Alcohol Abuse
Conditions
Brief summary
For an analytical validation of the method for the determination of blood hosphatidylethathanol, it is necessary to: * to compare the results of chronic and excessive ethanol patients with the cut-off proposed in the literature. * Also assess the stability of phosphatidylethanol in total blood collected, and in blotted dried blood stains (DBS), depending on temperature (ambient temperature and +4°C)
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Person with alcohol consumption ≥ 40g/day (women) and ≥ 60g/day (men) according to WHO criteria * Person hospitalized for a hospital withdrawal in the addiction service of Lille's hospital, without other distinctions.
Exclusion criteria
* Patient opposing the use of their personal data in the study * Patient subject to protective measures (guardianship or curatorship) * Person deprived of liberty
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of patients with a Peth concentration greater than 200 µg/L | at the end of study (at 6 months) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| the concentration of Peth in blood in ambiant temperature | between T0 and 96h and the end of study (at 6 months) | descrease expressed as a percentage of the initial concentration, in the primary blood tube (citrate tube) and stored at room temperature, |
| the concentration of Peth in blood at 4°C | between T0 and 96h and the end of study (at 6 months) | ecrease expressed as a percentage of the initial concentration, in the primary blood tube (citrate tube) and at 4°C. |
| the concentration of Peth in blood in DBS | between T0 and 4 weeks and the end of study (at 6 months) | decrease expressed as a percentage of the initial concentration, in the Dried Blood Spot (DBS) |
Contacts
University Hospital, Lille