Hutchinson D R, Tong S, Moon C A, Vince M, Clarke A
Brookwood Medical Research Group, Guildford, Surrey, UK.
Int Clin Psychopharmacol. 1992 Jun;6 Suppl 4:43-51. doi: 10.1097/00004850-199206004-00009.
A total of 101 patients entered a double-blind, parallel-group study in general practice, comparing the efficacy and tolerability of paroxetine and amitriptyline in elderly depressed patients. All patients received placebo for 1 week followed by active therapy for a total of 6 weeks. Medication was randomly allocated, two-thirds of the patients took paroxetine (20 mg daily) and one-third received amitriptyline (50 mg daily); this dose was increased to 30 mg and 100 mg, respectively, after 1 week. Of the patients who entered the placebo run-in, 90 took active treatment and were evaluable on an intention-to-treat basis (56 paroxetine, 32 amitriptyline). The mean age of the patients was 72 years. Significant reductions in Hamilton Depression Rating Scale (HAMD) from baseline to the end of treatment were seen for both groups (p < 0.01), with no difference between treatments. The HAMD score was reduced by half, or more, for 76% of patients taking paroxetine and 86% taking amitriptyline. Significant improvement was observed in the investigators' Clinical Global Impression (CGI) score for 57% of patients taking paroxetine and 52% on amitriptyline. Improvements after treatment were also observed in the Leeds Sleep Evaluation Questionnaire (LSEQ) scores. Significantly fewer patients taking paroxetine reported adverse events (34% vs 63% taking amitriptyline, p = 0.02). Those taking paroxetine experienced significantly fewer anticholinergic side effects (7% vs 25% taking amitriptyline, p = 0.04). Overall, this study confirmed the effectiveness of paroxetine as an antidepressant drug.(ABSTRACT TRUNCATED AT 250 WORDS)
共有101名患者进入一项全科医疗的双盲平行组研究,比较帕罗西汀和阿米替林在老年抑郁症患者中的疗效和耐受性。所有患者先接受1周的安慰剂治疗,随后接受为期6周的积极治疗。药物随机分配,三分之二的患者服用帕罗西汀(每日20毫克),三分之一的患者接受阿米替林(每日50毫克);1周后,剂量分别增至30毫克和100毫克。进入安慰剂导入期的患者中,90名接受了积极治疗,并可按意向性治疗原则进行评估(56名服用帕罗西汀,32名服用阿米替林)。患者的平均年龄为72岁。两组从基线到治疗结束时汉密尔顿抑郁量表(HAMD)评分均显著降低(p<0.01),治疗之间无差异。服用帕罗西汀的患者中有76%、服用阿米替林的患者中有86%的HAMD评分降低了一半或更多。服用帕罗西汀的患者中有57%、服用阿米替林的患者中有52%在研究者的临床总体印象(CGI)评分上有显著改善。治疗后利兹睡眠评估问卷(LSEQ)评分也有改善。服用帕罗西汀报告不良事件的患者明显较少(34%对比服用阿米替林的63%,p=0.02)。服用帕罗西汀的患者出现抗胆碱能副作用的明显较少(7%对比服用阿米替林的25%,p=0.04)。总体而言,本研究证实了帕罗西汀作为一种抗抑郁药物的有效性。(摘要截短至250字)