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

Centre Hospitalier Arras

Status: Withdrawn

Conditions: Emergencies; Intoxication;Alcohol;Acute

Treatments: Other: Medical Outcomes Study Short Form 36 (SF 36); Other: observationnal study

Study type: Observational

Funder types: Other

Identifiers

NCT05173116

2020-08

Details and patient eligibility

About

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

Full description

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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

0 participants in 2 patient groups

prospective study

Description:

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

Treatment:

Other: Medical Outcomes Study Short Form 36 (SF 36)

retrospective study

Description:

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)

Treatment:

Other: observationnal study