Anton R F
Institute of Psychiatry, Medical University of South Carolina, Charleston 29425-0742, USA.
Alcohol Clin Exp Res. 1996 Oct;20(7 Suppl):3A-9A. doi: 10.1111/j.1530-0277.1996.tb01183.x.
As the number of pharmacological agents for the treatment of alcoholism continues to proliferate, there is an increasing need to design studies that accurately measure the efficacy of these agents. Key study design issues include selecting subjects, calculating patient retention, determining medication compliance, maintaining adequate sample size to ensure that a clinically meaningful therapeutic effect will not be missed, and measuring the study outcome, including the amount of alcohol consumed and levels of craving. Because there is evidence that self-report of alcohol consumption and medication compliance can be unreliable in subjects, biological methods have been used. One type of direct measurement, carbohydrate-deficient transferrin levels, has been found to be a reasonably sensitive indicator of alcohol consumption that may provide meaningful outcome information. The ingestion of riboflavin with medication and its urinary measurement is an accepted method of compliance detection. Improved study design will lead to continued advances in pharmacotherapy for the treatment of patients with alcoholism.
随着用于治疗酒精中毒的药物数量不断增加,设计能够准确衡量这些药物疗效的研究变得愈发必要。关键的研究设计问题包括选择受试者、计算患者留存率、确定药物依从性、维持足够的样本量以确保不会错过具有临床意义的治疗效果,以及测量研究结果,包括饮酒量和渴望程度。由于有证据表明受试者对饮酒量和药物依从性的自我报告可能不可靠,因此采用了生物学方法。一种直接测量方法,即缺糖转铁蛋白水平,已被发现是饮酒量的一个相当敏感的指标,可能会提供有意义的结果信息。药物服用时同时摄入核黄素并对其尿液进行测量是一种公认的依从性检测方法。改进的研究设计将推动酒精中毒患者药物治疗的持续进展。