Clinical course and prediction of survival in idiopathic pulmonary fibrosis.

Abstract:

:Idiopathic pulmonary fibrosis (IPF) is a progressive, life-threatening, interstitial lung disease of unknown etiology. The median survival of patients with IPF is only 2 to 3 years, yet some patients live much longer. Respiratory failure resulting from disease progression is the most frequent cause of death. To date we have limited information as to predictors of mortality in patients with IPF, and research in this area has failed to yield prediction models that can be reliably used in clinical practice to predict individual risk of mortality. The goal of this concise clinical review is to examine and summarize the current data on the clinical course, individual predictors of survival, and proposed clinical prediction models in IPF. Finally, we will discuss challenges and future directions related to predicting survival in IPF.

authors

Ley B,Collard HR,King TE Jr

doi

10.1164/rccm.201006-0894CI

subject

Has Abstract

pub_date

2011-02-15 00:00:00

pages

431-40

issue

4

eissn

1073-449X

issn

1535-4970

pii

201006-0894CI

journal_volume

183

pub_type

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