Postinfarct ventricular tachycardia substrate: Characterization and ablation of conduction channels using ripple mapping.


Journal

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

Informations de publication

Date de publication:
10 2021
Historique:
received: 12 03 2021
revised: 27 04 2021
accepted: 11 05 2021
pubmed: 19 5 2021
medline: 15 2 2022
entrez: 18 5 2021
Statut: ppublish

Résumé

Conduction channels have been demonstrated within the postinfarct scar and seem to be co-located with the isthmus of ventricular tachycardia (VT). Mapping the local scar potentials (SPs) that define the conduction channels is often hindered by large far-field electrograms generated by healthy myocardium. The purpose of this study was to map conduction channel using ripple mapping to categorize SPs temporally and anatomically. We tested the hypothesis that ablation of early SPs would eliminate the latest SPs without direct ablation. Ripple maps of postinfarct scar were collected using the PentaRay (Biosense Webster) during normal rhythm. Maps were reviewed in reverse, and clusters of SPs were color-coded on the geometry, by timing, into early, intermediate, late, and terminal. Ablation was delivered sequentially from clusters of early SPs, checking for loss of terminal SPs as the endpoint. The protocol was performed in 11 patients. Mean mapping time was 65 ± 23 minutes, and a mean 3050 ± 1839 points was collected. SP timing ranged from 98.1 ± 60.5 ms to 214.8 ± 89.8 ms post QRS peak. Earliest SPs were present at the border, occupying 16.4% of scar, whereas latest SPs occupied 4.8% at the opposing border or core. Analysis took 15 ± 10 minutes to locate channels and identify ablation targets. It was possible to eliminate latest SPs in all patients without direct ablation (mean ablation time 16.3 ± 11.1 minutes). No VT recurrence was recorded (mean follow-up 10.1 ± 7.4 months). Conduction channels can be located using ripple mapping to analyze SPs. Ablation at channel entrances can eliminate the latest SPs and is associated with good medium-term results.

Sections du résumé

BACKGROUND
Conduction channels have been demonstrated within the postinfarct scar and seem to be co-located with the isthmus of ventricular tachycardia (VT). Mapping the local scar potentials (SPs) that define the conduction channels is often hindered by large far-field electrograms generated by healthy myocardium.
OBJECTIVE
The purpose of this study was to map conduction channel using ripple mapping to categorize SPs temporally and anatomically. We tested the hypothesis that ablation of early SPs would eliminate the latest SPs without direct ablation.
METHODS
Ripple maps of postinfarct scar were collected using the PentaRay (Biosense Webster) during normal rhythm. Maps were reviewed in reverse, and clusters of SPs were color-coded on the geometry, by timing, into early, intermediate, late, and terminal. Ablation was delivered sequentially from clusters of early SPs, checking for loss of terminal SPs as the endpoint.
RESULTS
The protocol was performed in 11 patients. Mean mapping time was 65 ± 23 minutes, and a mean 3050 ± 1839 points was collected. SP timing ranged from 98.1 ± 60.5 ms to 214.8 ± 89.8 ms post QRS peak. Earliest SPs were present at the border, occupying 16.4% of scar, whereas latest SPs occupied 4.8% at the opposing border or core. Analysis took 15 ± 10 minutes to locate channels and identify ablation targets. It was possible to eliminate latest SPs in all patients without direct ablation (mean ablation time 16.3 ± 11.1 minutes). No VT recurrence was recorded (mean follow-up 10.1 ± 7.4 months).
CONCLUSION
Conduction channels can be located using ripple mapping to analyze SPs. Ablation at channel entrances can eliminate the latest SPs and is associated with good medium-term results.

Identifiants

pubmed: 34004345
pii: S1547-5271(21)00443-4
doi: 10.1016/j.hrthm.2021.05.016
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

1682-1690

Subventions

Organisme : British Heart Foundation
ID : FS/15/12/31239
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RG/16/3/32175
Pays : United Kingdom

Informations de copyright

Copyright © 2021 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Auteurs

George Katritsis (G)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Vishal Luther (V)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Shahnaz Jamil-Copley (S)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Michael Koa-Wing (M)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Norman Qureshi (N)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Zachary Whinnett (Z)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Phang Boon Lim (PB)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Fu Siong Ng (FS)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Louisa Malcolme-Lawes (L)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Nicholas S Peters (NS)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Michael Fudge (M)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Elaine Lim (E)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Nicholas W F Linton (NWF)

Imperial College Healthcare NHS Trust, London, United Kingdom.

Prapa Kanagaratnam (P)

Imperial College Healthcare NHS Trust, London, United Kingdom. Electronic address: p.kanagaratnam@imperial.ac.uk.

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