Evaluation of the API-VIGIE Monitoring System: Program to Reduce Emergency Visits for Severe Paroxysmal Alcoholism

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2022-02-28

Study Completion Date

2023-08-31

Brief Summary

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The study was designed to evaluate the APIVIGIE program use at CH d'Arras. The objective of this program is to reduce repeated visits by the same patient to the emergency room for Alcoholism Severe Paroxysmal

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Detailed Description

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In France, between 10% and 30% of emergency room admissions are linked to problematic alcohol consumption. This considerable weight of alcohol-related problems in the current problematic of emergencies is largely unknown and can lead to blockages in emergencies.

For acute intoxication requiring emergency care, 80% of admissions concern people dependent on alcohol. Here again, this crucial clinical notion is largely ignored: when a patient in a state of intoxication arrives in the emergency room, this should not be considered as a banal and one-off event, it is necessary to put in place a care, if necessary, of addiction.

Supported by a call for projects from the Hauts-de-France Regional Health Agency, the Addictions Service of the Arras Hospital is setting up a monitoring system called APIVIGIE.

APIVIGIE program is offered to patients who present to the emergency room for a diagnosis of API after an evaluation by the liaison team of the addiction service. If the patient agrees to be part of the program, he will receive a resource card with the APIVIGIE phone number to contact if necessary.

The link will be maintained with the Addictology Care, Support and Prevention Center (CSAPA) for a period of 6 months, by telephone consultations, or by video-consultations or face-to-face consultations.

Conditions

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Intoxication;Alcohol;Acute Emergencies

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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prospective study

API-VIGIE program adult participant who agreed to participate in the study

Medical Outcomes Study Short Form 36 (SF 36)

Intervention Type OTHER

completion of questionnaire quality of life SF 36 (inclusion, Month 3, Month 6).

retrospective study

Any stay for adults patients in the emergency room of the ARRAS hospital for API during the period covered (from 1 year before to 1 year after the installation of the APIVIGIE program) (main diagnosis or associated with an API (F10.0 according to the ICD-10 classification used by Department of Medical Information)

observationnal study

Intervention Type OTHER

data collection

Interventions

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Medical Outcomes Study Short Form 36 (SF 36)

completion of questionnaire quality of life SF 36 (inclusion, Month 3, Month 6).

Intervention Type OTHER

observationnal study

data collection

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient 18 years or older;
* Participant at API-VIGIE program.

Exclusion Criteria

* Patient's opposition to participating in the research;
* Persons under legal protection (under tutorship or curatorship);
* Person deprived of liberty;
* Pregnant or breastfeeding women.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No