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Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea

Exercise pulmonary hypertension is an underappreciated form of physical limitation related to early pulmonary vascular disease. A low diffusing capacity of lungs for carbon monoxide (DLco) can be seen in patients with resting pulmonary hypertension as well as parenchymal lung disease. It remains unc...

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Autores principales: Zou, Richard H., Wallace, William D., Nouraie, S. Mehdi, Chan, Stephen Y., Risbano, Michael G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031800/
https://www.ncbi.nlm.nih.gov/pubmed/32128158
http://dx.doi.org/10.1177/2045894019891912
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author Zou, Richard H.
Wallace, William D.
Nouraie, S. Mehdi
Chan, Stephen Y.
Risbano, Michael G.
author_facet Zou, Richard H.
Wallace, William D.
Nouraie, S. Mehdi
Chan, Stephen Y.
Risbano, Michael G.
author_sort Zou, Richard H.
collection PubMed
description Exercise pulmonary hypertension is an underappreciated form of physical limitation related to early pulmonary vascular disease. A low diffusing capacity of lungs for carbon monoxide (DLco) can be seen in patients with resting pulmonary hypertension as well as parenchymal lung disease. It remains unclear whether low DLco% identifies early pulmonary vascular disease. We hypothesize that a reduced DLco% differentiates the presence of exercise pulmonary hypertension in patients with parenchymal lung disease. Fifty-six patients referred for unexplained exertional dyspnea with pulmonary function tests within six months of hemodynamic testing underwent exercise right heart catheterization. Exclusion criteria included resting pulmonary arterial or venous hypertension. Receiver operator characteristic curve determined the optimal DLco% cutoffs based on the presence or absence of parenchymal lung disease. Twenty-one (37%) patients had parenchymal lung disease, most common manifesting as chronic obstructive lung disease or interstitial lung disease. In patients with parenchymal lung disease, a DLco of 46% demonstrated 100% sensitivity and 73% specificity for detecting exercise pulmonary hypertension. In patients without parenchymal lung disease, a DLco of 73% demonstrated 58% sensitivity and 94% specificity for detecting exercise pulmonary hypertension. In both cohorts, DLco% below the optimum cutoffs were associated with higher peak mean pulmonary arterial pressure and peak total pulmonary resistance consistent with the hemodynamic definition of exercise pulmonary hypertension. Patients with a DLco < 46% were more often treated with pulmonary vasodilators and had a trend to higher mortality and lung transplant. DLco% is a simple non-invasive screening test for the presence of exercise pulmonary hypertension in our mixed referral population with progressive exertional dyspnea. DLco < 46% with parenchymal lung disease and DLco < 73% without parenchymal lung disease may play a role in differentiating the presence of pulmonary vascular disease prior to invasive hemodynamic testing.
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spelling pubmed-70318002020-03-03 Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea Zou, Richard H. Wallace, William D. Nouraie, S. Mehdi Chan, Stephen Y. Risbano, Michael G. Pulm Circ Research Article Exercise pulmonary hypertension is an underappreciated form of physical limitation related to early pulmonary vascular disease. A low diffusing capacity of lungs for carbon monoxide (DLco) can be seen in patients with resting pulmonary hypertension as well as parenchymal lung disease. It remains unclear whether low DLco% identifies early pulmonary vascular disease. We hypothesize that a reduced DLco% differentiates the presence of exercise pulmonary hypertension in patients with parenchymal lung disease. Fifty-six patients referred for unexplained exertional dyspnea with pulmonary function tests within six months of hemodynamic testing underwent exercise right heart catheterization. Exclusion criteria included resting pulmonary arterial or venous hypertension. Receiver operator characteristic curve determined the optimal DLco% cutoffs based on the presence or absence of parenchymal lung disease. Twenty-one (37%) patients had parenchymal lung disease, most common manifesting as chronic obstructive lung disease or interstitial lung disease. In patients with parenchymal lung disease, a DLco of 46% demonstrated 100% sensitivity and 73% specificity for detecting exercise pulmonary hypertension. In patients without parenchymal lung disease, a DLco of 73% demonstrated 58% sensitivity and 94% specificity for detecting exercise pulmonary hypertension. In both cohorts, DLco% below the optimum cutoffs were associated with higher peak mean pulmonary arterial pressure and peak total pulmonary resistance consistent with the hemodynamic definition of exercise pulmonary hypertension. Patients with a DLco < 46% were more often treated with pulmonary vasodilators and had a trend to higher mortality and lung transplant. DLco% is a simple non-invasive screening test for the presence of exercise pulmonary hypertension in our mixed referral population with progressive exertional dyspnea. DLco < 46% with parenchymal lung disease and DLco < 73% without parenchymal lung disease may play a role in differentiating the presence of pulmonary vascular disease prior to invasive hemodynamic testing. SAGE Publications 2020-02-19 /pmc/articles/PMC7031800/ /pubmed/32128158 http://dx.doi.org/10.1177/2045894019891912 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Article
Zou, Richard H.
Wallace, William D.
Nouraie, S. Mehdi
Chan, Stephen Y.
Risbano, Michael G.
Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title_full Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title_fullStr Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title_full_unstemmed Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title_short Lower DLco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
title_sort lower dlco% identifies exercise pulmonary hypertension in patients with parenchymal lung disease referred for dyspnea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031800/
https://www.ncbi.nlm.nih.gov/pubmed/32128158
http://dx.doi.org/10.1177/2045894019891912
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