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Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias

OBJECTIVES: To evaluate P-wave dispersion (PWD) and QT dispersion (QTd) in children with congenital heart disease and pulmonary arterial hypertension (PAH-CHD) and to investigate the predictive value of both PWD and QTd for prediction of arrhythmias in such children. MATERIALS AND METHODS: We includ...

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Autores principales: Saleh, Asmaa, Shabana, Ahmed, El Amrousy, Doaa, Zoair, Amr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312787/
https://www.ncbi.nlm.nih.gov/pubmed/30618481
http://dx.doi.org/10.1016/j.jsha.2018.11.006
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author Saleh, Asmaa
Shabana, Ahmed
El Amrousy, Doaa
Zoair, Amr
author_facet Saleh, Asmaa
Shabana, Ahmed
El Amrousy, Doaa
Zoair, Amr
author_sort Saleh, Asmaa
collection PubMed
description OBJECTIVES: To evaluate P-wave dispersion (PWD) and QT dispersion (QTd) in children with congenital heart disease and pulmonary arterial hypertension (PAH-CHD) and to investigate the predictive value of both PWD and QTd for prediction of arrhythmias in such children. MATERIALS AND METHODS: We included 40 children with PAH-CHD as Group I. Forty other children with CHD and no PAH were included as Group II. Forty healthy children of matched age and sex served as a Control group. Electrocardiography was performed to determine PWD and QTd. Furthermore, 24-hour Holter monitoring was performed to detect the presence of arrhythmias. Echocardiographic evaluation was also performed. RESULTS: QTd and PWD were significantly higher in Group I than in Group II and Control group. A significant positive correlation was present between both QTd and PWD and mean pulmonary artery pressure, right ventricular diameter, pulmonary vascular resistance (PVR), and PVR to systemic vascular resistance ratio. QTd showed 93% sensitivity, 80% specificity, and 85% accuracy for prediction of occurrence of arrhythmias in patients with PAH-CHD at a cutoff point of 61 ms, whereas PWD showed 87% sensitivity, 80% specificity, and 85% accuracy for prediction of arrhythmias at a cutoff point of 32.5 ms in such patients. Logistic regression analysis showed that both QTd and PWD were good predictors for the occurrence of arrhythmias in children with PAH-CHD (p = 0.003 and p = 0.01, respectively). CONCLUSIONS: PWD and QTd were good predictors for the occurrence of various arrhythmias in children with PAH-CHD.
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spelling pubmed-63127872019-01-07 Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias Saleh, Asmaa Shabana, Ahmed El Amrousy, Doaa Zoair, Amr J Saudi Heart Assoc Original Article OBJECTIVES: To evaluate P-wave dispersion (PWD) and QT dispersion (QTd) in children with congenital heart disease and pulmonary arterial hypertension (PAH-CHD) and to investigate the predictive value of both PWD and QTd for prediction of arrhythmias in such children. MATERIALS AND METHODS: We included 40 children with PAH-CHD as Group I. Forty other children with CHD and no PAH were included as Group II. Forty healthy children of matched age and sex served as a Control group. Electrocardiography was performed to determine PWD and QTd. Furthermore, 24-hour Holter monitoring was performed to detect the presence of arrhythmias. Echocardiographic evaluation was also performed. RESULTS: QTd and PWD were significantly higher in Group I than in Group II and Control group. A significant positive correlation was present between both QTd and PWD and mean pulmonary artery pressure, right ventricular diameter, pulmonary vascular resistance (PVR), and PVR to systemic vascular resistance ratio. QTd showed 93% sensitivity, 80% specificity, and 85% accuracy for prediction of occurrence of arrhythmias in patients with PAH-CHD at a cutoff point of 61 ms, whereas PWD showed 87% sensitivity, 80% specificity, and 85% accuracy for prediction of arrhythmias at a cutoff point of 32.5 ms in such patients. Logistic regression analysis showed that both QTd and PWD were good predictors for the occurrence of arrhythmias in children with PAH-CHD (p = 0.003 and p = 0.01, respectively). CONCLUSIONS: PWD and QTd were good predictors for the occurrence of various arrhythmias in children with PAH-CHD. Elsevier 2019-04 2018-12-01 /pmc/articles/PMC6312787/ /pubmed/30618481 http://dx.doi.org/10.1016/j.jsha.2018.11.006 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Saleh, Asmaa
Shabana, Ahmed
El Amrousy, Doaa
Zoair, Amr
Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title_full Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title_fullStr Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title_full_unstemmed Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title_short Predictive value of P-wave and QT interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
title_sort predictive value of p-wave and qt interval dispersion in children with congenital heart disease and pulmonary arterial hypertension for the occurrence of arrhythmias
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312787/
https://www.ncbi.nlm.nih.gov/pubmed/30618481
http://dx.doi.org/10.1016/j.jsha.2018.11.006
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