Key result
Pharmacist-initiated point-of-care CYP2C19 testing yields ~99% success and guides clopidogrel de-escalation.
Why the study?
Tailoring antiplatelet therapy based on CYP2C19 testing can improve outcomes, but widespread adoption, particularly in outpatient settings, remains limited.
Is community pharmacist-initiated point-of-care CYP2C19 genotype-guided de-escalation of oral P2Y12 inhibitors feasible?
Observational (n=144)
Yes
Is community pharmacist-initiated point-of-care CYP2C19 genotype-guided de-escalation of oral P2Y12 inhibitors feasible?
Point-of-care CYP2C19-guided de-escalation of P2Y12 inhibitors in community pharmacies is feasible and highly acceptable to patients and pharmacists, though actual de-escalation rates remain low.
Supports feasibility of pharmacist-led CYP2C19 testing in community pharmacies; leaves open effects on outcomes and adoption.
Tailoring antiplatelet therapy based on CYP2C19 pharmacogenetic (PGx) testing can improve cardiovascular outcomes and potentially reduce healthcare costs in patients on a P2Y12-inhibitor regime with prasugrel or ticagrelor. However, ubiquitous adoption—particularly in an outpatient setting—remains limited. We conducted a proof-of-concept study to evaluate the feasibility of CYP2C19-guided de-escalation of prasugrel/ticagrelor to clopidogrel through point-of-care (POC) PGx testing in the community pharmacy. Multiple feasibility outcomes were assessed. Overall, 144 patients underwent CYP2C19 PGx testing in 27 community pharmacies. Successful test results were obtained in 142 patients (98.6%). De-escalation to clopidogrel occurred in 19 patients (20%) out of 95 (67%) eligible for therapy de-escalation, which was mainly due to PGx testing not being included in cardiology guidelines. Out of the 119 patients (84%) and 14 pharmacists (100%) surveyed, 109 patients (92%) found the community pharmacy a suitable location for PGx testing, and the majority of pharmacists (86%) thought it has added value. Net costs due to PGx testing were estimated at €43 per patient, which could be reduced by earlier testing and could turn into savings if de-escalation would double to 40%. Although the observed de-escalation rate was low, POC CYP2C19-guided de-escalation to clopidogrel appears feasible in a community pharmacy setting.
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Levens et al. (2023) conducted an observational in Patients on a P2Y12-inhibitor regime with prasugrel or ticagrelor (n=144). Point-of-care CYP2C19 pharmacogenetic testing was evaluated on Feasibility outcomes (successful test results). Community pharmacist-initiated point-of-care CYP2C19 testing yielded successful results in 98.6% of patients, leading to de-escalation to clopidogrel in 20% of eligible patients.
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