Adjuvant low-dose ketamine for pediatric sickle cell vaso-occlusive
episodes in the emergency department
Abstract
Background: Sickle cell disease (SCD) vaso-occlusive episodes (VOEs) are
managed primarily with opioids that can lead to dependence and
tachyphylaxis. Ketamine mitigates opioid tolerance and appears
efficacious for all-cause pain in the adult emergency department (ED).
We hypothesized that ED treatment with low-dose adjuvant ketamine (LDK)
for acute VOE is safe and decreases opioid usage in children and young
adults with SCD. Procedure: In this exploratory study, patients with SCD
aged 10-25 years presenting to UCSF Benioff Children’s Hospital Oakland
ED with VOE were eligible for a single 0.2 mg/kg IV dose of LDK, after
receipt of the first IV opioid dose. Safety, tolerability, and
subjective experience were assessed prospectively. Pain scores, length
of stay, likelihood of discharge from the ED, time to 50% pain
reduction, and morphine equivalent usage (mg/kg/h) for the intervention
visits were compared to the patient’s historical data within the year
prior. Results: No serious treatment emergent adverse events occurred in
the 62 enrolled patient-encounters in 25 individual patients. LDK
decreased morphine equivalent usage by 0.06 mg/kg/h (15%; 95% CI
[2.3%, 28%], p=0.004), but did not affect pain scores on
discharge, time to or likelihood of 50% pain reduction, or likelihood
of discharge. Subjectively, when assessed in their first LDK encounter,
the majority of patients reported faster pain relief (60%) and desired
LDK in the future (68%). Conclusions: LDK for SCD VOE in the pediatric
ED is safe, subjectively improves the experience of pain, and decreases
opioid usage. Larger studies are needed to confirm these findings.