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DOI 10.1016/j.semarthrit.2024.152385

Медицинская библиотека · Seminars in arthritis and rheumatism · 2024

Identification of outcome domains in primary Sjögren's disease: A scoping review by the OMERACT Sjögren disease working group.

Nguyen Yann, Beydon Maxime, Foulquier Nathan, Gordon Rachael, Bouillot Coralie, Hammitt Katherine M, Bowman Simon J, Mariette Xavier, McCoy Sara S, Cornec Divi, Seror Raphaèle

СтатьяScoping ReviewПеревод пока не подготовлен

Аннотация

OBJECTIVES

Sjögren's disease (SjD) is a heterogenous disease with a wide range of manifestations, ranging from symptoms of dryness, fatigue, and pain, to systemic involvement. Considerable advances have been made to evaluate systemic activity or patient-reported outcomes, but most of the instruments were not able to assess all domains of this multifaceted disease. The aim of this scoping review was to generate domains that have been assessed in randomized controlled trials, as the first phase of the Outcome Measures in Rheumatology (OMERACT) process of core domain set development.

METHODS

We systematically searched Medline (Pubmed) and EMBASE between 2002 and March 2023 to identify all randomized controlled trials assessing relevant domains, using both a manual approach and an artificial intelligence software (BIBOT) that applies natural language processing to automatically identify relevant abstracts. Domains were mapped to core areas, as suggested by the OMERACT 2.1 Filter.

RESULTS

Among the 5,420 references, we included 60 randomized controlled trials, focusing either on overall disease manifestations (53%) or on a single organ/symptom: dry eyes (17%), xerostomia (15%), fatigue (12%), or pulmonary function (3%). The most frequently assessed domains were perceived dryness (52% for overall dryness), fatigue (57%), pain (52%), systemic disease activity (45%), lacrimal gland function (47%) and salivary function (55%), B-cell activation (60%), and health-related quality of life (40%).

CONCLUSION

Our scoping review highlighted the heterogeneity of SjD, in the study designs and domains. This will inform the OMERACT SjD working group to select the most appropriate core domains to be used in SjD clinical trials and to guide the future agenda for outcome measure research in SjD.

Для цитирования: Nguyen Yann, Beydon Maxime, Foulquier Nathan, Gordon Rachael, Bouillot Coralie, Hammitt Katherine M, Bowman Simon J, Mariette Xavier, McCoy Sara S, Cornec Divi, Seror Raphaèle. Identification of outcome domains in primary Sjögren's disease: A scoping review by the OMERACT Sjögren disease working group.. Seminars in arthritis and rheumatism. 2024. DOI: 10.1016/j.semarthrit.2024.152385.

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