Objectives: The aim of this study was to evaluate the effect of levetiracetam on tardive dyskinesia (TD), which is known to be a major limitation of chronic antipsychotic drug therapy, particularly with conventional antipsychotics. Methods: Sixteen patients suffering from chronic psychosis with TD were enrolled consecutively. Levetiracetam was given in gradually increasing doses, starting with 125 twice a day until the best clinical benefit was achieved (mean dosage, 2290 mg; range, 1000-3000 mg). Tardive dyskinesia was assessed using the Abnormal involuntary Movement Scale at baseline and after 1 month and 3 months of treatment with levetiracetam. Results: Compared with baseline, there was a significant improvement in the Abnormal involuntary Movement Scale score after 1 month still present after 3 months (P < 0.001). All patients well tolerated levetiracetam, except one who dropped out of the trial after the first 2 weeks owing to excessive drowsiness. Conclusions: The results of this open-label observational study suggest that levetiracetam is a well-tolerated drug and effectively controls TD.
Levetiracetam in tardive dyskinesia / Meco, Giuseppe; E., Fabrizio; Antonio, Epifanio; Francesca, Morgante; Valente, Marcella; Vanacore, Nicola; Antonio E., Di Rosa; Letterio, Morgante. - In: CLINICAL NEUROPHARMACOLOGY. - ISSN 0362-5664. - 29:5(2006), pp. 265-268. [10.1097/01.wnf.0000228807.49044.7d]
Levetiracetam in tardive dyskinesia
MECO, Giuseppe;VALENTE, Marcella;VANACORE, NICOLA;
2006
Abstract
Objectives: The aim of this study was to evaluate the effect of levetiracetam on tardive dyskinesia (TD), which is known to be a major limitation of chronic antipsychotic drug therapy, particularly with conventional antipsychotics. Methods: Sixteen patients suffering from chronic psychosis with TD were enrolled consecutively. Levetiracetam was given in gradually increasing doses, starting with 125 twice a day until the best clinical benefit was achieved (mean dosage, 2290 mg; range, 1000-3000 mg). Tardive dyskinesia was assessed using the Abnormal involuntary Movement Scale at baseline and after 1 month and 3 months of treatment with levetiracetam. Results: Compared with baseline, there was a significant improvement in the Abnormal involuntary Movement Scale score after 1 month still present after 3 months (P < 0.001). All patients well tolerated levetiracetam, except one who dropped out of the trial after the first 2 weeks owing to excessive drowsiness. Conclusions: The results of this open-label observational study suggest that levetiracetam is a well-tolerated drug and effectively controls TD.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.