Electrocardiographic localization of ventricular arrhythmias successfully ablated from the distal great cardiac vein.


Journal

Journal of cardiovascular electrophysiology
ISSN: 1540-8167
Titre abrégé: J Cardiovasc Electrophysiol
Pays: United States
ID NLM: 9010756

Informations de publication

Date de publication:
10 2020
Historique:
received: 30 04 2020
revised: 25 06 2020
accepted: 30 06 2020
pubmed: 4 7 2020
medline: 29 7 2021
entrez: 4 7 2020
Statut: ppublish

Résumé

Idiopathic ventricular arrhythmias (IVAs) from the left ventricular (LV) summit may be successfully ablated from the distal great cardiac vein (dGCV). Using a 12-lead electrocardiogram (ECG) to localize IVAs that can be ablated from the dGCV is valuable for ablation planning. To determine if a "w" wave, a notch in the Q wave in lead I, and other ECG features can identify IVAs that can be successfully ablated from the dGCV. We reviewed outflow tract premature ventricular contraction (PVC) ablations performed at two centers between September 2010 and June 2018. Successful PVC ablations, in which the PVCs were mapped from the right ventricular outflow tract, coronary cusps, commissures, endocardial LV, and the coronary venous system including the dGCV were included. ECG characteristics were compared between patients with successful ablations in the dGCV and non-dGCV sites. Of the 120 patients (age 56.8 ± 13.8 years, 45% female) that met the inclusion criteria, the dGCV was the successful ablation site in 18 patients (15%). Multivariate analysis with binary logistic regression showed that a "w" in lead I in combination with an early precordial pattern break and a maximum deflection index (MDI) ≥ 0.5 had sensitivity and specificity for a successful ablation in the dGCV of 94.4% and 96.1%, respectively. Combining a "w" wave in lead I with an early precordial pattern break and an MDI ≥ 0.5 is highly sensitive and specific for identifying the dGCV as a successful ablation site for PVCs.

Sections du résumé

BACKGROUND
Idiopathic ventricular arrhythmias (IVAs) from the left ventricular (LV) summit may be successfully ablated from the distal great cardiac vein (dGCV). Using a 12-lead electrocardiogram (ECG) to localize IVAs that can be ablated from the dGCV is valuable for ablation planning.
OBJECTIVE
To determine if a "w" wave, a notch in the Q wave in lead I, and other ECG features can identify IVAs that can be successfully ablated from the dGCV.
METHODS
We reviewed outflow tract premature ventricular contraction (PVC) ablations performed at two centers between September 2010 and June 2018. Successful PVC ablations, in which the PVCs were mapped from the right ventricular outflow tract, coronary cusps, commissures, endocardial LV, and the coronary venous system including the dGCV were included. ECG characteristics were compared between patients with successful ablations in the dGCV and non-dGCV sites.
RESULTS
Of the 120 patients (age 56.8 ± 13.8 years, 45% female) that met the inclusion criteria, the dGCV was the successful ablation site in 18 patients (15%). Multivariate analysis with binary logistic regression showed that a "w" in lead I in combination with an early precordial pattern break and a maximum deflection index (MDI) ≥ 0.5 had sensitivity and specificity for a successful ablation in the dGCV of 94.4% and 96.1%, respectively.
CONCLUSION
Combining a "w" wave in lead I with an early precordial pattern break and an MDI ≥ 0.5 is highly sensitive and specific for identifying the dGCV as a successful ablation site for PVCs.

Identifiants

pubmed: 32618396
doi: 10.1111/jce.14650
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2668-2676

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

David Chang (D)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

James Gabriels (J)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Aditi Vaishnav (A)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Beom S Kim (BS)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Kristie Coleman (K)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Mohammad Khan (M)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Kyle Maisel (K)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Haisam Ismail (H)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Bruce Goldner (B)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Jonathan Willner (J)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Raman Mitra (R)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Roy M John (RM)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Apoor Patel (A)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Laurence M Epstein (LM)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Stavros Mountantonakis (S)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

Stuart Beldner (S)

Division of Electrophysiology, Northwell Health, Manhasset, New York.

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