Evidence-Based Review of Clinical Outcomes of Guideline-Recommended Pharmacotherapies for Generalized Anxiety Disorder

被引:23
作者
Bereza, Basil G. [1 ]
Machado, Marcio [1 ,2 ]
Ravindran, Arun V. [3 ,4 ]
Einarson, Thomas R. [1 ]
机构
[1] Univ Toronto, Leslie Dan Fac Pharm, Toronto, ON M5S 3M2, Canada
[2] Univ Toronto, Toronto Hlth Technol Assessment Collaborat, Toronto, ON M5S 3M2, Canada
[3] Univ Toronto, Dept Psychiat, Toronto, ON M5S 3M2, Canada
[4] Ctr Addict & Mental Hlth, Toronto, ON, Canada
来源
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE | 2012年 / 57卷 / 08期
关键词
anxiety; meta-analysis; pharmacotherapy; VENLAFAXINE EXTENDED-RELEASE; PLACEBO-CONTROLLED TRIAL; COGNITIVE-BEHAVIOR-THERAPY; MAJOR DEPRESSIVE DISORDER; DOUBLE-BLIND; NONDEPRESSED OUTPATIENTS; EFFICACY; DIAZEPAM; BUSPIRONE; ALPRAZOLAM;
D O I
10.1177/070674371205700805
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To quantify the rates of clinical outcomes of Canadian Psychiatric Association (CPA) guideline-recommended pharmacotherapies for generalized anxiety disorder (GAD) by drug classification within each treatment line. Methods: Evidence from original research cited by the CPA was included. Pooled analyses, duplicates, and studies with nonextractable data were excluded. Response, remission, and baseline-endpoint or mean reductions scores of the Hamilton Anxiety Rating Scale (HARS) were extracted. The Cochrane Collaboration's computer program, Review Manager, version 5, with a random effects model, was used to pool results. Results: A total of 50 articles were cited as evidence for managing GAD by the CPA. There was sufficient evidence of remission with first- or third-line agents to pool reported rates, and with agents from all 3 treatment lines to pool response rates and reduction in HARS scores. The mean range of effect size varied considerably from study to study within each treatment line. Comparison of pooled remission rates between first- and second-line agents was not possible. While the range of values by drug and drug class overlapped, the summary results for the probability of response and reduction in HARS scores was greater for first-line, compared with second-line, treatments. Drug components for third-line treatments were heterogeneous and produced mixed results. Conclusion: Despite the abundance of evidence in its totality presented in the CPA guidelines, there is inadequate evidence to formulate recommendations based on the pooled results from this study alone. However, such analysis provides an additional resource for clinicians to make more effective treatment decisions for individual patients with GAD.
引用
收藏
页码:470 / 478
页数:9
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