Copyright ©ERS Journals Ltd 2001 Comparison of registries of interstitial lung diseases in three European countries1 Respiratory Division, University Hospital Gasthuisberg, Leuven, Belgium, 2 Abteilung Pneumologie/Allergologie, Ruhrlandklinik, Essen, Germany, 3 Ambulatorio della Sarcoidosi, Ente Ospedale Niguarda, Milano, and 4 Dipartemento Malattie del Torace, Ospedale Bellaria Maggiore, Bologna, Italy CORRESPONDENCE: M. Demedts, UZ Gasthuisberg, Respiratory Division, Herestraat 49, B-3000, Leuven, Belgium. Fax: 32 16346803 Keywords: connective tissue disease, epidemiology, hypersensitivity pneumonitis, idiopathic pulmonary fibrosis, interstitial lung diseases, sarcoidosis
Received: March 8, 2001
These registries show some striking similarities, but also discrepancies, which in part may be real, but may also be due to selection bias. Indeed, the registries in the European countries encompass the patients seen by pulmonologists, while the registry in Bernalillo County is based on a general population study in a limited area. In addition, in some studies, prevalences and incidences were registered, while in others, only prevalences or incidences were registered. Finally, most, but not all studies were prospective.
Nonetheless, the different studies showed that sarcoidosis, idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, interstitial lung diseases due to collagen vascular diseases and not-defined (or postinflammatory) fibrosis were most frequent. In the majority of disease entities a male predominance was found. Surprisingly large differences in the use of diagnostic techniques, such as high-resolution computed tomography, bronchoalveolar lavage, open lung biopsy and transbronchial lung biopsy, were noted between the different studies.
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