Glycoprotein IIb/IIIa inhibitors and cangrelor improve reperfusion success and stent patency during emergent carotid stenting for tandem lesions without consistently increasing hemorrhage risk.
Do rapid-acting intravenous antiplatelet agents improve technical success without increasing hemorrhagic risk in patients undergoing emergent carotid artery stenting for acute carotid tandem lesions?
Patients with acute carotid tandem lesions (concurrent cervical internal carotid artery stenosis or occlusion and intracranial large vessel occlusion) undergoing mechanical thrombectomy and emergent carotid artery stenting (review of 7 real-world studies and registry analyses).
Periprocedural antiplatelet therapies, including intravenous glycoprotein IIb/IIIa inhibitors (GPIs, particularly tirofiban), intravenous cangrelor, and oral dual antiplatelet therapy.
Acetylsalicylic acid (ASA) or other antiplatelet regimens.
In-stent thrombosis, reperfusion success, and symptomatic intracranial hemorrhage (sICH).
Observational data suggest rapid-acting IV antiplatelets like GPIs and cangrelor may improve technical success during emergent carotid stenting for tandem lesions without a clear excess in bleeding risk, though prospective RCTs are needed.
Background/Objectives: Acute carotid tandem lesions (TLs), defined by concurrent cervical internal carotid artery (ICA) stenosis or occlusion and intracranial large vessel occlusion, occur in 10–20% of patients undergoing mechanical thrombectomy (MT) for acute ischemic stroke (AIS). Optimal periprocedural antiplatelet management during emergent carotid artery stenting (eCAS) remains uncertain, particularly regarding the balance between preventing stent thrombosis and avoiding hemorrhagic complications. Methods: A narrative review was conducted using PubMed and Scopus (until 6 March 2026) to identify English-language studies evaluating antiplatelet therapies during eCAS for TLs. We included seven real-world studies and registry analyses. Data on study design, patient characteristics, procedural strategies, angiographic results, functional outcomes, and safety metrics were extracted. Results: No randomized controlled trials (RCTs) were identified. The available evidence is derived exclusively from observational studies. Across these cohorts, glycoprotein IIb/IIIa inhibitors (GPIs), particularly tirofiban, were generally associated with lower rates of in-stent thrombosis and higher reperfusion success, with symptomatic intracranial hemorrhage (sICH) rates that appeared comparable to or lower than those reported with acetylsalicylic acid (ASA). Cangrelor, an intravenous (IV) P2Y12 inhibitor, was associated with improved stent patency and increased likelihood of complete reperfusion, although reported effects on clinical outcomes were inconsistent when compared with GPIs or ASA. Aside from abciximab, potent IV antiplatelet agents did not consistently show an increased sICH signal. Oral dual antiplatelet therapy was also associated with improved technical outcomes without a clear excess in bleeding complications. Conclusions: Current real-world observational data suggest that rapid-acting IV antiplatelet agents—particularly GPIs and, increasingly, cangrelor—may represent feasible periprocedural options during eCAS for TLs, with potential benefits for technical success and no consistent evidence of increased hemorrhagic risk. However, interpretation is limited by study heterogeneity and non-randomized designs. The absence of RCTs highlights the need for prospective comparative studies and standardized periprocedural antiplatelet protocols.
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Matija Zupan
Lara Straus
Pawel Kermer
Journal of Clinical Medicine
National and Kapodistrian University of Athens
University of Ljubljana
Universitätsmedizin Göttingen
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Zupan et al. (Wed,) reported a other. Glycoprotein IIb/IIIa inhibitors and cangrelor improve reperfusion success and stent patency during emergent carotid stenting for tandem lesions without consistently increasing hemorrhage risk.
www.synapsesocial.com/papers/69eb0ac4553a5433e34b4b3b — DOI: https://doi.org/10.3390/jcm15093195