## Abstract ## Aim To assess the effectiveness of reminiscence and life review on late‐life depression across different target groups and treatment modalities. ## Method Twenty controlled outcome studies were retrieved from __Psychlit__, __Medline__ and __Dissertation Abstracts__. For each study
Citalopram versus other antidepressants for late-life depression: a systematic review and meta-analysis
✍ Scribed by Dallas P. Seitz; Sudeep S. Gill; David K. Conn
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 189 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0885-6230
- DOI
- 10.1002/gps.2483
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Objective
To determine the efficacy and tolerability of citalopram when compared to other antidepressants for late‐life depression (LLD).
Methods
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.
Results
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].
Conclusions
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. Copyright © 2010 John Wiley & Sons, Ltd.
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