Department of Psychiatry, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australia.
Neuropsychiatr Dis Treat. 2008 Dec;4(6):1169-80. doi: 10.2147/ndt.s2820.
Duloxetine, a medication with effects on both serotonin and noradrenaline transporter molecules, has recently been approved for the treatment of generalized anxiety disorder. The evidence for its efficacy lies in a limited number of double blind, placebo controlled comparisons. Statistically significant improvements in the Hamilton Anxiety Rating Scale from baseline were demonstrated in all studies at doses of 60 to 120 mg per day. The significance of such changes in terms of clinical improvements compared to placebo is less certain, particularly when the effect size of the change is calculated. In comparative trials with venlafaxine, duloxetine was as effective in providing relief of anxiety symptoms. In addition to improvements in clinical symptoms duloxetine has also been associated with restitution of role function as measured by disability scales. Duloxetine use is associated with nausea, dizziness, dry mouth, constipation, insomnia, somnolence, hyperhidrosis, decreased libido and vomiting. These treatment emergent side effects were generally of mild to moderate severity and were tolerated over time. Using a tapered withdrawal schedule over two weeks in the clinical trials, duloxetine was associated with only a mild withdrawal syndrome in up to about 30% of patients compared to about 17% in placebo treated patients. Duloxetine in doses of up to 200 mg twice daily did not prolong the QTc interval in healthy volunteers. Like other agents with dual neurotransmitter actions duloxetine reduces the symptoms of generalized anxiety disorder in short term treatments. Further evidence for its efficacy and safety in long term treatment is required.
度洛西汀是一种对 5-羟色胺和去甲肾上腺素转运体分子均有作用的药物,最近被批准用于治疗广泛性焦虑症。其疗效的证据来自于为数不多的双盲、安慰剂对照比较。在所有研究中,每天剂量为 60 至 120 毫克时,汉密尔顿焦虑量表(Hamilton Anxiety Rating Scale)基线均显示出显著改善。与安慰剂相比,这种变化在临床改善方面的意义不太确定,特别是在计算变化的效应大小时。在与文拉法辛的对照试验中,度洛西汀在缓解焦虑症状方面同样有效。除了改善临床症状外,度洛西汀还与残疾量表测量的角色功能恢复有关。度洛西汀的使用与恶心、头晕、口干、便秘、失眠、嗜睡、多汗、性欲降低和呕吐有关。这些治疗中出现的副作用通常为轻度至中度,随着时间的推移可以耐受。在临床试验中,使用两周的逐渐停药方案,与安慰剂组约 17%的患者相比,度洛西汀组只有约 30%的患者出现轻度停药综合征。度洛西汀在健康志愿者中的最高剂量为每天两次 200 毫克,不会延长 QTc 间期。与其他具有双重神经递质作用的药物一样,度洛西汀可在短期治疗中减轻广泛性焦虑症的症状。需要进一步的证据来证明其在长期治疗中的疗效和安全性。