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Heart rate variability in children with aortic valve stenosis – a pilot study
INTRODUCTION: The aim of our prospective study was to evaluate heart rate variability (HRV) in children with aortic valve stenosis (AS) and its relationship with left ventricular mass and peak transaortic valve pressure gradient (PG). MATERIAL AND METHODS: Sixty children with AS divided into 3 group...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701972/ https://www.ncbi.nlm.nih.gov/pubmed/23847678 http://dx.doi.org/10.5114/aoms.2013.34880 |
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author | Werner, Bozena Piorecka-Makula, Anna Bobkowski, Waldemar |
author_facet | Werner, Bozena Piorecka-Makula, Anna Bobkowski, Waldemar |
author_sort | Werner, Bozena |
collection | PubMed |
description | INTRODUCTION: The aim of our prospective study was to evaluate heart rate variability (HRV) in children with aortic valve stenosis (AS) and its relationship with left ventricular mass and peak transaortic valve pressure gradient (PG). MATERIAL AND METHODS: Sixty children with AS divided into 3 groups according to their PG and 60 healthy controls were studied. Holter ECG monitoring with time domain HRV analysis was performed. Left ventricular mass was calculated by echocardiography. RESULTS: Mean values of all HRV parameters were statistically significantly lower (p < 0.001) in children with AS than in controls (respectively: SDNN 127.8 ±28.2 ms; 162.6 ±38.0 ms, SDNN day 99.7 ±26.6 ms; 134.1 ±36.1 ms, SDNN night 99.9 ±32.8 ms; 123.4 ±45.7 ms, SDANN 112.2 ±27.7 ms; 142.4 ±34.6, SDNNi 62.2 ±16.2 ms; 75.9 ±21.6, RMSSD 39.6 ±12.1 ms; 50.3 ±16.7 ms, rMSSD day 33.6 ±10.9 ms; 43.1 ±14.7 ms, rMSSD night 49.8 ±18.1 ms; 64.4 ±24.9 ms, pNN50 16.4 ±9.5%; 23.5 ±11.7%, pNN50 day 12.0 ±8.5%; 18.4 ±10.7%, pNN50 night; 26.5 ±14.8%; 36.4 ±17.4%. No significant differences between the mean values of HRV parameters in children with different PG and with and without myocardial hypertrophy were found. In children with AS and ventricular arrhythmia SDNN day was significantly lower (p < 0.05) compared to patients without arrhythmia (94.9 ±22.1 ms vs. 109.3 ±22.5 ms). CONCLUSIONS: In children with AS the balance of the autonomic nervous systemic disturbed which manifests in an increase in sympathetic and decrease in parasympathetic activity. Transaortic valve pressure gradient and myocardial hypertrophy do not influence the HRV. The SDNN reduction during the day period may indicate the risk of ventricular arrhythmia in children with AS. |
format | Online Article Text |
id | pubmed-3701972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-37019722013-07-11 Heart rate variability in children with aortic valve stenosis – a pilot study Werner, Bozena Piorecka-Makula, Anna Bobkowski, Waldemar Arch Med Sci Short Communication INTRODUCTION: The aim of our prospective study was to evaluate heart rate variability (HRV) in children with aortic valve stenosis (AS) and its relationship with left ventricular mass and peak transaortic valve pressure gradient (PG). MATERIAL AND METHODS: Sixty children with AS divided into 3 groups according to their PG and 60 healthy controls were studied. Holter ECG monitoring with time domain HRV analysis was performed. Left ventricular mass was calculated by echocardiography. RESULTS: Mean values of all HRV parameters were statistically significantly lower (p < 0.001) in children with AS than in controls (respectively: SDNN 127.8 ±28.2 ms; 162.6 ±38.0 ms, SDNN day 99.7 ±26.6 ms; 134.1 ±36.1 ms, SDNN night 99.9 ±32.8 ms; 123.4 ±45.7 ms, SDANN 112.2 ±27.7 ms; 142.4 ±34.6, SDNNi 62.2 ±16.2 ms; 75.9 ±21.6, RMSSD 39.6 ±12.1 ms; 50.3 ±16.7 ms, rMSSD day 33.6 ±10.9 ms; 43.1 ±14.7 ms, rMSSD night 49.8 ±18.1 ms; 64.4 ±24.9 ms, pNN50 16.4 ±9.5%; 23.5 ±11.7%, pNN50 day 12.0 ±8.5%; 18.4 ±10.7%, pNN50 night; 26.5 ±14.8%; 36.4 ±17.4%. No significant differences between the mean values of HRV parameters in children with different PG and with and without myocardial hypertrophy were found. In children with AS and ventricular arrhythmia SDNN day was significantly lower (p < 0.05) compared to patients without arrhythmia (94.9 ±22.1 ms vs. 109.3 ±22.5 ms). CONCLUSIONS: In children with AS the balance of the autonomic nervous systemic disturbed which manifests in an increase in sympathetic and decrease in parasympathetic activity. Transaortic valve pressure gradient and myocardial hypertrophy do not influence the HRV. The SDNN reduction during the day period may indicate the risk of ventricular arrhythmia in children with AS. Termedia Publishing House 2013-05-07 2013-06-20 /pmc/articles/PMC3701972/ /pubmed/23847678 http://dx.doi.org/10.5114/aoms.2013.34880 Text en Copyright © 2013 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Werner, Bozena Piorecka-Makula, Anna Bobkowski, Waldemar Heart rate variability in children with aortic valve stenosis – a pilot study |
title | Heart rate variability in children with aortic valve stenosis – a pilot study |
title_full | Heart rate variability in children with aortic valve stenosis – a pilot study |
title_fullStr | Heart rate variability in children with aortic valve stenosis – a pilot study |
title_full_unstemmed | Heart rate variability in children with aortic valve stenosis – a pilot study |
title_short | Heart rate variability in children with aortic valve stenosis – a pilot study |
title_sort | heart rate variability in children with aortic valve stenosis – a pilot study |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701972/ https://www.ncbi.nlm.nih.gov/pubmed/23847678 http://dx.doi.org/10.5114/aoms.2013.34880 |
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