Why the study?
While periprocedural low-dose prasugrel is effective and safe for stent-assisted coil embolization of cerebral aneurysms, follow-up outcomes remained to be described.
Does a low-dose prasugrel regimen prevent delayed ischemic events in patients undergoing stent-assisted coil embolization for intracranial aneurysms?
Does a low-dose prasugrel regimen prevent delayed ischemic events in patients undergoing stent-assisted coil embolization for intracranial aneurysms?
A low-dose prasugrel regimen after stent-assisted coil embolization for intracranial aneurysms is associated with a low rate of delayed ischemic events and no hemorrhagic complications.
Low-dose prasugrel appears safe post-SACE with rare delayed infarcts; leaves open optimal duration and need for prospective trials.
OBJECTIVE: Much emphasis has been put on the use of antiplatelet medication for the prevention of ischemic events in the treatment of cerebral aneurysms with stent assistance. In this regard, the effectiveness and safety of a low-dose prasugrel regimen during the periprocedural period was recently reported. The purpose of this study was to present the outcomes of patients on low-dose prasugrel regimens during the follow-up period after stent-assisted coil embolization (SACE) of cerebral aneurysms. METHODS: For the 396 consecutive patients undergoing SACE procedures, low-dose prasugrel therapy (5 mg of prasugrel and 100 mg of aspirin) was recommended for 3 months after the endovascular treatment. The authors performed a retrospective review of a single-center experience focusing on delayed ischemic events beyond 1 month after treatment. The mean follow-up period was 24.6 ± 11.3 months. RESULTS: In this cohort of patients on a low-dose prasugrel regimen, cerebral infarction occurred in 1 patient (0.3%, 95% CI 0%-1.8%) beyond 1 month after SACE. No intracranial hemorrhage occurred. Overall ischemic events occurred in 14 patients (3.5%, 95% CI 2.1%-5.9%), all within 6 months of the coiling procedure. All patients had transient symptoms. The events occurred within 2 months after cessation of prasugrel in 11 patients (78.6%). Prasugrel maintenance for 6 months was found to result in lower ischemic events compared with maintenance for 3 months. CONCLUSIONS: For patients undergoing SACE, a low-dose prasugrel regimen was a safe and reliable treatment option for the prevention of delayed ischemic events. Transient ischemic events often occurred within 2 months of stopping prasugrel medication.
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Choi et al. (2023) studied this question.
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