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Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure

BACKGROUND: Assessment of ventricular dyssynchrony in patients with heart failure is used for selecting candidates for cardiac resynchronization therapy (CRT). The patterns of regional distribution of dyssynchrony in a population with LBBB with and without heart failure have not been well delineated...

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Autores principales: Rao, Hygriv B, Krishnaswami, Raghu, Kalavakolanu, Sharada, Calambur, Narasimhan
Formato: Texto
Lenguaje:English
Publicado: Indian Heart Rhythm Society 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836215/
https://www.ncbi.nlm.nih.gov/pubmed/20234808
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author Rao, Hygriv B
Krishnaswami, Raghu
Kalavakolanu, Sharada
Calambur, Narasimhan
author_facet Rao, Hygriv B
Krishnaswami, Raghu
Kalavakolanu, Sharada
Calambur, Narasimhan
author_sort Rao, Hygriv B
collection PubMed
description BACKGROUND: Assessment of ventricular dyssynchrony in patients with heart failure is used for selecting candidates for cardiac resynchronization therapy (CRT). The patterns of regional distribution of dyssynchrony in a population with LBBB with and without heart failure have not been well delineated. This aspect forms the object of the study. METHODS: Tissue Doppler Imaging (TDI) data of consecutive patients with heart failure and LBBB (Group A) was compared with those with LBBB and normal LV function (Group B). All patients had standard 2D-echocardigraphic examination and TDI. Tissue velocity curves obtained by placing sample volumes in opposing basal and mid segments of septal, lateral, inferior, anterior and posterior walls were analyzed. Inter ventricular dyssynchrony (IVD) was assessed by the difference between aortic and pulmonary pre ejection intervals. LV dyssynchrony (LVD) was assessed by the difference in times to peak velocity. A delay of ≥ 40 msec was considered significant for presence of IVD and LVD. RESULTS: There were 103 patients in Group A and 25 in Group B. The mean QRS duration and PR intervals respectively were 146 ± 25 vs. 152±20 msec and 182± 47 vs. 165±36 msec. (p=NS) LVEF in the 2 groups were (32 ± 6 % vs. 61± 11%; p< 0.01). Prevalence of dyssynchrony in the HF group compared to Group B was 72% vs. 16%, (P< 0.01). Lateral wall dyssynchrony in the 2 groups was 37% vs. 0% (p< 0.01) while septal dyssynchrony was 16% vs. 16% (p- NS). CONCLUSIONS: 72% of heart failure patients with LBBB have documented dyssynchrony on TDI, which has a heterogeneous regional distribution. Dyssynchrony may be seen in LBBB and normal hearts but it is does not involve the lateral wall. Septal dyssynchrony in heart failure patients may not have the same significance as lateral wall delay.
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spelling pubmed-28362152010-03-16 Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure Rao, Hygriv B Krishnaswami, Raghu Kalavakolanu, Sharada Calambur, Narasimhan Indian Pacing Electrophysiol J Original Article BACKGROUND: Assessment of ventricular dyssynchrony in patients with heart failure is used for selecting candidates for cardiac resynchronization therapy (CRT). The patterns of regional distribution of dyssynchrony in a population with LBBB with and without heart failure have not been well delineated. This aspect forms the object of the study. METHODS: Tissue Doppler Imaging (TDI) data of consecutive patients with heart failure and LBBB (Group A) was compared with those with LBBB and normal LV function (Group B). All patients had standard 2D-echocardigraphic examination and TDI. Tissue velocity curves obtained by placing sample volumes in opposing basal and mid segments of septal, lateral, inferior, anterior and posterior walls were analyzed. Inter ventricular dyssynchrony (IVD) was assessed by the difference between aortic and pulmonary pre ejection intervals. LV dyssynchrony (LVD) was assessed by the difference in times to peak velocity. A delay of ≥ 40 msec was considered significant for presence of IVD and LVD. RESULTS: There were 103 patients in Group A and 25 in Group B. The mean QRS duration and PR intervals respectively were 146 ± 25 vs. 152±20 msec and 182± 47 vs. 165±36 msec. (p=NS) LVEF in the 2 groups were (32 ± 6 % vs. 61± 11%; p< 0.01). Prevalence of dyssynchrony in the HF group compared to Group B was 72% vs. 16%, (P< 0.01). Lateral wall dyssynchrony in the 2 groups was 37% vs. 0% (p< 0.01) while septal dyssynchrony was 16% vs. 16% (p- NS). CONCLUSIONS: 72% of heart failure patients with LBBB have documented dyssynchrony on TDI, which has a heterogeneous regional distribution. Dyssynchrony may be seen in LBBB and normal hearts but it is does not involve the lateral wall. Septal dyssynchrony in heart failure patients may not have the same significance as lateral wall delay. Indian Heart Rhythm Society 2010-03-05 /pmc/articles/PMC2836215/ /pubmed/20234808 Text en Copyright: © 2010 Rao et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rao, Hygriv B
Krishnaswami, Raghu
Kalavakolanu, Sharada
Calambur, Narasimhan
Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title_full Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title_fullStr Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title_full_unstemmed Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title_short Ventricular Dyssynchrony Patterns in Left Bundle Branch Block, With and Without Heart Failure
title_sort ventricular dyssynchrony patterns in left bundle branch block, with and without heart failure
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836215/
https://www.ncbi.nlm.nih.gov/pubmed/20234808
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