The role of amantadine in cognitive recovery early after traumatic brain injury: A systematic review.


Journal

Clinical neurology and neurosurgery
ISSN: 1872-6968
Titre abrégé: Clin Neurol Neurosurg
Pays: Netherlands
ID NLM: 7502039

Informations de publication

Date de publication:
07 2020
Historique:
received: 27 02 2020
revised: 14 03 2020
accepted: 20 03 2020
pubmed: 4 4 2020
medline: 12 6 2021
entrez: 4 4 2020
Statut: ppublish

Résumé

We conducted an updated systematic review on the safety and efficacy of amantadine in cognitive recovery after traumatic brain injury (TBI), in order to determine if the current literature justifies its use in this clinical condition. A comprehensive search strategy was applied to three databases (PubMed, Scopus, and Cochrane). Only randomized clinical trials (RCTs) that compared the effect of amantadine and placebo in adults within 3 months of TBI were included in the review. Study characteristics, outcomes, and methodological quality were synthesized. This systematic review was conducted and presented in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). A quantitative synthesis (meta-analysis) was not feasible due to the large heterogeneity of studies identified. Three parallel RCTs and one cross-over RCT, with a total of 325 patients were included. All of the studies evaluated only severe TBI in adults. Amantadine was found to be well tolerated across the studies. Two RCTs reported improvement in the intermediate-term cognitive recovery (four to six weeks after end of treatment), using DRS (in both studies) and MMSE, GOS, and FIM-Cog (in one study). The effect of amantadine on the short-term (seven days to discharge) and long-term (six months from the injury) cognitive outcome was found not superior to placebo in two RCTs. The rate of severe adverse events was found to be consistently very low across the studies (the incidence of seizures, elevation in liver enzymes and cardiac death was 0.7 %, 1.9 %, and 0.3 %, respectively). In conclusion, amantadine seems to be well tolerated and might hasten the rate of cognitive recovery in the intermediate-term outcome. However, the long-term effect of amantadine in cognitive recovery is not well defined and further large randomized clinical trials in refined subgroups of patients are needed to better define its application.

Identifiants

pubmed: 32244036
pii: S0303-8467(20)30158-X
doi: 10.1016/j.clineuro.2020.105815
pii:
doi:

Substances chimiques

Nootropic Agents 0
Amantadine BF4C9Z1J53

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

105815

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Andrea Loggini (A)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States. Electronic address: andrea.loggini@uchospitals.edu.

Ruth Tangonan (R)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

Faten El Ammar (F)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

Ali Mansour (A)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

Fernando D Goldenberg (FD)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

Christopher L Kramer (CL)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

Christos Lazaridis (C)

Department of Neurology, University of Chicago Medicine and Biological Sciences, Chicago, IL, United States.

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Classifications MeSH