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Cross-Sectional Study on Adverse Events Linked to Ambulatory Care

France, 2008
Reference ID
FRESH-PEF9027-en
Producer(s)
Philippe Michel, Jean-Luc Quenon
Metadata
DDI/XML JSON
Created on
Nov 15, 2025
Last modified
Nov 15, 2025
Page views
2
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Study authorization
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Quality standards
  • Data Access
  • Contacts
  • Metadata production

    • Identification

    Survey ID number

    FRESH-PEF9027-en
    Title

    Cross-Sectional Study on Adverse Events Linked to Ambulatory Care
    Abbreviation or Acronym

    EVISA
    Country
    Name
    France
    Abstract

    To estimate the frequency, severity and preventability of adverse events linked to ambulatory care, as well as investigate the context and contributing factors on the occurrence of these events and to estimate the hospital treatment costs.
    Kind of Data

    ['Participant-reported health data']
    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Emergency medicine health theme
    cim-11 http://id.who.int/icd/entity/933902267
    Keywords
    iatrogenesis treatment-related adverse event medical accidents and incidents outpatient care patient safety nosocomial health safety risk

    Coverage

    Universe

    {
    "level_sex_clusion_I": [
    "Male",
    "Female"
    ],
    "level_age_clusion_I": [
    "Young Adult (19 to 24 years)",
    "Adult (25 to 44 years)",
    "Middle Aged (45 to 64 years)"
    ],
    "level_type_clusion_I": [
    "Patients population"
    ],
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Philippe Michel
    Jean-Luc Quenon
    Funding Agency/Sponsor
    Name
    MINISTERE DU TRAVAIL, DE LA SANTE, DES SOLIDARITES ET DES FAMILLES

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sample frame

    Unit Type

    ['Through organizations (health services or institutions, schools, businesses, etc.)']
    Sampling Procedure

    ['Probability: Stratified']

    Survey instrument

    Questionnaires

    Access on specific project only
    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start
    2008
    Time Method

    Cross-sectional study: one-time (excluding case-control studies)
    Mode of data collection
    • Interview with the participant (including clinical)

    Study activities

    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health event/mortality

    Quality standards

    Quality standards
    Standard
    ['Data quality control was carried out in three stages:']
    Other quality statement
    • The CCECQA (Coordination Committee for Clinical Evaluation and Quality in Aquitaine) carried out checks in institutions to verify proper data collection conduct, adherence to the method, as well as the completeness and quality of collected data. - Researchers and research associates coded questionnaires and checked for completeness and consistency. - All questionnaires were reviewed by CCECQA methodologists. Problematic records (unclear; inconsistent; complex clinical situation; episodes, causes or impact of an unusual event, etc.) were reviewed by a case review committee and, if required, by field experts.

    Data Access

    Access conditions

    Contact the principal investigator
    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Philippe Michel philippe.michel@ccecqa.asso.fr
    Jean-Luc Quenon jean-luc.quenon@ccecqa.asso.fr

    Metadata production

    DDI Document ID

    FRESH-PEF9027-en
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