Provocation and localization of atrial ectopy in patients with atrial septal defects.


Journal

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing
ISSN: 1572-8595
Titre abrégé: J Interv Card Electrophysiol
Pays: Netherlands
ID NLM: 9708966

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 26 03 2022
accepted: 07 06 2022
pubmed: 24 6 2022
medline: 13 10 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

Atrial fibrillation (AF) is associated with atrial septal defects (ASDs), but the mechanism of arrhythmia in these patients is poorly understood. We hypothesised that right-sided atrial ectopy may predominate in this cohort. Here, we aimed to localise the origin of spontaneous and provoked atrial ectopy in ASD patients. Following invasive calibration of P-wave axes, 24-h Holter monitoring was used to determine the chamber of origin of spontaneous atrial ectopy. Simultaneous electrogram recording from multiple intra-cardiac catheters was used to determine the chamber of origin of isoprenaline-provoked ectopy. Comparison was made to a group of non-congenital heart disease AF patients. Amongst ASD patients, a right-sided origin for spontaneous atrial ectopy was significantly more prevalent than a left-sided origin (24/30 patients with right-sided ectopy vs. 14/30 with left-sided ectopy, P = 0.015). Amongst AF patients, there was no difference in the prevalence of spontaneous right vs. left-sided ectopy. For isoprenaline-provoked ectopy, there was no significant difference in the proportions of patients with right-sided or left-sided ectopy in either group. When spontaneous atrial ectopy occurs in ASD patients, it is significantly more prevalent from a right-sided than left-sided origin. Isoprenaline infusion did not reveal the predilection for right-sided ectopy during electrophysiology study.

Sections du résumé

BACKGROUND BACKGROUND
Atrial fibrillation (AF) is associated with atrial septal defects (ASDs), but the mechanism of arrhythmia in these patients is poorly understood. We hypothesised that right-sided atrial ectopy may predominate in this cohort. Here, we aimed to localise the origin of spontaneous and provoked atrial ectopy in ASD patients.
METHODS METHODS
Following invasive calibration of P-wave axes, 24-h Holter monitoring was used to determine the chamber of origin of spontaneous atrial ectopy. Simultaneous electrogram recording from multiple intra-cardiac catheters was used to determine the chamber of origin of isoprenaline-provoked ectopy. Comparison was made to a group of non-congenital heart disease AF patients.
RESULTS RESULTS
Amongst ASD patients, a right-sided origin for spontaneous atrial ectopy was significantly more prevalent than a left-sided origin (24/30 patients with right-sided ectopy vs. 14/30 with left-sided ectopy, P = 0.015). Amongst AF patients, there was no difference in the prevalence of spontaneous right vs. left-sided ectopy. For isoprenaline-provoked ectopy, there was no significant difference in the proportions of patients with right-sided or left-sided ectopy in either group.
CONCLUSIONS CONCLUSIONS
When spontaneous atrial ectopy occurs in ASD patients, it is significantly more prevalent from a right-sided than left-sided origin. Isoprenaline infusion did not reveal the predilection for right-sided ectopy during electrophysiology study.

Identifiants

pubmed: 35737208
doi: 10.1007/s10840-022-01273-2
pii: 10.1007/s10840-022-01273-2
pmc: PMC9550781
doi:

Substances chimiques

Isoproterenol L628TT009W

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

227-237

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT 203148/Z/16/Z
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s).

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Auteurs

Louisa O'Neill (L)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK. louisa.oneill@kcl.ac.uk.

Iain Sim (I)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Daniel O'Hare (D)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

John Whitaker (J)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Rahul K Mukherjee (RK)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Steven Niederer (S)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Matthew Wright (M)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Vivienne Ezzat (V)

Bart's Heart Centre, London, UK.

Eric Rosenthal (E)

Guy's and St Thomas' NHS Foundation Trust, London, UK.

Matthew I Jones (MI)

Guy's and St Thomas' NHS Foundation Trust, London, UK.

Alessandra Frigiola (A)

Guy's and St Thomas' NHS Foundation Trust, London, UK.

Mark D O'Neill (MD)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.

Steven E Williams (SE)

Division of Imaging Sciences and Biomedical Engineering, King's College London, 4thFloor North Wing, St. Thomas' Hospital, London, SE1 7EH, UK.
The University of Edinburgh, Edinburgh, UK.

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Classifications MeSH