Connective tissue disease-associated interstitial lung diseases (CTD-ILD) - Report from OMERACT CTD-ILD working group

Dinesh Khanna, Shikha Mittoo, Rohit Aggarwal, Susanna M. Proudman, Nicola Dalbeth, Eric L. Matteson, Kevin Brown, Kevin Flaherty, Athol U. Wells, James R. Seibold, Vibeke Strand

Research output: Contribution to journalArticlepeer-review

74 Scopus citations

Abstract

Objective. Interstitial lung disease (ILD) is common in connective tissue disease (CTD) and is the leading cause of mortality. Investigators have used certain outcome measures in randomized controlled trials (RCT) in CTD-ILD, but the lack of a systematically developed, CTD-specific index that captures all measures relevant and meaningful to patients with CTD-ILD has left a large and conspicuous gap in CTD-ILD research. Methods. The CTD-ILD working group, under the aegis of the Outcome Measures in Rheumatology (OMERACT) initiative, has completed a consensus group exercise to reach harmony on core domains and items for inclusion in RCT in CTD-ILD. During the OMERACT 12 meeting, consensus was sought on domains and core items for inclusion in RCT. In addition, consensus was pursued on a definition of response in RCT. Consensus was defined as > 75% agreement among the participants. Results. OMERACT 12 participants endorsed the domains with minimal modifications. Clinically meaningful progression for CTD-ILD was proposed as > 10% relative decline in forced vital capacity (FVC) or > 5% to < 10% relative decline in FVC and > 15% relative decline in DLCO. Conclusion. There is consensus on domains for inclusion in RCT in CTD-ILD and on a definition of clinically meaningful progression. Data-driven approaches to validate these results in different cohorts and RCT are needed.

Original languageEnglish (US)
Pages (from-to)2168-2171
Number of pages4
JournalJournal of Rheumatology
Volume42
Issue number11
DOIs
StatePublished - Nov 2015

Keywords

  • Interstitial lung disease
  • Lung diseases
  • Outcome assessment omeract

ASJC Scopus subject areas

  • Rheumatology
  • Immunology and Allergy
  • Immunology

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