The University of Southampton
University of Southampton Institutional Repository

Global endocardial electrical restitution in human right and left ventricles determined by noncontact mapping

Global endocardial electrical restitution in human right and left ventricles determined by noncontact mapping
Global endocardial electrical restitution in human right and left ventricles determined by noncontact mapping
Objectives: This study was aimed at evaluating global characteristics of electrical restitution in the human ventricle using noncontact mapping.
Background: Steep action potential restitution (slope >1) and conduction velocity (CV) restitution have been linked with propensity to ventricular fibrillation, but clinical measurement of global electrical restitution had not been feasible.
Methods: Activation-recovery interval (ARI) and CV restitution curves were simultaneously constructed from 16 regional segments of the left and right ventricles in 8 patients (6 male, 2 female, age 42 ± 17 years) following successful ablation of idiopathic ventricular tachycardia in the absence of structural disease guided by the Ensite 3000 system (Endocardial Solutions Inc., St. Paul, Minnesota). The ARIs were determined from reconstructed unipolar electrograms as validated with monophasic action potential recordings. The ARI restitution slopes were determined using the overlapping least-squares linear segments.
Results: Global electrical restitution curves were heterogeneous in shape and distribution. ARI restitution slope was >1 at 25% of 128 sites. The overall mean slope was 0.79 and was greater in the left than the right ventricle (0.93 ± 0.49 vs. 0.65 ± 0.26, p < 0.001). Dispersion of ARI restitution slopes increased with decreasing diastolic intervals. The CV restitution operated over a narrower range of diastolic intervals compared with ARI restitution, reaching a plateau (10 ± 6 ms vs. 38 ± 13 ms, p < 0.001) after refractoriness. The magnitude of CV restitution was also greater (steeper) than ARI restitution (25 ± 10% vs. 18 ± 9%, p < 0.001).
Conclusions: Noncontact mapping can be used to examine global electrical restitution in the human ventricle. The ARI restitution is heterogeneous, with a slope >1 at 25% of all sites. The heterogeneity of ARI and CV restitution may be important in determining myocardial electrical stability.
0735-1097
1067-1075
Yue, Arthur M.
4040f8ec-0252-49e0-b838-58f37956acd2
Franz, Michael R.
c696330b-08fe-4432-a689-0ab0d3cdc399
Roberts, Paul R.
193431e8-f9d5-48d6-8f62-ed9052b2571d
Morgan, John M.
ac98099e-241d-4551-bc98-709f6dfc8680
Yue, Arthur M.
4040f8ec-0252-49e0-b838-58f37956acd2
Franz, Michael R.
c696330b-08fe-4432-a689-0ab0d3cdc399
Roberts, Paul R.
193431e8-f9d5-48d6-8f62-ed9052b2571d
Morgan, John M.
ac98099e-241d-4551-bc98-709f6dfc8680

Yue, Arthur M., Franz, Michael R., Roberts, Paul R. and Morgan, John M. (2005) Global endocardial electrical restitution in human right and left ventricles determined by noncontact mapping. Journal of the American College of Cardiology, 46 (6), 1067-1075. (doi:10.1016/j.jacc.2005.05.074).

Record type: Article

Abstract

Objectives: This study was aimed at evaluating global characteristics of electrical restitution in the human ventricle using noncontact mapping.
Background: Steep action potential restitution (slope >1) and conduction velocity (CV) restitution have been linked with propensity to ventricular fibrillation, but clinical measurement of global electrical restitution had not been feasible.
Methods: Activation-recovery interval (ARI) and CV restitution curves were simultaneously constructed from 16 regional segments of the left and right ventricles in 8 patients (6 male, 2 female, age 42 ± 17 years) following successful ablation of idiopathic ventricular tachycardia in the absence of structural disease guided by the Ensite 3000 system (Endocardial Solutions Inc., St. Paul, Minnesota). The ARIs were determined from reconstructed unipolar electrograms as validated with monophasic action potential recordings. The ARI restitution slopes were determined using the overlapping least-squares linear segments.
Results: Global electrical restitution curves were heterogeneous in shape and distribution. ARI restitution slope was >1 at 25% of 128 sites. The overall mean slope was 0.79 and was greater in the left than the right ventricle (0.93 ± 0.49 vs. 0.65 ± 0.26, p < 0.001). Dispersion of ARI restitution slopes increased with decreasing diastolic intervals. The CV restitution operated over a narrower range of diastolic intervals compared with ARI restitution, reaching a plateau (10 ± 6 ms vs. 38 ± 13 ms, p < 0.001) after refractoriness. The magnitude of CV restitution was also greater (steeper) than ARI restitution (25 ± 10% vs. 18 ± 9%, p < 0.001).
Conclusions: Noncontact mapping can be used to examine global electrical restitution in the human ventricle. The ARI restitution is heterogeneous, with a slope >1 at 25% of all sites. The heterogeneity of ARI and CV restitution may be important in determining myocardial electrical stability.

This record has no associated files available for download.

More information

Published date: 2005

Identifiers

Local EPrints ID: 26152
URI: http://eprints.soton.ac.uk/id/eprint/26152
ISSN: 0735-1097
PURE UUID: c5f14ae8-690c-4590-9c21-f5c2559197b4

Catalogue record

Date deposited: 19 Apr 2006
Last modified: 15 Mar 2024 07:08

Export record

Altmetrics

Contributors

Author: Arthur M. Yue
Author: Michael R. Franz
Author: Paul R. Roberts
Author: John M. Morgan

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×