Chest
Volume 130, Issue 4, Supplement, October 2006, Page 151S
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SEVERE PULMONARY HYPERTENSION IN IDIOPATHIC PULMONARY FIBROSIS

https://doi.org/10.1378/chest.130.1.93Get rights and content

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Abstract

PURPOSE: Severe pulmonary hypertension (PH) can complicate interstitial lung disease but both the prevalence and predictors of severe PH in idiopathic pulmonary fibrosis (IPF) are unknown.

METHODS: We reviewed the records of patients with IPF listed for lung transplant (LT) in the US (Jan. 1995 and June 2004) and defined severe PH as a mean pulmonary artery (PA) pressure of > 40 mm Hg. Patients with severe PH were compared to those with normal PA pressures, and we examined multiple demographic

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