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Ann Intern Med. 2012 May 15;156(10):684-91. doi: 10.7326/0003-4819-156-10-201205150-00004.

A multidimensional index and staging system for idiopathic pulmonary fibrosis.

Author information

1
Department of Medicine, University of California, San Francisco, 505 Parnassus Avenue, Box 0111, San Francisco, CA 94143, USA. brett.ley@ucsf.edu

Abstract

BACKGROUND:

Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with an overall poor prognosis. A simple-to-use staging system for IPF may improve prognostication, help guide management, and facilitate research.

OBJECTIVE:

To develop a multidimensional prognostic staging system for IPF by using commonly measured clinical and physiologic variables.

DESIGN:

A clinical prediction model was developed and validated by using retrospective data from 3 large, geographically distinct cohorts.

SETTING:

Interstitial lung disease referral centers in California, Minnesota, and Italy.

PATIENTS:

228 patients with IPF at the University of California, San Francisco (derivation cohort), and 330 patients at the Mayo Clinic and Morgagni-Pierantoni Hospital (validation cohort).

MEASUREMENTS:

The primary outcome was mortality, treating transplantation as a competing risk. Model discrimination was assessed by the c-index, and calibration was assessed by comparing predicted and observed cumulative mortality at 1, 2, and 3 years.

RESULTS:

Four variables were included in the final model: gender (G), age (A), and 2 lung physiology variables (P) (FVC and Dlco). A model using continuous predictors (GAP calculator) and a simple point-scoring system (GAP index) performed similarly in derivation (c-index of 70.8 and 69.3, respectively) and validation (c-index of 69.1 and 68.7, respectively). Three stages (stages I, II, and III) were identified based on the GAP index with 1-year mortality of 6%, 16%, and 39%, respectively. The GAP models performed similarly in pooled follow-up visits (c-index ≥71.9).

LIMITATION:

Patients were drawn from academic centers and analyzed retrospectively.

CONCLUSION:

The GAP models use commonly measured clinical and physiologic variables to predict mortality in patients with IPF.

[Indexed for MEDLINE]

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