Why the study?
Endovascular treatment of intracranial aneurysms requires tirofiban and dual antiplatelet therapy to prevent thromboembolic complications, but their safety in these cases needed determination.
Does tirofiban and DAPT increase the risk of haemorrhagic events in patients undergoing neuroendovascular surgery for intracranial aneurysms?
Does tirofiban and DAPT increase the risk of haemorrhagic events in patients undergoing neuroendovascular surgery for intracranial aneurysms?
The use of tirofiban and DAPT during stent-assisted coiling or flow diversion for intracranial aneurysms appears safe, with a low rate of symptomatic hemorrhages and no significant hematological changes.
May support tirofiban-DAPT safety after SAC or flow diversion; hypothesis-generating and requires prospective validation.
Background: Endovascular treatment of intracranial aneurysms usually involves stent-assisted coiling (SAC) and flow diverters. Glycoprotein IIb/IIIa inhibitors such as tirofiban and dual antiplatelet therapy (DAPT) are required to prevent thromboembolic complications afterwards. We sought to determine the safety of tirofiban and DAPT in these cases. Methods: We conducted a retrospective analysis of our database for patients with intracranial aneurysms who underwent SAC or flow diversion. The tirofiban-DAPT protocol used is described. Data regarding duration of infusion, placement of external ventricular devices (EVDs), complications, haemoglobin levels and platelet count before and 24 hours after antiplatelet therapy were collected and analysed. Results: One-hundred and forty-one patients with 148 aneurysms/procedures were included. 110 aneurysms were treated acutely and 38 electively. Minor and major haemorrhagic events were recognised in 20% (30/148) aneurysms. Only 5 (3.4%) intracerebral haemorrhages were symptomatic: 3 cortical/SAH and 2 EVD-related. The average blood volume in symptomatic haemorrhages was 24.8 cc versus 5.42 cc in asymptomatic haemorrhages (p=0.002). The rate of EVD-related haemorrhages was 15.7% (19/121) and only 2 (1.7%) were symptomatic. Most haemorrhagic events occurred in ruptured aneurysms (90.1%, p=0.01). No significant change in platelet count or haemoglobin levels before and 24 hours after administration of tirofiban and DAPT was documented. Concomitant administration of heparin did not increase haemorrhagic events. Conclusion: The use of the GP IIb/IIIa inhibitors tirofiban and DAPT in this series was safe. Tirofiban and DAPT did not affect platelet count or haemoglobin levels and did not increase rate of symptomatic haemorrhages or thromboembolic complications.
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Samaniego et al. (2019) studied this question.
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