Spatial Accuracy of a Clinically Established Noninvasive Electrocardiographic Imaging System for the Detection of Focal Activation in an Intact Porcine Model.


Journal

Circulation. Arrhythmia and electrophysiology
ISSN: 1941-3084
Titre abrégé: Circ Arrhythm Electrophysiol
Pays: United States
ID NLM: 101474365

Informations de publication

Date de publication:
11 2019
Historique:
entrez: 12 11 2019
pubmed: 12 11 2019
medline: 6 6 2020
Statut: ppublish

Résumé

Noninvasive electrocardiographic imaging (ECGi) is used clinically to map arrhythmias before ablation. Despite its clinical use, validation data regarding the accuracy of the system for the identification of arrhythmia foci is limited. Nine pigs underwent closed-chest placement of endocardial fiducial markers, computed tomography, and pacing in all cardiac chambers with ECGi acquisition. Pacing location was reconstructed from biplane fluoroscopy and registered to the computed tomography using the fiducials. A blinded investigator predicted the pacing location from the ECGi data, and the distance to the true pacing catheter tip location was calculated. A total of 109 endocardial and 9 epicardial locations were paced in 9 pigs. ECGi predicted the correct chamber of origin in 85% of atrial and 92% of ventricular sites. Lateral locations were predicted in the correct chamber more often than septal locations (97% versus 79%, The ECGi system is able to correctly identify the chamber of origin for focal activation in the vast majority of cases. Determination of the true site of origin is possible with sufficient accuracy with consideration of these error estimates.

Sections du résumé

BACKGROUND
Noninvasive electrocardiographic imaging (ECGi) is used clinically to map arrhythmias before ablation. Despite its clinical use, validation data regarding the accuracy of the system for the identification of arrhythmia foci is limited.
METHODS
Nine pigs underwent closed-chest placement of endocardial fiducial markers, computed tomography, and pacing in all cardiac chambers with ECGi acquisition. Pacing location was reconstructed from biplane fluoroscopy and registered to the computed tomography using the fiducials. A blinded investigator predicted the pacing location from the ECGi data, and the distance to the true pacing catheter tip location was calculated.
RESULTS
A total of 109 endocardial and 9 epicardial locations were paced in 9 pigs. ECGi predicted the correct chamber of origin in 85% of atrial and 92% of ventricular sites. Lateral locations were predicted in the correct chamber more often than septal locations (97% versus 79%,
CONCLUSIONS
The ECGi system is able to correctly identify the chamber of origin for focal activation in the vast majority of cases. Determination of the true site of origin is possible with sufficient accuracy with consideration of these error estimates.

Identifiants

pubmed: 31707808
doi: 10.1161/CIRCEP.119.007570
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007570

Auteurs

Stephan Hohmann (S)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Maryam E Rettmann (ME)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Hiroki Konishi (H)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Anna Borenstein (A)

Medtronic, Inc, Cleveland, OH (A.B.).

Songyun Wang (S)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Atsushi Suzuki (A)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Gregory J Michalak (GJ)

Department of Radiology (G.J.M.), Mayo Clinic, Rochester, MN.

Kristi H Monahan (KH)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Kay D Parker (KD)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

L Katie Newman (LK)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

Douglas L Packer (DL)

Translational Interventional Electrophysiology Laboratory (S.H., M.E.R., H.K., S.W., A.S., K.H.M., K.D.P., L.K.N., D.L.P.), Mayo Clinic, Rochester, MN.

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Classifications MeSH