Device-detected atrial sensing amplitudes as a marker of increased risk for new-onset and progression of atrial high-rate episodes.

AHRE Atrial fibrillation P-wave device-detected AF subclinical AF

Journal

Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317

Informations de publication

Date de publication:
15 Mar 2024
Historique:
received: 14 11 2023
revised: 09 03 2024
accepted: 13 03 2024
medline: 18 3 2024
pubmed: 18 3 2024
entrez: 17 3 2024
Statut: aheadofprint

Résumé

Atrial high-rate episodes (AHRE) are frequent in patients with cardiac implantable electronic devices. A decrease in device-detected P-wave amplitude may be an indicator of periods of increased risk of AHRE. To assess the association between P-wave amplitude and AHRE incidence. Remote monitoring data from 2,579 patients with no history of atrial fibrillation (23% pacemakers, 77% implantable cardioverter-defibrillators [ICDs] of which 40% providing cardiac resynchronization therapy [CRT]) were used to calculate the mean P-wave amplitude during 1 month after implantation. The association with AHRE incidence according to four strata of daily burden duration (≥15 minutes, ≥6 hours, ≥24 hours, ≥7 days) was investigated by adjusting the hazard ratio with the CHA The adjusted hazard ratio (HR) for 1-mV lower mean P-wave amplitude during the first month increased from 1.10 (95% confidence interval [CI], 1.05-1.15; p<0.001) to 1.18 (CI, 1.09-1.28; p<0.001) with AHRE duration strata from ≥15 minutes to ≥7 days independently of the CHA Device-detected P-wave amplitudes lower than 2.45 mV were associated with an increased risk of AHRE onset and progression to persistent forms of AHRE independently of the patient's risk profile.

Sections du résumé

BACKGROUND BACKGROUND
Atrial high-rate episodes (AHRE) are frequent in patients with cardiac implantable electronic devices. A decrease in device-detected P-wave amplitude may be an indicator of periods of increased risk of AHRE.
OBJECTIVE OBJECTIVE
To assess the association between P-wave amplitude and AHRE incidence.
METHODS METHODS
Remote monitoring data from 2,579 patients with no history of atrial fibrillation (23% pacemakers, 77% implantable cardioverter-defibrillators [ICDs] of which 40% providing cardiac resynchronization therapy [CRT]) were used to calculate the mean P-wave amplitude during 1 month after implantation. The association with AHRE incidence according to four strata of daily burden duration (≥15 minutes, ≥6 hours, ≥24 hours, ≥7 days) was investigated by adjusting the hazard ratio with the CHA
RESULTS RESULTS
The adjusted hazard ratio (HR) for 1-mV lower mean P-wave amplitude during the first month increased from 1.10 (95% confidence interval [CI], 1.05-1.15; p<0.001) to 1.18 (CI, 1.09-1.28; p<0.001) with AHRE duration strata from ≥15 minutes to ≥7 days independently of the CHA
CONCLUSION CONCLUSIONS
Device-detected P-wave amplitudes lower than 2.45 mV were associated with an increased risk of AHRE onset and progression to persistent forms of AHRE independently of the patient's risk profile.

Identifiants

pubmed: 38493989
pii: S1547-5271(24)00280-7
doi: 10.1016/j.hrthm.2024.03.034
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Mauro Biffi (M)

Policlinico Sant'Orsola-Malpighi, Bologna, Italy. Electronic address: mauro.biffi@aosp.bo.it.

Eduardo Celentano (E)

Humanitas Gavazzeni, Bergamo, Italy.

Massimo Giammaria (M)

Ospedali Martini e Maria Vittoria, Torino, Italy.

Antonio Curnis (A)

Spedali Civili, Brescia, Italy.

Giovanni Rovaris (G)

Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Matteo Ziacchi (M)

Policlinico Sant'Orsola-Malpighi, Bologna, Italy.

Gennaro Miracapillo (G)

Ospedale della Misericordia, Grosseto, Italy.

Davide Saporito (D)

Ospedale degli Infermi, Rimini, Italy.

Matteo Baroni (M)

ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Fabio Quartieri (F)

Arcispedale Santa Maria Nuova, Reggio Emilia, Italy.

Massimiliano Marini (M)

Ospedale Santa Chiara, Trento, Italy.

Patrizia Pepi (P)

Ospedale Carlo Poma, Mantova, Italy.

Gaetano Senatore (G)

Ospedale di Ciriè, Ciriè (TO), Italy.

Fabrizio Caravati (F)

ASST dei sette laghi, Ospedale di Circolo, Varese, Italy.

Valeria Calvi (V)

Azienda O.U. Policlinico G. Rodolico - San Marco, Catania, Italy.

Luca Tomasi (L)

Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy.

Gerardo Nigro (G)

Università Vanvitelli - AO Monaldi, Napoli, Italy.

Luca Bontempi (L)

Ospedale Bolognini, Seriate (BG), Italy.

Francesca Notarangelo (F)

Azienda Ospedaliero-Unviversitaria di Parma, Parma, Italy.

Vincenzo Ezio Santobuono (VE)

Dipartimento Interdisciplinare di Medicina (DIM) - Università degli Studi di Bari "Aldo Moro", Bari, Italy.

Giulio Boggian (G)

Ospedale di Bentivoglio, Bentivoglio (BO), Italy.

Giuseppe Arena (G)

Ospedale Apuane, Massa, Italy.

Francesco Solimene (F)

Clinica Montevergine, Mercogliano (AV), Italy.

Marzia Giaccardi (M)

Ospedale Santa Maria Annunziata, Bagno a Ripoli (FI), Italy.

Giampiero Maglia (G)

Ospedale Pugliese-Ciaccio, Catanzaro, Italy.

Alessandro Paoletti Perini (AP)

Ospedale Santa Maria Nuova, Firenze, Italy.

Mario Volpicelli (M)

Ospedale Santa Maria della Pietà, Nola (NA), Napoli, Italy.

Daniele Giacopelli (D)

Biotronik Italia S.p.a., Cologno Monzese (MI), Italy.

Alessio Gargaro (A)

Biotronik Italia S.p.a., Cologno Monzese (MI), Italy.

Saverio Iacopino (S)

Maria Cecilia Hospital, Cotignola (RA), Italy.

Classifications MeSH