Safety of antiplatelet medication discontinuation more than 12 months after stent-assisted coil embolization: a

Chang Hyeun Kim1, Young Hoon Choi2, Jae Sang Oh3

  • 1Department of Neurosurgery, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea (the Republic of).

Insights

Discontinuing antiplatelet medication more than 12 months after stent-assisted coiling (SAC) appears safe for patients not at high risk for ischemia. This study investigated outcomes following antiplatelet medication discontinuation (AMD) in a large patient cohort.

Area of Science:

  • Neurology
  • Cardiovascular Medicine
  • Interventional Neuroradiology

Background:

  • Antiplatelet therapy is crucial after stent-assisted coiling (SAC) to prevent ischemic events.
  • The optimal timing for discontinuing antiplatelet medication (AMD) post-SAC remains unclear and debated.
  • This study addresses the safety of AMD initiated over 12 months after SAC procedures.

Purpose of the Study:

  • To evaluate the safety of antiplatelet medication discontinuation (AMD) in patients more than 12 months after stent-assisted coiling (SAC).
  • To analyze clinical outcomes following delayed AMD in a diverse patient population.

Main Methods:

  • A multicenter, prospective, non-interventional study involving 495 patients who underwent AMD >12 months post-SAC.
  • Data collected from January 2021 to December 2023, with a minimum 6-month follow-up post-AMD.
  • Physician discretion guided maintenance duration and cessation based on patient clinical status.

Main Results:

  • No ischemic events were observed in relation to AMD, even in the 41.0% of patients considered high-risk.
  • The mean time to AMD was 20.0±12.9 months after SAC.
  • Internal carotid artery aneurysms were most commonly treated (67.1%), with open-cell laser-cut stents being prevalent (60.5%).

Conclusions:

  • Antiplatelet medication discontinuation over 12 months after SAC is a safe strategy for patients not at high risk for ischemia.
  • Further confirmation through randomized controlled trials is recommended to solidify these findings.
Abstract

Related Concept Videos

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
436
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
583
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants01:18

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants

Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.1K