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Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD
BACKGROUND: Exercise tolerance decreases as COPD progresses. Pulmonary hypertension (PH) is common in COPD and may reduce performance further. COPD patients with and without PH could potentially be identified by cardiopulmonary exercise test (CPET). However, results from previous studies are divergi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744745/ https://www.ncbi.nlm.nih.gov/pubmed/29339921 http://dx.doi.org/10.2147/COPD.S150034 |
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author | Skjørten, Ingunn Hilde, Janne Mykland Melsom, Morten Nissen Hisdal, Jonny Hansteen, Viggo Steine, Kjetil Humerfelt, Sjur |
author_facet | Skjørten, Ingunn Hilde, Janne Mykland Melsom, Morten Nissen Hisdal, Jonny Hansteen, Viggo Steine, Kjetil Humerfelt, Sjur |
author_sort | Skjørten, Ingunn |
collection | PubMed |
description | BACKGROUND: Exercise tolerance decreases as COPD progresses. Pulmonary hypertension (PH) is common in COPD and may reduce performance further. COPD patients with and without PH could potentially be identified by cardiopulmonary exercise test (CPET). However, results from previous studies are diverging, and a unified conclusion is missing. We hypothesized that CPET combined with arterial blood gases is useful to discriminate between COPD outpatients with and without PH. METHODS: In total, 93 COPD patients were prospectively included. Pulmonary function tests, right heart catheterization, and CPET with blood gases were performed. The patients were divided, by mean pulmonary artery pressure, into COPD-noPH (<25 mmHg) and COPD-PH (≥25 mmHg) groups. Linear mixed models (LMMs) were fitted to estimate differences when repeated measurements during the course of exercise were considered and adjusted for gender, age, and airway obstruction. RESULTS: Ventilatory and/or hypoxemic limitation was the dominant cause of exercise termination. In LMM analyses, significant differences between COPD-noPH and COPD-PH were observed for PaO(2), SaO(2), PaCO(2), ventilation, respiratory frequency, and heart rate. PaO(2) <61 mmHg (8.1 kPa) during unloaded pedaling, the only load level achieved by all the patients, predicted PH with a sensitivity of 86% and a specificity of 78%. CONCLUSION: During CPET, low exercise performance and PaO(2) strongly indicated PH in COPD patients. |
format | Online Article Text |
id | pubmed-5744745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57447452018-01-16 Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD Skjørten, Ingunn Hilde, Janne Mykland Melsom, Morten Nissen Hisdal, Jonny Hansteen, Viggo Steine, Kjetil Humerfelt, Sjur Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Exercise tolerance decreases as COPD progresses. Pulmonary hypertension (PH) is common in COPD and may reduce performance further. COPD patients with and without PH could potentially be identified by cardiopulmonary exercise test (CPET). However, results from previous studies are diverging, and a unified conclusion is missing. We hypothesized that CPET combined with arterial blood gases is useful to discriminate between COPD outpatients with and without PH. METHODS: In total, 93 COPD patients were prospectively included. Pulmonary function tests, right heart catheterization, and CPET with blood gases were performed. The patients were divided, by mean pulmonary artery pressure, into COPD-noPH (<25 mmHg) and COPD-PH (≥25 mmHg) groups. Linear mixed models (LMMs) were fitted to estimate differences when repeated measurements during the course of exercise were considered and adjusted for gender, age, and airway obstruction. RESULTS: Ventilatory and/or hypoxemic limitation was the dominant cause of exercise termination. In LMM analyses, significant differences between COPD-noPH and COPD-PH were observed for PaO(2), SaO(2), PaCO(2), ventilation, respiratory frequency, and heart rate. PaO(2) <61 mmHg (8.1 kPa) during unloaded pedaling, the only load level achieved by all the patients, predicted PH with a sensitivity of 86% and a specificity of 78%. CONCLUSION: During CPET, low exercise performance and PaO(2) strongly indicated PH in COPD patients. Dove Medical Press 2017-12-22 /pmc/articles/PMC5744745/ /pubmed/29339921 http://dx.doi.org/10.2147/COPD.S150034 Text en © 2018 Skjørten et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Skjørten, Ingunn Hilde, Janne Mykland Melsom, Morten Nissen Hisdal, Jonny Hansteen, Viggo Steine, Kjetil Humerfelt, Sjur Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title | Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title_full | Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title_fullStr | Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title_full_unstemmed | Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title_short | Cardiopulmonary exercise test and PaO(2) in evaluation of pulmonary hypertension in COPD |
title_sort | cardiopulmonary exercise test and pao(2) in evaluation of pulmonary hypertension in copd |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744745/ https://www.ncbi.nlm.nih.gov/pubmed/29339921 http://dx.doi.org/10.2147/COPD.S150034 |
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