Abstract | OBJECTIVE: Beta-blocking agents, particularly propranolol, are considered effective in the treatment of neuroleptic-induced akathisia, but considerable controversy exists about the involved receptor subtype(s). The authors conducted a randomized, controlled trial comparing the effects of propranolol and betaxolol to determine whether central beta 1-adrenoceptor blockade is sufficient to correct neuroleptic-induced akathisia. METHOD: The subjects were 19 patients whose neuroleptic-induced akathisia responded to 20 mg/day of propranolol and subsequently reemerged during a placebo washout period. They were randomly assigned to propranolol (20 or 40 mg/day) or betaxolol (10 or 20 mg/day) and, after another placebo period, were switched to the second beta blocker. RESULTS: CONCLUSIONS: The lack of difference between propranolol and betaxolol suggests that beta 1-adrenoceptor blockade is sufficient to improve neuroleptic-induced akathisia. The results of this explanatory study need therapeutic confirmation.
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Authors | J P Dumon, J Catteau, F Lanvin, B A Dupuis |
Journal | The American journal of psychiatry
(Am J Psychiatry)
Vol. 149
Issue 5
Pg. 647-50
(May 1992)
ISSN: 0002-953X [Print] United States |
PMID | 1349458
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Antipsychotic Agents
- Placebos
- Propranolol
- Betaxolol
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Topics |
- Adult
- Akathisia, Drug-Induced
- Antipsychotic Agents
(adverse effects)
- Betaxolol
(therapeutic use)
- Double-Blind Method
- Humans
- Middle Aged
- Placebos
- Propranolol
(therapeutic use)
- Psychomotor Agitation
(drug therapy)
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