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Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients

OBJECTIVE: The aim of our study was to evaluate the effect of cardiac resyncronization therapy (CRT) on QT dispersion (QTd), JT dispersion (JTd) and transmural dispersion of re-polarization (TDR), markers of heterogeneity of ventricular repolarization in a study population with severe heart failure....

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Autores principales: SANTANGELO, LUCIO, RUSSO, VINCENZO, AMMENDOLA, ERNESTO, CAVALLARO, CIRO, VECCHIONE, FILIPPO, GAROFALO, SALVATORE, D’ONOFRIO, ANTONIO, MININNI, NICOLA, CALABRÒ, RAFFAELE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184659/
https://www.ncbi.nlm.nih.gov/pubmed/21977248
http://dx.doi.org/10.4081/hi.2006.27
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author SANTANGELO, LUCIO
RUSSO, VINCENZO
AMMENDOLA, ERNESTO
CAVALLARO, CIRO
VECCHIONE, FILIPPO
GAROFALO, SALVATORE
D’ONOFRIO, ANTONIO
MININNI, NICOLA
CALABRÒ, RAFFAELE
author_facet SANTANGELO, LUCIO
RUSSO, VINCENZO
AMMENDOLA, ERNESTO
CAVALLARO, CIRO
VECCHIONE, FILIPPO
GAROFALO, SALVATORE
D’ONOFRIO, ANTONIO
MININNI, NICOLA
CALABRÒ, RAFFAELE
author_sort SANTANGELO, LUCIO
collection PubMed
description OBJECTIVE: The aim of our study was to evaluate the effect of cardiac resyncronization therapy (CRT) on QT dispersion (QTd), JT dispersion (JTd) and transmural dispersion of re-polarization (TDR), markers of heterogeneity of ventricular repolarization in a study population with severe heart failure. METHODS AND RESULTS: Fifty patients (43 male, 7 female, aged 60.2 ± 3.1 years) suffering from congestive heart failure (N = 39 NYHA class III; N = 11 NYHA class IV) as a result of coronary artery disease (N = 19) or of dilated cardiomyopathy (N = 31), sinus rhythm, QRS duration >130 ms (mean QRS duration >156 ± 21 ms), an ejection fraction < 35%, left ventricular end-diastolic diameter >55 mm, underwent permanent biventricular DDDR pacemaker implantation. A 12-lead standard electrocardiogram was performed at baseline, during right-, left-, and biventricular pacing and QTd, JTd and TDR were assessed. Biventricular pacing significantly reduced QTd (73.93 ± 19.4 ms during BiVP vs 91 ± 6.7 ms at sinus rhythm, p = 0.004), JTd (73.18 ± 17.16 ms during BiVP vs 100.72 ± 39.04 at baseline p = 0.003), TDR (93.16 ± 15.60 vs 101.55 ± 19.08 at baseline; p<0.004), as compared to sinus rhythm. Right ventricular endocardial pacing and left ventricular epicardial pacing both enhanced QTd (RVendoP 94 ± 51 ms, p<0.03; LVepiP 116 ±71 ms, p<0.02) and TDR (RVendoP 108.13 ± 19.94 ms; p<0.002; LVepiP 114.71 ± 26.1; p<0.05).There was no effect on JTd during right and left ventricular stimulation. CONCLUSIONS: Biventricular pacing causes a statistically significant reduction of ventricular heterogeneity of ripolarization and has an electrophysiological antiarrhythmic influence on arrhythmogenic substrate of dilatative cardiomiopathy.
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spelling pubmed-31846592011-10-05 Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients SANTANGELO, LUCIO RUSSO, VINCENZO AMMENDOLA, ERNESTO CAVALLARO, CIRO VECCHIONE, FILIPPO GAROFALO, SALVATORE D’ONOFRIO, ANTONIO MININNI, NICOLA CALABRÒ, RAFFAELE Heart Int Article OBJECTIVE: The aim of our study was to evaluate the effect of cardiac resyncronization therapy (CRT) on QT dispersion (QTd), JT dispersion (JTd) and transmural dispersion of re-polarization (TDR), markers of heterogeneity of ventricular repolarization in a study population with severe heart failure. METHODS AND RESULTS: Fifty patients (43 male, 7 female, aged 60.2 ± 3.1 years) suffering from congestive heart failure (N = 39 NYHA class III; N = 11 NYHA class IV) as a result of coronary artery disease (N = 19) or of dilated cardiomyopathy (N = 31), sinus rhythm, QRS duration >130 ms (mean QRS duration >156 ± 21 ms), an ejection fraction < 35%, left ventricular end-diastolic diameter >55 mm, underwent permanent biventricular DDDR pacemaker implantation. A 12-lead standard electrocardiogram was performed at baseline, during right-, left-, and biventricular pacing and QTd, JTd and TDR were assessed. Biventricular pacing significantly reduced QTd (73.93 ± 19.4 ms during BiVP vs 91 ± 6.7 ms at sinus rhythm, p = 0.004), JTd (73.18 ± 17.16 ms during BiVP vs 100.72 ± 39.04 at baseline p = 0.003), TDR (93.16 ± 15.60 vs 101.55 ± 19.08 at baseline; p<0.004), as compared to sinus rhythm. Right ventricular endocardial pacing and left ventricular epicardial pacing both enhanced QTd (RVendoP 94 ± 51 ms, p<0.03; LVepiP 116 ±71 ms, p<0.02) and TDR (RVendoP 108.13 ± 19.94 ms; p<0.002; LVepiP 114.71 ± 26.1; p<0.05).There was no effect on JTd during right and left ventricular stimulation. CONCLUSIONS: Biventricular pacing causes a statistically significant reduction of ventricular heterogeneity of ripolarization and has an electrophysiological antiarrhythmic influence on arrhythmogenic substrate of dilatative cardiomiopathy. PAGEPress Publications 2006-05-28 /pmc/articles/PMC3184659/ /pubmed/21977248 http://dx.doi.org/10.4081/hi.2006.27 Text en © Wichtig Editore, 2006
spellingShingle Article
SANTANGELO, LUCIO
RUSSO, VINCENZO
AMMENDOLA, ERNESTO
CAVALLARO, CIRO
VECCHIONE, FILIPPO
GAROFALO, SALVATORE
D’ONOFRIO, ANTONIO
MININNI, NICOLA
CALABRÒ, RAFFAELE
Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title_full Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title_fullStr Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title_full_unstemmed Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title_short Biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
title_sort biventricular pacing and heterogeneity of ventricular repolarization in heart failure patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184659/
https://www.ncbi.nlm.nih.gov/pubmed/21977248
http://dx.doi.org/10.4081/hi.2006.27
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