Evidence map›Paper›PMID 40169281›Full record

ArticleRMD open2025

Patient-reported outcomes as early warning signs of flare following drug cessation in rheumatoid arthritis.

Leher Gumber, Fiona Rayner, Theophile Bigirumurame, Bernard Dyke, Andrew Melville, Sean Kerrigan, Andrew McGucken, Najib Naamane, Jonathan Prichard, Christopher D Buckley and 10 more

Abstract read
In one paragraph

Article in RMD open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Leher Gumber *Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0003-0154-1207
Fiona Rayner *Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0003-4302-0899
Theophile BigirumuramePopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Bernard DykeNIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Andrew MelvilleSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Sean KerriganSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Andrew McGuckenSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.
Najib NaamaneTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Jonathan PrichardNewcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, UK.
Christopher D BuckleyKennedy Institue for Rheumatology, University of Oxford, Oxford, UK.
Andrew FilerNIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.ORCID 0000-0001-8164-6249
Iain B McInnesSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.ORCID 0000-0002-6462-4280
Karim RazaNIHR Birmingham Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.ORCID 0000-0003-1570-1232
Stefan SiebertSchool of Infection and Immunity, University of Glasgow, Glasgow, UK.ORCID 0000-0002-1802-7311
James Ms WasonPopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Wan-Fai NgTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Amy E AndersonTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
John D IsaacsTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK john.isaacs@newcastle.ac.uk.
Kenneth F Baker *Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
Arthur G Pratt *Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDrug withdrawal in rheumatoid arthritis (RA) in remission can reduce toxicity, but with the risk of flare which requires close monitoring. We explored the potential of patient-reported outcomes (PROs) for flare detection among RA patients in sustained remission after conventional synthetic disease-modifying antirheumatic drug (csDMARD) cessation.

methodsFour PROs (Factors that Limit sustAined Remission in rhEumatoid arthritis (FLARE-RA), EuroQol-5 Dimensions (EQ5D), Routine Assessment of Patient Index Data-3 (RAPID-3) and RA Flare Questionnaire (RA-FQ)) were captured at baseline and at sequential visits until time-of-flare or end of 6-month follow-up as part of the BIO-FLARE prospective cohort study. Flare was defined as any of (i) Disease Activity Score 28 (DAS28)-C reactive protein (CRP) ≥3.2 at any visit, (ii) DAS28-CRP≥2.4 on two visits within 2 weeks or (iii) resuming DMARD and/or steroid therapy despite DAS28-CRP<2.4. Cox regression models with time-varying covariates were fitted to evaluate associations between PRO changes and likelihood of flare. Receiver-operating characteristic (ROC) curves enabled discriminatory changes in each PRO to be compared as a means of identifying flare.

results58/121 (47.9%) participants (70.1% females, mean age 64.8 years) experienced a flare. A 1-point change in each PRO score was strongly associated with flare development in the multivariate Cox regression model (p<0.001 in each case). ROC curve analysis confirmed that monitoring adverse changes in PROs from baseline offered robust discriminatory utility for identifying flare occurrence. This was most evident for RA-FQ and FLARE-RA (both areas under the curves 0.90, 95% CI 0.84 to 0.96; p=0.001); for example, an RA-FQ increment of ≥5.5 from baseline identified objective flare with positive and negative predictive values of 80% and 91%, respectively.

conclusionsOur data support the potential value of remote PRO monitoring of RA patients in drug-free remission to identify flare occurrence.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidPatient Reported Outcome MeasuresAdultAgedFemaleHumansMaleMiddle AgedProspective StudiesRemission InductionSeverity of Illness IndexSymptom Flare UpWithholding TreatmentAntirheumatic AgentsAutoimmune DiseasesPatient Reported Outcome MeasuresRheumatoid Arthritis

Identifiers

PMID40169281
PMCPMC11962807

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.