The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.
Détails
ID Serval
serval:BIB_47B1D03F4DF5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
The ventricular ectopic QRS interval (VEQSI): Diagnosis of arrhythmogenic right ventricular cardiomyopathy in patients with incomplete disease expression.
Périodique
Heart rhythm
ISSN
1556-3871 (Electronic)
ISSN-L
1547-5271
Statut éditorial
Publié
Date de publication
07/2016
Peer-reviewed
Oui
Volume
13
Numéro
7
Pages
1504-1512
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
The ventricular ectopic QRS interval (VEQSI) has been shown to identify structural heart disease and predict mortality. In arrhythmogenic right ventricular cardiomyopathy (ARVC), early diagnosis is difficult using current methods, and life-threatening arrhythmias are common and difficult to predict.
The purpose of this study was to assess the utility of ventricular ectopic indices including VEQSI in ARVC diagnosis.
We studied 70 patients with ARVC [30 with definite disease (age 47 ± 12 years; 60% male), 40 with incomplete disease expression (age 44 ± 18 years; 44% male)], 116 healthy controls (age 40 ± 15 years; 56% male), and 26 patients with normal heart right ventricular outflow tract (RVOT) ectopy (age 46 ± 17 years; 27% male). The duration of the broadest ventricular ectopic beat during 12-lead Holter monitoring was recorded as VEQSI max.
VEQSI max was associated with age and gender, but not with conducted QRS duration. Adjusted VEQSI max was greater in ARVC patients than in control groups. In healthy males (44.5 years), estimated VEQSI max was 163 ms (95% confidence interval [CI] 159-167 ms); in definite ARVC 212 ms (95% CI 206-217 ms); in incompletely expressed ARVC 204 ms (95% CI 199-210 ms); and in normal heart RVOT ectopy 171 ms (95% CI 165-178 ms). VEQSI max >180 ms had 98% sensitivity and specificity for diagnosis of ARVC (area under the curve 0.99, 95% CI 0.980-0.998). In our incompletely expressed ARVC patients, VEQSI max >180 ms identified 88% as affected.
VEQSI max distinguishes ARVC patients, including those with incomplete disease expression, from healthy controls and patients with normal heart RVOT ectopy.
The purpose of this study was to assess the utility of ventricular ectopic indices including VEQSI in ARVC diagnosis.
We studied 70 patients with ARVC [30 with definite disease (age 47 ± 12 years; 60% male), 40 with incomplete disease expression (age 44 ± 18 years; 44% male)], 116 healthy controls (age 40 ± 15 years; 56% male), and 26 patients with normal heart right ventricular outflow tract (RVOT) ectopy (age 46 ± 17 years; 27% male). The duration of the broadest ventricular ectopic beat during 12-lead Holter monitoring was recorded as VEQSI max.
VEQSI max was associated with age and gender, but not with conducted QRS duration. Adjusted VEQSI max was greater in ARVC patients than in control groups. In healthy males (44.5 years), estimated VEQSI max was 163 ms (95% confidence interval [CI] 159-167 ms); in definite ARVC 212 ms (95% CI 206-217 ms); in incompletely expressed ARVC 204 ms (95% CI 199-210 ms); and in normal heart RVOT ectopy 171 ms (95% CI 165-178 ms). VEQSI max >180 ms had 98% sensitivity and specificity for diagnosis of ARVC (area under the curve 0.99, 95% CI 0.980-0.998). In our incompletely expressed ARVC patients, VEQSI max >180 ms identified 88% as affected.
VEQSI max distinguishes ARVC patients, including those with incomplete disease expression, from healthy controls and patients with normal heart RVOT ectopy.
Mots-clé
Adult, Age Factors, Arrhythmogenic Right Ventricular Dysplasia/complications, Arrhythmogenic Right Ventricular Dysplasia/diagnosis, Arrhythmogenic Right Ventricular Dysplasia/physiopathology, Early Diagnosis, Electrocardiography, Ambulatory/methods, Female, Heart Conduction System/physiopathology, Heart Ventricles/physiopathology, Humans, Male, Middle Aged, Risk Factors, Sensitivity and Specificity, Sex Factors, Tachycardia, Ventricular/diagnosis, Tachycardia, Ventricular/physiopathology, Tachycardia, Ventricular/prevention & control, United Kingdom, Ventricular Premature Complexes/diagnosis, Ventricular Premature Complexes/etiology, Ventricular Premature Complexes/physiopathology, Arrhythmogenic right ventricular cardiomyopathy, Implantable cardioverter-defibrillator, Sudden cardiac death, Ventricular ectopic QRS interval (VEQSI), Ventricular ectopic beat
Pubmed
Web of science
Création de la notice
03/03/2024 17:57
Dernière modification de la notice
11/03/2024 7:17