Predictive Tracking of Patient Flow in the Emergency Services During the Virus Winter Epidemics (PREDAFLU)

Epidemics and infectious diseases in general, punctuate much of the activity of an emergency service. The impact of winter infections is particularly important to vulnerable populations such as infant during bronchiolitis epidemics and the elderly during seasonal influenza. Each year, these epidemic phenomena lead to disorganization of emergency services and healthcare teams by lack of anticipation and organizational measures in particular to manage the approval of emergency services for the most vulnerable populations requiring hospitalization.

For 2 years, the pediatric emergency department of St Etienne University Hospital has a decision support tool for the periods of winter epidemics. Through a retrospective analysis of Passages of Emergency summary, this tool provides an estimate of infants with bronchiolitis flow day to day, and the availability in real time of an abnormally high flow of patients to pediatric emergencies. These data can help to affirm that the epidemic begins in this hospital.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

760000

Contacts and Locations

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

Study Contact

Study Contact Backup

Study Locations

      • Grenoble, France, 38000
        • CHU de Grenoble (adult emergency service)
      • Grenoble, France, 38000
        • CHU de Grenoble (pediatric service)
      • Lyon, France, 69000
        • CHU de Lyon (adult emergency service)
      • Lyon, France, 69000
        • CHU de Lyon (laboratory of virology)
      • Lyon, France, 69000
        • CHU de Lyon HFME (pediatric service)
      • Saint Etienne, France, 42055
        • CHU de Saint Etienne (adult emergency service)
      • Saint Etienne, France, 42055
        • CHU de Saint Etienne (Pediatric service)
      • Valence, France, 26000
        • CH de Valence (adult emergency service)
      • Valence, France, 26000
        • CH de Valence (pediatric service)
      • Villefranche Sur Saone, France, 69655
        • CH de Villefranche (adult emergency service)
      • Villefranche Sur Saone, France, 69655
        • CH de Villefranche (pediatric service)

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

1 month and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

child < 24 months with bronchiolitis or elderly < 60 years with acute renal failure

Description

Inclusion Criteria:

  • child < 24 months with bronchiolitis
  • elderly < 60 years with acute renal failure or breathing problem

Exclusion Criteria:

  • refuse of transmission of their data

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: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
patients < 24 months or 60 years with bronchiolitis or ARF
ARF = Acute Renal Failure
data retrieval with the Hospital Information System

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
build a predictive tool
Time Frame: at inclusion

a tool with different levels of alerts of the influx of people aged to emergencies during winter epidemics.

Variables in the model : activity database in emergency services, computer data, virology database and average length of stay.

at inclusion

Secondary Outcome Measures

Outcome Measure
Time Frame
Difference between the estimated date and the effective date of the activity peak on the average length of stay of patients in the hospital of Saint Etienne
Time Frame: at inclusion
at inclusion
Difference between the estimated date and the effective date of the activity peak on the average length of stay of patients in the other hospitals
Time Frame: at inclusion
at inclusion
Comparison virological databases with clinical diagnosis of patients
Time Frame: at inclusion
at inclusion
Percentage of elderly staying more than 10 hours in the emergency services.
Time Frame: at inclusion
at inclusion

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Olivier MORY, MD, Centre Hospitalier Universitaire de Saint Etienne

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)

September 1, 2016

Primary Completion (Actual)

December 31, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

August 1, 2016

First Submitted That Met QC Criteria

August 3, 2016

First Posted (Estimated)

August 8, 2016

Study Record Updates

Last Update Posted (Actual)

March 22, 2024

Last Update Submitted That Met QC Criteria

March 21, 2024

Last Verified

March 1, 2024

More Information

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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