M. Roelandt et al., EPIDEMIOLOGY OF INTERSTITIAL LUNG-DISEASE (ILD) IN FLANDERS - REGISTRATION BY PNEUMOLOGISTS IN 1992-1994, Acta Clinica Belgica, 50(5), 1995, pp. 260-268
Worldwide almost no epidemiologic data are available on the prevalence
or incidence of interstitial lung diseases (ILD) in the general popul
ation. Therefore, a registration programme of ILD-prevalence was organ
ised by the VRGT (Vereniging voor Respiratoire Gezondheidszorg en Tube
rculosebestrijding), among about 100 Flemish pneumologists since 1990.
Most categories of the classification by Crystal et al. (1) were incl
uded and the diagnostic criteria (histology, laboratory tests, clinic,
radiology) were registered. The present paper presents the results of
1992-1994: twenty pneumologists had forwarded the summary files of 23
7 patients to the central office in 1992 (n=68), 1993 (n=90) and 1994
(n=79). The diagnoses that were most frequently made were: sarcoidosis
in 27%, idiopathic pulmonary fibrosis in 20%, hypersensitivity pneumo
nitis in 14% (of which 68% by birds) and collagen-vascular disease in
10% (of which 54% in rheumatoid arthritis). Less frequent causes were
eosinophilic pneumonia (4%), inhalation of inorganic material (4%, ant
hracosilicosis being excluded), histiocytosis X (3%), drugs (3%), angi
itis and granulomatosis (2%), pulmonary hemosiderosis (1%), lymphocyti
c infiltrative lung disease (1%) and lymphangioleiomyomatosis (1%). Th
e order of relative frequencies of the different categories of disease
s was the same in the 3 registration years. In 9% of the patients the
diagnosis was confined to ''undefined fibrosis''. The diagnosis was co
nfirmed by histology in 63% of the cases. The overall male-female rati
o was nearly one, with, however, a male preponderance in hypersensitiv
ity pneumonitis (22/12), UIP(8/3) and ''undefined fibrosis'' (14/7). A
ll age groups were represented but 65% of the patients were over 50 ye
ars old. Analysis of the postal codes showed following regional distri
bution (for the whole study period): 51 patients lived in Flemish Brab
ant, 111 in Antwerp, 31 in Limburg, 24 in East-Flanders, and 13 in Wes
t-Flanders. Although this registration undoubtedly underestimates the
real prevalence of interstitial lung diseases and may contain some bia
s due to different approaches among the participating centers (despite
the instructions in the protocol), it provides important information
on the relative frequency of the different forms.