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Safety and Depth of Sedation With Ketamine Alone Versus Ketamine With Midazolam in Pediatric Fracture Reduction: A
Kimberly Wells1, Vincent Calleo
1From the Department of Emergency Medicine, SUNY Upstate Medical University, Syracuse, NY.
Insights
Ketamine alone or with midazolam for pediatric fracture reduction sedation showed similar safety and efficacy. Midazolam coadministration slightly increased hypoxia risk and sedation length but did not impact sedation depth.
Area of Science:
- Emergency Medicine
- Pediatric Sedation
- Orthopedic Procedures
Background:
- Pediatric extremity fractures frequently necessitate procedural sedation in the pediatric emergency department (PED).
- While combination sedation may enhance orthopedic fracture reduction efficacy, concerns exist regarding increased adverse events in pediatric populations.
- Evidence comparing ketamine alone versus ketamine with midazolam for pediatric procedural sedation in orthopedic fracture reduction is limited.
Purpose of the Study:
- To compare the depth of sedation and incidence of adverse events using intravenous ketamine alone versus ketamine with midazolam for pediatric procedural sedation.
- To evaluate the safety and efficacy of ketamine-based sedation regimens for orthopedic fracture reduction in pediatric patients.
Main Methods:
- Retrospective cohort study of pediatric patients (2-18 years) undergoing sedation for fracture reduction in a PED.
- Comparison of adverse events, sedation depth (Ramsey score), medication doses, sedation duration, and discharge time between ketamine-alone and ketamine-midazolam groups.
- Logistic regression models were utilized to adjust for potential confounding variables.
Main Results:
- Hypoxia occurred more frequently with ketamine-midazolam coadministration (5% vs. 0%), though it was mild and resolved with supportive care.
- Sedation length was longer by approximately 3.5 minutes in the ketamine-midazolam group; time to PED discharge was not significantly different.
- No significant differences were observed in sedation depth, ketamine dosage, positive pressure ventilation, vomiting, agitation, or overall adverse events. No apnea or laryngospasm occurred.
Conclusions:
- Both ketamine alone and ketamine with midazolam demonstrate a low rate of adverse events for pediatric orthopedic fracture reduction.
- Coadministration of midazolam with ketamine is associated with a slight increase in hypoxia and sedation duration without affecting sedation depth.
- Further research is needed as information on orthopedic reduction quality and provider satisfaction was not collected in this study.
Objectives:
Pediatric patients with extremity fractures often require sedation for fracture reduction in the pediatric emergency department (PED). Although orthopedic literature suggests combination sedation regimens may be more effective for fracture reduction, some pediatric literature suggests adverse events are more frequent. The primary objective of this study is to determine the comparable depth of sedation and incidence of adverse events when intravenous ketamine is used alone versus with midazolam for pediatric procedural sedation and orthopedic fracture reduction.
Methods:
This is a retrospective cohort study of pediatric patients 2-18 years old who underwent sedation for fracture reduction in the PED at a single level 1 trauma center over a 2-year period. Medical records were reviewed, and occurrence of adverse events, depth of sedation (Ramsey score), midazolam dose, total ketamine administration, opiate administration, total sedation time, and time to PED discharge were compared in patients who received ketamine alone versus those who received ketamine with midazolam. Logistic regression models were adjusted to evaluate for potential confounders.
Results:
There was a statistically significant increase in the occurrence of hypoxia with coadministration of midazolam (5% vs 0%). When hypoxia occurred, it was mild and resolved with repositioning or administration of supplemental oxygen. Length of sedation was increased in sedations with coadministration of benzodiazepines by approximately 3.5 minutes. Time to PED discharge was not significantly different. There was no significant difference in depth of sedation, ketamine dose administered, end-tidal CO 2 measurements, administration of positive pressure ventilation, vomiting, agitation, or overall occurrence of adverse events. No patients developed apnea or laryngospasm.
Conclusions:
This study showed a low rate of adverse events in pediatric sedation for orthopedic reduction with ketamine alone or ketamine with midazolam. There was an increased occurrence of hypoxia with coadministration of midazolam and an increase in the length of sedation. This study showed no difference in depth of sedation based on Ramsay scores when midazolam was coadministered. Information on the orthopedic reduction and provider satisfaction was not collected.
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