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Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke

INTRODUCTION: Stroke is the second leading cause of death in the world. However, there is still no approved neuroprotective drug for acute ischaemic stroke. To clarify the neuroprotective efficacy and safety of dextromethorphan in stroke, the following study was carried out. MATERIAL AND METHODS: Fo...

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Autores principales: Mousavi, Seyed Ali, Saadatnia, Mohammad, Khorvash, Faribourz, Hoseini, Tahereh, Sariaslani, Payam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258743/
https://www.ncbi.nlm.nih.gov/pubmed/22295030
http://dx.doi.org/10.5114/aoms.2011.23413
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author Mousavi, Seyed Ali
Saadatnia, Mohammad
Khorvash, Faribourz
Hoseini, Tahereh
Sariaslani, Payam
author_facet Mousavi, Seyed Ali
Saadatnia, Mohammad
Khorvash, Faribourz
Hoseini, Tahereh
Sariaslani, Payam
author_sort Mousavi, Seyed Ali
collection PubMed
description INTRODUCTION: Stroke is the second leading cause of death in the world. However, there is still no approved neuroprotective drug for acute ischaemic stroke. To clarify the neuroprotective efficacy and safety of dextromethorphan in stroke, the following study was carried out. MATERIAL AND METHODS: Forty patients with acute stroke causing moderate deficit were randomized to be treated with either dextromethorphan 300 mg per day or placebo for 5 days. Plasma level of dextromethorphan and its active metabolite was not evaluated in this study. The NIHSS score was calculated on day 5 and the Barthel activities of daily living index and Rankin score were checked after 3 months by a blinded investigator. Collected data were analysed using the t-test and χ(2) test. RESULTS: In the dextromethorphan-treated group, the mean NIHSS score was 16.8 ±3.9 at baseline, and was 14.2 ±4.8 for the placebo-treated group (p = 0.069). At day 5, there was also no significant difference regarding NIHSS score (p = 0.167). At the 3-month follow-up, there was no significant difference regarding Barthel scale and Rankin score between the dextromethorphan and placebo groups. CONCLUSIONS: The results of our study suggest that although low-dose and short-term oral administration of dextromethorphan seems to be not neuroprotective, it does not worsen either patients’ condition or NIHSS score. Moreover, patients treated with dextromethorphan showed a significant reduction in seizures (complication after stroke), but had increased chance of MI and renal failure by almost 5% when compared to the placebo-treated groups. More prolonged studies with a higher number of cases are recommended.
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spelling pubmed-32587432012-01-31 Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke Mousavi, Seyed Ali Saadatnia, Mohammad Khorvash, Faribourz Hoseini, Tahereh Sariaslani, Payam Arch Med Sci Clinical Research INTRODUCTION: Stroke is the second leading cause of death in the world. However, there is still no approved neuroprotective drug for acute ischaemic stroke. To clarify the neuroprotective efficacy and safety of dextromethorphan in stroke, the following study was carried out. MATERIAL AND METHODS: Forty patients with acute stroke causing moderate deficit were randomized to be treated with either dextromethorphan 300 mg per day or placebo for 5 days. Plasma level of dextromethorphan and its active metabolite was not evaluated in this study. The NIHSS score was calculated on day 5 and the Barthel activities of daily living index and Rankin score were checked after 3 months by a blinded investigator. Collected data were analysed using the t-test and χ(2) test. RESULTS: In the dextromethorphan-treated group, the mean NIHSS score was 16.8 ±3.9 at baseline, and was 14.2 ±4.8 for the placebo-treated group (p = 0.069). At day 5, there was also no significant difference regarding NIHSS score (p = 0.167). At the 3-month follow-up, there was no significant difference regarding Barthel scale and Rankin score between the dextromethorphan and placebo groups. CONCLUSIONS: The results of our study suggest that although low-dose and short-term oral administration of dextromethorphan seems to be not neuroprotective, it does not worsen either patients’ condition or NIHSS score. Moreover, patients treated with dextromethorphan showed a significant reduction in seizures (complication after stroke), but had increased chance of MI and renal failure by almost 5% when compared to the placebo-treated groups. More prolonged studies with a higher number of cases are recommended. Termedia Publishing House 2011-06 2011-07-11 /pmc/articles/PMC3258743/ /pubmed/22295030 http://dx.doi.org/10.5114/aoms.2011.23413 Text en Copyright © 2011 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Mousavi, Seyed Ali
Saadatnia, Mohammad
Khorvash, Faribourz
Hoseini, Tahereh
Sariaslani, Payam
Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title_full Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title_fullStr Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title_full_unstemmed Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title_short Evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
title_sort evaluation of the neuroprotective effect of dextromethorphan in the acute phase of ischaemic stroke
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258743/
https://www.ncbi.nlm.nih.gov/pubmed/22295030
http://dx.doi.org/10.5114/aoms.2011.23413
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