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Association of Race and Ethnicity with Sedation Management in Pediatric Intensive Care
JoAnne E Natale1, Lisa A Asaro2, Jill G Joseph3
1Department of Pediatrics, University of California, Davis, Sacramento, California.
Insights
This study found scattered differences in pain management and sedation for critically ill Black, Hispanic, and white children. While no group consistently benefited, implicit bias in racial disparities cannot be ruled out.
Area of Science:
- Pediatric Critical Care Medicine
- Pain Management and Sedation
- Health Disparities Research
Background:
- Racial disparities in pediatric pain management are documented, particularly in emergency care settings.
- Understanding these disparities in critically ill, mechanically ventilated children is crucial for equitable care.
- The RESTORE trial provides a unique dataset to investigate race and ethnicity's impact on sedation and pain management.
Purpose of the Study:
- To investigate associations between patient race/ethnicity and pain management/sedation goals.
- To analyze differences in opioid and benzodiazepine use among diverse pediatric populations.
- To assess outcomes like pain episodes, withdrawal syndrome, and 'awake and calm' status by race/ethnicity.
Main Methods:
- Secondary analysis of the RESTORE cluster-randomized clinical trial data.
- Inclusion of 2,271 pediatric patients from 31 U.S. pediatric intensive care units.
- Categorization of patients into non-Hispanic white, non-Hispanic Black, and Hispanic groups.
Main Results:
- No significant differences in opioid or benzodiazepine selection or cumulative dosing across race/ethnicity groups.
- Black patients experienced fewer pain episodes and less iatrogenic withdrawal syndrome compared to white and Hispanic patients in specific arms.
- No significant differences in the percentage of days awake and calm while intubated across groups.
Conclusions:
- Sedation management in critically ill children showed varied, inconsistent differences across racial and ethnic groups.
- The findings suggest complex factors influencing care, without a clear advantage for any single group.
- The potential role of implicit bias in persistent racial disparities in pediatric critical care warrants further investigation.
Abstract:
Rationale: Racial disparities in pain management have been previously reported for children receiving emergency care.Objectives: To determine whether patient race or ethnicity is associated with the broader goal of pain management and sedation among pediatric patients mechanically ventilated for acute respiratory failure.Methods: Planned secondary analysis of RESTORE (Randomized Evaluation of Sedation Titration for Respiratory Failure). RESTORE, a cluster-randomized clinical trial conducted in 31 U.S. pediatric intensive care units, compared protocolized sedation management (intervention arm) with usual care (control arm). Participants included 2,271 children identified as non-Hispanic white (white, n = 1,233), non-Hispanic Black (Black, n = 502), or Hispanic of any race (Hispanic, n = 536).Results: Within each treatment arm, neither opioid nor benzodiazepine selection, nor cumulative dosing, differed significantly among race and ethnicity groups. Black patients experienced fewer days with an episode of pain (compared with white patients in the control arm and with Hispanic patients in the intervention arm) and experienced less iatrogenic withdrawal syndrome (compared with white patients in either arm or with Hispanic patients in the intervention arm). The percentage of days awake and calm while intubated was not significantly different in pairwise comparisons by race and ethnicity groups in either the control arm (median: white, 75%; Black, 71%; Hispanic, 75%) or the intervention arm (white, 86%; Black, 88%; Hispanic, 85%).Conclusions: Across multiple measures, our study found scattered differences in sedation management among critically ill Black, Hispanic, and white children that did not consistently favor any group. However, racial disparities related to implicit bias cannot be completely ruled out.Clinical trial registered with clinicaltrials.gov (NCT00814099).
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