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氟西汀在中国患者广泛性焦虑障碍中的临床疗效与安全性。

Clinical efficacy and safety of fluoxetine in generalized anxiety disorder in Chinese patients.

作者信息

Zou Chuan, Ding Xiang, Flaherty Joseph H, Dong Birong

机构信息

The Center of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, People's Republic of China.

出版信息

Neuropsychiatr Dis Treat. 2013;9:1661-70. doi: 10.2147/NDT.S38899. Epub 2013 Nov 1.

Abstract

BACKGROUND

Generalized anxiety disorder (GAD) is a prevalent, disabling disease and is highly comorbid with other psychiatric disorders both in Western countries and the People's Republic of China. Fluoxetine, a selective inhibitor of serotonin reuptake (SSRI), is widely utilized in the management of GAD in clinical practice despite the lack of strong evidence. This article reviews fluoxetine trials to investigate fluoxetine's efficacy and tolerability in Chinese patients with GAD.

METHODS

A literature review was conducted using the following databases up to and including April 2013: Chinese BioMedical Literature, China National Knowledge Infrastructure, EMBASE, MEDLINE, and PsycINFO. We selected clinical studies that utilized fluoxetine for GAD in which all participants were Chinese.

RESULTS

Fifteen open-label, non-placebo trials were identified and analyzed; eleven anxiolytics were compared with fluoxetine separately. Short-term efficacy of fluoxetine had been established in these open-label, head-to-head controlled trials. Fluoxetine had rapid onset of action (approximately 1-2 weeks) and seemed to be effective in maintenance treatment. Fluoxetine was generally well-tolerated with the most common side effect of dry month and nausea. Compared to other anxiolytic agents, fluoxetine was equivalent with all of the comparative anxiolytics in terms of efficacy except mirtazapine which showed conflicting results with fluoxetine in two studies. In terms of side effects, fluoxetine was better tolerated than diazepam, doxepine, and amitriptyline, less tolerated than escitalopram, and had similar tolerability with duloxetine as well as alprazolam.

CONCLUSION

Given the high risk of bias of the included studies, the overall small sample size of the studies, the lack of placebo control groups as well as the lack of certain clinically meaningful outcomes, it is not possible to recommend fluoxetine as a reliable first-line treatment in Chinese patients with GAD. Furthermore, no definitive implications for clinical practice in choosing anxiolytics can be drawn from this review. Trials with larger sample sizes, better quality, longer duration, and more clinically meaningful outcomes are needed in future research.

摘要

背景

广泛性焦虑障碍(GAD)是一种常见的致残性疾病,在西方国家和中华人民共和国均与其他精神障碍高度共病。氟西汀是一种5-羟色胺再摄取选择性抑制剂(SSRI),尽管缺乏有力证据,但在临床实践中广泛用于GAD的治疗。本文回顾氟西汀试验,以研究氟西汀在中国GAD患者中的疗效和耐受性。

方法

截至2013年4月,使用以下数据库进行文献回顾:中国生物医学文献数据库、中国知网、EMBASE、MEDLINE和PsycINFO。我们选择了所有参与者均为中国人、使用氟西汀治疗GAD的临床研究。

结果

确定并分析了15项开放标签、非安慰剂试验;分别将11种抗焦虑药与氟西汀进行比较。在这些开放标签、直接对照试验中确定了氟西汀的短期疗效。氟西汀起效迅速(约1-2周),似乎在维持治疗中有效。氟西汀总体耐受性良好,最常见的副作用是口干和恶心。与其他抗焦虑药相比,氟西汀在疗效方面与所有比较的抗焦虑药相当,但米氮平在两项研究中与氟西汀的结果存在冲突。在副作用方面,氟西汀的耐受性优于地西泮、多塞平和阿米替林,耐受性低于艾司西酞普兰,与度洛西汀以及阿普唑仑的耐受性相似。

结论

鉴于纳入研究的偏倚风险高、研究总体样本量小、缺乏安慰剂对照组以及缺乏某些具有临床意义的结果,无法推荐氟西汀作为中国GAD患者可靠的一线治疗药物。此外,本综述无法得出在选择抗焦虑药方面对临床实践的确切启示。未来研究需要样本量更大、质量更高、持续时间更长以及具有更多临床意义结果的试验。

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