Fabre L F, Scharf M B, Itil T M
Fabre Clinic, Houston, TX 77004.
J Clin Psychiatry. 1991 Jun;52 Suppl:62-7.
The safety and efficacy of nortriptyline and fluoxetine were compared in a double-blind, randomized, multicenter 5-week trial involving 205 outpatients with acute major depression of moderate severity. Seventy-two nortriptyline and 84 fluoxetine patients completed at least 2 weeks of medication and were included in the efficacy analysis; all patients were evaluated for side effects. Average total scores on the Hamilton Rating Scale for Depression (HAM-D) for both treatment groups declined from 22-23 at baseline to 11.5 at the conclusion of the 5-week period. At Week, 5, 71% of nortriptyline patients and 65% of fluoxetine patients were much or very much improved. Fluoxetine was associated more frequently with nausea (p less than .05), while nortriptyline was associated more frequently with dry mouth (p less than .05). These results are discussed in the context of selecting between nortriptyline and fluoxetine for a particular depressed patient.
在一项为期5周的双盲、随机、多中心试验中,对去甲替林和氟西汀的安全性和有效性进行了比较,该试验涉及205名中度严重急性重度抑郁症门诊患者。72名服用去甲替林的患者和84名服用氟西汀的患者完成了至少2周的药物治疗,并被纳入疗效分析;对所有患者进行了副作用评估。两个治疗组的汉密尔顿抑郁评定量表(HAM-D)平均总分从基线时的22 - 23降至5周疗程结束时的11.5。在第5周时,71%服用去甲替林的患者和65%服用氟西汀的患者有显著或非常显著的改善。氟西汀更常与恶心相关(p小于0.05),而去甲替林更常与口干相关(p小于0.05)。在为特定抑郁症患者选择去甲替林和氟西汀时,对这些结果进行了讨论。