EULAR recommendations for the treatment of systemic sclerosis: 2023 update

医学 重症监护医学 多发性硬化 物理疗法 免疫学
作者
Francesco Del Galdo,Alain Lescoat,Philip G. Conaghan,Eugenia Bertoldo,Jelena Čolić,Tânia Santiago,Yossra A. Suliman,Marco Matucci‐Cerinic,Armando Gabrielli,Oliver Distler,Anna‐Maria Hoffmann‐Vold,I. Castellví,Alexandra Balbir‐Gurman,Madelon C Vonk,L. P. Ananyeva,Simona Rednic,А. Тарасова,Pedrag Ostojic,Vladimira Boyadzhieva,Khadija El Aoufy
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:84 (1): 29-40 被引量:26
标识
DOI:10.1136/ard-2024-226430
摘要

Objectives

To update the 2017 European Alliance of Associations for Rheumatology (EULAR) recommendations for treatment of systemic sclerosis (SSc), incorporating new evidence and therapies.

Methods

An international task force was convened in line with EULAR standard operating procedures. A nominal group technique exercise was performed in two rounds to define questions underpinning a subsequent systematic literature review. The evidence derived was discussed and overarching principles, recommendations and future research agenda were iteratively developed with voting rounds.

Results

The task force agreed on 22 recommendations covering 8 clinical/organ domains including Raynaud's phenomenon, digital ulcers, pulmonary arterial hypertension, scleroderma renal crisis, skin fibrosis, interstitial lung disease (ILD), gastrointestinal manifestations and arthritis. Most new recommendations are related to skin fibrosis and ILD. These included novel recommendations for the use of mycophenolate mofetil, nintedanib, rituximab and tocilizumab for the treatment of these crucial disease manifestations. The recommendations also included first-line and second-line interventions, providing increased utility for rheumatology practitioners. Important additions to the future research agenda included consideration of novel interventions for the management of vascular, musculoskeletal and gastrointestinal manifestations and calcinosis, as well as for the local management of digital ulcers.

Conclusion

These updated recommendations include the first set of synthetic and biological targeted therapies recommended for key fibrotic manifestations of SSc as well as first-line combination treatment for newly diagnosed pulmonary artery hypertension and prioritise a new research agenda for the coming years.
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