Emergency Medicine

Comprehensive Summary

In Australia, oral olanzapine and diazepam are commonly used to manage acute severe behavioral disturbances in children presenting to emergency departments. Bourke et al., conducted a multicenter randomized controlled trial (RCT) (October 2021-November 2023) across nine Australian emergency departments to compare the efficacy of oral olanzapine versus diazepam for behavioral sedation. The trial enrolled 348 patients aged 9-17 whose symptoms persisted despite nonpharmacologic interventions. Dosing was weight-based: patients < 40 kg received 5 mg, and those ≥ 40 kg received 10 mg of their assigned study drug. A successful sedation was defined as behavior containment without additional sedatives within one hour of administration. Successful sedation was achieved in 103 patients (61%) in the olanzapine group and in 90 patients (57%) in the diazepam group (p = 0.49). Secondary outcomes, including adverse effects, staff-directed aggression, length of stay, and satisfaction with care, did not differ significantly between groups. Notably, 40% of patients did not reach successful sedation within the first hour. The authors note that a success rate of approximately 60% may be suboptimal for clinical practice. They advocate for protocols to ensure timely recognition of acute behavioral disturbances and consideration of alternative or additional pharmacological agents when needed.

Outcomes and Implications

This RCT of 348 children found no significant difference between olanzapine and diazepam in sedation success, adverse effects, or secondary outcomes. Acute severe behavioral disturbance represents a high-risk emergency requiring rapid intervention to protect patients, families, and staff.

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