Abstract

We investigated the hemodynamic and mortality effects of continuous ketamine infusion in critically ill pediatric patients. We conducted a retrospective cohort study in a tertiary pediatric intensive care unit (PICU). Patients who used continuous sedative from 2015 to 2017 for 24 hours or more were included. We compared blood pressure, heart and respiratory rates, vasogenic medications, and sedation and pain scores for 12 hours before and after initiation of continuous ketamine. The mortality rates for continuous ketamine and Non-ketamine groups were compared by multivariate logistic regression. A total of 240 patients used continuous sedation, and 82 used continuous ketamine. The median infusion rate of ketamine was 8.1 mcg/kg/min, and the median duration was 6 days. Heart rates (138 vs. 135 beat/minute, P = .033) and respiratory rates (31 vs. 25 respiration/minute, P = .001) decreased, but blood pressure (99.9 vs. 101.1 mm Hg, P = .124) and vasogenic medications did not change after ketamine infusion. Continuous ketamine was not a significant risk factor for mortality (hazard ratio 1.352, confidence interval 0.458–3.996). Continous ketamine could be used in PICU without hemodynamic instability. Further studies in randomized controlled design about the effects of continuous ketamine infusion on hemodynamic changes, sedation, and mortality are required.

Highlights

  • Pediatric patients in intensive care units (ICUs) are frequently treated with sedatives and analgesics because critical care is a stressful, painful experience [1]

  • In the pediatric intensive care unit (PICU) under study, opioid-based analgosedatives were used as an initial sedative for most mechanically ventilated patients according to analgesia-first sedation suggested in the guideline for pain, agitation, and delirium management [13]

  • A total of 730 patients were admitted to the PICU, and 297 received at least one sedative agent

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Summary

Introduction

Pediatric patients in intensive care units (ICUs) are frequently treated with sedatives and analgesics because critical care is a stressful, painful experience [1]. Based on concerns about benzodiazepine-induced delirium and opioid tolerance, healthcare providers are seeking alternative or additive agents.

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