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The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients

Pulmonary hypertension (PHT) is associated with increased mortality in hemodialysis (HD) patients. The ventricular gradient optimized for right ventricular pressure overload (VG-RVPO) is sensitive to early changes in right ventricular overload. The study aimed to assess the ability of the VG-RVPO to...

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Autores principales: Jaroszyński, A., Schlegel, T. T., Zaborowski, T., Zapolski, T., Załuska, W., Janion-Sadowska, A., Kozieł, D., Głuszek, S., Dąbrowski, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748426/
https://www.ncbi.nlm.nih.gov/pubmed/35013477
http://dx.doi.org/10.1038/s41598-021-04186-8
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author Jaroszyński, A.
Schlegel, T. T.
Zaborowski, T.
Zapolski, T.
Załuska, W.
Janion-Sadowska, A.
Kozieł, D.
Głuszek, S.
Dąbrowski, W.
author_facet Jaroszyński, A.
Schlegel, T. T.
Zaborowski, T.
Zapolski, T.
Załuska, W.
Janion-Sadowska, A.
Kozieł, D.
Głuszek, S.
Dąbrowski, W.
author_sort Jaroszyński, A.
collection PubMed
description Pulmonary hypertension (PHT) is associated with increased mortality in hemodialysis (HD) patients. The ventricular gradient optimized for right ventricular pressure overload (VG-RVPO) is sensitive to early changes in right ventricular overload. The study aimed to assess the ability of the VG-RVPO to detect PHT and predict all-cause and cardiac mortality in HD patients. 265 selected HD patients were enrolled. Clinical, biochemical, electrocardiographic, and echocardiographic parameters were evaluated. Patients were divided into normal and abnormal VG-RVPO groups, and were followed-up for 3 years. Abnormal VG-RVPO patients were more likely to be at high or intermediate risk for PHT, were older, had longer HD vintage, higher prevalence of myocardial infarction, higher parathormone levels, shorter pulmonary flow acceleration time, lower left ventricular ejection fraction, higher values of left atrial volume index, left ventricular mass index, and peak tricuspid regurgitant velocity. Both all-cause and CV mortality were higher in abnormal VG-RVPO group. In multivariate Cox analysis, VG-RVPO remained an independent and strong predictor of all-cause and CV mortality. In HD patients, abnormal VG-RVPO not only predicts PHT, but also all-cause and CV mortality.
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spelling pubmed-87484262022-01-11 The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients Jaroszyński, A. Schlegel, T. T. Zaborowski, T. Zapolski, T. Załuska, W. Janion-Sadowska, A. Kozieł, D. Głuszek, S. Dąbrowski, W. Sci Rep Article Pulmonary hypertension (PHT) is associated with increased mortality in hemodialysis (HD) patients. The ventricular gradient optimized for right ventricular pressure overload (VG-RVPO) is sensitive to early changes in right ventricular overload. The study aimed to assess the ability of the VG-RVPO to detect PHT and predict all-cause and cardiac mortality in HD patients. 265 selected HD patients were enrolled. Clinical, biochemical, electrocardiographic, and echocardiographic parameters were evaluated. Patients were divided into normal and abnormal VG-RVPO groups, and were followed-up for 3 years. Abnormal VG-RVPO patients were more likely to be at high or intermediate risk for PHT, were older, had longer HD vintage, higher prevalence of myocardial infarction, higher parathormone levels, shorter pulmonary flow acceleration time, lower left ventricular ejection fraction, higher values of left atrial volume index, left ventricular mass index, and peak tricuspid regurgitant velocity. Both all-cause and CV mortality were higher in abnormal VG-RVPO group. In multivariate Cox analysis, VG-RVPO remained an independent and strong predictor of all-cause and CV mortality. In HD patients, abnormal VG-RVPO not only predicts PHT, but also all-cause and CV mortality. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748426/ /pubmed/35013477 http://dx.doi.org/10.1038/s41598-021-04186-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Jaroszyński, A.
Schlegel, T. T.
Zaborowski, T.
Zapolski, T.
Załuska, W.
Janion-Sadowska, A.
Kozieł, D.
Głuszek, S.
Dąbrowski, W.
The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title_full The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title_fullStr The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title_full_unstemmed The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title_short The value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
title_sort value of ventricular gradient for predicting pulmonary hypertension and mortality in hemodialysis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748426/
https://www.ncbi.nlm.nih.gov/pubmed/35013477
http://dx.doi.org/10.1038/s41598-021-04186-8
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