Evidence map›Paper›PMID 32907801›Full record

Trial reportAnnals of the rheumatic diseases2020

Two-year cost effectiveness between two gradual tapering strategies in rheumatoid arthritis: cost-utility analysis of the TARA trial.

Elise van Mulligen, Angelique E Weel, Tjallingius Martijn Kuijper, N H A M Denissen, Andreas H Gerards, Mike H de Jager, Wai-Kwan Lam-Tse, J M Hazes, Annette van der Helm-van Mil, Pascal Hendrik Pieter de Jong and 1 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Annals of the rheumatic diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

10 citing papers in PubMed, 19 citations in OpenAlex.

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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

11 authors at 6 institutions in 1 country.

Elise van MulligenRheumatology, Erasmus MC, Rotterdam, The Netherlands elise.vanmulligen@erasmusmc.nl.ORCID 0000-0003-1900-790X
Angelique E WeelRheumatology, Erasmus MC, Rotterdam, The Netherlands.
Tjallingius Martijn KuijperRheumatology, Maasstad Hospital, Rotterdam, Zuid-Holland, The Netherlands.
N H A M DenissenRheumatology, Amphia Hospital, Breda, North Brabant, The Netherlands.
Andreas H GerardsRheumatology, Franciscus Gasthuis en Vlietland, Rotterdam, Zuid-Holland, The Netherlands.
Mike H de JagerRheumatology, Albert Schweitzer Hospital, Dordrecht, Zuid-Holland, The Netherlands.
Wai-Kwan Lam-TseRheumatology, Franciscus Gasthuis en Vlietland, Rotterdam, Zuid-Holland, The Netherlands.
J M HazesRheumatology, Erasmus MC, Rotterdam, The Netherlands.
Annette van der Helm-van MilRheumatology, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0001-8572-1437
Pascal Hendrik Pieter de Jong *Rheumatology, Erasmus MC, Rotterdam, The Netherlands.
Jolanda J Luime *Rheumatology, Erasmus MC, Rotterdam, The Netherlands.ORCID 0000-0002-1071-7932
Erasmus MC · NLSint Franciscus Gasthuis · NLAlbert Schweitzer Ziekenhuis · NLAmphia Ziekenhuis · NLLeiden University Medical Center · NLMaasstad Ziekenhuis · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of the current study was to evaluate the 2-year cost-utility ratio between tapering conventional synthetic disease-modifying antirheumatic drugs (csDMARD) first followed by the tumour necrosis factor (TNF)-inhibitor, or vice versa, in patients with rheumatoid arthritis (RA).

methodsTwo-year data of the Tapering strategies in Rheumatoid Arthritis trial were used. Patients with RA, who used both a csDMARD and a TNF-inhibitor and had a well-controlled disease (disease activity score ≤2.4 and swollen joint count≤1) for at least 3 months, were randomised into gradual tapering the csDMARD first followed by the TNF-inhibitor, or vice versa. Quality-adjusted life years (QALYs) were derived from the European Quality of life questionnaire with 5 dimensions. Healthcare and productivity costs were calculated with data from patient records and questionnaires. The incremental cost-effectiveness ratio and the incremental net monetary benefit were used to assess cost effectiveness between both tapering strategies.

results94 patients started tapering their TNF-inhibitor first, while the other 95 tapered their csDMARD first. QALYs (SD) were, respectively, 1.64 (0.22) and 1.65 (0.22). Medication costs were significantly lower in the patients who tapered the TNF-inhibitor first, while indirect cost were higher due to more productivity loss (p=0.10). Therefore, total costs (SD) were €38 833 (€39 616) for tapering csDMARDs first, and €39 442 (€47 271) for tapering the TNF-inhibitor (p=0.88). For willingness-to-pay (WTP) levels <€83 800 tapering, the csDMARD first has the highest probability of being cost effective, while for WTP levels >€83 800 tapering the TNF-inhibitor first has the highest probability.

conclusionOur economic evaluation shows that costs are similar for both tapering strategies. Regardless of the WTP, tapering either the TNF-inhibitor or the csDMARD first is equally cost effective. TRIAL REGISTRATION NUMBER: NTR2754.

Indexed as

Cost-Benefit AnalysisAdultAgedAntirheumatic AgentsArthritis, RheumatoidFemaleHumansMaleMiddle AgedQuality-Adjusted Life YearsSingle-Blind MethodSymptom Flare UpTreatment OutcomeTumor Necrosis Factor InhibitorsAntirheumatic AgentsTumor Necrosis Factor Inhibitorseconomicshealth caremethotrexateoutcome assessmentrheumatoid arthritistumour necrosis factor inhibitors

Identifiers

PMID32907801
PMCPMC7677489
OpenAlexW3042161981

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.