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

医学 间质性肺病 肺科医生 混合性结缔组织病 未分化结缔组织病 痹症科 疾病 重症监护医学 分级(工程) 物理疗法 内科学 结缔组织病 自身免疫性疾病 工程类 土木工程
作者
Κατερίνα Αντωνίου,Oliver Distler,Ana-Maria Gheorghiu,Catharina C. Moor,Jens Vikse,Nikoleta Bizymi,Ilaria Galetti,G. R. Brown,Elena Bargagli,Yannick Allanore,Tamera J. Corte,Philippe Dieudé,Vincent Cottin,Benjamin A. Fisher,Aurélie Fabre,Jon T. Giles,Michael Kreuter,Ingrid E. Lundberg,Venerino Poletti,Britta Maurer
出处
期刊:The European respiratory journal [European Respiratory Society]
卷期号:67 (1): 2402533-2402533 被引量:26
标识
DOI:10.1183/13993003.02533-2024
摘要

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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