Systemic sclerosis & Raynaud's

Heterogeneity of determining disease severity, clinical course and outcomes in systemic sclerosis-associated interstitial lung disease: a systematic literature review

RMD OpenPublished Systematic literature review

Authors' conclusion

The studies presenting definitions of SSc-ILD 'progression', 'severity' and 'outcome' show a large heterogeneity.

Study context

Population
Studies of SSc-ILD recording definitions of severity, progression and outcomes342 papers included of 9054 reviewed
Participants
342 participants
Outcome
Definitions of severity, progression and outcomes recorded for SSc-ILD
Methodological detailsPRISMA guidelines, Medline, Embase, Web of Science and Cochrane Library up to 1 August 2023
  • PRISMA guidelines
  • Medline, Embase, Web of Science and Cochrane Library up to 1 August 2023

Main finding

As reported in the abstract

  • Most frequent tools: combined DLCO and forced vital capacity (FVC) changes, isolated FVC or DLCO changes, high-resolution CT (HRCT) extension, and composite algorithms (pulmonary function test, clinical signs and HRCT data)
  • Mortality (all-cause or ILD related) was the most frequently reported long-term event

Original publication

Heterogeneity of determining disease severity, clinical course and outcomes in systemic sclerosis-associated interstitial lung disease: a systematic literature review. RMD Open. Published 8 November 2023. doi:10.1136/rmdopen-2023-003426

Composed by AI from the published abstract and checked against it. How Briefs are made →

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