首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Efficacy and tolerability of Hypericum perforatum in major depressive disorder in comparison with selective serotonin reuptake inhibitors: A meta-analysis.
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Efficacy and tolerability of Hypericum perforatum in major depressive disorder in comparison with selective serotonin reuptake inhibitors: A meta-analysis.

机译:与选择性5-羟色胺再摄取抑制剂相比,贯叶连翘在主要抑郁症中的疗效和耐受性:一项荟萃分析。

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Hypericum perforatum is a medicinal plant with established antidepressant properties. The aim of this meta-analysis was to compare the efficacy and tolerability of this antidepressant with selective serotonin reuptake inhibitors (SSRIs) as a group of standard antidepressants. For this purpose, Pubmed, Embase, Scopus, Web of Science, and Cochrane Central Register of Controlled Trials were searched for studies comparing efficacy and/or tolerability of Hypericum with SSRIs in the management of major depressive disorder (MDD). The search terms were: "Hypericum" or "St. John's wort" and "fluoxetine", "paroxetine", citalopram collected from 1966 to 2008 (up to June). "Clinical response", "remission", "mean reduction in Hamilton Rating Scale for Depression (HAMD) score from baseline", total adverse events outcomes of interest. Thirteen randomized placebo controlled clinical trials met our criteria and were included. Comparison of SSRIs with placebo yielded a significant relative risk (RR) of 1.22 (95% confidence interval: 1.03-1.45, P=0.02) for clinical response (n=4), a non significant RR of 0.96 (95% CI: 0.71-1.29, P=0.76) for remission (n=4), and a significant effect size [weighted mean difference (wmd+)] of 1.33 (95% CI: 1.15-1.51, P<0.0001) for mean reduction in HAMD score from baseline (n=3). Comparison of Hypericum with SSRIs yielded a non significant relative risk (RR) of 0.99 (95% confidence interval: 0.91-1.08, P=0.83) for clinical response, a non significant RR of 1.1 (95% CI: 0.90-1.35, P=0.35) for remission, and a non-significant wmd+ of 0.32 (95% CI: -1.28-0.64, P=0.52) for mean reduction in HAMD score from baseline, a non significant RR of 0.85 (95% CI: 0.7-1.04, P=0.11) for any adverse events, and a significant RR of 0.53 (95% CI: 0.35-0.82, P=0.004) for withdrawals due to adverse events. Hypericum does not differ from SSRIs according to efficacy and adverse events in MDD. Lower withdrawal from study due to adverse events by Hypericum is an advantage in management of MDD.
机译:贯叶连翘是具有确定的抗抑郁特性的药用植物。这项荟萃分析的目的是比较该抗抑郁药与选择性5-羟色胺再摄取抑制剂(SSRI)作为一组标准抗抑郁药的疗效和耐受性。为此目的,搜寻Pubmed,Embase,Scopus,Web of Science和Cochrane对照试验中央注册机构,以研究比较贯叶连翘与SSRIs在治疗重性抑郁症(MDD)中的功效和/或耐受性。搜索词是:1966年至2008年(截至6月)收集的西酞普兰的“金丝桃”或“圣约翰草”和“氟西汀”,“帕罗西汀”。 “临床反应”,“缓解”,“汉密尔顿抑郁量表(HAMD)得分相对于基线的平均降低”,总不良事件相关的结果。符合我们标准的13项随机安慰剂对照临床试验已包括在内。 SSRI与安慰剂的比较显示临床反应(n = 4)的相对风险(RR)为1.22(95%置信区间:1.03-1.45,P = 0.02),非显着RR为0.96(95%CI:0.71)缓解(n = 4)时为-1.29,P = 0.76),而HAMD得分的平均降低幅度为1.33(95%CI:1.15-1.51,P <0.0001),显着影响大小[加权平均差异(wmd +)]基线(n = 3)。金丝桃与SSRI的临床反应相对非危险性(RR)为0.99(95%置信区间:0.91-1.08,P = 0.83),非显着相对危险度为1.1(95%CI:0.90-1.35,P缓解率= 0.35),HAMD得分较基线平均降低的wmd +为0.32(95%CI:-1.28-0.64,P = 0.52),无显着性,RR为0.85(95%CI:0.7-不良反应为1.04,P = 0.11),不良事件引起的停药的显着RR为0.53(95%CI:0.35-0.82,P = 0.004)。金丝桃属植物与MDRI中的功效和不良事件没有区别。金丝桃属植物因不良事件而退出研究的人数减少,是管理MDD的优势。

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