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首页> 外文期刊>British journal of clinical pharmacology >Melatonin for sedative withdrawal in older patients with primary insomnia: a randomized double-blind placebo-controlled trial
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Melatonin for sedative withdrawal in older patients with primary insomnia: a randomized double-blind placebo-controlled trial

机译:褪黑素用于老年原发性失眠患者的镇静药戒断:一项随机双盲安慰剂对照试验

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We compared the efficacy of melatonin and placebo as adjuvants in the withdrawal of patients from long term temazepam, zopiclone or zolpidem (here ‘BZD’) use.MethodsA double-blind, placebo-controlled, randomized trial was conducted in a primary health care outpatient clinic. Ninety-two men or women (≥55?years) with primary insomnia and chronic BZD use received controlled release melatonin 2?mg (CRM) (n?=?46) or placebo (n?=?46) during the 1?month withdrawal from BZDs. Psychosocial support was provided. Follow-up continued for up to 6?months. Successful BZD withdrawal by the end of 1?month was confirmed by BZD plasma determinations, while reduction in BZD use and abstinence continuing for 6?months were noted.ResultsThere were two drop-outs on CRM and one on placebo. After a 1?month withdrawal, 31 participants (67%; 95% CI 54, 81) on CRM and 39 (85%; 74, 95) on placebo had withdrawn completely (intention-to-treat analysis between groups, P?=?0.051; per protocol P?=?0.043). Reduction in BZD use was similar or even more rare in the CRM than in the placebo group (P = 0.052 per protocol). After 6?months, 14 participants in the CRM group and 20 in the placebo group remained non-users of BZD (NS between groups). BZD doses were higher in the CRM than in the placebo group at the end of the 6?month follow-up (P?=?0.025). Withdrawal symptoms did not differ between the groups.ConclusionsGradual dose reduction of BZDs combined with CRM or placebo, and psychosocial support produced high short term and moderate long term BZD abstinence. CRM showed no withdrawal benefit compared with placebo.
机译:我们比较了褪黑素和安慰剂作为佐剂在长期使用替马西epa,佐匹克隆或唑吡坦(此处简称为BZD)患者的戒断中的功效。方法在初级保健门诊进行了一项双盲,安慰剂对照,随机试验诊所。患有原发性失眠和慢性BZD的92名男性或女性(≥55岁)在1个月内接受了2毫克褪黑激素(CRM)(n?=?46)或安慰剂(n?=?46)的控制释放。从BZD中退出。提供了社会心理支持。随访持续长达6个月。通过BZD血浆测定证实在1个月末成功撤出BZD,同时注意到BZD使用减少和禁欲持续6个月。结果CRM出现2次退出,安慰剂退出1次。撤出1个月后,接受CRM的31名参与者(67%; 95%CI 54,81)和接受安慰剂的39名参与者(85%; 74,95)已完全退出(组间意向治疗分析,P = 0.051;根据方案P,P = 0.043)。与安慰剂组相比,CRM中减少BZD的使用率相似甚至更为罕见(每个方案P = 0.052)。 6个月后,CRM组的14位参与者和安慰剂组的20位参与者仍未使用BZD(两组之间为NS)。在6个月的随访结束时,CRM中的BZD剂量高于安慰剂组(P≤0.025)。两组间的戒断症状无差异。结论逐渐降低BZD联合CRM或安慰剂的剂量以及社会心理支持产生了短期和中期长期较高的BZD戒断。与安慰剂相比,CRM没有撤出收益。

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