Article Text

Download PDFPDF
Validation of the definition of rheumatoid arthritis flare based on SDAI and CDAI in clinical practice in two French independent cohorts
  1. Jérôme Avouac,
  2. Sophie Hecquet,
  3. Marion Thomas,
  4. Alice Combier,
  5. Sandrine Carvès,
  6. Yannick Allanore
  1. Service de Rhumatologie, Hôpital Cochin, AP-HP. Centre - Université Paris Cité, Paris, Île-de-France, France
  1. Correspondence to Professor Jérôme Avouac, Service de Rhumatologie, Hôpital Cochin, AP-HP. Centre - Université Paris Cité, Paris, France; javouac{at}me.com

Statistics from Altmetric.com

New definitions for flares in rheumatoid arthritis (RA) based on the Simplified and Clinical Disease Activity Indices (SDAI, CDAI) have been recently introduced.1 In this article, the authors defined flare as an absolute increase of 4.7 in SDAI and 4.5 in CDAI. Following this proposal we aimed at studying these cut-off values for absolute increases in SDAI and CDAI in diagnosing self-reported flares and treatment escalation in two separate real-world cohorts of patients with RA in France.

The first cohort included 101 patients with established RA,2 recruited between May 2016 and February 2018 and annually evaluated in day hospitalisation (table 1). We collected data from their initial visit and their 12-month follow-up. The second cohort consisted of 272 patients with established RA in remission or low disease activity, defined by SDAI ≤11 and CDAI ≤10. Among these patients, 73 had a second visit with data available 6.5±2 months after the first visit (table 1). Self-reported flares were reported in the first cohort and defined as a worsening in RA accompanied by at least one swollen and tender joint, as perceived by the patient. Treatment …

View Full Text

Footnotes

  • Handling editor Dimitrios T Boumpas

  • Contributors Study design: JA, YA. Data Acquisition: JA, MT, AC, SH, SC. Data analysis: JA. Writing/drafting and revisiting the manuscript: JA, YA. Final Approval of the manuscript: JA, MT, AC, SH, SC, YA.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.