Baclofen Combined With Psychosocial Care is Useful and Safe in Alcohol-Related Cirrhosis Patients: A Real-Life Multicenter Study.


Journal

Alcohol and alcoholism (Oxford, Oxfordshire)
ISSN: 1464-3502
Titre abrégé: Alcohol Alcohol
Pays: England
ID NLM: 8310684

Informations de publication

Date de publication:
10 Mar 2023
Historique:
received: 09 06 2022
revised: 10 11 2022
accepted: 14 11 2022
pubmed: 18 12 2022
medline: 15 3 2023
entrez: 17 12 2022
Statut: ppublish

Résumé

Alcohol-related cirrhosis is a frequent and difficult-to-treat disease. Despite the low hepatic metabolism of baclofen, data on its use in this subgroup are scarce. The French multicenter Observatory of patients treated with Baclofen for Alcohol DEpendence real-life cohort assessed: (a) prescription modalities of baclofen in liver units; (b) safety profile of baclofen; and (c) declared alcohol intake, biological markers of excessive alcohol intake and hepatic function at 12 months. All consecutive patients with cirrhosis who received baclofen to reduce alcohol consumption or maintain abstinence were prospectively included. Psychosocial management was always associated. Clinical and biological data were collected every 3 months for 1 year. Between November 2013 and December 2016, 71 in- or outpatients were included from 10 liver units. Of the patients, 25% had ascites. After 12 months, 52 patients (73%) were still being followed, and 41 (57.7%) were still receiving baclofen at a mean dosage of 75 mg/day (r30-210). The overall declared consumption decreased from 100.2 to 14.7 g/day (P < 0.0001), and 29 patients (40.8%) reached abstinence. Significant improvement in the usual biomarkers of excessive alcohol intake (AST, GGT and MCV) and liver function (Prothrombin ratio (PTr), albumin levels) were observed. The usual side effects such as drowsiness were frequent (22%) but no serious adverse events (AEs) or overt encephalopathy related to baclofen was reported. In this 1-year follow-up series, baclofen was combined with psychosocial treatment in patients with cirrhosis and was well tolerated. This treatment was associated with a significant decrease in declared alcohol consumption as well as improvement in hepatic function.

Sections du résumé

BACKGROUND BACKGROUND
Alcohol-related cirrhosis is a frequent and difficult-to-treat disease. Despite the low hepatic metabolism of baclofen, data on its use in this subgroup are scarce. The French multicenter Observatory of patients treated with Baclofen for Alcohol DEpendence real-life cohort assessed: (a) prescription modalities of baclofen in liver units; (b) safety profile of baclofen; and (c) declared alcohol intake, biological markers of excessive alcohol intake and hepatic function at 12 months.
METHODS METHODS
All consecutive patients with cirrhosis who received baclofen to reduce alcohol consumption or maintain abstinence were prospectively included. Psychosocial management was always associated. Clinical and biological data were collected every 3 months for 1 year.
RESULTS RESULTS
Between November 2013 and December 2016, 71 in- or outpatients were included from 10 liver units. Of the patients, 25% had ascites. After 12 months, 52 patients (73%) were still being followed, and 41 (57.7%) were still receiving baclofen at a mean dosage of 75 mg/day (r30-210). The overall declared consumption decreased from 100.2 to 14.7 g/day (P < 0.0001), and 29 patients (40.8%) reached abstinence. Significant improvement in the usual biomarkers of excessive alcohol intake (AST, GGT and MCV) and liver function (Prothrombin ratio (PTr), albumin levels) were observed. The usual side effects such as drowsiness were frequent (22%) but no serious adverse events (AEs) or overt encephalopathy related to baclofen was reported.
CONCLUSION CONCLUSIONS
In this 1-year follow-up series, baclofen was combined with psychosocial treatment in patients with cirrhosis and was well tolerated. This treatment was associated with a significant decrease in declared alcohol consumption as well as improvement in hepatic function.

Identifiants

pubmed: 36527321
pii: 6918726
doi: 10.1093/alcalc/agac065
doi:

Substances chimiques

Baclofen H789N3FKE8

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-124

Informations de copyright

© The Author(s) 2022. Medical Council on Alcohol and Oxford University Press. All rights reserved.

Auteurs

Camille Barrault (C)

Liver, Digestive Disease and Addiction Unit, CH Intercommunal, Créteil 83056, France.

Shuaib Alqallaf (S)

Liver, Digestive Disease and Addiction Unit, CH Intercommunal, Créteil 83056, France.

Hortensia Lison (H)

Liver and Digestive Diseases Nutrition and Addiction Department, GHPSO, Creil 60100, France.

Isabelle Lamote-Chaouche (I)

Addiction Unit, Liver, Digestive Disease and Addiction Unit, GHEF, Meaux 44730, France.

Valérie Bourcier (V)

Liver Unit, AP-HP, Hôpitaux Universitaires Paris Seine Saint-Denis, Bobigny 93143, France.

Joëlle Laugier (J)

Liver, Digestive Disease and Addiction Unit, CH Delafontaine, Saint Denis, Bobigny 93200, France.

Thierry Thevenot (T)

Liver Unit and Intensive Care Unit, Hôpital Jean Minjoz, 25030 Besançon Cedex, France.
CIC-1431 INSERM, CHU de Besançon, Besançon 25030, France.

Damien Labarriere (D)

Liver, Digestive Disease and Addiction Unit, CH Régional, Orléans 75008, France.

Marie-Pierre Ripault (MP)

Liver, Digestive Disease and Addiction Unit, CH, Narbonne 11108, France.

Antonia Le Gruyer (A)

Liver, Digestive Disease and Addiction Unit, CH Yves Le Foll, Saint Brieuc 22000, France.

Charlotte Costentin (C)

Liver Unit, CHU Grenoble 38043, France.

Véronique Behar (V)

Liver, Digestive Disease and Addiction Unit, CH Intercommunal, Créteil 83056, France.

Hervé Hagege (H)

Liver, Digestive Disease and Addiction Unit, CH Intercommunal, Créteil 83056, France.

Camille Jung (C)

CRC CH Intercommunal, Créteil 94010, France.

Jean-François Cadranel (JF)

Liver and Digestive Diseases Nutrition and Addiction Department, GHPSO, Creil 60100, France.

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Classifications MeSH