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Korean guidelines for diagnosis and management of interstitial lung diseases: Part 2. Idiopathic pulmonary fibrosis

Title
Korean guidelines for diagnosis and management of interstitial lung diseases: Part 2. Idiopathic pulmonary fibrosis
Authors
Lee S.H.Yeo Y.Kim T.-H.Lee H.L.Lee J.H.Park Y.B.Park J.S.Kim Y.H.Song J.W.Jhun B.W.Kim H.J.Park J.Uh S.-T.Kim Y.W.Kim D.S.Park M.S.
Ewha Authors
이진화
SCOPUS Author ID
이진화scopus
Issue Date
2019
Journal Title
Tuberculosis and Respiratory Diseases
ISSN
1738-3536JCR Link
Citation
Tuberculosis and Respiratory Diseases vol. 82, no. 2, pp. 102 - 117
Keywords
DiagnosisDisease ManagementIdiopathic Pulmonary FibrosisKorea
Publisher
Korean National Tuberculosis Association
Indexed
SCOPUS; KCI scopus
Document Type
Review
Abstract
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrosing interstitial pneumonia, which presents with a progressive worsening dyspnea, and thus a poor outcome. The members of the Korean Academy of Tuberculosis and Respiratory Diseases as well as the participating members of the Korea Interstitial Lung Disease Study Group drafted this clinical practice guideline for IPF management. This guideline includes a wide range of topics, including the epidemiology, pathogenesis, risk factors, clinical features, diagnosis, treatment, prognosis, and acute exacerbation of IPF in Korea. Additionally, we suggested the PICO for the use of pirfenidone and nintendanib and for lung transplantation for the treatment of patients with IPF through a systemic literature review using experts’ help in conducting a meta-analysis. We recommend this guideline to physicians, other health care professionals, and government personnel in Korea, to facilitate the treatment of patients with IPF. Copyright © 2019 The Korean Academy of Tuberculosis and Respiratory Diseases.
DOI
10.4046/trd.2018.0091
Appears in Collections:
의과대학 > 의학과 > Journal papers
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