Risperidone, haloperidol, and placebo in the treatment of aggressive challenging behaviour in patients with intellectual disability: a randomised controlled trial
| Autor: | Zed Ahmed, Nick Bouras, Shoumitro Deb, Patricia C Oliver-Africano, Bernard V. North, Ben Reece, Adrienne Regan, Mike J. Crawford, David Thomas, Sherva Cooray, Michael Meade, David Harley, Sabyasachi Bhaumik, Kofi Kramo, Joseph Eliahoo, Anju Soni, Bharti Rao, Shamshad Karatela, Monica Hare, Peter Tyrer, Declan G. Murphy |
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| Rok vydání: | 2008 |
| Předmět: |
Adult
Male medicine.medical_specialty Challenging behaviour medicine.medical_treatment Poison control Placebo law.invention Randomized controlled trial law Internal medicine medicine Haloperidol Humans Mental Competency Psychiatry Antipsychotic Modified Overt Aggression Scale Aged Risperidone business.industry Mental Disorders General Medicine Middle Aged Aggression Patient Compliance Female business medicine.drug Antipsychotic Agents |
| Zdroj: | Lancet (London, England). 371(9606) |
| ISSN: | 1474-547X |
| Popis: | Summary Background Aggressive challenging behaviour is frequently reported in adults with intellectual disability and it is often treated with antipsychotic drugs. However, no adequate evidence base for this practice exists. We compared flexible doses of haloperidol (a typical, first-generation antipsychotic drug), risperidone (an atypical, second-generation antipsychotic), and placebo, in the treatment of this behaviour. Methods 86 non-psychotic patients presenting with aggressive challenging behaviour from ten centres in England and Wales, and one in Queensland, Australia, were randomly assigned to haloperidol (n=28), risperidone (n=29), or placebo (n=29). Clinical assessments of aggression, aberrant behaviour, quality of life, adverse drug effects, and carer uplift (positive feelings about the care of the disabled person) and burden, together with total costs, were recorded at 4, 12, and 26 weeks. The primary outcome was change in aggression after 4 weeks' treatment, which was recorded with the modified overt aggression scale (MOAS). Analysis was by intention to treat. This study is registered as ISRCTN 11736448. Findings 80 patients had adherence of 80% or more to prescribed drug. Aggression decreased substantially with all three treatments by 4 weeks, with the placebo group showing the greatest change (median decrease in MOAS score after 4 weeks=9 [95% CI 5–14] for placebo, 79% from baseline; 7 [4–14] for risperidone, 58% from baseline; 6·5 [5–14] for haloperidol, 65% from baseline; p=0·06). Furthermore, although no important differences between the treatments were recorded, including adverse effects, patients given placebo showed no evidence at any time points of worse response than did patients assigned to either of the antipsychotic drugs. Interpretation Antipsychotic drugs should no longer be regarded as an acceptable routine treatment for aggressive challenging behaviour in people with intellectual disability. |
| Databáze: | OpenAIRE |
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