Incidence of idiopathic pulmonary fibrosis in Korea based on the 2011 ATS/ERS/JRS/ALAT statement

Authors
J. GjonbratajW-I. ChoiY. E. BahnB. H. RhoJ. J. LeeC. W. Lee
Department
Dept. of Internal Medicine (내과학); Dept. of Radiology (영상의학)
Issue Date
2015
Citation
International Journal of Tuberculosis and Lung Disease, Vol.19(6) : 742-746, 2015
ISSN
1027-3719
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
URI
http://kumel.medlib.dsmc.or.kr/handle/2015.oak/35941
Appears in Collections:
1. Journal Papers (연구논문) > 1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
1. Journal Papers (연구논문) > 1. School of Medicine (의과대학) > Dept. of Radiology (영상의학)
Keimyung Author(s)
최원일; 노병학
Full Text
http://www.ingentaconnect.com/content/iuatld/ijtld/2015/00000019/00000006/art00024
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