Bromperidolo decanoato del disturbo schizofrenico in fase residua

Translated title of the contribution: Bromperidol decanoate in the residual phase of schizophrenia

E. Smeraldi, C. Cocconcelli, L. Canova, C. Faravelli, F. P. Marchetti, G. Mariani, V. Rapisarda

Research output: Contribution to journalArticle

Abstract

We assessed the safety and therapeutic efficacy of bromperidol decanoate in a six-month open trial on 21 patients (13 males and 8 females), mean age 41.3 years, who were no longer in the acute phase and were being treated as outpatients. The recommended initial dosage was 150 mg bromperidol (one 3 ml ampoule), and this did not in fact have to be increased during the trial. The scores for psychotic symptom rating scales (SAPS, SANS, BPRS, HAM-D and social adaptation scale) were analysed by analysis of variance, which indicated that bromperidol decanoate was effective on almost all parameters. Adverse reactions were reported for 14.3% of the patients, indicating that the drug was very well tolerated; only three patients complained of a total of seven adverse events. In conclusion, bromperidol decanoate was effective in the treatment of residual schizophrenia, with significant differences between before and after treatment ratings for symptoms. The drug was well tolerated, only one patient dropping out on account of adverse reactions.

Translated title of the contributionBromperidol decanoate in the residual phase of schizophrenia
Original languageItalian
Pages (from-to)39-44
Number of pages6
JournalMinerva Psichiatrica
Volume37
Issue number1
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Psychiatry and Mental health

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