Sepsis Electronic Prompting for Timely Intervention and Care for Emergency Department Patients (SEPTIC-ED)
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About
The goal of this clinical trial is to study systemic inflammatory response syndrome (SIRS) electronic health record (EHR) alerts for sepsis in the emergency department (ED). The main question it aims to answer is: do nurse alerts, prescribing clinician alerts, or both nurse and prescribing clinician alerts improve time to sepsis treatment for patients in the ED?
Nurses and prescribing clinicians will receive SIRS alerts based on the group to which the patient is randomly assigned. Researchers will compare four groups: no alerts, nurse alerts only, prescribing clinician alerts only, or both nurse and prescribing clinician alerts.
Full description
SEPTIC is a master protocol for two trials on distinct subpopulations: emergency department (ED) patients and inpatients. This protocol "ID: AAAU1002 - ED" describes the ED subpopulation study while "ID: AAAU1002 - IP" describes the inpatient subpopulation study.
Sepsis is a major cause of death both globally and in the United States. Early identification and treatment of sepsis are crucial for improving outcomes. International guidelines recommend hospital sepsis screening programs, which are commonly implemented in the electronic health record (EHR) as an interruptive screening alert based on systemic inflammatory response syndrome (SIRS) criteria. Despite widespread use, it is unknown whether these sepsis screening and alert tools improve the delivery of high-quality sepsis care. This study tests interruptive (pop-up) EHR alerts. Epic Systems, the company that produces the EHR, refers to these types of alerts as BestPractice Advisories (BPAs).
Enrollment
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Inclusion and exclusion criteria
Patient Inclusion Criteria:
- age > 18 years-old
- meets SIRS criteria
- physically located in the emergency department
- not located in a hospital unit that takes care of pregnant and peri-partum patients
- not SARS-COV-2 PCR positive in past 7 days
- does not have an active order for "comfort measures only"
Patient Exclusion Criteria:
- already having sepsis treatment ordered (if prescribing clinician alert) or collected/completed (if nurse alert)
- already enrolled in the SEPTIC study (including as an emergency department patient or as an inpatient)
Trial design
Primary purpose
Allocation
Interventional model
Masking
25,668 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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