VerifyNow-guided antiplatelet modification linked to lower stroke recurrence in atherothrombotic or lacunar infarction
This was a single-center retrospective observational study involving 243 analyzed patients (122 in a modified group, 121 in an unmodified group) with atherothrombotic or lacunar infarction. The intervention was VerifyNow-guided antiplatelet therapy modification, where selection was based on VerifyNow Aspirin Reaction Units and P2Y12 Reaction Units, with switching to prasugrel or cilostazol if both aspirin and clopidogrel showed inadequate inhibition. The comparator was empirically selected antiplatelet agent (unmodified group).
For the primary outcome of recurrent ischemic stroke, the modified group had 1 patient (0.8%) versus 8 patients (6.6%) in the unmodified group over a mean follow-up of 1.62 +/- 0.61 years. The hazard ratio was 0.10, with a 95% CI of 0.012-0.84, an adjusted P=0.033, and an unadjusted log-rank P=0.018, indicating a lower risk in the modified group. For safety, intracranial hemorrhage occurred in 0 patients (0%) in the modified group versus 1 patient (0.8%) in the unmodified group; other adverse events, serious adverse events, discontinuations, and tolerability were not reported.
Key limitations include the single-center retrospective design and small sample size. Funding or conflicts of interest were not reported. The practice relevance is that validation in a multicenter randomized controlled trial is warranted, as this study reports an association without claiming causality, and the evidence is limited due to the retrospective observational design.