4.3 Article

Continuous intravenous tirofiban can improve the 90-day functional outcome and decrease 90-day mortality without increasing bleeding risk in acute ischemic stroke patients treated by endovascular therapy: A meta-analysis

Journal

JOURNAL OF CLINICAL NEUROSCIENCE
Volume 99, Issue -, Pages 109-116

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jocn.2022.03.008

Keywords

Acute ischemic stroke; Tirofiban; Intravenous; Endovascular therapy; Meta-analysis

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This meta-analysis study demonstrated that intravenous administration of tirofiban, either alone or in combination, improves the 90-day functional prognosis, reduces the risk of 90-day mortality, and increases the possibility of early recanalization in acute ischemic stroke patients treated by endovascular therapy. There was no increase in the rates of symptomatic intracranial hemorrhage and intracranial hemorrhage.
Background: The role of continuous intravenous administration of tirofiban in endovascular therapy is still unclear. This meta-analysis aims to evaluate the 90-day functional prognosis in acute ischemic stroke patients (AIS) treated by endovascular treatment and intravenous administration of tirofiban. Methods: We searched PubMed, Embase, and CENTRAL databases with the subject terms tirofiban , brain ischemia , and some related free words. Inclusion criteria were: (1) cohort study or randomized control trials; (2) AIS patients who received endovascular therapy; (3) the intervention or exposure was intravenous tirofiban monotherapy or combined with intra-arterial tirofiban; (4) containing data on modified Rankin Scale at 90 days and including at least one of the following indicators: mortality, symptomatic intracranial hemorrhage (sICH), intracranial hemorrhage (ICH), and recanalization. A summary odds ratio was calculated. Results: Twelve eligible studies, consisting of 3268 AIS participants, were identified. There was a significant trend of favorable outcomes (measured by mRS at three months) in the tirofiban group (ORs = 1.36; 95% CI = 1.09-1.70). In addition, compared with the non-tirofiban group, intravenous tirofiban was significantly associated with decreased risk of 90-day mortality (ORs = 0.73; 95% CI:0.59-0.89) and increased recanalization rate (ORs = 1.50; 95% CI:1.08-2.09) but no significant difference in rates of sICH (ORs = 0.93; 95% CI = 0.70-1.24) or ICH (ORs = 0.84; 95% CI = 0.62-1.15). Conclusions: Intravenous tirofiban appears to be safe and effective when used following intra-arterial tirofiban or as monotherapy in AIS patients treated by endovascular therapy, which can improve the 90-day functional outcome, decrease the 90-day mortality and increase the possibility of early recanalization without increasing rates of sICH and ICH.

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