Movement Disorders (revue)

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A pilot tolerability and efficacy trial of sodium oxybate in ethanol‐responsive movement disorders

Identifieur interne : 003A45 ( Main/Exploration ); précédent : 003A44; suivant : 003A46

A pilot tolerability and efficacy trial of sodium oxybate in ethanol‐responsive movement disorders

Auteurs : Steven J. Frucht [États-Unis] ; Yvette Bordelon [États-Unis] ; William H. Houghton [États-Unis] ; Dayton Reardan [États-Unis]

Source :

RBID : ISTEX:13DB9E68088F40250D33A2690DEBC082CC1E3214

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English descriptors

Abstract

Sodium oxybate is currently approved in the United States exclusively for the treatment of cataplexy in narcoleptic patients. In a prior article published in this journal, we reported a patient with severe posthypoxic myoclonus whose myoclonus improved with ethanol and also with treatment with sodium oxybate. We extend this preliminary observation to five other patients with ethanol‐responsive movement disorders in an open‐label, dose‐titration, add‐on, 8‐week trial. All five patients (one with severe alcohol‐responsive posthypoxic myoclonus, two with ϵ‐sarcoglycan–linked myoclonus–dystonia, and two with essential tremor) experienced improvement from baseline of 50% or greater as measured by blinded videotape review. Tolerability was satisfactory, with dose‐dependent sedation as the most common side effect. Further studies of this drug in hyperkinetic movement disorders are warranted. © 2005 Movement Disorder Society

Url:
DOI: 10.1002/mds.20605


Affiliations:


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<term>Aged</term>
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<div type="abstract" xml:lang="en">Sodium oxybate is currently approved in the United States exclusively for the treatment of cataplexy in narcoleptic patients. In a prior article published in this journal, we reported a patient with severe posthypoxic myoclonus whose myoclonus improved with ethanol and also with treatment with sodium oxybate. We extend this preliminary observation to five other patients with ethanol‐responsive movement disorders in an open‐label, dose‐titration, add‐on, 8‐week trial. All five patients (one with severe alcohol‐responsive posthypoxic myoclonus, two with ϵ‐sarcoglycan–linked myoclonus–dystonia, and two with essential tremor) experienced improvement from baseline of 50% or greater as measured by blinded videotape review. Tolerability was satisfactory, with dose‐dependent sedation as the most common side effect. Further studies of this drug in hyperkinetic movement disorders are warranted. © 2005 Movement Disorder Society</div>
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