Fluoxetine for stroke recovery: Meta-analysis of randomized controlled trials

  • Gillian E Mead
    Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK
  • Lynn Legg
    Department of Medicine for the Elderly, Royal Alexandra Hospital, Paisley
  • Russel Tilney
    Department of Neuroscience, Mater Dei Hospital, Msida, Malta
  • Cheng Fang Hsieh
    Division of Geriatrics and Gerontology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung
  • Simiao Wu
    Department of Neurology, West China Hospital, Sichuan University, Chengdu, China
  • Erik Lundström
    Department of Clinical Neuroscience, Karolinska Institutet, Solna, Sweden
  • Ann Sofie Rudberg
    Department of Clinical Neuroscience, Karolinska Institutet, Solna, Sweden
  • Mansur Kutlubaev
    Department of Neurology, G.G. Kuvatov Republican Clinical Hospital, Ufa, Russia
  • Martin S Dennis
    Stroke Medicine, University of Edinburgh, Edinburgh, UK
  • Babak Soleimani
    NHS Lothian, Edinburgh, UK
  • Amanda Barugh
    NHS Lothian, Edinburgh, UK
  • Maree L Hackett
    Faculty of Medicine, UNSW Sydney, Sydney, Australia
  • Graeme J Hankey
    Medical School, The University of Western Australia, Perth, Australia

この論文をさがす

説明

<jats:sec><jats:title>Objective</jats:title><jats:p> To determine whether fluoxetine, at any dose, given within the first year after stroke to patients who did not have to have mood disorders at randomization reduced disability, dependency, neurological deficits and fatigue; improved motor function, mood, and cognition at the end of treatment and follow-up, with the same number or fewer adverse effects. </jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p> Searches (from 2012) in July 2018 included databases, trials registers, reference lists, and contact with experts. Co-primary outcomes were dependence and disability. Dichotomous data were synthesized using risk ratios (RR) and continuous data using standardized mean differences (SMD). Quality was appraised using Cochrane risk of bias methods. Sensitivity analyses explored influence of study quality. </jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p> The searches identified 3414 references of which 499 full texts were assessed for eligibility. Six new completed RCTs (n = 3710) were eligible, and were added to the seven trials identified in a 2012 Cochrane review (total: 13 trials, n = 4145). There was no difference in the proportion independent (3 trials, n = 3249, 36.6% fluoxetine vs. 36.7% control; RR 1.00, 95% confidence interval 0.91 to 1.09, p = 0.99, I<jats:sup>2</jats:sup> = 78%) nor in disability (7 trials n = 3404, SMD 0.05, −0.02 to 0.12 p = 0.15, I<jats:sup>2</jats:sup> = 81%) at end of treatment. Fluoxetine was associated with better neurological scores and less depression. Among the four (n = 3283) high-quality RCTs, the only difference between groups was lower depression scores with fluoxetine. </jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p> This class I evidence demonstrates that fluoxetine does not reduce disability and dependency after stroke but improves depression. </jats:p></jats:sec>

収録刊行物

被引用文献 (1)*注記

もっと見る

問題の指摘

ページトップへ