Key result
CYP2C19-guided DAPT proves cost-effective in ACS, costing ~£569 per QALY gained in STEMI.
Why the study?
Prescribing guidelines recommend prasugrel or ticagrelor with aspirin after PCI for ACS, but the cost-effectiveness of CYP2C19-guided DAPT prescribing compared with current practice was unknown.
Does point-of-care CYP2C19 genetic testing to guide dual antiplatelet therapy improve cost-effectiveness (QALYs and costs) compared to current prescribing practice in patients with acute coronary syndrome undergoing percutaneous coronary intervention?
Does point-of-care CYP2C19 genetic testing to guide dual antiplatelet therapy improve cost-effectiveness (QALYs and costs) compared to current prescribing practice in patients with acute coronary syndrome undergoing percutaneous coronary intervention?
A CYP2C19-guided strategy for dual antiplatelet therapy prescription in ACS patients undergoing PCI is highly cost-effective within the UK NHS, generating health gains at very low incremental costs.
Answers are grounded in this paper and cite their sources.
May support CYP2C19-guided DAPT adoption in NHS ACS care; modeling leaves open confirmation by prospective trials.
Background Prescribing guidelines recommend prasugrel or ticagrelor with aspirin as dual antiplatelet therapy (DAPT) following percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS), with clopidogrel reserved for people at high bleeding risk or with contraindications. We evaluated the cost-effectiveness of a point-of-care CYP2C19 genetic test to guide prescribing of DAPT compared with current prescribing practice in the Nathinal Health Service (NHS) in England. Methods We designed a hybrid decision-tree and state transition Markov model (40-year horizon) to calculate the costs and Quality-Adjusted Life-Years (QALYs) of CYP2C19-guided DAPT compared with current prescribing for two post-PCI populations: ST-segment elevation myocardial infarction (STEMI) and non-ST-segment elevation myocardial infarction or unstable angina (UA/NSTEMI). In CYP2C19-guided DAPT, loss of function (LoF) carriers were prescribed prasugrel or ticagrelor; non-LoF carriers prescribed clopidogrel. Costs (£, 2024/25 prices, NHS and Social Services), event rates, and utility values were sourced from published data. Sensitivity analyses measured uncertainty in the analysis results. The R programming language implementation of our decision-analytic model is available at https://github.com/JBHilton/pg-ap-analytics and archived at https://doi.org/10.5281/zenodo.20629081 . Results CYP2C19-guided DAPT generated an additional 0.0439 QALYs at an additional cost of £25 for STEMI, giving an incremental cost-effectiveness ratio (ICER) of £569 per QALY. For UA/NSTEMI, CYP2C19-guided DAPT generated an additional 0.0358 QALYs at an additional cost of £83, giving an ICER of £2,318 per QALY. At a cost-effectiveness threshold of £20,000 per QALY, CYP2C19-guided DAPT had a probability of being cost-effective of 87.6% in the STEMI population and 94.3% in the UA/NSTEMI population. Conclusions CYP2C19-guided DAPT is likely to be a cost-effective use of the NHS budget when compared with current prescribing practice for both STEMI and UA/NSTEMI populations.
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Ahari et al. (2026) studied Acute coronary syndrome (STEMI and UA/NSTEMI) treated with percutaneous coronary intervention (n=102,938). CYP2C19-guided dual antiplatelet therapy vs. Current prescribing practice (DAPT with aspirin plus P2Y12 inhibitor without genotype testing) was evaluated on Incremental cost-effectiveness ratio (ICER) in £ per QALY (ICER £569 per QALY (STEMI); £2,318 per QALY (UA/NSTEMI)). CYP2C19-guided DAPT generated additional QALYs at an incremental cost of £569 per QALY for STEMI and £2,318 per QALY for UA/NSTEMI, proving cost-effective compared to current prescribing practice.
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