Abstract
Purpose
The management of acute stroke is challenging. The aim of this meta-analysis was to
determine the efficacy and tolerability of edaravone, with or without thrombolytic therapy,
in the treatment of patients with acute ischemic stroke.
Methods
The PubMed, EMBASE, and Cochrane databases were searched for randomized controlled
trials (RCTs) and cohort studies. Mean differences (MD), risk ratios (RR), 95% confidence
interval (CI), and heterogeneity were calculated.
Findings
Totals of nine RCTs and four cohort studies were included, for a total of 2102 patients.
In patients with acute ischemic stroke, edaravone monotherapy was associated with
significantly improved Barthel Index of functioning in activities for daily living
(MD, 23.95; 95% CI, 18.48 to 29.41; P < 0.001) and neurologic deficit, (as measured using the National Institutes of Health
Stroke Scale score) (MD = –3.49; 95% CI, –5.76 to 1.22; P = 0.003), on short-term follow-up. However, edaravone was not associated with an
improved rate of death or disability (RR = 0.75; 95% CI, 0.45 to 1.23; P = 0.25) on long-term follow-up.When plus to thrombolytic therapy, edaravone was associated
with significant improvements in recanalization rate (RR = 1.71; 95% CI, 1.05 to 2.77;
P = 0.03) and neurologic deficit (MD = 3.97; 95% CI, 5.14 to 2.79; P < 0.001), without an increase in the prevalence of bleeding events (RR = 1.11; 95%
CI, 0.76 to 1.62; P = 0.59). However, edaravone did not have a significant effect on death or disability
(RR = 0.85; 95% CI, 0.69 to 1.04; P = 0.12).
Implications
Based on the findings from the present meta-analysis, edaravone was an effective and
well-tolerated neuroprotective agent in these patients with ischemic stroke. With
the use of edaravone, activities of daily living and neurologic deficits, along with
recanalization rates, were improved on short-term follow-up, but the long-term effects
still need confirmation in larger-scale clinical trials.
Key words
Abbreviations:
IV (Intravenouss), RCT (randomized controlled trial)To read this article in full you will need to make a payment
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Article info
Publication history
Published online: December 03, 2022
Accepted:
November 8,
2022
Identification
Copyright
© 2022 Elsevier Inc.