374 - Pediatric Electronic Sepsis Alert Performance in Rural Community Emergency Department
Saturday, April 29, 2023
3:30 PM – 6:00 PM ET
Poster Number: 374 Publication Number: 374.211
Nancy Clemens, Janet Weis Children's Hospital at Geisinger, Cogan Station, PA, United States; Megan Zelonis, Janet Weis Children's Hospital at Geisinger, Pittston, PA, United States; Sarah Alander, Geisinger Medical Center, Danville, PA, United States
Assistant Professor of Emergency Medicine and Pediatrics Janet Weis Children's Hospital at Geisinger Medical Center Cogan Station, Pennsylvania, United States
Background: Most children seek emergency care at community emergency departments (ED) and not at specialized pediatric hospitalEDs. A two-stage electronic sepsisalert (ESA) screening tool has been shown to be highlysensitive and specific for recognizing sepsiswhen studied at an academic pediatric ED. It is unknown how pediatric electronic sepsis alerts perform in the community ED setting. Objective: To evaluate the performance of a pediatricESA in a rural community ED. Design/Methods: We evaluated the test characteristics of a pediatric ESA by completing asingle-site retrospective observational study in children presenting to a rural community EDbetween March 1, 2022 and August 31, 2022.We calculated sensitivity, specificity, positive and negative predictive value of the ESA, whether the patient was treated for sepsis in the ED, and whether sepsis was missed. A positive ESA (Table 1.) was defined as a high heart rate or low blood pressure that alerted the nurse to assess other risk factors and physical findings concerning for potential sepsis. We defined sepsis treatment as obtaining blood culture and receivingIV antibiotics and IV fluids. We defined missed sepsis as no ED sepsis treatment with subsequent ICU admission with IV antibiotics within 24 hours of admission. Results: 4264 children under 18 years presented to the ED over 6 months. Step one of the ESA triggered in 803(18.8%). A sepsis huddle was documented in 94(2.2%), and 40of those received sepsis treatment. Sepsis treatment was given to 86 children without a positive ESA. Sensitivity of ESA was 28.8% (95% CI: 21.4-37.1), specificity was 98.7% (95% CI: 98.3-99.0), positive predictive value42.6% (95% CI: 33.8-51.8%), and negative predictive value97.6% (95% CI: 97.4-97.9).There were 13 cases of missed sepsis; 8 had a positive step 1 which was dismissed and did not progress to the rest of the ESA (Figure 1.).
Conclusion(s): Use of the 2-stage ESA showed poor sensitivityin a community ED.The majority of missed sepsis cases had an initial alert due to abnormal vitals that did not progress to bedside huddle and treatment.Further research is required to determine how ESAs can be improved in community EDsto aid in identifying pediatric sepsis.