Evidence map›Paper›PMID 41238359›Full record

ArticleBMJ open2025

Early-stage cost-utility analysis of novel diagnostic tests for giant cell arteritis: a modelling study in UK secondary care.

Miaoqing Yang, Paola Cocco, Sarah L Mackie, Ann W Morgan

Abstract read
In one paragraph

Article in BMJ 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.

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1 · What the graph read from it

What it found

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2 · The registry

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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

4 authors.

Miaoqing YangSchool of Medicine, University of Leeds, Leeds, UK.ORCID http://orcid.org/0000-0001-7975-374X
Paola CoccoSchool of Medicine, University of Leeds, Leeds, UK.
Sarah L MackieSchool of Medicine, University of Leeds, Leeds, UK.
Ann W MorganSchool of Medicine, University of Leeds, Leeds, UK a.w.morgan@leeds.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo identify the key characteristics required for hypothetical diagnostic tests to be cost-effective for diagnosing giant cell arteritis (GCA).

designCombined decision tree and Markov cohort state-transition models were used to evaluate the cost-utility of new diagnostic tests compared with the standard pathways of biopsy and clinical judgement, with and without ultrasound. Input parameters were derived from secondary data and expert opinions. The analysis adopted a lifetime horizon and the UK National Health Service (NHS) perspective, using a willingness-to-pay threshold of £20 000 per quality-adjusted life year (QALY). Bivariate deterministic sensitivity analyses identified the maximum test price at varying diagnostic performance levels, and probabilistic sensitivity analyses over 5000 simulations provided 95% CIs.

settingUK.

participantsPatients with symptoms suggestive of GCA.

main outcome measurePercentage of GCA-related and glucocorticoid-related complications avoided, maximum test price and incremental QALYs at each sensitivity and specificity combination.

resultsA biomarker test incorporated into a hypothetical diagnostic pathway with perfect accuracy (100% sensitivity and specificity) can be priced up to £7245 (95% CI £5763 to £8727) and remain cost-effective compared with a standard pathway of temporal artery biopsy and clinical judgement. Against a standard pathway including ultrasound, the biomarker test can be priced up to £8606 (£6741 to £10 471). The test's value was more strongly influenced by improvements in specificity than in sensitivity. The maximum prices decreased with earlier starting age, lower clinician adherence, shorter time horizons and shorter durations of glucocorticoid-related effects.

conclusionsThe study highlights the potential for hypothetical tests to improve GCA diagnosis and reduce glucocorticoid toxicity, while demonstrating their market viability for use within the NHS. It also illustrates how early-stage economic models can provide valuable insights into potential cost-effectiveness to inform the test development process.

Indexed as

Giant Cell ArteritisSecondary Health CareBiomarkersBiopsyCost-Benefit AnalysisDecision TreesFemaleHumansMarkov ChainsQuality-Adjusted Life YearsSensitivity and SpecificityState MedicineUltrasonographyUnited KingdomBiomarkersHEALTH ECONOMICSRare DiseasesRheumatology

Identifiers

PMID41238359
PMCPMC12625940

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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.