Korean Guidelines for the Diagnosis and Management of Interstitial Lung Diseases: Hypersensitivity Pneumonitis

Hypersensitivity pneumonitis (HP) is characterized as an immune-mediated interstitial lung disease with heterogeneous clinical manifestations and presents complex diagnostic challenges. This clinical guideline provides a comprehensive framework for diagnosing and managing HP, accentuating the evolving classification into fibrotic and nonfibrotic subtypes. By integrating current clinical guidelines and expert consensus, it addresses essential aspects such as radiologic and histopathologic findings, diagnostic strategies, and pharmacologic management. Tailored to the healthcare context in Korea, this guideline presents clinicians with a structured approach to diagnose and manage HP, considering regional variations in antigen exposure and clinical presentation. The recommendations are based on both international and local data, aiming to enhance outcomes for Korean patients through timely and accurate diagnosis, individualized treatment plans, and meticulous monitoring.

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Publication Details

Journal
Tuberculosis & respiratory diseases
Published
2025-03-06
DOI
https://doi.org/10.4046/trd.2024.0190
Citations
1
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
1.52
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article

Korean Guidelines for the Diagnosis and Management of Interstitial Lung Diseases: Hypersensitivity Pneumonitis

Jinkyeong Park, Sooim Sin, Byoung Soo Kwon, Hongseok Yoo et al.
1 citations
Tuberculosis & respiratory diseases
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
article

Korean Guidelines for the Diagnosis and Management of Interstitial Lung Diseases: Hypersensitivity Pneumonitis

Jinkyeong Park, Sooim Sin, Byoung Soo Kwon, Hongseok Yoo, Beomsu Shin, Kyung-Hoon Kim, Yong Hyun Kim
article en
1 citations

Abstract

Hypersensitivity pneumonitis (HP) is characterized as an immune-mediated interstitial lung disease with heterogeneous clinical manifestations and presents complex diagnostic challenges. This clinical guideline provides a comprehensive framework for diagnosing and managing HP, accentuating the evolving classification into fibrotic and nonfibrotic subtypes. By integrating current clinical guidelines and expert consensus, it addresses essential aspects such as radiologic and histopathologic findings, diagnostic strategies, and pharmacologic management. Tailored to the healthcare context in Korea, this guideline presents clinicians with a structured approach to diagnose and manage HP, considering regional variations in antigen exposure and clinical presentation. The recommendations are based on both international and local data, aiming to enhance outcomes for Korean patients through timely and accurate diagnosis, individualized treatment plans, and meticulous monitoring.

Tuberculosis & respiratory diseasesVol. 88(3)
Gachon University (KR), Samsung Medical Center (KR), Seoul National University Bundang Hospital (KR), Gachon University Gil Medical Center (KR), The Catholic University of Korea Incheon St. Mary's Hospital (KR), St. Mary's Hospital (US), The Catholic University of Korea Bucheon St. Mary's Hospital (KR), National Medical Center (KR), Kyung Hee University Hospital at Gangdong (KR), Sungkyunkwan University (KR), Catholic University of Korea (KR)
Good health and well-being
Openalex Percentile: Top 21%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
1.52
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