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Clinical Trials/NCT05042804
NCT05042804
Completed
Not Applicable

Perioperative Outcome Risk Assessment With Computer Learning Enhancement

Washington University School of Medicine1 site in 1 country5,114 target enrollmentSeptember 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Morality
Sponsor
Washington University School of Medicine
Enrollment
5114
Locations
1
Primary Endpoint
Area under receiver-operating characteristic curve of clinician prediction for postoperative death
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This study will test whether anesthesiology clinicians working in a telemedicine setting can predict patient risk for postoperative complications (death and acute kidney injury) more accurately with access to a machine learning display than without it.

Detailed Description

The Perioperative Outcome Risk Assessment with Computer Learning Enhancement (Periop ORACLE) study will be a sub-study nested within the ongoing TECTONICS trial (NCT03923699). TECTONICS is a single-center randomized clinical trial assessing the impact of an anesthesiology control tower (ACT) on postoperative 30-day mortality, delirium, respiratory failure, and acute kidney injury. As part of the TECTONICS trial, investigators in the ACT perform medical record case reviews during the early part of surgery and document how likely they feel each patient is to experience postoperative death and acute kidney injury (AKI). In Periop ORACLE, these case reviews will be randomized to be performed with or without access to machine learning (ML) predictions. Investigators in the ACT will conduct all case reviews by viewing the patient's records in AlertWatch (AlertWatch, Ann Arbor, MI) and Epic (Epic, Verona, WI). AlertWatch is an FDA-approved patient monitoring system designed for use in the operating room. The version of AlertWatch used in this study has been customized for use in a telemedicine setting. Epic is the electronic health record system utilized at Barnes-Jewish Hospital. Each case review will be randomized in a 1:1 fashion to be completed with or without ML assistance. If the case review is randomized to ML assistance, the investigator will access a display interface (currently deployed as a web application on a secure server) that shows real-time ML predicted likelihood for postoperative death and postoperative AKI. If the case review is not randomized to ML assistance, the investigator will not access this display. After viewing the patient's data, the investigator will predict how likely the patient is to experience postoperative death and postoperative AKI and will document this prediction. The area under the receiver operating characteristic curves for predictions made with ML assistance and without ML assistance will be compared.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
November 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bradley Fritz

Instructor in Anesthesiology

Washington University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Surgery in the main operating suite at Barnes-Jewish Hospital
  • Surgery during hours of ACT operation (weekdays 7:00am-4:00pm)
  • Enrolled in the TECTONICS randomized clinical trial (NCT03923699)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Area under receiver-operating characteristic curve of clinician prediction for postoperative death

Time Frame: 30 days

Clinicians will predict the likelihood of postoperative death for each case using a categorical scale. A logistic regression will be constructed using the clinician predictions as inputs, and the area under the receiver-operating characteristic curve will be determined.

Area under receiver-operating characteristic curve of clinician prediction for postoperative acute kidney injury

Time Frame: 7 days

Clinicians will predict the likelihood of postoperative acute kidney injury for each case using a categorical scale. A logistic regression will be constructed using the clinician predictions as inputs, and the area under the receiver-operating characteristic curve will be determined.

Study Sites (1)

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