Diagnosis and Treatment of Hypersensitivity Pneumonitis: S2k Guideline of the German Respiratory Society and the German Society for Allergology and Clinical Immunology

German recommendations for the diagnosis of hypersensitivity pneumonitis (HP), also known as extrinsic allergic alveolitis, were last published in 2007. The current S2k Guideline for the Diagnosis and Treatment of Hypersensitivity Pneumonitis replaces these diagnostic recommendations. They were supplemented by the aspect of chronic, and in particular of the chronic fibrotic phenotype of HP, and also, as the first HP guideline, include treatment recommendations. Based on current scientific evidence and on expert opinion, 12 consensus recommendations were developed. They include important statements summarizing the diagnostic process, the treatment indication and therapeutic strategies for patients with HP. Particular emphasis was placed on the different clinical courses (acute and chronic) and their characteristics (inflammatory and/or fibrotic pattern), which present differential diagnostic challenges and ultimately result in different treatment approaches. In addition to general information (diagnosis, classification, clinical disease course, epidemiology, pathogenesis, risk factors, prognosis, and special aspects associated with occupational disease), the guideline will present the various clinical disease entities of HP, some in detail, others in tabular form. A major focus is on the various diagnostic steps and the different treatment approaches. The background information serves to provide a deeper understanding and inform the implementation of the recommendations. In particular, other current international guidelines for the diagnosis of HP as well as German guidelines for the diagnosis of interstitial lung diseases (ILDs) (Leitlinien zur Diagnostik interstitieller Lungenerkrankungen) in general and for the pharmacotherapy of fibrotic ILDs were integrated and considered in this guideline.

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Journal
Respiration
Published
2025-01-27
DOI
https://doi.org/10.1159/000543675
Citations
5
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
7.59

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article

Diagnosis and Treatment of Hypersensitivity Pneumonitis: S2k Guideline of the German Respiratory Society and the German Society for Allergology and Clinical Immunology

Michael Kreuter, Dennis Nowak, Okka W. Hamer, Dirk Theegarten et al.
5 citations
Respiration
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
7.59
article

Diagnosis and Treatment of Hypersensitivity Pneumonitis: S2k Guideline of the German Respiratory Society and the German Society for Allergology and Clinical Immunology

Michael Kreuter, Dennis Nowak, Okka W. Hamer, Dirk Theegarten, Francesco Bonella, Gabriela Leuschner, Markus Berger, Monika Raulf, Jens Schreiber, B. Rehbock, Danny Jonigk, Jürgen Behr, Marcus Joest, D. Koschel, H. Sitter, Ulrich Costabel
article en
5 citations

Abstract

German recommendations for the diagnosis of hypersensitivity pneumonitis (HP), also known as extrinsic allergic alveolitis, were last published in 2007. The current S2k Guideline for the Diagnosis and Treatment of Hypersensitivity Pneumonitis replaces these diagnostic recommendations. They were supplemented by the aspect of chronic, and in particular of the chronic fibrotic phenotype of HP, and also, as the first HP guideline, include treatment recommendations. Based on current scientific evidence and on expert opinion, 12 consensus recommendations were developed. They include important statements summarizing the diagnostic process, the treatment indication and therapeutic strategies for patients with HP. Particular emphasis was placed on the different clinical courses (acute and chronic) and their characteristics (inflammatory and/or fibrotic pattern), which present differential diagnostic challenges and ultimately result in different treatment approaches. In addition to general information (diagnosis, classification, clinical disease course, epidemiology, pathogenesis, risk factors, prognosis, and special aspects associated with occupational disease), the guideline will present the various clinical disease entities of HP, some in detail, others in tabular form. A major focus is on the various diagnostic steps and the different treatment approaches. The background information serves to provide a deeper understanding and inform the implementation of the recommendations. In particular, other current international guidelines for the diagnosis of HP as well as German guidelines for the diagnosis of interstitial lung diseases (ILDs) (Leitlinien zur Diagnostik interstitieller Lungenerkrankungen) in general and for the pharmacotherapy of fibrotic ILDs were integrated and considered in this guideline.

RespirationVol. 104(7)
Witten/Herdecke University (DE), Philipps University of Marburg (DE), Johannes Gutenberg University Mainz (DE), Federal Institute for Risk Assessment (DE), LMU Klinikum (DE), University Hospital Regensburg (DE), Ruhrlandklinik (DE), University Medical Center of the Johannes Gutenberg University Mainz (DE), Essen University Hospital (DE), Institute for Prevention and Occupational Medicine (DE), Center for Assessment (US), Kliniken der Stadt Köln (DE), German Center for Lung Research (DE), University Hospital Magdeburg (DE), Klinik Donaustauf (DE), Helios Kliniken (DE), Institut für Soziale Arbeit (DE), University Hospital Carl Gustav Carus (DE), Ludwig-Maximilians-Universität München (DE), RWTH Aachen University (DE)
Bristol-Myers Squibb, Pfizer, AstraZeneca, Sanofi, United Therapeutics Corporation, CSL Behring, aTyr, Savara Pharmaceuticals
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Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
7.59
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