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A Prospective Study of the Safety and Effectiveness of Droperidol in Children for Prehospital Acute Behavioral
Insights
Droperidol effectively and safely sedated children experiencing acute behavioral disturbance in prehospital settings. This study found a low rate of adverse events, demonstrating droperidol
Area of Science:
- Emergency Medicine
- Pediatric Emergency Care
- Pharmacology
Background:
- Acute behavioral disturbance in children presents challenges for emergency medical services.
- Prehospital sedation is crucial for managing agitated pediatric patients.
- Limited data exists on droperidol's safety and efficacy in pediatric prehospital settings.
Purpose of the Study:
- To evaluate the safety and effectiveness of droperidol for children (<16 years) with acute behavioral disturbance.
- To assess adverse events and time to sedation following droperidol administration.
Main Methods:
- Prospective observational study over one year.
- Inclusion of children (<16 years) with acute behavioral disturbance (sedation assessment tool score ≥2).
- Administration of droperidol (0.1-0.2 mg/kg) with monitoring of primary outcomes (adverse effects) and secondary outcomes (time to sedation, need for additional sedation, sedation success).
Main Results:
- 96 pediatric patients (102 occasions) received droperidol.
- 8% of patients experienced adverse events, including asymptomatic hypotension and one case of respiratory depression.
- Successful sedation was achieved in 87% of patients, with a median time to sedation of 14 minutes and minimal need for additional sedation.
Conclusions:
- Droperidol is a safe and effective option for managing acute behavioral disturbance in pediatric patients in the prehospital setting.
- The study supports the use of droperidol for rapid and effective sedation in pediatric emergencies.
- Low rates of adverse events indicate a favorable safety profile for droperidol in this population.
Abstract:
Study objective: Although uncommon, children (<16 years) with acute behavioral disturbance are a significant issue for emergency medical service providers. In this study, we aimed to investigate the safety and effectiveness of droperidol in children with prehospital acute behavioral disturbance. Methods: This was a prospective observational study over 1 year investigating the use of droperidol (0.1-0.2 mg/kg) for children (< 16 years) with acute behavioral disturbance. Inclusion criteria for acute behavioral disturbance were defined by a sedation assessment tool score of ≥2 determined by the attending paramedic. The primary outcome was the proportion of adverse effects (need for airway intervention, oxygen saturation <90% and/or respiratory rate <12, systolic blood pressure <90 mmHg, sedation assessment tool score of -3 and dystonic reactions). Secondary outcomes included time to sedation (sedation assessment tool score decreased by 2 or more, or a score of zero), requirement for additional sedation, failure to sedate and proportion of sedation success defined as the number of patients successfully sedated who did not suffer any adverse events or receive additional sedation. Results: There were 96 patients (males 51 [53%], median age 14 years [range 7-15 years]) who presented on 102 occasions over the one year study period. Self-harm and/or harm to others was the commonest (74/105 [70%]) cause of acute behavioral disturbance followed by alcohol (16/105 [15%]). There were 9 adverse events in 8 patients (8/102 [8%]; 95% confidence intervals [CI]: 3-13%) Five patients had hypotension, all asymptomatic and only one required treatment; 2 dystonic reactions managed with benztropine and one patient with respiratory depression. Median time to sedation was 14 min (interquartile range (IQR): 10-20 min; range: 3-85 min). There was no requirement for prehospital additional sedation (0/102 [0%]; 95% CI: 0-4%) and additional sedation in the first hour of arrival to hospital was required by 4 patients (4/102 [4%]; 95% CI: 1-10%). Overall successful sedation was achieved in 89 (87%) patients. Conclusions: The use of droperidol in children for acute behavioral disturbance in the prehospital setting is both safe and effective.
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