Abstract |
While haloperidol is still widely used in the treatment of psychoses, the optimal daily dose remains a topic of controversy, particularly in first-episode psychosis. Previous studies have suggested that doses as low as 2 mg/d may be effective, whereas others have indicated superiority for higher over lower doses. This double-blinded, randomized controlled study compared the efficacy and tolerability of 2 vs. 8 mg/d of haloperidol over 6 wk in 40 subjects with first-episode psychosis. Both treatments were equally effective in reducing the PANSS Total and subscale scores. The low dose of haloperidol was better tolerated, with fewer extrapyramidal side-effects, less frequent use of anticholinergic medication and smaller elevations in prolactin levels. Using a low dose of haloperidol is at least as effective as, and better tolerated than a high dose of haloperidol in the treatment of first-episode psychosis.
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Authors | Piet Oosthuizen, Robin Emsley, H Jadri Turner, Natasha Keyter |
Journal | The international journal of neuropsychopharmacology
(Int J Neuropsychopharmacol)
Vol. 7
Issue 2
Pg. 125-31
(Jun 2004)
ISSN: 1461-1457 [Print] England |
PMID | 15003147
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antipsychotic Agents
- Prolactin
- Haloperidol
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Topics |
- Adolescent
- Adult
- Antipsychotic Agents
(administration & dosage, adverse effects, therapeutic use)
- Double-Blind Method
- Drug Interactions
- Dyskinesia, Drug-Induced
(epidemiology)
- Female
- Haloperidol
(administration & dosage, adverse effects, therapeutic use)
- Humans
- Male
- Middle Aged
- Prolactin
(blood)
- Psychiatric Status Rating Scales
- Psychotic Disorders
(drug therapy, psychology)
- Schizophrenia
(drug therapy)
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