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Published online before print December 5, 2007, 10.1183/09031936.00063706
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Eur Respir J 2008; 31:585-591
Copyright ©ERS Journals Ltd 2008

Multidisciplinary interobserver agreement in the diagnosis of idiopathic pulmonary fibrosis

M. Thomeer1,2, M. Demedts1, J. Behr3, R. Buhl4, U. Costabel5, C. D. R. Flower6, J. Verschakelen1, F. Laurent7, A. G. Nicholson8, E. K. Verbeken1, F. Capron9, M. Sardina10, G. Corvasce10, I. Lankhorst10 the Idiopathic Pulmonary Fibrosis International Group Exploring N-Acetylcysteine I Annual (IFIGENIA) study group

1 University Hospitals, Catholic University of Leuven, Leuven, and 2 East Limburg Hospital, Genk, Belgium, 3 Dept of Internal Medicine I, Grosshadern Clinic, Ludwig Maximilian University, Munich, 4 Dept of Internal Medicine III, Johannes Gutenberg University Clinic, Mainz, and 5 Dept of Respiratory Medicine, Ruhrland Clinic, Essen, Germany, 6 Evelyn Hospital, Cambridge, and 8 Royal Brompton Hospital, London, UK, 7 Cardiological Hospital, Bordeaux University Hospital, Bordeaux, and 9 Pitie-Salpetriere Hospital, Paris, France, 10 Zambon Group, Bresso, Italy.

CORRESPONDENCE: M. Thomeer, UZ Leuven, Afdeling Longziekten, Herestraat 49, B - 3000 Leuven, Belgium. Fax: 32 16346803. E-mail: michiel.thomeer{at}scarlet.be

Keywords: Idiopathic pulmonary fibrosis, kappa coefficient, lung biopsy, radiology

Received: May 11, 2006
Accepted November 21, 2007

The purpose of the present study was to evaluate the accuracy of the diagnosis of idiopathic pulmonary fibrosis (IPF) by respiratory physicians in six European countries, and to calculate the interobserver agreement between high-resolution computed tomography reviewers and histology reviewers in IPF diagnosis.

The diagnosis of usual interstitial pneumonia (UIP) was assessed by a local investigator, following the American Thoracic Society/European Respiratory Society consensus statement, and confirmed when a minimum of two out of three expert reviewers from each expert panel agreed with the diagnosis. The level of agreement between readers within each expert panel was calculated by weighted kappa.

The diagnosis of UIP was confirmed by the expert panels in 87.2% of cases. A total of 179 thoracic high-resolution computed tomography scans were independently reviewed, and an interobserver agreement of 0.40 was found. Open or thoracoscopic lung biopsy was performed in 97 patients, 82 of whom could be reviewed by the expert committee. The weighted kappa between histology readers was 0.30.

It is concluded that, although the level of agreement between the readers within each panel was only fair to moderate, the overall accuracy of a clinical diagnosis of idiopathic pulmonary fibrosis in expert centres is good (87.2%).






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Copyright © 2008 by the European Respiratory Society.