Treatment of severe, incapacitating action myoclonus is difficult. Piraceta
m has been shown to be a very potent antimyoclonic agent, but only at very
high, impractical doses, ranging from 24 to 40 g/d. Levetiracetam (LEV), a
new antiepileptic drug, is a structurally related compound that has a disti
nct pharmacological profile and appears to be efficient at much lower doses
. We gave LEV, 4,000 mg/d, without titration, to three volunteers with post
-anoxic myoclonus (PAM) (one case) and Unverricht-Lundborg disease (two cas
es), over 2, 2 and 10 weeks, respectively. LEV produced a clear abatement o
f myoclonus, which is demonstrated on video for the patient with post-anoxi
c myoclonus, without any unwanted side-effects. These preliminary findings
suggest that LEV may have interesting antimyoclonic properties that deserve
further investigation.