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Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure
An accurate distinction between isolated post-capillary pulmonary hypertension (Ipc-PH) and combined post- and pre-capillary pulmonary hypertension (Cpc-PH) is integral to therapy and prognosis in heart failure (HF). This study aimed to compare the ability of four previously validated Doppler estima...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669188/ https://www.ncbi.nlm.nih.gov/pubmed/31123846 http://dx.doi.org/10.1007/s10554-019-01591-z |
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author | Venkateshvaran, Ashwin Hamade, Jasmin Kjellström, Barbro Lund, Lars H. Manouras, Aristomenis |
author_facet | Venkateshvaran, Ashwin Hamade, Jasmin Kjellström, Barbro Lund, Lars H. Manouras, Aristomenis |
author_sort | Venkateshvaran, Ashwin |
collection | PubMed |
description | An accurate distinction between isolated post-capillary pulmonary hypertension (Ipc-PH) and combined post- and pre-capillary pulmonary hypertension (Cpc-PH) is integral to therapy and prognosis in heart failure (HF). This study aimed to compare the ability of four previously validated Doppler estimates of pulmonary vascular resistance (PVR(Doppler)) to distinguish Ipc-PH from Cpc-PH in a well-defined HF population. Consecutive subjects referred for HF assessment underwent standard echocardiography immediately followed by right heart catheterization (RHC). Subjects with atrial fibrillation, acute coronary syndrome, significant valvular disease or poor image quality were excluded. PVR(Doppler) estimates were correlated with invasive PVR and agreement was studied using Bland–Altman analysis. Receiver operating characteristics analyses were performed to determine the ability of PVR(Doppler) methods to identify PVR > 3WU. 55 HF subjects (58 ± 16 years, 55% Ipc-PH) were analyzed. PVR(Doppler) estimates demonstrated weak to modest associations with invasive PVR. The Doppler method proposed by Abbas et al. demonstrated relatively strong discriminatory ability to distinguish Ipc-PH from Cpc-PH (AUC = 0.79; 95% CI 0.63–0.96; p = 0.001). However, Bland–Altman analysis revealed wide limits of agreement (bias = 0; SD = 1.83WU) and greater variability at higher mean PVR. Conclusions: PVR(Doppler) estimates demonstrate reasonable ability to distinguish Ipc-PH from Cpc-PH but may not be reliable independent PH distinguishers in HF. |
format | Online Article Text |
id | pubmed-6669188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-66691882019-08-14 Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure Venkateshvaran, Ashwin Hamade, Jasmin Kjellström, Barbro Lund, Lars H. Manouras, Aristomenis Int J Cardiovasc Imaging Original Paper An accurate distinction between isolated post-capillary pulmonary hypertension (Ipc-PH) and combined post- and pre-capillary pulmonary hypertension (Cpc-PH) is integral to therapy and prognosis in heart failure (HF). This study aimed to compare the ability of four previously validated Doppler estimates of pulmonary vascular resistance (PVR(Doppler)) to distinguish Ipc-PH from Cpc-PH in a well-defined HF population. Consecutive subjects referred for HF assessment underwent standard echocardiography immediately followed by right heart catheterization (RHC). Subjects with atrial fibrillation, acute coronary syndrome, significant valvular disease or poor image quality were excluded. PVR(Doppler) estimates were correlated with invasive PVR and agreement was studied using Bland–Altman analysis. Receiver operating characteristics analyses were performed to determine the ability of PVR(Doppler) methods to identify PVR > 3WU. 55 HF subjects (58 ± 16 years, 55% Ipc-PH) were analyzed. PVR(Doppler) estimates demonstrated weak to modest associations with invasive PVR. The Doppler method proposed by Abbas et al. demonstrated relatively strong discriminatory ability to distinguish Ipc-PH from Cpc-PH (AUC = 0.79; 95% CI 0.63–0.96; p = 0.001). However, Bland–Altman analysis revealed wide limits of agreement (bias = 0; SD = 1.83WU) and greater variability at higher mean PVR. Conclusions: PVR(Doppler) estimates demonstrate reasonable ability to distinguish Ipc-PH from Cpc-PH but may not be reliable independent PH distinguishers in HF. Springer Netherlands 2019-05-23 2019 /pmc/articles/PMC6669188/ /pubmed/31123846 http://dx.doi.org/10.1007/s10554-019-01591-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Paper Venkateshvaran, Ashwin Hamade, Jasmin Kjellström, Barbro Lund, Lars H. Manouras, Aristomenis Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title | Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title_full | Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title_fullStr | Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title_full_unstemmed | Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title_short | Doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
title_sort | doppler estimates of pulmonary vascular resistance to phenotype pulmonary hypertension in heart failure |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669188/ https://www.ncbi.nlm.nih.gov/pubmed/31123846 http://dx.doi.org/10.1007/s10554-019-01591-z |
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