Efficacy and Safety of Replase for Acute Ischemic Stroke: a Systematic Review and Meta-Analysis
Natasha Maranhao Vieira Rodrigues1, Frederico De Sousa Marinho Mendes Filho1, Eva Maia1, Emanuelly Maria Barbosa1, Julia Cauduro1, Pablo Feitoza2
1Universidade Federal do Amazonas (UFAM), 2Department of Neurology, Universidade Federal do Amazonas (UFAM)
Objective:
This study aimed to assess the safety and efficacy of reteplase compared with alteplase in acute ischemic stroke.
Background:

Alteplase is widely used in early reperfusion therapy and is currently the standard drug in Acute Ischemic stroke (AIS). However, there are new and more affordable drugs with a prolonged half-life such as Reteplase that need further research.

Design/Methods:

We systematically searched Pubmed, Embase and Cochrane databases for studies comparing the use of reteplase and ateplase for reperfusion therapy in patients with AIS that reported the outcomes of interest: mortality (1), any adverse events (2), any Intracranial Hemorrhage (ICH) (3) and Symptomatic ICH (4). Heterogeneity was examined with I² statics. Statistical analyses were performed using R (version 4.3.1).


Results:
Out of 725 database results, 3 studies and 1.759 patients were included. In a pooled analysis, there were no significant differences in mortality (OR 1.19; CI 0.71-1.98; p=0.509; I² 0%), symptomatic ICH (OR 1.08; CI 0.63-1.87; p=0.775; I² 0%), any ICH (OR 1.29; CI 0.83-2.01; p=0.265; I² 6%) and any adverse events (OR 1.67; CI 0.83-3.38; p = 0.03; I² 71%) between these two groups.  
Conclusions:

There were no significant differences in the efficacy and safety of reteplase compared with alteplase in treating AIS. However, it was not possible to analyze excellent functional outcomes, such as a decrease of points in the Rankin scale at 30 and 90 days, and just 2 RCT had been published in the AIS context. Reteplase is a more affordable drug that could be viable in low and middle-income countries considering cost-effectiveness, but more RCTs are needed for further evaluation.

10.1212/WNL.0000000000211830
Disclaimer: Abstracts were not reviewed by Neurology® and do not reflect the views of Neurology® editors or staff.