Trial reportPharmacoEconomics2008
Escitalopram and duloxetine in major depressive disorder: a pharmacoeconomic comparison using UK cost data.
Trial report in PharmacoEconomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 5 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
20 citing papers in PubMed, 5 syntheses or guidelines pooled it, 41 citations in OpenAlex.
- Interventions to improve return to work in depressed people.The Cochrane database of systematic reviews · 2020Pooled it
- Economic evidence for the clinical management of major depressive disorder: a systematic review and quality appraisal of economic evaluations alongside randomised controlled trials.Epidemiology and psychiatric sciences · 2017Pooled it
- Economic Evaluation alongside Multinational Studies: A Systematic Review of Empirical Studies.PloS one · 2015Pooled it
- Interventions to facilitate return to work in adults with adjustment disorders.The Cochrane database of systematic reviews · 2012Pooled it
- Duloxetine versus other anti-depressive agents for depression.The Cochrane database of systematic reviews · 2012Pooled it
- A Digital Intervention Addressing Alcohol Use Problems (the "Daybreak" Program): Quasi-Experimental Randomized Controlled Trial.Journal of medical Internet research · 2019Trial
- Article
- Article
- Practical pathway for the management of depression in the workplace: a Canadian perspective.Frontiers in psychiatry · 2023Review
- Validation of a novel online depression symptom severity rating scale: the R8 Depression.Health and quality of life outcomes · 2021Article
- Trends in Antidepressant Use and Expenditure in Six Major Cities in China From 2013 to 2018.Frontiers in psychiatry · 2020Article
- A Participatory Health Promotion Mobile App Addressing Alcohol Use Problems (The Daybreak Program): Protocol for a Randomized Controlled Trial.JMIR research protocols · 2018Article
- Safety and effectiveness of escitalopram in an 8-week open study in Chinese patients with depression and anxiety.Neuropsychiatric disease and treatment · 2018Article
- An observational study of duloxetine versus SSRI monotherapy for the treatment of painful physical symptoms in Japanese patients with major depressive disorder: primary analysis.Neuropsychiatric disease and treatment · 2017Article
- Cognitive Deficits as a Mediator of Poor Occupational Function in Remitted Major Depressive Disorder Patients.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2016Article
- A comparative review of escitalopram, paroxetine, and sertraline: Are they all alike?International clinical psychopharmacology · 2014Review
- Depression treatment with duloxetine and reduction of inability to work.Depression research and treatment · 2012Article
- Escitalopram, an antidepressant with an allosteric effect at the serotonin transporter--a review of current understanding of its mechanism of action.Psychopharmacology · 2012Review
- Escitalopram: a review of its use in the management of major depressive disorder in adults.CNS drugs · 2010Review
- Escitalopram--translating molecular properties into clinical benefit: reviewing the evidence in major depression.Journal of psychopharmacology (Oxford, England) · 2010Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSelective serotonin reuptake inhibitors (SSRIs) and serotonin-noradrenaline reuptake inhibitors (SNRIs) are approved for the treatment of major depressive disorder (MDD). The allosteric SSRI escitalopram has been shown to be at least as clinically effective as the SNRIs venlafaxine and duloxetine in MDD, with a better tolerability profile. In addition, escitalopram has been shown to be cost saving compared with venlafaxine.
objectiveTo evaluate the cost effectiveness of escitalopram versus duloxetine in the treatment of MDD, and to identify key cost drivers.
methodsThe pharmacoeconomic evaluation was conducted alongside a 24-week, double-blind, multinational randomized study (escitalopram 20 mg/day and duloxetine 60 mg/day) in outpatients with MDD, aged 18-65 years, with Montgomery-Asberg Depression Rating Scale (MADRS) score >or=26 and Clinical Global Impression Severity (CGI-S) score >or=4, and baseline duration of the current depressive episode of 12 weeks to 1 year.The analysis was conducted on the full analysis set (FAS), which included all patients with >or=1 valid post-baseline health economic assessment. Effectiveness outcomes of the cost-effectiveness analyses (CEA) included the change in Sheehan Disability Scale (SDS) score (primary CEA), treatment response (MADRS score decrease >or=50%) and remission (MADRS score <or=12) rates at week 24. Cost outcomes were assessed from the societal perspective. Healthcare resource use and sick leave were evaluated using a health economic assessment questionnaire. Unit costs of healthcare services were obtained from standard UK sources ( pound, year 2006 values).
resultsOver the total 24-week study period, escitalopram was associated with significant cost savings compared with duloxetine (total per-patient monthly cost pound 188 vs pound 334, respectively). In the primary CEA, escitalopram dominated duloxetine (i.e. was more effective on the disability scale and less costly). Treatment with escitalopram resulted in significantly lower mean sick leave duration per patient over 24 weeks than duloxetine (30.7 days vs 62.2 days).In multivariate analyses, escitalopram as a treatment choice was associated with a 54% reduction in sick leave duration (p < 0.001). Treatment with escitalopram also resulted in 49% lower total costs than treatment with duloxetine (p = 0.002). Absenteeism accounted for about two-thirds of the overall cost. Early clinical improvement (mean change in MADRS total score, response and remission) had an independent significant impact on the sick leave duration, after controlling for key co-variates.
conclusionsEscitalopram was associated with significantly lower duration of sick leave and significant savings in the total cost compared with duloxetine; it dominated duloxetine when effectiveness was assessed on the SDS scale. Indirect costs due to sick leave accounted for the most substantial portion of the total cost and should, therefore, be an important consideration when pharmacoeconomic comparisons between treatments are made from the societal perspective. The link between decrease in absenteeism and early (8-week) clinical improvement suggested in the additional analyses may explain the reduced sick leave observed with escitalopram, given its superior short-term efficacy compared with duloxetine (demonstrated in the underlying clinical trial).
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