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Improving the Management of Vaso-Occlusive Episodes in the Pediatric Emergency Department
Patricia L Kavanagh1, Philippa G Sprinz2, Tahlia L Wolfgang2
1Department of Pediatrics, Boston University School of Medicine/Boston Medical Center, Boston, Massachusetts; and patricia.kavanagh@bmc.org.
Insights
Quality improvement initiatives significantly reduced emergency department wait times for pediatric sickle cell disease patients experiencing vaso-occlusive episodes. This led to faster pain management and increased patient discharges, without compromising safety.
Area of Science:
- Pediatric Emergency Medicine
- Hematology
- Quality Improvement Science
Background:
- Vaso-occlusive episodes (VOEs) are the primary cause of emergency department (ED) visits for children with sickle cell disease (SCD).
- Inefficiencies in ED care for VOEs can lead to delayed pain management and prolonged hospital stays.
- Addressing barriers to timely and effective VOE care is crucial for improving patient outcomes.
Purpose of the Study:
- To implement and evaluate a quality improvement (QI) initiative aimed at streamlining care for pediatric patients with SCD experiencing VOEs.
- To reduce the time to analgesic administration and decision-making for VOE management in the ED.
- To assess the impact of interventions on patient outcomes and safety.
Main Methods:
- A QI initiative was conducted in an urban pediatric ED from September 2010 to April 2014.
- Key interventions included a standardized VOE protocol, intranasal fentanyl, an SCD pain calculator, and provider/patient education.
- Data on process, outcome, and balancing measures were collected and analyzed.
Main Results:
- Significant reductions in the mean time to first parenteral opioid (56 to 23 minutes) and admission/discharge decisions were observed.
- The proportion of patients discharged from the ED increased from 32% to 48%.
- No adverse effects on safety measures, such as 24-hour readmission or respiratory depression, were noted.
Conclusions:
- Targeted interventions can significantly improve the efficiency and effectiveness of emergency care for pediatric sickle cell disease patients with VOEs.
- The implemented QI strategies led to faster pain relief and increased ED discharges.
- Further studies are warranted to confirm the replicability of these findings.
Objectives:
Vaso-occlusive episodes (VOEs) account for the majority of emergency department (ED) visits for children with sickle cell disease (SCD). We hypothesized that addressing key barriers to VOE care would improve receipt of analgesics and outcomes.
Methods:
A quality improvement (QI) initiative was conducted from September 2010 to April 2014 to streamline VOE care in an urban pediatric ED. Four interventions were used: a standardized time-specific VOE protocol; intranasal fentanyl as the first parenteral pain medication; an SCD pain medication calculator; and provider and patient/family education. Data were collected for 3 outcome measures (mean time from triage to first parenteral opioid and admission/discharge decision, and proportion discharged from the ED); 1 process measure (mean time from triage to initiation of patient-controlled analgesia); and 4 balancing measures (mean time from triage to second intravenous opioid dose, 24-hour ED readmission, respiratory depression, and length of stay).
Results:
There were 289 ED visits in the study period. Improvements were seen in mean time to: first dose of parenteral opioid (56 to 23 minutes); second opiate intravenous dose (106 to 83 minutes); admission and discharge decisions (163 to 109 minutes and 271 to 178 minutes, respectively); and initiation of patient-controlled analgesia (216 to 141 minutes). The proportion discharged from the ED increased from 32% to 48% (χ(2) = 6.5402, P = .01). No increase in 24-hour readmission, respiratory depression, or inpatient length of stay was observed.
Conclusions:
Using VOE-specific interventions, we significantly improved VOE care for children. Studies are needed to determine if these results can be replicated.
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