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ERS/EULAR clinical practice guidelines for connective tissue disease-associated interstitial lung disease

Katerina M. Antoniou, Oliver Distler, Ana-Maria Gheorghiu, Catharina C. Moor, Jens Vikse, Nikoleta Bizymi, Ilaria Galetti, Graham Brown, Elena Bargagli, Yannick Allanore, Tamera J. Corte, Philippe Dieudé, Vincent Cottin, Benjamin A. Fisher, Aurelie Fabre, Jon T. Giles, Michael Kreuter, Ingrid E. Lundberg, Venerino Poletti, Britta Maurer, Elisabetta A. Renzoni, Ulf Müller-Ladner, Mary E. Strek, Nicola Sverzellati, Paul Studenic, Jibril Mohammed, Blin Nagavci, Tanja Stamm, Thomy Tonia, Bruno Crest

Year:

2025

Type:

Clinical practice guidelines

Produced by:

ERS / EULAR

DOI: https://doi.org/10.1183/13993003.02533-2024

Background

Interstitial lung disease (ILD) is a frequent manifestation of connective tissue diseases (CTDs) and is associated with high morbidity and mortality. Clinical practice guidelines to standardise screening, diagnosis, treatment and follow-up for CTD-ILD are of high importance for optimised patient care.

Methods

A European Respiratory Society and European Alliance of Associations for Rheumatology task force committee, composed of pulmonologists, rheumatologists, pathologists, radiologists, methodologists and patient representatives, developed recommendations based on PICO (Patients, Intervention, Comparison, Outcomes) questions with grading of the evidence according to the GRADE (Grading of Recommendations, Assessment, Development and Evaluations) methodology and complementary narrative questions agreed on by both societies. For both PICO and narrative questions, the Evidence to Decision framework was used to formulate the recommendations.

Results

The task force committee concluded with recommendations for 25 PICO and 28 narrative questions, regarding ILD in the context of systemic sclerosis, rheumatoid arthritis (RA), idiopathic inflammatory myopathies, Sjögren disease (SjD), systemic lupus erythematosus (SLE) and mixed connective tissue disease (MCTD). In four narrative questions, regarding screening and assessment of risk for ILD progression in MCTD, SjD and SLE and one PICO question regarding pirfenidone in CTD-ILD other than RA-ILD, the task force had insufficient evidence to support recommendations. Screening, diagnostic, monitoring and treatment algorithms were developed based on the recommendations and usual clinical practice.

Conclusions

We provide practical guidance by evidence-based recommendations to clinicians for each of the CTDs. In many cases there is low certainty or absence of evidence and we encourage further research to fill these gaps.

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