A review of therapeutic agents for the management of pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is an uncommon, progressive and life threatening disease characterized by a proliferative vasculopathy of the small muscular pulmonary arterioles resulting in elevated pulmonary vascular resistance and eventually right ventricular failure. An increasing understa...

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Main Authors: Stella S Hahn, Mina Makaryus, Arunabh Talwar, Mangala Narasimhan, Gulrukh Zaidi
Format: Article
Language:English
Published: SAGE Publishing 2017-01-01
Series:Therapeutic Advances in Respiratory Disease
Online Access:https://doi.org/10.1177/1753465816665289
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author Stella S Hahn
Mina Makaryus
Arunabh Talwar
Mangala Narasimhan
Gulrukh Zaidi
author_facet Stella S Hahn
Mina Makaryus
Arunabh Talwar
Mangala Narasimhan
Gulrukh Zaidi
author_sort Stella S Hahn
collection DOAJ
description Pulmonary arterial hypertension (PAH) is an uncommon, progressive and life threatening disease characterized by a proliferative vasculopathy of the small muscular pulmonary arterioles resulting in elevated pulmonary vascular resistance and eventually right ventricular failure. An increasing understanding of the pathobiology of PAH and its natural history has led to the development of numerous targeted therapies. Despite these advances there is significant progression of disease and the survival rate remains low. This article reviews the agents currently available for the medical management of PAH.
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spelling doaj.art-5ad90c45a81048ce86e08ae76a3541fa2022-12-21T23:04:02ZengSAGE PublishingTherapeutic Advances in Respiratory Disease1753-46581753-46662017-01-011110.1177/1753465816665289A review of therapeutic agents for the management of pulmonary arterial hypertensionStella S HahnMina MakaryusArunabh TalwarMangala NarasimhanGulrukh ZaidiPulmonary arterial hypertension (PAH) is an uncommon, progressive and life threatening disease characterized by a proliferative vasculopathy of the small muscular pulmonary arterioles resulting in elevated pulmonary vascular resistance and eventually right ventricular failure. An increasing understanding of the pathobiology of PAH and its natural history has led to the development of numerous targeted therapies. Despite these advances there is significant progression of disease and the survival rate remains low. This article reviews the agents currently available for the medical management of PAH.https://doi.org/10.1177/1753465816665289
spellingShingle Stella S Hahn
Mina Makaryus
Arunabh Talwar
Mangala Narasimhan
Gulrukh Zaidi
A review of therapeutic agents for the management of pulmonary arterial hypertension
Therapeutic Advances in Respiratory Disease
title A review of therapeutic agents for the management of pulmonary arterial hypertension
title_full A review of therapeutic agents for the management of pulmonary arterial hypertension
title_fullStr A review of therapeutic agents for the management of pulmonary arterial hypertension
title_full_unstemmed A review of therapeutic agents for the management of pulmonary arterial hypertension
title_short A review of therapeutic agents for the management of pulmonary arterial hypertension
title_sort review of therapeutic agents for the management of pulmonary arterial hypertension
url https://doi.org/10.1177/1753465816665289
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