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KMID : 1044520190820020102
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Tuberculosis and Respiratory Diseases
2019 Volume.82 No. 2 p.102 ~ p.117
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Korean Guidelines for Diagnosis and Management of Interstitial Lung Diseases: Part 2. Idiopathic Pulmonary Fibrosis
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Lee Sang-Hoon
Yeo Yoo-Mi
Kim Tae-Hyung
Lee Hong-Lyeol
Lee Jin-Hwa
Park Yong-Bum
Park Jong-Sun
Kim Yee-Hyung
Song Jin-Woo
Jhun Byung-Woo
Kim Hyun-Jung
Park Jin-Kyeong
Uh Soo-Taek
Kim Young-Whan
Kim Dong-Soon
Park Moo-Suk
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Abstract
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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.
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KEYWORD
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Idiopathic Pulmonary Fibrosis, Diagnosis, Disease Management, Korea
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