A Systematic Review and Meta-Analysis on the Safety of Antiplatelet Discontinuation Following Stent-Assisted Coil

Mohammed Maan Al-Salihi1, Maryam Sabah Al-Jebur2, Ahmed Abd Elazim3

  • 1Zeenat Qureshi Stroke Institute, University of Missouri, Columbia, MO 65211, USA.

Neurosci
|April 23, 2025
PubMed

Insights

Discontinuing antiplatelet therapy after stent-assisted coil embolization (SACE) for brain aneurysms carries a low risk of thromboembolic complications. Further research is needed to determine optimal antiplatelet durations to balance risks.

Area of Science:

  • Neurology
  • Cardiovascular Medicine
  • Interventional Radiology

Background:

  • Stent-assisted coil embolization (SACE) is a prevalent endovascular method for treating intracranial aneurysms.
  • Post-SACE management requires antiplatelet therapy due to the permanent stent presence.
  • Optimal duration of antiplatelet therapy post-SACE remains a clinical question.

Purpose of the Study:

  • To systematically review and quantify the risk of ischemic complications following antiplatelet therapy discontinuation after SACE.
  • To analyze existing literature for evidence on thromboembolic events post-SACE antiplatelet cessation.

Main Methods:

  • Systematic literature search of PubMed, Cochrane Library, Scopus, and Web of Science (WOS).
  • Inclusion of five observational cohort studies with data from 18,425 cases (2009-2020).
  • Meta-analysis using a random-effects model to calculate the pooled event rate of ischemic complications.

Main Results:

  • The pooled rate of thromboembolism within 6 to 24 months after antiplatelet discontinuation was 0.01 (95% CI: 0.006 to 0.018).
  • Included studies predominantly originated from Korea and Japan.
  • Follow-up duration in most studies exceeded 24 months post-discontinuation.

Conclusions:

  • The risk of thromboembolic complications after discontinuing antiplatelet therapy post-SACE is low.
  • A definitive consensus on the ideal duration for dual- or single-antiplatelet therapy is lacking.
  • Prospective studies are necessary to establish optimal antiplatelet durations balancing thromboembolic and hemorrhagic risks.
Abstract