PAthwAy of Dyspneic patIent in Emergency (PArADIsE)

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT02800122
Collaborator
(none)
4,000
1
56
71.4

Study Details

Study Description

Brief Summary

This is an observational retrospective single-center study (CHRU of Nancy) in patients cared for acute dyspnea by a medical team of the emergencies of the CHRU of Nancy.

The main purpose of the study is to evaluate the outcome of patients cared for acute dyspnea by a medical team of emergencies of CHRU of Nancy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This observational retrospective single-center study will be conducted using data from medical records, acquired as part of usual care, patients cared for acute dyspnea in the last 5 years (from the date of authorization of data processing). About 4,000 patients will be affected, including more than 800 patients with acute heart failure.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    4000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    PAthwAy of Dyspneic patIent in Emergency
    Actual Study Start Date :
    Mar 1, 2016
    Actual Primary Completion Date :
    Dec 1, 2018
    Anticipated Study Completion Date :
    Nov 1, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with acute dyspnea

    Patients with acute dyspnea treated by a medical team of emergencies of CHRU of Nancy. All patients admitted to the emergencies in the last 5 years matching the inclusion criteria will be evaluated. About 4,000 patients will be affected, including more than 800 patients with acute heart failure. (Figures based on export of ICD X codes (R06.0: Dyspnea) of patients cared in extra-hospital for acute dyspnea (diagnosis Dyspnea + Heart Failure) over the last 5 years).

    Outcome Measures

    Primary Outcome Measures

    1. All cause in-hospital mortality [in the last 5 years]

    Secondary Outcome Measures

    1. Demographic and clinical data of patients cared by a medical team of emergencies [in the last 5 years]

    2. Duration of total hospitalization (including emergency stay and conventional hospitalization) [in the last 5 years]

    3. The main diagnosis of the initial hospitalization [in the last 5 years]

    4. Rate of Brain Natriuretic Peptide (BNP) [in the last 5 years]

    5. Administration of non-invasive ventilation and / or diuretics and / or nitrates [in the last 5 years]

    6. Administration time of non-invasive ventilation and / or diuretics and / or nitrates [in the last 5 years]

    7. Service type admitting the patient after the emergency care (intensive care, cardiology, intensive care cardiology, other ...) [in the last 5 years]

    8. Admission time in a service after the emergency care [in the last 5 years]

    9. Mortality and re-hospitalization of included patients [in the last 5 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Man or women ≥ 18 years

    • Patients with acute dyspnea cared by a medical team of the emergencies of CHRU of Nancy.

    Exclusion Criteria:
    • Cardiorespiratory arrest before the care by a medical team of the emergencies of the CHRU of Nancy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHRU Nancy - Service des Urgences Nancy France 54000

    Sponsors and Collaborators

    • Central Hospital, Nancy, France

    Investigators

    • Principal Investigator: Tahar CHOUIHED, MD, Central Hospital, Nancy, France
    • Principal Investigator: Nicolas GIRERD, MD, Central Hospital, Nancy, France

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Central Hospital, Nancy, France
    ClinicalTrials.gov Identifier:
    NCT02800122
    Other Study ID Numbers:
    • R2016-08
    First Posted:
    Jun 15, 2016
    Last Update Posted:
    Nov 25, 2019
    Last Verified:
    Nov 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Central Hospital, Nancy, France
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 25, 2019