Department of Psychiatry, Baycrest Centre, Toronto, Ontario, Canada.
Int J Geriatr Psychiatry. 2010 Dec;25(12):1296-305. doi: 10.1002/gps.2483.
To determine the efficacy and tolerability of citalopram when compared to other antidepressants for late-life depression (LLD).
We searched electronic databases and trial registries to identify randomized controlled trials comparing citalopram to other antidepressants for LLD. Study quality was assessed using the Cochrane collaboration risk of bias tool. We summarized the efficacy of citalopram compared to other antidepressants by examining rates of depression remission, depression response and change in depression symptom scores. Medication tolerability was assessed through trial withdrawals due adverse events and withdrawals due to any cause. We used meta-analysis to determine the odds ratios (OR) of efficacy and tolerability outcomes for citalopram compared to other antidepressants.
Seven studies comparing citalopram (N = 647) to other antidepressants (N = 641) for LLD were identified including four studies with tricyclic comparators and three studies with non-tricyclic comparators. Most of the studies had methodological limitations that placed them at risk for potential bias. The majority of studies reported no significant differences between citalopram and comparator medications for depression efficacy or tolerability outcomes. Meta-analysis did not find any significant differences between citalopram and other antidepressants for depression remission [OR = 0.84; 95%CI: 0.56-1.28] or for trial withdrawals due to adverse effects [OR = 0.70; 95%CI: 0.48-1.02].
Currently there are few studies directly comparing citalopram to other antidepressants for LLD. The small number of studies and methodological issues in many studies limit any conclusions about the relative efficacy and tolerability of citalopram compared to other antidepressants. Well-designed studies comparing citalopram to other antidepressants for LLD are required.
评估西酞普兰治疗老年抑郁症(LLD)的疗效和耐受性,并与其他抗抑郁药进行比较。
我们检索了电子数据库和试验注册库,以确定比较西酞普兰与其他抗抑郁药治疗 LLD 的随机对照试验。使用 Cochrane 协作风险偏倚工具评估研究质量。我们通过比较西酞普兰与其他抗抑郁药治疗后的抑郁缓解率、抑郁反应率和抑郁症状评分变化,来评估西酞普兰的疗效。通过因不良反应和任何原因停药评估药物的耐受性。我们使用荟萃分析来确定西酞普兰与其他抗抑郁药相比的疗效和耐受性结果的优势比(OR)。
共确定了 7 项比较西酞普兰(N = 647)与其他抗抑郁药(N = 641)治疗 LLD 的研究,其中包括 4 项与三环类抗抑郁药比较的研究和 3 项与非三环类抗抑郁药比较的研究。大多数研究存在方法学局限性,存在潜在偏倚的风险。大多数研究报告西酞普兰与对照药物在抑郁疗效或耐受性结果方面没有显著差异。荟萃分析未发现西酞普兰与其他抗抑郁药在抑郁缓解方面有任何显著差异[OR = 0.84;95%CI:0.56-1.28]或因不良反应导致的试验停药方面有任何显著差异[OR = 0.70;95%CI:0.48-1.02]。
目前直接比较西酞普兰与其他抗抑郁药治疗 LLD 的研究较少。由于许多研究的研究数量较少和方法学问题,限制了关于西酞普兰与其他抗抑郁药相比的相对疗效和耐受性的任何结论。需要设计良好的比较西酞普兰与其他抗抑郁药治疗 LLD 的研究。