Diagnosis and Management of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension is a rare disease, which requires a high index of suspicion to diagnose when patients initially present. Initial symptoms can be nonspecific and include complaints such as fatigue and mild dyspnea. Once the disease is suspected, echocardiography is used to estimate th...

Full description

Saved in:
Bibliographic Details
Main Authors: Jeanne Houtchens, Douglas Martin, James R. Klinger
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Pulmonary Medicine
Online Access:http://dx.doi.org/10.1155/2011/845864
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832559042126413824
author Jeanne Houtchens
Douglas Martin
James R. Klinger
author_facet Jeanne Houtchens
Douglas Martin
James R. Klinger
author_sort Jeanne Houtchens
collection DOAJ
description Pulmonary arterial hypertension is a rare disease, which requires a high index of suspicion to diagnose when patients initially present. Initial symptoms can be nonspecific and include complaints such as fatigue and mild dyspnea. Once the disease is suspected, echocardiography is used to estimate the pulmonary arterial (PA) pressure and to exclude secondary causes of elevated PA pressures such as left heart disease. Right heart catheterization with vasodilator challenge is critical to the proper assessment of pulmonary hemodynamics and to determine whether patients are likely to benefit from vasodilator therapy. Pathologically, the disease is characterized by deleterious remodeling of the distal pulmonary arterial and arteriolar circulation, which results in increased pulmonary vascular resistance. In the last fifteen years, medications from three different classes have been approved for the treatment of pulmonary arterial hypertension. These include the prostanoids, endothelin receptor antagonists, and phosphodiesterase-5 inhibitors.
format Article
id doaj-art-f464b01a97d74757a72f05167591aaf4
institution Kabale University
issn 2090-1836
2090-1844
language English
publishDate 2011-01-01
publisher Wiley
record_format Article
series Pulmonary Medicine
spelling doaj-art-f464b01a97d74757a72f05167591aaf42025-02-03T01:31:08ZengWileyPulmonary Medicine2090-18362090-18442011-01-01201110.1155/2011/845864845864Diagnosis and Management of Pulmonary Arterial HypertensionJeanne Houtchens0Douglas Martin1James R. Klinger2Division of Pulmonary, Sleep and Critical Care Medicine, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI 02903, USADivision of Pulmonary, Sleep and Critical Care Medicine, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI 02903, USADivision of Pulmonary, Sleep and Critical Care Medicine, Rhode Island Hospital, Alpert Medical School of Brown University, Providence, RI 02903, USAPulmonary arterial hypertension is a rare disease, which requires a high index of suspicion to diagnose when patients initially present. Initial symptoms can be nonspecific and include complaints such as fatigue and mild dyspnea. Once the disease is suspected, echocardiography is used to estimate the pulmonary arterial (PA) pressure and to exclude secondary causes of elevated PA pressures such as left heart disease. Right heart catheterization with vasodilator challenge is critical to the proper assessment of pulmonary hemodynamics and to determine whether patients are likely to benefit from vasodilator therapy. Pathologically, the disease is characterized by deleterious remodeling of the distal pulmonary arterial and arteriolar circulation, which results in increased pulmonary vascular resistance. In the last fifteen years, medications from three different classes have been approved for the treatment of pulmonary arterial hypertension. These include the prostanoids, endothelin receptor antagonists, and phosphodiesterase-5 inhibitors.http://dx.doi.org/10.1155/2011/845864
spellingShingle Jeanne Houtchens
Douglas Martin
James R. Klinger
Diagnosis and Management of Pulmonary Arterial Hypertension
Pulmonary Medicine
title Diagnosis and Management of Pulmonary Arterial Hypertension
title_full Diagnosis and Management of Pulmonary Arterial Hypertension
title_fullStr Diagnosis and Management of Pulmonary Arterial Hypertension
title_full_unstemmed Diagnosis and Management of Pulmonary Arterial Hypertension
title_short Diagnosis and Management of Pulmonary Arterial Hypertension
title_sort diagnosis and management of pulmonary arterial hypertension
url http://dx.doi.org/10.1155/2011/845864
work_keys_str_mv AT jeannehoutchens diagnosisandmanagementofpulmonaryarterialhypertension
AT douglasmartin diagnosisandmanagementofpulmonaryarterialhypertension
AT jamesrklinger diagnosisandmanagementofpulmonaryarterialhypertension