Predictors of the need for atrioventricular nodal ablation following redo ablation for atrial fibrillation.

ablation atrial fibrillation atrioventricular nodal ablation pace and ablate pacemaker

Journal

Journal of arrhythmia
ISSN: 1880-4276
Titre abrégé: J Arrhythm
Pays: Japan
ID NLM: 101263026

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 30 11 2023
revised: 28 01 2024
accepted: 03 03 2024
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 28 6 2024
Statut: epublish

Résumé

Patients who have recurrent atrial fibrillation (AF) following redo catheter ablation may eventually be managed with a pace-and-ablate approach, involving pacemaker implant followed by We analyzed patients undergoing redo AF ablations between 2013 and 2019 at our institution. Follow-up was censored on December 31, 2021. Patients with no available follow-up data were excluded. Time-to-event analysis with Cox proportional hazard regression was used to compare those who underwent AVNA to those who did not. A total of 467 patients were included, of whom 39 (8.4%) underwent AVNA. After multivariable adjustment, female sex (aHR 4.68 [95% CI 2.30-9.50]; Female sex, ischemic heart disease, and persistent AF may be useful clinical predictors of the requirement for subsequent AVNA and may be considered as part of shared clinical decision making.

Sections du résumé

Background UNASSIGNED
Patients who have recurrent atrial fibrillation (AF) following redo catheter ablation may eventually be managed with a pace-and-ablate approach, involving pacemaker implant followed by
Methods UNASSIGNED
We analyzed patients undergoing redo AF ablations between 2013 and 2019 at our institution. Follow-up was censored on December 31, 2021. Patients with no available follow-up data were excluded. Time-to-event analysis with Cox proportional hazard regression was used to compare those who underwent AVNA to those who did not.
Results UNASSIGNED
A total of 467 patients were included, of whom 39 (8.4%) underwent AVNA. After multivariable adjustment, female sex (aHR 4.68 [95% CI 2.30-9.50];
Conclusion UNASSIGNED
Female sex, ischemic heart disease, and persistent AF may be useful clinical predictors of the requirement for subsequent AVNA and may be considered as part of shared clinical decision making.

Identifiants

pubmed: 38939768
doi: 10.1002/joa3.13023
pii: JOA313023
pmc: PMC11199796
doi:

Types de publication

Journal Article

Langues

eng

Pagination

501-507

Informations de copyright

© 2024 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of Japanese Heart Rhythm Society.

Déclaration de conflit d'intérêts

DG reports: institutional research grants from Boston Scientific and Medtronic, and speaker fees from Boston Scientific. AB reports consultant or speaker fees from Medtronic. The other authors report no conflicts of interest.

Auteurs

Peter Calvert (P)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital Liverpool UK.
Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Wern Yew Ding (WY)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital Liverpool UK.
Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Michael Griffin (M)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Arnaud Bisson (A)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.
Centre Hospitalier Régional Universitaire et Faculté de Médecine de Tours Tours France.

Ioanna Koniari (I)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Noel Fitzpatrick (N)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Richard Snowdon (R)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Simon Modi (S)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Vishal Luther (V)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Saagar Mahida (S)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Johan Waktare (J)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Zoltan Borbas (Z)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Reza Ashrafi (R)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Derick Todd (D)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Archana Rao (A)

Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Dhiraj Gupta (D)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital Liverpool UK.
Liverpool Heart & Chest Hospital NHS Foundation Trust Liverpool UK.

Classifications MeSH