Skip to main content
Clinical Trials/NCT05502107
NCT05502107
Completed
Not Applicable

A Multicenter, Stepped Wedge, Cluster Randomized Study of a Prehospital Sepsis Protocol and Its Impact on Timely Antibiotic Administration in the Emergency Department and Subsequent Adverse Events

Emory University3 sites in 1 country984 target enrollmentJune 27, 2023
ConditionsSepsis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sepsis
Sponsor
Emory University
Enrollment
984
Locations
3
Primary Endpoint
Time to First Antibiotic Administration in the ED
Status
Completed
Last Updated
8 months ago

Overview

Brief Summary

The primary purpose of this study is to evaluate the impact of an Emergency Medical Services (EMS) based sepsis screening and early warning protocol on the timing of early sepsis care in the Emergency Department (ED).

Detailed Description

Sepsis is life-threatening medical emergency and a common cause of morbidity and mortality among hospitalized patients. Recognizing and treating sepsis immediately is key to achieving optimal patient outcomes after sepsis. The prehospital, EMS setting represents a unique opportunity to implement best practice by operationalizing guideline-recommended, system-wide sepsis screening protocols in an effort to facilitate earlier recognition of sepsis and minimize delays in evaluation and treatment. Unfortunately, evidence-based screening tools to assist EMS providers in recognizing this heterogenous syndrome are lacking, and recognition by EMS providers is generally poor. The purpose of this study is to evaluate the prehospital sepsis (PRESS) protocol, which is an evidence-based sepsis screening and early communication protocol designed for use in the prehospital, EMS environment. The PRESS protocol pairs a validated sepsis screening tool with a prehospital sepsis alert to the receiving ED for patients who are screen positive. This innovative approach has been used to improve patient care and outcomes in other life-threatening, time-sensitive medical emergencies including heart attack and stroke. Prehospital screening and an early warning call to the ED before patient arrival provides valuable lead time that makes immediate evaluation and treatment by EMS providers possible once a patient arrives in the ED. This study includes three study sites which are each comprised of cluster pairs of one EMS organization and one partnered acute care hospital. Each cluster pair will participate in both a baseline and intervention phase of study. EMS providers will be trained to screen for sepsis according to the PRESS protocol. The PRESS EMS protocol includes 2 major components: 1) an evidence-based sepsis screening tool, and 2) a prehospital sepsis alert call to the receiving hospital for participants who screen positive. Upon arrival to the ED, ED providers will provide immediate medical assessment to the patient to determine whether there is concern for sepsis. The overarching hypothesis is that implementation of an EMS-based sepsis screening and early warning protocol will be associated with a reduction in time first antibiotic administration in the ED among patients with sepsis.

Registry
clinicaltrials.gov
Start Date
June 27, 2023
End Date
July 15, 2025
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Carmen Polito

Assistant Professor

Emory University

Eligibility Criteria

Inclusion Criteria

  • Lowest EMS systolic blood pressure \<110 mmHg
  • Highest EMS pulse rate \>90 beats per minute
  • Highest EMS respiratory rate \>20 breaths per minute
  • EMS transport to a participating study ED/hospital
  • At least one of the following present:
  • Lowest systolic blood pressure \<90 mmHg
  • Age 40 years or greater
  • Hot temperature assessment or temp \>38 degrees Celsius
  • Oxygen saturation \<90%
  • Nursing home patient

Exclusion Criteria

  • Any of the following EMS conditions present:
  • Trauma injury
  • Cardiac arrest
  • Psychiatric emergency
  • Toxic ingestion
  • Pregnant patient
  • Inability to administratively link EMS and ED/hospital records
  • Patient left emergency department prior to being evaluated by a medical provider (inability to classify sepsis status)

Outcomes

Primary Outcomes

Time to First Antibiotic Administration in the ED

Time Frame: During ED stay on Day 1

Among eligible EMS patients with sepsis, the time from ED arrival to first antibiotic administration (parenteral only) in the ED will be examined. Time will be censored at the time of hospital admission or ED discharge.

Secondary Outcomes

  • Time to Sepsis Bundle from ED Arrival(During ED stay on Day 1)
  • In-hospital Death(During hospital stay (up to 20 days, on average))
  • EMS Documentation of a Prehospital Sepsis Alert(During ED stay on Day 1)
  • Proportion of Patients Admitted to the ICU(During hospital stay (up to 20 days, on average))
  • Hospital Length of Stay(During hospital stay (up to 20 days, on average))
  • Proportion of Patients Without Sepsis Receiving Antibiotics in the ED(During ED stay on Day 1)
  • Antibiotic Days of Therapy(Up to 10 days (on average))
  • EMS Documentation of Sepsis(During ED stay on Day 1)
  • Time to First Care Provider Documentation(During ED stay on Day 1)

Study Sites (3)

Loading locations...

Similar Trials