Reorientation of Tripped Patients 4 and 5 in Emergency Department

Sponsor
Centre Hospitalier de Saint-Denis (Other)
Overall Status
Recruiting
CT.gov ID
NCT05392829
Collaborator
(none)
368
1
5.9
61.9

Study Details

Study Description

Brief Summary

The increase in emergency room visits is partly related to the growing increase in unscheduled care, paradoxically associated with a decrease in the outpatient supply in the city. The "avoidable" passing rate is estimated at 43% in the last major DREES survey on hospital emergencies. Emergency services have been facing this challenge for years, but there is an urgent need to rethink its organizational model with the liberal system to meet this growing demand. Reorientation from the reception of emergencies is one of the avenues envisaged to face this challenge. It offers a different course from that of emergencies, provided that there are care structures equipped and adapted to unscheduled care. The Hospital in Saint-Denis is particularly faced with these challenges given a particular social ecosystem.

Methodology :

This single-center prospective observational study includes all adult patients sorted 4 and 5 by the reception organizing nurse, present during the survey.

The reorientation is one of the solutions proposed in the context of reorganizing access to care throughout the territory, appearing as one of the major public health issues in the coming years, it is appropriate to ask the question on a local scale. particularly exposed to the problem of unscheduled care, if patients are eligible for reorientation The non-medical factors identified as limiting the reorientation are: the absence of social cover, the language barrier, the patients referred by the samu or the fire brigade or a doctor, the patients who came by ambulance (because considered in theory as in the impossibility to move or having already been the subject of a "regulation")

Each 4 or 5 redirected patient is included and completes a questionnaire allowing the collection of information relating to their care pathways.

Primary endpoint :

Determine the proportion of patients not eligible for reorientation on non-medical criteria via a questionnaire, and identify the distribution of factors complicating reorientation

Secondary endpoints :

Identify the needs of patients re-orientated towards city medicine via the analysis of their passage to the emergency room, the reasons for their recourse to the emergency room (reasons, means and modes of arrival) their knowledge of the health system, and their relationship to general medicine

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    368 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Reorientation of Tripped Patients 4 and 5 in Emergency Department to the City Medicine
    Actual Study Start Date :
    Feb 15, 2022
    Actual Primary Completion Date :
    Jun 30, 2022
    Anticipated Study Completion Date :
    Aug 15, 2022

    Outcome Measures

    Primary Outcome Measures

    1. socio-demographic characteristics [Day 1]

      medical history, social security coverage, french language

    2. reason for consultation [Day 1]

      emergency assessment

    Secondary Outcome Measures

    1. care pathway [Day 1]

      time spent in the emergency room, additional examinations, diagnosic, becoming

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • patients tripped 4 and 5 at the IOA

    • patients aged 18 years or older

    • patients presenting to the emergency room every day of the week during the day and in the evening

    Exclusion Criteria:
    • patients triaged 1, 2, 3 at the IOA

    • consulting patients for reasons requiring psychiatric advice

    • unaccompanied minor patients

    • patients brought by the police

    • refusal or impossibility to participate

    • protected adult patients

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hôpital DELAFONTAINE Saint-Denis Ile De France France 93200

    Sponsors and Collaborators

    • Centre Hospitalier de Saint-Denis

    Investigators

    • Principal Investigator: Aurélie GIRARD, Centre Hospitalier de Saint-Denis

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Centre Hospitalier de Saint-Denis
    ClinicalTrials.gov Identifier:
    NCT05392829
    Other Study ID Numbers:
    • CHSD_0015_URGENCES
    • 2021-A01989-32
    First Posted:
    May 26, 2022
    Last Update Posted:
    Aug 11, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 11, 2022