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高剂量巴氯芬治疗酒精障碍患者的耐受性:一项回顾性研究。

Tolerability of High-dose Baclofen in the Treatment of Patients with Alcohol Disorders: A Retrospective Study.

作者信息

Rigal Laurent, Legay Hoang Léa, Alexandre-Dubroeucq Constance, Pinot Juliette, Le Jeunne Claire, Jaury Philippe

机构信息

Département de Médecine Générale, Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France

Département de Médecine Générale, Université Paris Descartes, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.

出版信息

Alcohol Alcohol. 2015 Sep;50(5):551-7. doi: 10.1093/alcalc/agv052. Epub 2015 Jun 2.

Abstract

AIMS

The aim of this study was to describe the tolerability of high-dose baclofen taken by patients with alcohol disorders during their first year of treatment.

METHODS

The medical records of all patients prescribed baclofen by one general practitioner were examined and all patients who could be contacted were retrospectively interviewed about adverse effects.

RESULTS

Of the 146 eligible patients, 116 (79%) could be interviewed. Ninety (78%) reported at least one adverse effect (mean number per patient: 2.8 ± 2.7). The mean dosage of baclofen at the onset of the first adverse effect was 83 ± 57 mg/day. The most frequent group of adverse effects involved disruption of the wake-sleep cycle and affected 73 patients (63%). Persistent adverse effects occurred in 62 patients (53%). Eight patients (7%) had adverse effects that led them to stop taking baclofen. Their dosages were <90 mg/day at that time. Alertness disorders and depression were the adverse effects that most frequently led to stopping baclofen. Bouts of somnolence and hypomanic episodes were the most potentially dangerous adverse effects. Women reported significantly more adverse effects than men.

CONCLUSION

High-dose baclofen exposes patients with alcohol disorders to many adverse effects. Generally persistent, some adverse effects appear at low doses and may be dangerous.

摘要

目的

本研究旨在描述酒精障碍患者在接受高剂量巴氯芬治疗的第一年中的耐受性。

方法

检查了由一名全科医生开具巴氯芬处方的所有患者的病历,并对所有能够联系到的患者进行了关于不良反应的回顾性访谈。

结果

在146名符合条件的患者中,116名(79%)接受了访谈。90名(78%)患者报告了至少一种不良反应(每位患者的平均不良反应数:2.8±2.7)。首次出现不良反应时巴氯芬的平均剂量为83±57毫克/天。最常见的不良反应组涉及睡眠-觉醒周期紊乱,有73名患者(63%)受影响。62名患者(53%)出现持续性不良反应。8名患者(7%)因不良反应而停止服用巴氯芬。当时他们的剂量<90毫克/天。警觉性障碍和抑郁是最常导致停止服用巴氯芬的不良反应。发作性嗜睡和轻躁狂发作是最具潜在危险性的不良反应。女性报告的不良反应明显多于男性。

结论

高剂量巴氯芬使酒精障碍患者面临许多不良反应。一些不良反应通常具有持续性,在低剂量时就可能出现且可能很危险。

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