Barrault Camille, Lison Hortensia, Roudot-Thoraval Françoise, Garioud Armand, Costentin Charlotte, Béhar Véronique, Medmoun Mourad, Pulwermacher Georges, Hagège Hervé, Cadranel Jean-François
aLiver and Addiction Unit, Intercommunal Hospital bPublic Health Department cLiver Unit, Universitary Hospital Henri Mondor, Créteil dLiver and Addiction Unit, Federation of Public Hospitals of South of Oise, Creil, France.
Eur J Gastroenterol Hepatol. 2017 Oct;29(10):1155-1160. doi: 10.1097/MEG.0000000000000922.
Several studies have suggested the efficacy of baclofen in reducing alcohol consumption, leading to a temporary recommendation for use in France.
Our aim was to report our experience in using baclofen in alcohol-dependant patients with or without liver cirrhosis.
Consecutive patients from two liver and alcohol units were recruited over a 3-year period and received increasing doses of baclofen associated with social, psychological, and medical care.
One hundred patients were treated, of whom 65 were cirrhotic. After 1 year, 86 patients were still being followed up. At a mean dosage of 40 mg/day (extremes: 30-210), the median daily alcohol consumption reduced from 80 to 0 g/day (P<0.001). Twenty patients drank a small amount of alcohol of up to 30 g/day and 44 patients were completely abstinent. These declarative results were associated with a significant improvement in alcohol-related biological markers in this 'low-consumption' group of 64 patients: the median γ-glutamyl transferase decreased from 3.9 to 2.0 UNL (P<0.001), the mean aspartate transaminase decreased from 2.6 to 1.2 UNL (P<0.001), and the mean corpuscular volume decreased from 101 to 93 µm (P<0.001). In cirrhotic patients, bilirubinemia decreased significantly from 22 to 11 µmol/l (P=0.026), prothrombin time increased from 68 to 77% (P<0.001), and albuminemia increased from 34.1 to 37.4 g/l (P<0.001). Twenty patients reported grades 1-2 adverse events. No liver or renal function deterioration occurred in cirrhotic patients.
In our cohort, baclofen associated with a global care was very well tolerated even in cirrhotic patients. The marked reduction in alcohol consumption in 64 patients translated into a significant improvement in biological markers and in liver function tests. Baclofen could be very useful, especially in cases of severe alcoholic liver disease.
多项研究表明巴氯芬在减少酒精摄入量方面具有疗效,这使得法国曾临时推荐使用该药。
我们的目的是报告我们在使用巴氯芬治疗有或无肝硬化的酒精依赖患者中的经验。
在3年期间招募了来自两个肝脏与酒精治疗科室的连续患者,并给予逐渐增加剂量的巴氯芬,同时提供社会、心理和医疗护理。
共治疗了100例患者,其中65例患有肝硬化。1年后,86例患者仍在接受随访。平均剂量为每日40毫克(范围:30 - 210毫克)时,每日酒精摄入量中位数从80克降至0克/天(P<0.001)。20例患者每天饮用少量酒精,最多30克,44例患者完全戒酒。在这64例“低饮酒量”患者中,这些陈述性结果与酒精相关生物学标志物的显著改善相关:γ-谷氨酰转移酶中位数从3.9降至2.0 UNL(P<0.001),天冬氨酸转氨酶平均值从2.6降至1.2 UNL(P<0.001),平均红细胞体积从101降至93 µm(P<0.001)。在肝硬化患者中,胆红素血症从22显著降至11 µmol/l(P = 0.026),凝血酶原时间从68%增至77%(P<0.001),白蛋白血症从34.1增至37.4 g/l(P<0.001)。20例患者报告了1 - 2级不良事件。肝硬化患者未出现肝或肾功能恶化。
在我们的队列中,即使在肝硬化患者中,巴氯芬联合全面护理的耐受性也非常好。64例患者酒精摄入量的显著减少转化为生物学标志物和肝功能检查的显著改善。巴氯芬可能非常有用,尤其是在严重酒精性肝病的病例中。