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Evaluation, Diagnosis, and Classification of Pulmonary Hypertension
Pulmonary hypertension (PH) is a rare heterogenous disease characterized by elevated blood pressure in the lungs. Patients with PH require careful evaluation and management at an expert center. Understanding of the mechanisms underlying the development of PH has increased over the past two decades,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Houston Methodist DeBakey Heart & Vascular
Center
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298121/ https://www.ncbi.nlm.nih.gov/pubmed/34326927 http://dx.doi.org/10.14797/OCDF4453 |
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author | Sarah, Beshay Ashrith, Guha Sandeep, Sahay |
author_facet | Sarah, Beshay Ashrith, Guha Sandeep, Sahay |
author_sort | Sarah, Beshay |
collection | PubMed |
description | Pulmonary hypertension (PH) is a rare heterogenous disease characterized by elevated blood pressure in the lungs. Patients with PH require careful evaluation and management at an expert center. Understanding of the mechanisms underlying the development of PH has increased over the past two decades, and several treatment options for pulmonary arterial hypertension have emerged. Despite this progress, PH continues to carry high morbidity and mortality. The 6th World Symposium on Pulmonary Hypertension that occurred in late 2018 modified the clinical classification of PH into five groups. In this review, we focus on the evaluation and diagnosis of PH and discuss the updated clinical classification. |
format | Online Article Text |
id | pubmed-8298121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Houston Methodist DeBakey Heart & Vascular
Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-82981212021-07-28 Evaluation, Diagnosis, and Classification of Pulmonary Hypertension Sarah, Beshay Ashrith, Guha Sandeep, Sahay Methodist Debakey Cardiovasc J Review Article Pulmonary hypertension (PH) is a rare heterogenous disease characterized by elevated blood pressure in the lungs. Patients with PH require careful evaluation and management at an expert center. Understanding of the mechanisms underlying the development of PH has increased over the past two decades, and several treatment options for pulmonary arterial hypertension have emerged. Despite this progress, PH continues to carry high morbidity and mortality. The 6th World Symposium on Pulmonary Hypertension that occurred in late 2018 modified the clinical classification of PH into five groups. In this review, we focus on the evaluation and diagnosis of PH and discuss the updated clinical classification. Houston Methodist DeBakey Heart & Vascular Center 2021-07-01 /pmc/articles/PMC8298121/ /pubmed/34326927 http://dx.doi.org/10.14797/OCDF4453 Text en Copyright: © 2021 The Author(s) https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC-BY-NC 4.0), which permits unrestricted use, distribution, and reproduction in any noncommercial medium, provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Article Sarah, Beshay Ashrith, Guha Sandeep, Sahay Evaluation, Diagnosis, and Classification of Pulmonary Hypertension |
title | Evaluation, Diagnosis, and Classification of Pulmonary
Hypertension |
title_full | Evaluation, Diagnosis, and Classification of Pulmonary
Hypertension |
title_fullStr | Evaluation, Diagnosis, and Classification of Pulmonary
Hypertension |
title_full_unstemmed | Evaluation, Diagnosis, and Classification of Pulmonary
Hypertension |
title_short | Evaluation, Diagnosis, and Classification of Pulmonary
Hypertension |
title_sort | evaluation, diagnosis, and classification of pulmonary
hypertension |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298121/ https://www.ncbi.nlm.nih.gov/pubmed/34326927 http://dx.doi.org/10.14797/OCDF4453 |
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