Pulmonary arterial hypertension: evaluation and management.

Abstract:

:Pulmonary arterial hypertension (PAH), a rare disease involving the pulmonary vascular circuit, is defined as an elevation in pulmonary arterial pressures and is characterized by symptoms of dyspnea, chest pain, and syncope. If left untreated, the disease carries a high mortality rate, with the most common cause of death being decompensated right heart failure. Over the past 5 years, there have been significant advances in this field in regards to understanding the pathogenesis, diagnosis, and classification of PAH. The availability of newer drugs has resulted in a radical change in the management of this disease with significant improvement in both quality of life and mortality. Ongoing research promises to lead to a more comprehensive understanding of the genetics, etiology, and pathogenesis of pulmonary arterial hypertension, which may ultimately translate into more effective therapeutic options.

journal_name

South Med J

journal_title

Southern medical journal

authors

LaRaia AV,Waxman AB

doi

10.1097/SMJ.0b013e31802f2ff1

subject

Has Abstract

pub_date

2007-04-01 00:00:00

pages

393-9

issue

4

eissn

0038-4348

issn

1541-8243

journal_volume

100

pub_type

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