Performance and limitations of noninvasive cardiac activation mapping.


Journal

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

Informations de publication

Date de publication:
03 2019
Historique:
received: 08 03 2018
pubmed: 6 11 2018
medline: 10 10 2020
entrez: 3 11 2018
Statut: ppublish

Résumé

Activation mapping using noninvasive electrocardiographic imaging (ECGi) has recently been used to describe the physiology of different cardiac abnormalities. These descriptions differ from prior invasive studies, and both methods have not been thoroughly confronted in a clinical setting. The goal of the present study was to provide validation of noninvasive activation mapping in a clinical setting through direct confrontation with invasive epicardial contact measures. Fifty-nine maps were obtained in 55 patients and aligned on a common geometry. Nearest-neighbor interpolation was used to avoid map smoothing. Quantitative comparison was performed by computing between-map correlation coefficients and absolute activation time errors. The mean activation time error was 20.4 ± 8.6 ms, and the between-map correlation was poor (0.03 ± 0.43). The results suggested high interpatient variability (correlation -0.68 to 0.82), wide QRS patterns, and paced rhythms demonstrating significantly better mean correlation (0.68 ± 0.17). Errors were greater in scarred regions (21.9 ± 10.8 ms vs 17.5 ± 6.7 ms; P < .01). Fewer epicardial breakthroughs were imaged using noninvasive mapping (1.3 ± 0.5 vs 2.3 ± 0.7; P < .01). Primary breakthrough locations were imaged 75.7 ± 38.1 mm apart. Lines of conduction block (jumps of ≥50 ms between contiguous points) due to structural anomalies were recorded in 27 of 59 contact maps and were not visualized at these same sites noninvasively. Instead, artificial lines appeared in 33 of 59 noninvasive maps in regions of reduced bipolar voltage amplitudes (P = .03). An in silico model confirms these artificial constructs. Overall, agreement of ECGi activation mapping and contact mapping is poor and heterogeneous. The between-map correlation is good for wide QRS patterns. Lines of block and epicardial breakthrough sites imaged using ECGi are inaccurate. Further work is required to improve the accuracy of the technique.

Sections du résumé

BACKGROUND
Activation mapping using noninvasive electrocardiographic imaging (ECGi) has recently been used to describe the physiology of different cardiac abnormalities. These descriptions differ from prior invasive studies, and both methods have not been thoroughly confronted in a clinical setting.
OBJECTIVE
The goal of the present study was to provide validation of noninvasive activation mapping in a clinical setting through direct confrontation with invasive epicardial contact measures.
METHODS
Fifty-nine maps were obtained in 55 patients and aligned on a common geometry. Nearest-neighbor interpolation was used to avoid map smoothing. Quantitative comparison was performed by computing between-map correlation coefficients and absolute activation time errors.
RESULTS
The mean activation time error was 20.4 ± 8.6 ms, and the between-map correlation was poor (0.03 ± 0.43). The results suggested high interpatient variability (correlation -0.68 to 0.82), wide QRS patterns, and paced rhythms demonstrating significantly better mean correlation (0.68 ± 0.17). Errors were greater in scarred regions (21.9 ± 10.8 ms vs 17.5 ± 6.7 ms; P < .01). Fewer epicardial breakthroughs were imaged using noninvasive mapping (1.3 ± 0.5 vs 2.3 ± 0.7; P < .01). Primary breakthrough locations were imaged 75.7 ± 38.1 mm apart. Lines of conduction block (jumps of ≥50 ms between contiguous points) due to structural anomalies were recorded in 27 of 59 contact maps and were not visualized at these same sites noninvasively. Instead, artificial lines appeared in 33 of 59 noninvasive maps in regions of reduced bipolar voltage amplitudes (P = .03). An in silico model confirms these artificial constructs.
CONCLUSION
Overall, agreement of ECGi activation mapping and contact mapping is poor and heterogeneous. The between-map correlation is good for wide QRS patterns. Lines of block and epicardial breakthrough sites imaged using ECGi are inaccurate. Further work is required to improve the accuracy of the technique.

Identifiants

pubmed: 30385382
pii: S1547-5271(18)31026-9
doi: 10.1016/j.hrthm.2018.10.010
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

435-442

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Josselin Duchateau (J)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France. Electronic address: josselin.duchateau@ihu-liryc.fr.

Frédéric Sacher (F)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Thomas Pambrun (T)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Nicolas Derval (N)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Judit Chamorro-Servent (J)

IHU LIRYC, Bordeaux University, Bordeaux, France.

Arnaud Denis (A)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Sylvain Ploux (S)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Mélèze Hocini (M)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Pierre Jaïs (P)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Olivier Bernus (O)

IHU LIRYC, Bordeaux University, Bordeaux, France.

Michel Haïssaguerre (M)

Bordeaux University Hospital, Bordeaux, France; IHU LIRYC, Bordeaux University, Bordeaux, France.

Rémi Dubois (R)

IHU LIRYC, Bordeaux University, Bordeaux, France.

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