Cheeloo College of Medicine Shandong University, Jinan, China.

Yundai Chen (Y)

Senior Department of Cardiology, The Sixth Medical Center of PLA General Hospital, Beijing, China.

Changfu Liu (C)

Senior Department of Cardiology, The Sixth Medical Center of PLA General Hospital, Beijing, China.

Jianzeng Dong (J)

Department of Cardiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Jianfang Luo (J)

Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Cardiovascular Institute, Guangzhou, China.

Jie Li (J)

Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Cardiovascular Institute, Guangzhou, China.

Guosheng Fu (G)

Department of Cardiology, Sir Run Shaw Hospital, Zhejiang University of Medicine, Hangzhou, China.

Sheng Wang (S)

Department of Cardiology, Fuwai Central China Cardiovascular Hospital, Zhengzhou, China.

Hui Huang (H)

Department of Cardiology, General Hospital of Ningxia Medical University, Yinchuan, China.

Yuewu Zhao (Y)

Department of Cardiology, Xuzhou Municipal Hospital Affiliated to Xuzhou Medical University, Xuzhou, China.

Xijin Zhuang (X)

Department of Cardiology, Dalian Municipal Central Hospital, Dalian, China.

Hasan Jilaihawi (H)

NYU Langone Health, New York, USA.

Nicolo Piazza (N)

Division of Cardiology, Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.

Feicheng Yu (F)

Department of Cardiology, Sir Run Shaw Hospital, Zhejiang University of Medicine, Hangzhou, China.

Thomas Modine (T)

UMCV, Hôpital Haut Leveque, Centre Hospitalier Universitaire (CHU) de Bordeaux, France.

Guangyuan Song (G)

Interventional Center of Valvular Heart Disease, Beijing AnZhen Hospital, Capital Medical University, National Clinical Research Centre for Cardiovascular Diseases, Beijing, China.

Classifications MeSH