Pittler M H, Edzard E
Department of Complementary Medicine, University of Exeter, 25 Victoria Park Road, Exeter, UK, EX2 4NT.
Cochrane Database Syst Rev. 2001(4):CD003383. doi: 10.1002/14651858.CD003383.
Synthetic anxiolytic drugs are effective for anxiety, but they are burdened with adverse events. Constraints on resources and time often render treatments such as psychological interventions impracticable. Thus, an effective and safe oral medication would be of considerable interest and a welcome addition to the therapeutic repertoire.
To systematically review the evidence regarding the efficacy and safety of kava extract for the symptomatic treatment of anxiety.
Computerized literature searches were performed in the databases Medline, Embase, Biosis, AMED, CISCOM and the Cochrane Library (all from their respective inception to June 1998). The search terms used were kava, kawa, kavain, Piper methysticum and Rauschpfeffer (German common name for Piper methysticum). Manufacturers of kava preparations and experts on the subject were contacted and asked to contribute published and unpublished material. In addition, our own files were searched and the bibliographies of all of the studies identified were scanned for further trials. There were no restrictions regarding the language of publication.
Randomized, double-blind trials of oral kava extract mono-preparations for the treatment of anxiety were included. Trials comparing kava with placebo were included. Trials assessing kava as one of several active constituents in a combination preparation or as a part of a combination treatment were excluded.
All publications were blinded prior to assessment by a person not involved in the study. Data on patients, interventions, methods, results and adverse events were extracted systematically. Methodological quality of all trials was evaluated using the scoring system developed by Jadad and colleagues. The screening of studies, selection, data extraction and the assessment of methodological quality were performed independently by the two reviewers. Disagreements in the evaluation of individual trials were resolved through discussion.
Seven trials met the inclusion criteria. All of the reviewed trials suggest superiority of kava extract over placebo. The meta-analysis of three studies using the Hamilton Anxiety Score as a common outcome measure suggests a significant differential treatment effect in favour of kava extract (weighted mean difference: 9.69, 95% confidence interval: 3.54 - 15.83). Adverse events as reported in the reviewed trials were mild, transient and infrequent.
REVIEWER'S CONCLUSIONS: These data imply that kava extract is superior to placebo and relatively safe as a symptomatic treatment for anxiety. These findings warrant further and more rigorous investigations into the efficacy and safety of kava extract.
合成抗焦虑药物对焦虑症有效,但存在不良事件负担。资源和时间的限制常常使心理干预等治疗方法难以实施。因此,一种有效且安全的口服药物将备受关注,并成为治疗方法中的一项受欢迎补充。
系统评价卡瓦提取物对症治疗焦虑症的疗效和安全性证据。
在Medline、Embase、Biosis、AMED、CISCOM和Cochrane图书馆数据库(均从各自起始时间至1998年6月)进行计算机文献检索。使用的检索词为卡瓦、卡哇、卡瓦因、胡椒科植物卡瓦胡椒和Rauschpfeffer(卡瓦胡椒的德语通用名)。联系了卡瓦制剂制造商和该领域专家,请求提供已发表和未发表的资料。此外,检索了我们自己拥有的资料,并浏览了所有已识别研究的参考文献以查找更多试验。对发表语言没有限制。
纳入口服卡瓦提取物单一制剂治疗焦虑症的随机、双盲试验。纳入卡瓦与安慰剂比较的试验。排除将卡瓦作为复方制剂中几种活性成分之一或作为联合治疗一部分进行评估的试验。
所有出版物在由未参与该研究的人员进行评估之前均进行了盲法处理。系统提取关于患者、干预措施、方法、结果和不良事件的数据。使用Jadad及其同事开发的评分系统评估所有试验的方法学质量。两项评价者独立进行研究筛选、选择、数据提取和方法学质量评估。对个别试验评价中的分歧通过讨论解决。
七项试验符合纳入标准。所有纳入评价的试验均表明卡瓦提取物优于安慰剂。三项使用汉密尔顿焦虑量表作为共同结局指标的研究进行的荟萃分析表明,卡瓦提取物有显著的差异治疗效果(加权均数差:9.69,95%置信区间:3.54 - 15.83)。纳入评价的试验中报告的不良事件轻微、短暂且不常见。
这些数据表明卡瓦提取物优于安慰剂,作为焦虑症的对症治疗相对安全。这些发现值得对卡瓦提取物的疗效和安全性进行进一步更严格的研究。