Department of Neurology, Beichen Traditional Chinese Medical Hospital, Tianjin, China.
Department of Internal Medicine, Characteristic Medical Center of Chinese People's Armed Police, Tianjin,China.
J Clin Neurosci. 2020 Oct;80:112-120. doi: 10.1016/j.jocn.2020.07.040. Epub 2020 Aug 18.
Although tirofiban therapy is considered a potentially effective treatment to reduce the incidence of thrombotic complications in patients receiving endovascular treatment (EVT), the safety and efficacy of tirofiban remain controversial. Our objective was to investigate the efficacy and safety of EVT plus tirofiban therapy in patients with emergent large artery occlusion.
Relevant articles from randomized controlled trials (RCTs) or observational studies that compared treatment with tirofiban to treatment without tirofiban in patients undergoing EVT were retrieved from the PubMed and Embase databases. We calculated odds ratios (ORs) with corresponding 95% confidence intervals (CIs) for the safety and efficacy outcomes based on a random effects model.
Twelve studies including 2533 patients were identified for the analysis. Overall, the risk of fatal intracranial haemorrhage (ICH) was higher for the treatment with tirofiban group than for the treatment without tirofiban group in patients with large artery occlusion who underwent EVT (p = 0.002), whereas the risk of any ICH, symptomatic ICH, parenchymal haematoma type 2, in-hospital mortality and 3-month mortality did not differ significantly (p > 0.05). No significant differences in reocclusion rate, recanalization rate or excellent functional outcome were found between the patients treated with or without tirofiban, but significantly favourable functional outcome at 3 months occurred in the tirofiban group (p = 0.017).
Tirofiban administration in patients receiving EVT significantly improved 3-month favourable functional outcomes, whereas an increased risk of fatal ICH was also observed. Further rigorous trials are needed to verify the safety of tirofiban.
替罗非班治疗被认为是一种潜在有效的治疗方法,可以降低接受血管内治疗(EVT)的患者发生血栓并发症的发生率,但替罗非班的安全性和疗效仍存在争议。我们的目的是研究 EVT 联合替罗非班治疗紧急大动脉闭塞患者的疗效和安全性。
从 PubMed 和 Embase 数据库中检索了比较替罗非班组与不使用替罗非班组接受 EVT 治疗的患者的随机对照试验(RCT)或观察性研究的相关文章。我们根据随机效应模型计算了安全性和疗效结局的比值比(OR)及其相应的 95%置信区间(CI)。
共纳入 12 项研究,共 2533 例患者。总体而言,接受 EVT 的大动脉闭塞患者中,替罗非班组致命性颅内出血(ICH)的风险高于不使用替罗非班组(p=0.002),但任何 ICH、症状性 ICH、脑实质血肿 2 型、住院死亡率和 3 个月死亡率无显著差异(p>0.05)。替罗非班组与不使用替罗非班组患者的再闭塞率、再通率或良好的功能结局无显著差异,但替罗非班组患者在 3 个月时的功能结局显著更优(p=0.017)。
在接受 EVT 的患者中使用替罗非班可显著改善 3 个月时的良好功能结局,但也观察到致命性 ICH 的风险增加。需要进一步的严格试验来验证替罗非班的安全性。