Quality improvement initiative reduced non-indicated antibiotic use for febrile neutropenia in children, indicating better alignment with guidelines.
Background Management of febrile neutropenia in previously healthy, presumed immunocompetent children varies. Overtreatment impacts the patients, families, and the healthcare system. With guidance from a Canadian Paediatric Society (CPS) Practice Point, most well-appearing children with an episode of febrile neutropenia can be managed with reduced exposure to antibiotics and close outpatient follow-up. Objectives The aim of this initiative was to safely reduce antibiotic use in this low-risk patient population presenting to the emergency department (ED). Design/Methods A multidisciplinary team designed a quality improvement (QI) initiative from July 2023 – July 2024. Treatment with antibiotics was classified as indicated or non-indicated according to guidance from the CPS Practice Point. Patient management from the year prior to guideline publication (baseline) was compared to the intervention period. Interventions involved guideline dissemination, provider education, and point of care tools to facilitate clinical decision-making and follow-up. Outcome measures included the proportion of children receiving antibiotics, hospital admission, and appropriate laboratory follow-up. Re-presentation to ED and missed serious bacterial infections (SBI) were monitored as balancing measures. Outcomes were evaluated using descriptive statistics and statistical process control (SPC) charts. Results Three hundred and ninety-eight (398) children with febrile neutropenia were included. The proportion of non-indicated antibiotics was 6.7% at baseline. Due to the low baseline use of non-indicated antibiotics, an SPC was used to detect special cause variation. Special cause was demonstrated with 97 consecutive cases occurring without error (non-indicated antibiotics). Following the occurrence of special cause variation until the end of the study, only 1.6% of children received non-indicated antibiotics. There was no increase in re-presentations to ED (9% vs 8%; p= 0.65) nor missed SBI (0% vs 0%). Influenza was prevalent during the intervention period, accounting for 71% of positive viral tests (n=64/90) in children with febrile neutropenia. Severe neutropenia resolved in 90% of evaluable children, with a median duration of 44 days. Four children had persistent neutropenia and were referred to Paediatric Hematology; all were diagnosed with benign or immune neutropenia. Conclusion QI methodology can facilitate the timely adoption of best practices to align local clinical care with new national guidelines. Implementation of the CPS recommendations allowed low-risk children with febrile neutropenia to avoid unnecessary antibiotic exposure and hospital admission. This work demonstrates an excellent opportunity for ED providers and paediatricians to reduce low-value treatment while simultaneously enhancing patient- and family-centered care.Figure 1.(A) P chart: Administration of non-indicated antibiotics in patients presenting to the Alberta Children’s Hospital ED with fever and neutropenia, presented as a proportion of the total patients per month. (B) G chart: Number of cases between errors (error = receipt of non-indicated antibiotics) among patients presenting to the Alberta Children’s Hospital ED with fever and neutropenia. The mean from the baseline period was used as the center line, with upper (UCL) and lower control limits (LCL) at 3-sigma above and below the mean.
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