Portrayal of Hospital Alcohol Detoxification in France (Alcostop)

October 18, 2021 updated by: University Hospital, Montpellier

Portrayal of Hospital Alcohol Detoxifications and Factors Associated With Longer or Ulterior Hospitalizations in France From 2011 to 2020

Even if hospital alcohol detoxifications are frequent in France, their caracteristicscharacteristics remain unknown. The investigators aim to describe the clinical and paraclinical caracteristicscharacteristics of their patients, their length and geographical repartition, etc… The investigators also aim to evaluate factors associated with longer stays or ulterior re-hospitalization for the same reason. Finally, The investigators aim to compare the stays by facility type.

Study Overview

Detailed Description

Context:

In France, the consequences of excessive alcohol use are one of the primary reasons for hospitalization. When stopping the substance, patients with an alcohol use disorder can suffer from a potentially fatal alcohol withdrawal syndrome. To mitigate these risks, a withdrawal under medical supervision is possible, either in an outpatient setting or in hospital, where the detoxification can be programmed or imposed. In the course of an alcohol dependent patient's life, re-drinking is not exceptional and the patient may undergo several withdrawals during his or her life.

Psychiatric pathologies, especially anxiety and depression, are more frequent in these patients than in the rest of the population, just as can be somatic pathologies.e. Withdrawal accidents, represented by comital seizures and delirium tremens, can be critical.

In hospital detoxifications, studies do not show any benefit in continuing the stay beyond 10 days, except in the case of somatic or psychiatric complication. However, little information is available on the average length of stay for hospital alcohol detoxification.

Although alcohol dependence issues are very frequent and the resulting withdrawals are relatively common and associated with numerous comorbidities, little data exists at a national level in France.

The aim of this study is to describe these hospital detoxifications: course, duration, frequency and clinical and paraclinical characteristics of the patients. We also wish to analyze which characteristics are associated with longer stays or re-hospitalization and to compare the care according to the facility type.

Objectives:

Main:

- To describe the clinical, paraclinical, and stay characteristics of hospital alcohol detoxification in France

Secondary:

  • To describe the regional distribution of hospital alcohol detoxification
  • To evaluate whether certain clinical characteristics are associated with a longer hospital stays
  • To evaluate whether certain clinical characteristics are associated with subsequent re-hospitalization for the same reason
  • To compare the characteristics of patient stays by type of facility

Methods:

In this descriptive observational study using pre-existing data accessed via the PMSI (Programme de Médicalisation des Systèmes d'Information), we will use all hospital stays from 2011 to 2020 for alcohol detoxification in France, both in public and private settings.

For each hospital stay will be collected the length, the antecedents of hospital alcohol detoxification, clinical and psychiatric comorbidities, withdrawals complication, alcohol use complication, further examinations.

We will describe the stays using median and quartiles for continuous variables and number and percentage for dichotomous variables. For secondary objectives, we will use a multivariate linear regression model if the length of stay is normal, an ordinal regression model otherwise. The characteristics of the stays will be compared regarding the type of facility using univariate comparative tests: Chi² or Fisher for dichotomous variables and Student or Mann-Whitney for continuous variables.

Study Type

Observational

Enrollment (Actual)

50000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Montpellier, France, 34295
        • Uhmontpellier

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

French patients hospitalized for alcohol detoxification from 2011 to 2020

Description

Inclusion criteria:

Inclusion criteria:

  • French patients of at least 18 years old
  • Inpatients of a public or private care facility for alcohol detoxification
  • From 01/01/2011 to 12/31/2020
  • In a medical or psychiatric hospital

Exclusion criteria:

- age < 18 years

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Inpatients for alcohol detoxifications
French patients who were hospitalized for alcohol detoxification from 2011 to 2020
Stay for alcohol detoxification : routine care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
description of age
Time Frame: day 1 (At hospital inclusion)
Age at admission (in years), calculated by the difference of the year of admission and the year of birth through the PMSI.
day 1 (At hospital inclusion)
description of sex
Time Frame: day 1 (At hospital inclusion)
Sex collected through the PMSI.
day 1 (At hospital inclusion)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
description of geographic code
Time Frame: day 1 (At hospital inclusion)
Sex collected through the PMSI.
day 1 (At hospital inclusion)
description of CMU-C
Time Frame: day 1 (At hospital inclusion)
CMU-C (universal complementary health insurance, collected through the PMSI.
day 1 (At hospital inclusion)
Length of stay
Time Frame: During the stay (day 1 - day 15)
Length of stay (in days), calculated by the difference between the discharge date and the entry date, collected through the PMSI.
During the stay (day 1 - day 15)
Care establishment
Time Frame: During the stay (day 1 - day 15)
Name and type of the care establishment, collected through the PMSI.
During the stay (day 1 - day 15)
Number of previous hospital detoxification stays in the studied period
Time Frame: During the stay (day 1 - day 15)
Number of previous hospital detoxification stays in the studied period, collected through the PMSI.
During the stay (day 1 - day 15)
Psychiatric comorbidities
Time Frame: During the stay (day 1 - day 15)
Psychiatric comorbidities (Major depression episode, anxiety, psychotic trouble, personality diseases), collected through the PMSI.
During the stay (day 1 - day 15)
Withdrawal complication
Time Frame: During the stay (day 1 - day 15)
Withdrawal complications (delirium tremens, comitial seizures), collected through the PMSI.
During the stay (day 1 - day 15)
Further examination
Time Frame: During the stay (day 1 - day 15)
Further examination (biology, imagery, etc…), collected through the PMSI.
During the stay (day 1 - day 15)
Re-hospitalization for same reason
Time Frame: day 1
For each patient, and each stay, we will evaluate if the patient had an ulterior re-hospitalization for alcohol withdrawal. Collected through the PMSI.
day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lionel MOULIS, University Hospital, Montpellier

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2021

Primary Completion (Actual)

August 30, 2021

Study Completion (Actual)

August 30, 2021

Study Registration Dates

First Submitted

July 6, 2021

First Submitted That Met QC Criteria

July 21, 2021

First Posted (Actual)

July 22, 2021

Study Record Updates

Last Update Posted (Actual)

October 19, 2021

Last Update Submitted That Met QC Criteria

October 18, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

NC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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