Tirofiban for acute ischemic stroke: systematic review and meta-analysis

被引:61
作者
Gong, Jinhong [1 ,2 ]
Shang, Jingjing [1 ]
Yu, Hai [3 ]
Wan, Qian [4 ]
Su, Dan [1 ]
Sun, Zhiqiang [5 ]
Liu, Guangjun [1 ]
机构
[1] Nanjing Med Univ, Affiliated Changzhou 2 Peoples Hosp, Dept Pharm, Changzhou, Jiangsu, Peoples R China
[2] Soochow Univ, Dept Pharmaceut, Coll Pharmaceut Sci, Suzhou, Peoples R China
[3] Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China
[4] Fudan Univ, Zhongshan Hosp, Qingpu Branch, Dept Pharm, Shanghai, Peoples R China
[5] Nanjing Med Univ, Affiliated Changzhou 2 Peoples Hosp, Dept Radiotherapy, Changzhou 213003, Jiangsu, Peoples R China
关键词
Stroke; Tirofiban; Symptomatic intracranial hemorrhage; Fatal intracranial hemorrhage; ENDOVASCULAR TREATMENT; INTRAVENOUS TIROFIBAN; PRELIMINARY EFFICACY; BLEEDING RISK; THROMBOLYSIS; ALTEPLASE; SAFETY; OCCLUSION; THERAPY; TRIAL;
D O I
10.1007/s00228-019-02817-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background The safety and efficacy of tirofiban for patients with acute ischemic stroke (AIS) remains controversial. We therefore conducted a systematic review and meta-analysis. Methods We searched PubMed, EMBASE, Cochrane Library, Web of Science, and related international clinical trials registries through March 31, 2019, using the terms "tirofiban" and "stroke". All apparently unconfounded randomized controlled trials (RCTs) and cohort studies with two arms comparing treatment with and without tirofiban for AIS were included in this review. Primary outcomes included symptomatic intracranial hemorrhage (sICH), fatal ICH, mortality, and modified Rankin Scale (mRS 0-2) at 3 months. Results Seventeen studies including 2914 AIS patients were identified. Pooled results showed that tirofiban treatment in AIS did not increase the risk of sICH (OR, 0.95; 95% CI, 0.71-1.28; p = 0.75) or mortality (OR, 0.80; 95% CI; 0.64-1.02; p = 0.07). However, fatal ICH increased significantly in the tirofiban treatment group (OR, 2.84; 95% CI, 1.38-5.85; p = 0.005), and subgroup analysis showed that tirofiban via intra-arterial (IA) administration was associated with increased risk of fatal ICH (OR, 2.90; 95% CI, 1.12-7.55; p = 0.03), while intravenous (IV) administration was not (OR, 2.75; 95% CI, 0.92-8.20; p = 0.07). In addition, tirofiban showed no obvious improvement in functional outcome (mRS 0-2) (OR, 1.29; 95% CI, 0.97-1.71; p = 0.08). Conclusion Tirofiban seems to be safe in systemic treatment and may represent a potential choice for management of AIS. However, intra-arterial administration requires further adequately controlled studies in order to develop an appropriate protocol, similar to that in cardiology.
引用
收藏
页码:475 / 481
页数:7
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