Department of Neurosurgery, Thomas Jefferson University and Jefferson Hospital for Neuroscience, Philadelphia, Pennsylvania, USA.
Neurosurgery. 2012 Sep;71(3):710-4; discussion 714. doi: 10.1227/NEU.0b013e31826213f9.
Thromboembolic complications are a major concern in stent-assisted coiling of intracranial aneurysms that may be prevented with adequate antiplatelet therapy.
To assess the safety and efficacy of tirofiban in stent-assisted coiling.
Two protocols were used. In the initial protocol, tirofiban was administered intravenously as a 0.4 μg/kg per min bolus for 30 minutes followed by 0.10 μg·kg min maintenance infusion. The revised protocol consisted of a 0.10 μg·kg min maintenance infusion alone.
Sixty-seven patients received tirofiban, 16 under the initial protocol and 51 under the revised protocol. Thirty (44.8%) patients had sustained a subarachnoid hemorrhage (SAH). Tirofiban infusion was initiated after thromboembolic events in 9 (13.4%) patients and prophylactically in 58 (86.6%). Four (6.0%) intracranial hemorrhages were noted. Three (18.8%) intracranial hemorrhages occurred with the initial protocol in patients treated electively and were fatal in 2 (66.7%) cases. The only complication (1.9%) under the revised protocol was a subclinical worsening of the computed tomographic appearance of an SAH. There was no tirofiban-related morbidity or deaths with the revised protocol. Of 9 patients that received tirofiban as a rescue treatment, 7 (77.8%) had complete and 2 (22.2%) had partial arterial recanalization. No thromboembolic events occurred in patients receiving prophylactic tirofiban.
A bolus followed by a maintenance dose of tirofiban appears to have a high risk of cerebral hemorrhage. A maintenance infusion without an initial bolus, however, has an exceedingly low risk of hemorrhage and appears to be very safe and effective, even in the setting of SAH.
血栓栓塞并发症是颅内动脉瘤支架辅助栓塞的主要关注点,充分的抗血小板治疗可能预防此类并发症。
评估替罗非班在支架辅助栓塞中的安全性和有效性。
采用两种方案。在初始方案中,替罗非班静脉推注 0.4 μg/kg 剂量,持续 30 分钟,然后以 0.10 μg·kg·min 的剂量维持输注。修订方案仅使用 0.10 μg·kg·min 的维持输注。
67 例患者接受了替罗非班治疗,其中 16 例采用初始方案,51 例采用修订方案。30 例(44.8%)患者发生蛛网膜下腔出血(SAH)。9 例(13.4%)患者发生血栓栓塞事件后开始输注替罗非班,58 例(86.6%)患者预防性输注替罗非班。4 例(6.0%)患者发生颅内出血。3 例(18.8%)采用初始方案的颅内出血患者为择期治疗,2 例(66.7%)患者死亡。修订方案唯一的并发症(1.9%)是 CT 显示的 SAH 程度恶化,但无临床症状。修订方案无与替罗非班相关的发病率或死亡率。9 例接受替罗非班抢救治疗的患者中,7 例(77.8%)完全再通,2 例(22.2%)部分再通。接受预防性替罗非班治疗的患者未发生血栓栓塞事件。
推注加维持剂量的替罗非班似乎有很高的脑出血风险。不使用初始推注,仅用维持剂量,脑出血风险极低,安全性和有效性极高,即使在蛛网膜下腔出血的情况下也是如此。