Sultan Asquad, Gaskell Helen, Derry Sheena, Moore R Andrew
Nuffield Department of Anaesthetics, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
BMC Neurol. 2008 Aug 1;8:29. doi: 10.1186/1471-2377-8-29.
Duloxetine hydrochloride is a reuptake inhibitor of 5-hydroxytryptamine and norepinephrine used to treat depression, generalized anxiety disorder, neuropathic pain, and stress incontinence in women. We investigated the efficacy of duloxetine in painful diabetic neuropathy and fibromyalgia to allow comparison with other antidepressants.
We searched PubMed, EMBASE (via Ovid), and Cochrane CENTRAL up to June 2008 for randomised controlled trials using duloxetine to treat neuropathic pain.
We identified six trials with 1,696 patients: 1,510 were treated with duloxetine and 706 with placebo. All patients had established baseline pain of at least moderate severity. Trial duration was 12 to 13 weeks. Three trials enrolled patients with painful diabetic neuropathy (PDN) and three enrolled patients with fibromyalgia. The number needed to treat (NNT) for at least 50% pain relief at 12 to 13 weeks with duloxetine 60 mg versus placebo (1,211 patients in the total comparison) was 5.8 (95% CI 4.5 to 8.4), and for duloxetine 120 mg (1,410 patients) was 5.7 (4.5 to 5.7). There was no difference in NNTs between PDN and fibromyalgia. With all doses of duloxetine combined (20/60/120 mg) there were fewer withdrawals for lack of efficacy than with placebo (number needed to treat to prevent one withdrawal 20 (13 to 42)), but more withdrawals due to adverse events (number needed to harm (NNH) 15 (11 to 25)). Nausea, somnolence, constipation, and reduced appetite were all more common with duloxetine than placebo (NNH values 6.3, 11, 11, and 18 respectively). The results for duloxetine are compared with published data for other antidepressants in neuropathic pain.
Duloxetine is equally effective for the treatment of PDN and fibromyalgia, judged by the outcome of at least 50% pain relief over 12 weeks, and is well tolerated. The NNT of 6 for 50% pain relief suggests that this is likely to be a useful drug in these difficult-to-treat conditions, where typically only a minority of patients respond. Comparing duloxetine with antidepressants for pain relief in DPN shows inadequacies in the evidence for efficacy of antidepressants, which are currently recommended in PDN care pathways.
盐酸度洛西汀是一种5-羟色胺和去甲肾上腺素再摄取抑制剂,用于治疗抑郁症、广泛性焦虑症、神经性疼痛及女性压力性尿失禁。我们研究了度洛西汀治疗糖尿病性疼痛性神经病变和纤维肌痛的疗效,以便与其他抗抑郁药进行比较。
我们检索了截至2008年6月的PubMed、EMBASE(通过Ovid)和Cochrane CENTRAL,以查找使用度洛西汀治疗神经性疼痛的随机对照试验。
我们确定了6项试验,共1696例患者:1510例接受度洛西汀治疗,706例接受安慰剂治疗。所有患者均有至少中度严重程度的既定基线疼痛。试验持续时间为12至13周。3项试验纳入了糖尿病性疼痛性神经病变(PDN)患者,3项试验纳入了纤维肌痛患者。与安慰剂相比(总比较中有1211例患者),度洛西汀60mg在12至13周时使至少50%的疼痛得到缓解的治疗所需人数(NNT)为5.8(95%CI 4.5至8.4),度洛西汀120mg(1410例患者)的NNT为5.7(4.5至5.7)。PDN和纤维肌痛之间的NNT没有差异。将所有剂量的度洛西汀(20/60/120mg)合并使用时,因缺乏疗效而退出的人数比安慰剂少(预防1例退出所需治疗人数为20(13至42)),但因不良事件导致的退出人数更多(伤害所需人数(NNH)为15(11至25))。与安慰剂相比,度洛西汀引起的恶心、嗜睡、便秘和食欲减退更为常见(NNH值分别为6.3、11、11和18)。将度洛西汀的结果与其他抗抑郁药治疗神经性疼痛的已发表数据进行了比较。
以12周内至少50%的疼痛缓解为评判标准,度洛西汀治疗PDN和纤维肌痛同样有效,且耐受性良好。50%疼痛缓解的NNT为6,这表明在这些难以治疗的疾病中,度洛西汀可能是一种有用的药物,因为通常只有少数患者有反应。将度洛西汀与用于缓解DPN疼痛的抗抑郁药进行比较,结果显示目前在PDN治疗途径中推荐使用的抗抑郁药的疗效证据不足。