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Antiplatelet therapy discontinuation after stent-assisted coil embolization for intracranial aneurysms: a
Insights
Discontinuing single antiplatelet therapy (SAPT) after stent-assisted coil embolization (SACE) for intracranial aneurysms appears safe after two years if no complications arise. T- or Y-stent use increases risks for delayed ischemic events.
Area of Science:
- Neurosurgery
- Interventional Neuroradiology
- Vascular Neurology
Background:
- The optimal antiplatelet therapy protocol following stent-assisted coil embolization (SACE) for intracranial aneurysms is not well-defined.
- Discontinuation of single antiplatelet therapy (SAPT) remains a controversial topic in managing patients post-SACE.
Purpose of the Study:
- To investigate the long-term outcomes associated with discontinuing SAPT after SACE.
- To identify risk factors for antiplatelet therapy reduction or discontinuation and analyze outcomes post-discontinuation.
Main Methods:
- Retrospective analysis of 240 patients undergoing SACE between 2010-2020 with >1 year follow-up.
- Evaluation of delayed ischemic and hemorrhagic complication rates, and risk factors for antiplatelet therapy modification.
Main Results:
- Nine (3.8%) patients experienced delayed ischemic complications; 3 (1.3%) had modified Rankin Scale score decline.
- T- or Y-stent configuration was the sole risk factor for delayed ischemic complications (p < 0.001).
- SAPT was discontinued in 71.7% of 205 patients with >2 years follow-up, with no observed ischemic complications.
Conclusions:
- Discontinuing SAPT is safe for patients without ischemic complications and with stable MRA findings 2 years post-SACE.
- T- or Y-stent use is a significant risk factor for delayed ischemic complications, warranting cautious consideration of antiplatelet therapy reduction or discontinuation.
Objective:
The protocol for antiplatelet therapy after stent-assisted coil embolization (SACE) for intracranial aneurysms is not well established. In particular, the indications for single antiplatelet therapy (SAPT) discontinuation remain controversial. The authors investigated the long-term outcomes of SAPT discontinuation after SACE among patients at a single institution.
Methods:
Patients who underwent SACE during the period from 2010 to 2020 and who were followed up for > 1 year were included in this study. The delayed ischemic and hemorrhagic complication rates were examined during follow-up. Moreover, the risk factors of antiplatelet therapy reduction or discontinuation and the outcomes of SAPT discontinuation were examined.
Results:
In total, 240 patients were included in the analysis. The average patient age was 60.3 years, and the average follow-up period was 46.7 months. Nine (3.8%) patients presented with symptomatic delayed ischemic complication, and 3 (1.3%) patients experienced a decline in modified Rankin Scale score. The stent configuration (T- or Y-stent) was the only risk factor associated with delayed ischemic complication (p < 0.001). SAPT was discontinued in 147 (71.7%) of 205 patients who were followed up for > 2 years, and no ischemic complications were observed.
Conclusions:
It is safe to discontinue SAPT in patients without ischemic complications and with stable intraaneurysmal signals on MRA 2 years after SACE. The T- or Y-stent is a high-risk factor for delayed ischemic complications, and antiplatelet therapy reduction or discontinuation should be cautiously considered.
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