MedPath

Effect of Automated Real-time Feedback on Early Sepsis Care

Not Applicable
Completed
Conditions
Sepsis
Interventions
Other: SCTP
Registration Number
NCT05625464
Lead Sponsor
Massachusetts General Hospital
Brief Summary

Sepsis is the leading cause of death among US hospitals, accounting for 6% of all hospitalizations and 35% of all inpatient deaths. International guidelines and the CMS SEP-1 bundle stress the importance of adhering to specific steps in the diagnosis and management of sepsis. This can be very difficult, especially in the setting of a busy ED, ward, or ICU where there are multiple simultaneous demands on providers' attention and time. Critical steps can be missed or delayed. The CMS SEP-1 bundle is a measure of compliance with sepsis care that is being tracked nationally across hospitals.

Unfortunately, a recent study demonstrated that every hour of delay to the completion of a sepsis bundle, including antibiotic administration, was associated with a 4% increase in risk-adjusted hospital mortality.

One strategy to improve the care and outcomes of patients with sepsis is the use of information technology to support our providers in a targeted manner. Technology has already been developed and deployed to help with the early identification of patients with sepsis using a Best Practice Alert (BPA), which has been in place at our hospital since 2017. This pop-up window alerts the team to the possibility of sepsis based on data within the medical record. However, once the alert is accepted or declined, the BPA does not offer ongoing support to clinicians, leaving the clinician to track and execute multiple time-based and inter-dependent sepsis bundle measures in a busy, hectic environment. To augment this existing tool, here we propose to study the efficacy of a novel technology called the Sepsis Care Tracking Platform (SCTP) to provide ongoing support at the bedside to providers, thus improving the care we deliver to patients.

SCTP is a monitoring and notification platform that aims to increase the timely delivery of key elements of evidence-based sepsis care. This platform, which was built by clinicians for clinicians, leverages the electronic medical record (EMR) to track real-time compliance with key components of the CMS SEP-1 bundle - timely antibiotics, blood cultures prior to antibiotics, initial lactate, and repeat lactate for those patients with an initially elevated level. SCTP underwent technical validation in Fall 2019 with a pilot in the MGH Emergency Department. The pilot confirmed that SCTP correctly identified missing bundle elements and paged the appropriate team members connected with the patient's care. The pilot also did not find alarm fatigue to be an issue. We hypothesize that SCTP will increase our hospital's compliance with sepsis process metrics and improve patient outcomes.

By monitoring real-time data and automatically alerting bedside providers to missing elements within an actionable timeframe, SCTP has the potential to drive improvements in clinical care even in the extremely busy and complex environment of the emergency department and inpatient units.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3269
Inclusion Criteria
  1. Adult patients aged 18 years old and over
  2. Who triggered a sepsis best practice advisory that was subsequently acknowledged by a treating clinician as "yes, sepsis possible"
Exclusion Criteria
  1. Transfer from an outside hospital
  2. Sepsis best practice advisory triggered while the patient is in an intensive care unit
  3. Sepsis best practice advisory triggered while the patient is in a perioperative care area

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionSCTPReceived SCTP monitoring and standard of care
Primary Outcome Measures
NameTimeMethod
3-hour sepsis bundle order complianceWithin 3 hours of sepsis BPA trigger (time zero)

Overall 3-hour bundle ordering compliance, defined as orders for all 3-hour bundle measures monitored by the study platform completed within the bundle time limits - i.e., orders for antibiotics, blood cultures, and lactate measurement measured from the electronic medical record at the end of the study period

Secondary Outcome Measures
NameTimeMethod
Early intensive care unit admissionwithin 72 hours of time-zero

Early intensive care unit (ICU) admission, defined as ICU admission or death within 72 hours of time-zero

Repeat lactate delivery compliancewithin 6 hours of time-zero and within 3 hours of initial lactate measurement

Repeat lactate delivery compliance, defined as the measurement of a repeat lactate within 6 hours of time-zero and within 3 hours of initial lactate measurement, among patients with an initial lactate \> 2.0mmol/L

Hospital length of stayThrough day 28 after time zero

Hospital length of stay, defined as hospital days from time-zero through day 28

Mortality by Day 28Within 28 days of time zero

Mortality by Day 28

3-hour sepsis bundle care delivery complianceWithin 3 hours of sepsis BPA trigger (time zero)

Overall 3-hour bundle care delivery compliance, defined as the implementation of all 3-hour bundle measures monitored by the study platform completed within the bundle time limits - i.e., administration of antibiotics, collection of blood cultures prior to antibiotic administration, and lactate measurement.

Antibiotic delivery compliancewithin 3 hours of timezero

Antibiotic delivery compliance, defined as administration of antibiotics within 3 hours of timezero

Mechanical ventilation during hospitalizationwithin 28 days of time-zero

Mechanical ventilation during hospitalization, defined as receipt of mechanical ventilation or death within 28 days of time-zero

Early antibiotic discontinuationat least 24 hours by 48 hours post-time-zero

Early antibiotic discontinuation, defined as discontinuation of all antibiotics for at least 24 hours by 48 hours post-time-zero

Antibiotic order compliancewithin 3 hours of timezero

Antibiotic ordering compliance, defined as orders for antibiotics placed within 3 hours of timezero

Initial lactate delivery compliancewithin 3 hours of time-zero

Initial lactate delivery compliance, defined measurement of initial lactate within 3 hours of time-zero

Early mechanical ventilationwithin 72 hours of time-zero

Early mechanical ventilation, defined as the receipt of mechanical ventilation or death within 72 hours of time-zero

Blood culture order compliancewithin 3 hours of time-zero

Blood culture ordering compliance, defined as orders for blood cultures placed within 3 hours of time-zero

Initial lactate order compliancewithin 3 hours of time-zero

Initial blood lactate level ordering compliance, defined as orders for initial blood lactate level within 3 hours of time-zero

Repeat lactate order complianceplaced within 6 hours of time-zero and within 3 hours of initial lactate measurement

Repeat blood lactate level ordering compliance, defined as orders for repeat blood lactate level placed within 6 hours of time-zero and within 3 hours of initial lactate measurement, among patients with initial lactate \> 2.0mmol/L

Blood culture delivery compliancewithin 3 hours of timezero and prior to antibiotic administration

Blood cultures delivery compliance, defined collection of blood cultures within 3 hours of timezero and prior to antibiotic administration

Any culture positivity24 hours before or 7 days after time zero

Any culture positivity, defined as a composite of positive results from either the blood or non-blood culture positivity outcome

Blood culture positivity24 hours before or 7 days after time zero

Blood culture positivity, defined as bacterial growth recovered from any blood culture collected 24 hours before or 7 days after time zero

Non-blood culture positivity24 hours before or 7 days after time zero

Non-blood culture positivity, defined as bacterial pathogen recovery from any urine, respiratory, peritoneal, pleural, joint, or cerebrospinal fluid culture collected 24 hours before or 7 days after time zero

Trial Locations

Locations (1)

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

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