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1710. Clostridioides difficile Bundle Implementation Reduces Unnecessary Testing in Pediatric Patients

BACKGROUND: Failure to follow proper guidelines can lead to inappropriate Clostridioides difficile infection (CDI) testing in pediatric patients, resulting in incorrect diagnoses and antibiotic overuse. The Infectious Diseases Society of America and Society for Healthcare Epidemiology of America rec...

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Detalles Bibliográficos
Autores principales: Sietsema, Lydia, Maples, Holly, Honeycutt, Michele, Boyanton, Bobby, Forbus, John, Snowden, Jessica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677042/
http://dx.doi.org/10.1093/ofid/ofad500.1543
Descripción
Sumario:BACKGROUND: Failure to follow proper guidelines can lead to inappropriate Clostridioides difficile infection (CDI) testing in pediatric patients, resulting in incorrect diagnoses and antibiotic overuse. The Infectious Diseases Society of America and Society for Healthcare Epidemiology of America recommend a 2-step testing algorithm incorporating restrictions based on age, exposure, and underlying conditions. With these recommendations, a CDI bundle was implemented to reduce unnecessary testing in pediatric patients. Outcomes were measured via National Healthcare Safety Network (NHSN) LabID reporting. METHODS: An interdisciplinary team reviewed the CDI ordering process in a 24-bed community pediatric hospital with an Emergency Department (ED). Previous testing only used toxigenic C. difficile PCR without order restrictions. In September 2021, a CDI bundle was implemented, including a 2-step algorithm (toxigenic C. difficile PCR, toxin A/B immunoassay), a physician guidance pathway, and Epic order restrictions (Table 1). Outcomes were measured by examining NHSN LabID data before and after bundle implementation. Inpatient and ED data were reported under the appropriate NHSN patient safety module. CDI rates were calculated by the number of infections/1000 inpatient days and number of infections/1000 ED encounters. There was a 12-month pre-implementation period (August 2020-July 2021), a 3-month implementation period (August 2021-October 2021), and a 12-month post-implementation period (November 2021-October 2022). [Figure: see text] RESULTS: A statistically significant decrease in the CDI incidence was seen after CDI bundle implementation (P< 0.05 for both inpatient and ED using test of proportions). The average CDI incidence decreased from 2.24 to zero infections/1000 inpatient days (Figure 1) and from 0.58 to 0.02 infections/1000 ED encounters (Figure 2). [Figure: see text] [Figure: see text] CONCLUSION: CDI diagnostic bundle implementation effectively decreased the number of abnormal CDI test results, and positively impacted data reported to NHSN. Further analysis is warranted to delineate the impact of CDI bundle implementation on patient treatment, antimicrobial stewardship, and healthcare costs. DISCLOSURES: Jessica Snowden, MD, MHPTT, Pfizer: Advisor/Consultant