Incidence of idiopathic pulmonary fibrosis in Korea based on the
2011 ATS/ERS/JRS/ALAT statement
- Author(s)
- J. Gjonbrataj; W-I. Choi; Y. E. Bahn; B. H. Rho; J. J. Lee; C. W. Lee
- Keimyung Author(s)
- Choi, Won Il; Rho, Byung Hak
- Department
- Dept. of Internal Medicine (내과학)
Dept. of Radiology (영상의학)
- Journal Title
- International Journal of Tuberculosis and Lung Disease
- Issued Date
- 2015
- Volume
- 19
- Issue
- 6
- Abstract
- O B J E C T IVE : To estimate the annual incidence rate of
interstitial lung disease (ILD) and idiopathic pulmonary
fibrosis (IPF) in Korea.
D E S I G N : A retrospective cohort design using the Korean
Health Insurance Review and Assessment Service
(HIRA) database spanned the period from January
2008 to December 2012. Patients with ILD and IPF
were identified based on the International Classification
of Disease-10 (ICD-10) diagnosis and procedure codes.
Definition 1 is code J84 (ILD); Definition 2 is code J84
plus high-resolution computed tomography (HRCT),
bronchoalveolar lavage (BAL) or lung biopsy; Definition
3 is code J84.1 (ILD with fibrosis); Definition 4 is code
J84.1 and HRCT, BAL or lung biopsy; and Definition 5
is code J84.1A (IPF), and was specifically implemented
for IPF.
RESULTS : The incidence rates of ILD per 100 000
population based on Definitions 1–5 were respectively
48.5, 32.2, 16.2, 11.4 and 1.7.
CONCLUSION: The incidence of ILD with fibrosis was
approximately 23% of overall ILD incidence. IPF
incidence was approximately 10% of the incidence of
ILD with fibrosis. Based on the new ATS/ERS/JRS/
ALATstatement published in 2011, the incidence rate of
IPF was 1.7/100 000.
KEY WORD S : epidemiology; IPF; interstitial lung disease;
usual interstitial pneumonia
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