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Quetiapine versus haloperidol in the treatment of delirium: a double-blind, randomized, controlled trial

Authors Maneeton B, Maneeton N, Srisurapanont M, Chittawatanarat K

Received 22 March 2013

Accepted for publication 28 May 2013

Published 24 July 2013 Volume 2013:7 Pages 657—667

DOI https://doi.org/10.2147/DDDT.S45575

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 3


Benchalak Maneeton,1 Narong Maneeton,1 Manit Srisurapanont,1 Kaweesak Chittawatanarat2

1Department of Psychiatry, 2Department of Surgery, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand

Background: Atypical antipsychotic drugs may have low propensity to induce extrapyramidal side effects in delirious patients. This study aimed to compare the efficacy and tolerability between quetiapine and haloperidol in controlling delirious behavior.
Methods: A 7-day prospective, double-blind, randomized controlled trial was conducted from June 2009 to April 2011 in medically ill patients with delirium. Measures used for daily assessment included the Delirium Rating Scale-revised-98 (DRS-R-98) and total sleep time. The Clinical Global Impression, Improvement (CGI–I) and the Modified (nine-item) Simpson–Angus Scale were applied daily. The primary outcome was the DRS-R-98 severity scores. The data were analyzed on an intention-to-treat basis.
Results: Fifty-two subjects (35 males and 17 females) were randomized to receive 25–100 mg/day of quetiapine (n = 24) or 0.5–2.0 mg/day of haloperidol (n = 28). Mean (standard deviation) doses of quetiapine and haloperidol were 67.6 (9.7) and 0.8 (0.3) mg/day, respectively. Over the trial period, means (standard deviation) of the DRS-R-98 severity scores were not significantly different between the quetiapine and haloperidol groups (-22.9 [6.9] versus -21.7 [6.7]; P = 0.59). The DRS-R-98 noncognitive and cognitive subscale scores were not significantly different. At end point, the response and remission rates, the total sleep time, and the Modified (nine-item) Simpson–Angus scores were also not significantly different between groups. Hypersomnia was common in the quetiapine-treated patients (33.3%), but not significantly higher than that in the haloperidol-treated group (21.4%).
Limitations: Patients were excluded if they were not able to take oral medications, and the sample size was small.
Conclusion: Low-dose quetiapine and haloperidol may be equally effective and safe for controlling delirium symptoms.
Clinical trials registration number: clinicaltrials.gov NCT00954603.

Keywords: delirium, quetiapine, haloperidol, extrapyramidal symptoms

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