Feighner J, Hendrickson G, Miller L, Stern W
J Clin Psychopharmacol. 1986 Feb;6(1):27-32.
A double-blind controlled study comparing the effects of bupropion to doxepin in outpatients with primary depression was conducted to evaluate efficacy and safety differences between the two drugs. Following a 7-day placebo washout period, patients could be treated for up to 13 weeks on either treatment. Antidepressant response was assessed by the Hamilton Depression and Anxiety Scales, Clinical Global Severity and Improvement Ratings, and the Zung Self-Rating Depression Scale. Comparable efficacy between the compounds was found across the 13-week study. Doxepin differed from bupropion mainly on the sleep factor of the Hamilton Depression Scale, with doxepin improving sleep to a greater extent than bupropion. Doxepin produced a greater incidence of anticholinergic side effects, including dry mouth, constipation, sleepiness, and tiredness, in comparison to bupropion. Also, increased appetite and weight gain were consistent side effects of doxepin relative to bupropion.
开展了一项双盲对照研究,比较安非他酮与多塞平对原发性抑郁症门诊患者的疗效,以评估这两种药物在疗效和安全性上的差异。经过7天的安慰剂洗脱期后,患者可接受长达13周的任一治疗。通过汉密尔顿抑郁与焦虑量表、临床总体严重程度和改善评定量表以及zung自评抑郁量表评估抗抑郁反应。在为期13周的研究中,发现这两种化合物具有相当的疗效。多塞平与安非他酮的主要差异在于汉密尔顿抑郁量表的睡眠因子,多塞平在改善睡眠方面比安非他酮效果更好。与安非他酮相比,多塞平产生抗胆碱能副作用的发生率更高,包括口干、便秘、嗜睡和疲劳。此外,与安非他酮相比,食欲增加和体重增加是多塞平的常见副作用。