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Impact of point-of-care high-sensitivity troponin testing on index admission and 30-day costs: secondary analysis of a randomised controlled trial

I. V. L. Thulin S. M. F. Jordalen J. J. Gangstoe J. Krishnapillai O. C. Lekven R. Body P. Collinson F. Apple L. Cullen T. M. Norekval T. Wisloff K. Vikenes R. O. Bjorneklett T. Omland K. M. Aakre
Oct 2026 · European Heart Journal · 0 citations

Abstract

Point-of-care (POC) high-sensitivity cardiac troponin (hs-cTn) assays provide rapid turnaround times and are increasingly considered for use within guideline recommended 0/1-hour accelerated diagnostic protocols (ADPs). However, higher per-test costs raise concerns regarding overall economic impact. Randomised evaluations of real-world implementation remain limited. To assess the effect of implementing POC hs-cTnI testing within a 0/1-hour ADP on total index admission costs and 30-day specialist care costs. This pre-specified secondary analysis of a single-centre randomised controlled trial included 1,494 adults presenting with suspected acute coronary syndrome. Participants were randomised 1:1 to 0/1-hour POC hs-cTnI testing or central laboratory hs-cTnT testing. Costs were estimated from the healthcare provider perspective using Norwegian patient-level costing and Diagnosis-Related Group frameworks. Resource use was extracted from electronic hospital records. Unadjusted mean cost differences were estimated using non-parametric bootstrap resampling. To account for potential confounders, a generalised linear model with gamma distribution and log link was fitted, adjusting for age, sex, adjudicated diagnosis, and disposition. Mean total index admission cost was €3,083 in the POC group and €3,126 in the control group (mean difference −€43; 95%CI −510 to 423). In adjusted analyses, costs remained similar between groups (adjusted mean difference €11; 95%CI −183 to 204). Mean total specialist care costs from admission to 30 days were €3,517 in the POC group and €3,413 in the control group (mean difference €105; 95%CI −405 to 615). Cost patterns were consistent across diagnostic and disposition subgroups. In this randomised evaluation, implementation of POC hs-cTnI testing within a 0/1-hour ADP was cost-neutral at both index admission and 30 days. Despite higher per-test costs, overall episode costs were not increased. These findings suggest that biomarker pricing alone is unlikely to be a major driver of total healthcare expenditure when POC hs-cTn testing is integrated into emergency department pathways.Mean total index admission costs

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