Article Text
Abstract
Objectives To assess if the Juvenile Arthritis Disease Activity Score (JADAS71) could be used to correctly identify patients with juvenile idiopathic arthritis (JIA) in need of antitumour necrosis factor therapy (anti-TNF) therapy 3 and 6 months after start of methotrexate (MTX).
Methods Monocentric retrospective cohort study from 2011 to 2015 analysing all patients with oligoarticular JIA (OJIA) (n=39) and polyarticular course JIA (PJIA) (n=74) first starting MTX. Three and 6 months after MTX start, clinical and laboratory features and the 2011 American College of Rheumatology (ACR) JIA treatment recommendations (ACR clinical practice guideline (ACR-CPG)) were compared between groups starting and not starting anti-TNF therapy. The sensitivity and specificity of the ACR-CPG, JADAS71 and the clinical JADAS to identify non-responders after 12 months were calculated.
Results Physicians escalated patients with significantly higher physician global assessment, clinical JADAS (cJADAS) and patient Visual Analogue Scale (VAS). The decision not to escalate was correct in 70%–75% as shown by MTX response. The implementation of the ACR-CPG would increase the current anti-TNF use from 12% to 65%. The use of (c)JADAS in identifying patients in need of anti-TNF therapy outperformed the ACR-CPG with a much higher sensitivity, specificity and accuracy. The cJADAS threshold for treatment escalation at month 3 and 6 was >5 and >3 for OJIA and >7 and >4 for PJIA, respectively. The performance of the cJADAS decreased when the patient VAS contribution to the total score was restricted and overall did not improve by adding the erythrocyte sedimentation rate.
Conclusions The cJADAS identifies patients in need of anti-TNF and is a user-friendly tool ready to be used for treat to target in JIA. The patient VAS is a critical item in the cJADAS for the decision to escalate to anti-TNF.
- juvenile idiopathic arthritis
- treatment
- anti-TNF
- disease activity
- patient perspective
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Footnotes
Handling editor Tore K Kvien
Contributors JFS, NMW and SdR planned the study. JFS and NMW shaped the electronic medical records in such a way that meaningful data could be extracted. SdR built the research data platform used for the analyses of this study. JFS checked 100% of the data from the research data platform with the source (electronic medical records). JFS, EHPvD and SdR analysed the data. JFS wrote the manuscript. EHPvD, NMW and SdR critically reviewed and edited the manuscript before submission. All authors contributed substantially to discussion of content.
Funding This study was supported by Pfizer (grant no WI189796) and by the Dutch Arthritis Foundation (Reumafonds) grant RF 901.
Competing interests None declared.
Ethics approval Utrecht Medical Ethical Committee.
Provenance and peer review Not commissioned; externally peer reviewed.