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Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 2. Idiopathic Pulmonary Fibrosis

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Affiliated Author(s)
김현정
Alternative Author(s)
Kim, Hyun Jung
Journal Title
Tuberculosis and Respiratory Diseases
ISSN
2005-6184
Issued Date
2019
Keyword
Idiopathic Pulmonary FibrosisDiagnosisDisease ManagementKorea
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.
Department
Dept. of Internal Medicine (내과학)
Publisher
School of Medicine (의과대학)
Citation
Sang Hoon Lee et al. (2019). Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 2. Idiopathic Pulmonary Fibrosis. Tuberculosis and Respiratory Diseases, 82(2), 102–117. doi: 10.4046/trd.2018.0091
Type
Article
ISSN
2005-6184
DOI
10.4046/trd.2018.0091
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/41949
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
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