Rapid tranquillisation of violent or agitated patients in a psychiatric emergency setting. Pragmatic randomised trial of intramuscular lorazepam v. haloperidol plus promethazine
- PMID: 15231557
- DOI: 10.1192/bjp.185.1.63
Rapid tranquillisation of violent or agitated patients in a psychiatric emergency setting. Pragmatic randomised trial of intramuscular lorazepam v. haloperidol plus promethazine
Abstract
Background: The pharmacological management of violence in people with psychiatric disorders is under-researched.
Aims: To compare interventions commonly used for controlling agitation or violence in people with serious psychiatric disorders.
Method: We randomised 200 people to receive intramuscular lorazepam (4 mg) or intramuscular haloperidol (10 mg) plus promethazine (25-50 mg mix).
Results: At blinded assessments 4 h later (99.5% follow-up), equal numbers in both groups (96%) were tranquil or asleep. However, 76% given the haloperidol-promethazine mix were asleep compared with 45% of those allocated lorazepam (RR=2.29,95% CI 1.59-3.39; NNT=3.2,95% CI 2.3-5.4). The haloperidol-promethazine mix produced a faster onset of tranquillisation/sedation and more clinical improvement over the first 2 h. Neither intervention differed significantly in the need for additional intervention or physical restraints, numbers absconding, or adverse effects.
Conclusions: Both interventions are effective for controlling violent/agitated behaviour. If speed of sedation is required, the haloperidol-promethazine combination has advantages over lorazepam.
Comment in
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Intramuscular haloperidol-promethazine sedates violent or agitated patients more quickly than intramuscular lorazepam.Evid Based Ment Health. 2005 Feb;8(1):7. doi: 10.1136/ebmh.8.1.7. Evid Based Ment Health. 2005. PMID: 15671498 No abstract available.
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Limitations of rapid tranquillisation trial.Br J Psychiatry. 2005 Aug;187:193-4; author reply 194. Br J Psychiatry. 2005. PMID: 16110594 No abstract available.
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Drug combinations for rapid tranquillisation.Br J Psychiatry. 2005 Aug;187:192-3; author reply 193. Br J Psychiatry. 2005. PMID: 16110595 No abstract available.
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