Evidence map›Paper›PMID 39718801›Full record

ArticleRheumatology (Oxford, England)2025

Association of patient- and hospital-level predictors with patterns of initial treatment in patients with rheumatoid arthritis: findings from a national cohort study.

Zijing Yang, Edward Alveyn, Mark Russell, Katie Bechman, Callum Coalwood, Elizabeth Price, Abhishek Abhishek, Sam Norton, James Galloway

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Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Zijing YangDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.
Edward AlveynDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.
Mark RussellDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID 0000-0001-8171-7772
Katie BechmanDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.
Callum CoalwoodBritish Society for Rheumatology, Bride House, London, UK.
Elizabeth PriceDepartment of Rheumatology, Great Western Hospital NHS Foundation Trust, Swindon, UK.ORCID 0000-0003-3042-0201
Abhishek AbhishekThe University of Nottingham, Nottingham NIHR-BRC, Nottingham, UK.ORCID 0000-0003-0121-4919
Sam NortonDepartment of Inflammation Biology, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID 0000-0003-1714-9963
James GallowayDepartment of Inflammation Biology, Centre for Rheumatic Diseases, King's College London, London, UK.ORCID 0000-0002-1230-2781

Funding

AbbVieNIHR
6 · The paper itself

Abstract

objectivesTo update the first-line conventional synthetic DMARDs (csDMARDs) prescribing pattern, describe change and variation across demographical and geographical factors in the RA population, and identify individual and hospital factors associated with it.

methodsThis retrospective cohort study included newly diagnosed RA adult patients from 1 May 2018 to 1 April 2023 in the UK. We used adjusted multinomial logistic regression with random effect to explore associations with different first-line csDMRAD prescription and to account for hospital-level clustering.

resultsWe identified 15 462 RA patients who received csDMARD treatment. Overall, 57% received MTX monotherapy and 14% received MTX combination therapy as first-line treatment. MTX is the most frequently medication, following by HCQ and SSZ. Compared with non-MTX prescription, prescription of MTX monotherapy [adjusted odds ratio (aOR) 1.25 95% CI (1.22-1.29)] and MTX combination therapy [aOR 1.45 (1.38-1.52)] was significantly higher in patients with higher DAS28, but lower in the non-White individuals with comorbidities: lung disease, cancer, fracture and heart attack. Among those who received MTX, monotherapy is more likely be prescribed in patients with higher DAS28 [aOR 1.08 (1.05-1.11)] and without lung disease [aOR 0.5 (0.44-0.56)], compared with combination therapy. Around 20% of the variability in first-line csDMARD prescribing was attributed to the hospital level.

conclusionIn this cohort study of new-onset RA population, both individual- and institution-level variation in first-line csDMARD treatment strategy was evident. Gender, ethnicity, disease activity, and comorbidities, especially lung disease, were associated with disparities at the individual level.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidMethotrexatePractice Patterns, Physicians'AdultAgedCohort StudiesDrug Therapy, CombinationFemaleHumansMaleMiddle AgedRetrospective StudiesUnited KingdomAntirheumatic AgentsMethotrexateconventional synthetic disease-modifying antirheumatic drugsmethotrexaterheumatoid arthritistreatment strategy

Identifiers

PMID39718801
PMCPMC12107036

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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.