ER2 and Deep Learning for Prediction of Adverse Health Outcomes

July 22, 2024 updated by: Olivier Beauchet, Jewish General Hospital

Emergency Room Evaluation for Older Users of Emergency Departments: Predicting Adverse Health Outcomes With Deep Learning Algorithms

An Emergency Department (ED) visit for an older adult is a high-risk medical intervention. Known adverse events (AE) include delirium, prolonged ED or hospital stay, hospitalization, recurrent ED visits and hospital death. These happen in a growing proportion in ED visitors over age 65 are over who are represented in ED visits.

Tools predicting AEs in the ED are of paramount importance to help decision-making on patient triage and disposition. They can help identify areas of unmet needs for seniors in order to develop targeted actions. Multiple scoring systems including "Programme de recherche sur l'intégration des services de maintien de l'autonomie" (PRISMA-7), Identification of Seniors at Risk (ISAR), Clinical Frailty Scale (CFS), Brief Geriatric Assessment (BGA) have extensively been studied in the ED and other settings for various outcomes. These tools rely on a simple scoring system that minimally trained staff can reliably and quickly administer. Doing otherwise is unlikely to be applicable to daily clinical practice.

As prediction accuracy has not significantly improved in the past decade, perhaps new analysis strategies are necessary. The current hype surrounding deep learning comes from better and cheaper hardware and the availability of simple and open-source libraries supported by large companies and a broad community of users. Hence, implementing deep learning (DL) algorithms is now open to a wide range of settings, including medical care in a standard clinical practice. DL has been shown to be more accurate than the average board-certified specialist on very specific tasks. Prediction of various clinical outcomes has produced less dramatic results, perhaps as traditional (non-DL) models already outperformed clinicians for many disease states. Published DL approaches applied to outcome prediction in the ED have focused on acutely ill adults in general, specific conditions or administrative issues such as admitting department or ED overcrowding. None have targeted a specific age group like older ED visitors.

An important caveat to many DL approaches is interpretation of results. To develop interventions based on targeted features associated with AEs in a given model, it has to be somewhat transparent. If multiple layers of NNs improve prediction compared to linear regression, they often provide no clinically relevant insight on how and which variables interact to yield that result.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Study Type

Observational

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Montréal, Quebec, Canada, H3T 1E2
        • Jewish General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

71 years and older (Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Between September 2017 and July 2020, 47 000 Emergency Department visits met the selection criteria. Training DL models on tabular data has been shown to be less effective than on unstructured sources such as images or sound. An appropriate mitigation strategy is to increase the quantity of data. Hence, all participants of the ER2 database will be included in the analysis. All visits will be included in the analysis.

Description

Inclusion Criteria:

  • Age above 75 years old
  • Unplanned Emergency department visit

Exclusion Criteria:

  • Do not meet inclusion criteria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
ER2 participants
all participants of ER2 database will be included in the analysis
No intervention, data analysis only

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ED length of stay
Time Frame: through database constitution, from September 2017 to July 2020
The length of emergencey department stay is defined as the average number of hours that patients spend in Emergency department.
through database constitution, from September 2017 to July 2020

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prolonged hospital stay
Time Frame: through database constitution, from September 2017 to July 2020
The prolonged length of hospital stay is defined as a stay above the average number of days that patients spend in hospital
through database constitution, from September 2017 to July 2020
Number of partciipants with at least one hospitalizations
Time Frame: through database constitution, from September 2017 to July 2020
Defined as the admission in hospital after an admission in Emergency department
through database constitution, from September 2017 to July 2020
recurrent ED visits
Time Frame: through database constitution, from September 2017 to July 2020
Defined as all the Emergency department recurrent visit within 30 days
through database constitution, from September 2017 to July 2020
Number of partciipants with diagnosis of delirium
Time Frame: through database constitution, from September 2017 to July 2020
Defined as a diagnosis of delirium in teh medical chart of the patient
through database constitution, from September 2017 to July 2020
Number of partciipants with hospital death
Time Frame: through database constitution, from September 2017 to July 2020
Defined as a reported death during hospitalization
through database constitution, from September 2017 to July 2020

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Olivier Beauchet, MD, McGill University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 24, 2023

Primary Completion (Actual)

February 24, 2023

Study Completion (Actual)

February 24, 2023

Study Registration Dates

First Submitted

December 14, 2020

First Submitted That Met QC Criteria

December 17, 2020

First Posted (Actual)

December 22, 2020

Study Record Updates

Last Update Posted (Actual)

July 23, 2024

Last Update Submitted That Met QC Criteria

July 22, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2021-2699

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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