Systemic sclerosis & Raynaud's

Domain reporting in systemic sclerosis-related Raynaud's phenomenon: An OMERACT scoping review

Semin Arthritis RheumPublished Scoping review

Authors' conclusion

The outcome domains and the associated outcomes used to assess the impact of SSc-RP in research studies are broad and have varied across studies.

Study context

Population
Clinical studies of adult participants with SSc-associated raynaud's phenomenon (RP) (randomized control trials (RCTs), quasi-randomised, case-control, cohort, case series, cross-sectional), in English; Embase, MEDLINE, Cochrane CENTRAL58 studies (24 RCTs)
Outcome
Outcome domains studied and outcome measures used in clinical studies of SSc-RP
Methodological detailsOMERACT
  • OMERACT

Main finding

As reported in the abstract

Commonest outcome domains captured (number of studies)

Severity of attacks

35

Frequency of attacks

28

Duration of attacks

19

Original publication

Domain reporting in systemic sclerosis-related Raynaud's phenomenon: An OMERACT scoping review. Semin Arthritis Rheum. Published 27 April 2023. doi:10.1016/j.semarthrit.2023.152208

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