氟伏沙明与舍曲林治疗抑郁症门诊患者的双盲多中心比较

Depression Pub Date : 1995-01-01 DOI:10.1002/depr.3050030402
Charles B. Nemeroff M.D., Ph.D., Philip T. Ninan M.D., James Ballenger M.D., R. Bruce Lydiard M.D., Ph.D., John Feighner M.D., William M. Patterson M.D., John H. Greist M.D.
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引用次数: 45

摘要

氟伏沙明和舍曲林均为选择性5-羟色胺再摄取抑制剂(SSRIs),在一项5中心、7周的双盲研究中,对经DSM-III-R诊断为重度抑郁症的门诊患者进行了比较。95例患者滴注氟伏沙明50 ~ 150mg /天(n = 49)或舍曲林50 ~ 200mg /天(n = 46)。第3-1周的平均给药剂量氟伏沙明为123.8 mg/天,舍曲林为137.1 mg/天。47%的氟伏沙明治疗患者和30%的舍曲林治疗患者滴定至最大允许剂量。氟伏沙明和舍曲林在改善抑郁方面同样有效,汉密尔顿抑郁评定量表(HAMD)总得分平均较基线分别降低10.61±7.53和10.98±6.08。93.5%的舍曲林患者和85.7%的氟伏沙明患者报告了轻中度的不良事件。舍曲林组最常见的事件是失眠(34.8%)、头痛(32.6%)、腹泻(23.9%)和射精困难(22.2%),氟伏沙明组最常见的事件是恶心(30.6%)、头痛(26.5%)、失眠(26.5%)和嗜睡(24.5%)。舍曲林组(28%)报告性功能障碍的患者明显多于氟伏沙明组(10%)。与氟伏沙明组(18.4%)相比,舍曲林组(2.2%)的不良事件辍学率异常低。在五个中心中,有四个中心氟伏沙明组(0-2例患者/中心)因不良事件而停药的比率与舍曲林组(1例患者)相当;第五中心氟伏沙明组有4例停药。这两种SSRIs的临床特征差异为医生提供了针对个体患者特征的抗抑郁治疗的有意义的选择。抑郁症:163 - 169(1995)。©1995 Wiley-Liss, Inc
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Double-blind multicenter comparison of fluvoxamine versus sertraline in the treatment of depressed outpatients

Fluvoxamine and sertraline, both selective serotonin reuptake inhibitors (SSRIs), were compared in a 5-center, 7-week double-blind study in outpatients with major depression diagnosed by DSM-III-R criteria. Ninety-five patients were titrated from 50 to 150 mg/day offluvoxamine (n = 49) or 50 to 200 mg/day of sertraline (n = 46). The mean dose administered in Weeks 3-1 was 123.8 mg/day for fluvoxamine, and 137.1 mg/day for sertraline. Forty-seven percent (47%) of fluvoxamine-treated patients and 30% of sertraline-treated patients were titrated to the maximum permissible dose. Fluvoxamine and sertraline were similarly effective in ameliorating depression as demonstrated by a mean reduction from baseline in the Hamilton Rating Scale for Depression (HAMD) total score of 10.61 ± 7.53 and 10.98 ± 6.08, respectively. Adverse events, mostly mild to moderate in severity, were reported for 93.5% of sertraline patients and 85.7% offluvoxamine patients. The most common events in the sertraline group were insomnia (34.8%), headache (32.6%), diarrhea (23.9%), and ejaculatory difficulty (22.2% of males), and in the fluvoxamine group, nausea (30.6%), headache (26.5%), insomnia (26.5%), and somnolence (24.5%). Significantly more patients reported sexual dysfunction in the sertraline (28%) than in the fluvoxamine (10%) group. An uncharacteristically low dropout rate due to adverse events was observed in the sertraline group (2.2%) compared with the fluvoxamine group (18.4%). The rate of withdrawal due to adverse events in the fluvoxamine group (0–2 patients/center) was comparable to that in the sertraline group (1 patient) for four of the five centers; the fifth center had 4 withdrawals in the fluvoxamine group. The differences in clinical profile of these two SSRIs provide physicians with meaningful choices in antidepressant therapy attuned to individual patient characteristics. Depression 3:163–169 (1995). © 1995 Wiley-Liss, Inc.

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