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Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study

OBJECTIVE: Screening of drug-induced performance impairment is needed to provide meaningful information for users and prescribers regarding the impact of drugs on driving. The main objective was to assess the effects of oxazepam 10 mg (OXA10), oxazepam 30 mg (OXA30), and diazepam 10 mg (DIA10) on st...

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Autores principales: Jongen, S., Vuurman, E. F. P. M., Ramaekers, J. G., Vermeeren, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869943/
https://www.ncbi.nlm.nih.gov/pubmed/29500585
http://dx.doi.org/10.1007/s00213-018-4844-5
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author Jongen, S.
Vuurman, E. F. P. M.
Ramaekers, J. G.
Vermeeren, A.
author_facet Jongen, S.
Vuurman, E. F. P. M.
Ramaekers, J. G.
Vermeeren, A.
author_sort Jongen, S.
collection PubMed
description OBJECTIVE: Screening of drug-induced performance impairment is needed to provide meaningful information for users and prescribers regarding the impact of drugs on driving. The main objective was to assess the effects of oxazepam 10 mg (OXA10), oxazepam 30 mg (OXA30), and diazepam 10 mg (DIA10) on standard deviation of lateral position (SDLP) in a highway driving test in actual traffic and to determine the ability of eight neurocognitive tests to detect comparable effects. METHODS: Twenty-three healthy volunteers participated in a four-way double-blind, placebo-controlled, crossover study. The highway driving test was conducted between 4 and 5 h after drug intake. A range of neurocognitive tests was conducted before and after driving, 2 and 6 h post-treatment, respectively. RESULTS: Mean SDLP increased by 1.83, 3.03, and 7.57 cm after OXA10, DIA10, and OXA30, respectively. At 2 h post-treatment, all neurocognitive tests, except the useful field of view, showed performance impairment in all active treatments. Effect sizes (ES) were moderate for OXA10, large ES for DIA10, and largest ES for OXA30. Modest correlations were found between changes in SDLP and performance in the attention network test (ANT), the divided attention test (DAT), and the psychomotor vigilance test (PVT). CONCLUSION: OXA10 caused minor, DIA10 moderate, and OXA30 severe driving impairment. No neurocognitive test was both dose dependently sensitive and able to be associated with driving impairment. No neurocognitive test can replace the on-the-road highway driving test.
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spelling pubmed-58699432018-03-28 Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study Jongen, S. Vuurman, E. F. P. M. Ramaekers, J. G. Vermeeren, A. Psychopharmacology (Berl) Original Investigation OBJECTIVE: Screening of drug-induced performance impairment is needed to provide meaningful information for users and prescribers regarding the impact of drugs on driving. The main objective was to assess the effects of oxazepam 10 mg (OXA10), oxazepam 30 mg (OXA30), and diazepam 10 mg (DIA10) on standard deviation of lateral position (SDLP) in a highway driving test in actual traffic and to determine the ability of eight neurocognitive tests to detect comparable effects. METHODS: Twenty-three healthy volunteers participated in a four-way double-blind, placebo-controlled, crossover study. The highway driving test was conducted between 4 and 5 h after drug intake. A range of neurocognitive tests was conducted before and after driving, 2 and 6 h post-treatment, respectively. RESULTS: Mean SDLP increased by 1.83, 3.03, and 7.57 cm after OXA10, DIA10, and OXA30, respectively. At 2 h post-treatment, all neurocognitive tests, except the useful field of view, showed performance impairment in all active treatments. Effect sizes (ES) were moderate for OXA10, large ES for DIA10, and largest ES for OXA30. Modest correlations were found between changes in SDLP and performance in the attention network test (ANT), the divided attention test (DAT), and the psychomotor vigilance test (PVT). CONCLUSION: OXA10 caused minor, DIA10 moderate, and OXA30 severe driving impairment. No neurocognitive test was both dose dependently sensitive and able to be associated with driving impairment. No neurocognitive test can replace the on-the-road highway driving test. Springer Berlin Heidelberg 2018-03-02 2018 /pmc/articles/PMC5869943/ /pubmed/29500585 http://dx.doi.org/10.1007/s00213-018-4844-5 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Investigation
Jongen, S.
Vuurman, E. F. P. M.
Ramaekers, J. G.
Vermeeren, A.
Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title_full Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title_fullStr Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title_full_unstemmed Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title_short Comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
title_sort comparing the effects of oxazepam and diazepam in actual highway driving and neurocognitive test performance: a validation study
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869943/
https://www.ncbi.nlm.nih.gov/pubmed/29500585
http://dx.doi.org/10.1007/s00213-018-4844-5
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