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Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia
Pulmonary hypertension (PH) is caused by a range of conditions and is important to recognize as it is associated with increased mortality. Pulmonary arterial hypertension refers to a group of PH subtypes affecting the distal pulmonary arteries for which effective treatment is available. The hemodyna...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823284/ https://www.ncbi.nlm.nih.gov/pubmed/36624795 http://dx.doi.org/10.1016/j.jacasi.2022.04.008 |
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author | Anderson, James J. Lau, Edmund M. |
author_facet | Anderson, James J. Lau, Edmund M. |
author_sort | Anderson, James J. |
collection | PubMed |
description | Pulmonary hypertension (PH) is caused by a range of conditions and is important to recognize as it is associated with increased mortality. Pulmonary arterial hypertension refers to a group of PH subtypes affecting the distal pulmonary arteries for which effective treatment is available. The hemodynamic definition of pulmonary arterial hypertension has recently changed which may lead to greater case recognition and earlier treatment. The prevalence of specific PH etiologies may differ depending on geographic region. PH caused by left heart disease is the most common cause of PH worldwide. In Asia, there is greater proportion of congenital heart disease– and connective tissue disease– (especially systemic lupus erythematosus) related PH relative to the West. This review summarizes the definition, classification, and epidemiology of PH as it pertains to Asia. |
format | Online Article Text |
id | pubmed-9823284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98232842023-01-08 Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia Anderson, James J. Lau, Edmund M. JACC Asia State-of-the-Art Review Pulmonary hypertension (PH) is caused by a range of conditions and is important to recognize as it is associated with increased mortality. Pulmonary arterial hypertension refers to a group of PH subtypes affecting the distal pulmonary arteries for which effective treatment is available. The hemodynamic definition of pulmonary arterial hypertension has recently changed which may lead to greater case recognition and earlier treatment. The prevalence of specific PH etiologies may differ depending on geographic region. PH caused by left heart disease is the most common cause of PH worldwide. In Asia, there is greater proportion of congenital heart disease– and connective tissue disease– (especially systemic lupus erythematosus) related PH relative to the West. This review summarizes the definition, classification, and epidemiology of PH as it pertains to Asia. Elsevier 2022-08-02 /pmc/articles/PMC9823284/ /pubmed/36624795 http://dx.doi.org/10.1016/j.jacasi.2022.04.008 Text en © 2022 The Authors https://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 | State-of-the-Art Review Anderson, James J. Lau, Edmund M. Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title | Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title_full | Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title_fullStr | Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title_full_unstemmed | Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title_short | Pulmonary Hypertension Definition, Classification, and Epidemiology in Asia |
title_sort | pulmonary hypertension definition, classification, and epidemiology in asia |
topic | State-of-the-Art Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823284/ https://www.ncbi.nlm.nih.gov/pubmed/36624795 http://dx.doi.org/10.1016/j.jacasi.2022.04.008 |
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