Fluoxetine for motor recovery after acute ischaemic stroke (FLAME): a randomised placebo-controlled trial
- PMID: 21216670
- DOI: 10.1016/S1474-4422(10)70314-8
Fluoxetine for motor recovery after acute ischaemic stroke (FLAME): a randomised placebo-controlled trial
Erratum in
- Lancet Neurol. 2011 Mar;10(3):205
Abstract
Background: Hemiplegia and hemiparesis are the most common deficits caused by stroke. A few small clinical trials suggest that fluoxetine enhances motor recovery but its clinical efficacy is unknown. We therefore aimed to investigate whether fluoxetine would enhance motor recovery if given soon after an ischaemic stroke to patients who have motor deficits.
Methods: In this double-blind, placebo-controlled trial, patients from nine stroke centres in France who had ischaemic stroke and hemiplegia or hemiparesis, had Fugl-Meyer motor scale (FMMS) scores of 55 or less, and were aged between 18 years and 85 years were eligible for inclusion. Patients were randomly assigned, using a computer random-number generator, in a 1:1 ratio to fluoxetine (20 mg once per day, orally) or placebo for 3 months starting 5-10 days after the onset of stroke. All patients had physiotherapy. The primary outcome measure was the change on the FMMS between day 0 and day 90 after the start of the study drug. Participants, carers, and physicians assessing the outcome were masked to group assignment. Analysis was of all patients for whom data were available (full analysis set). This trial is registered with ClinicalTrials.gov, number NCT00657163.
Findings: 118 patients were randomly assigned to fluoxetine (n=59) or placebo (n=59), and 113 were included in the analysis (57 in the fluoxetine group and 56 in the placebo group). Two patients died before day 90 and three withdrew from the study. FMMS improvement at day 90 was significantly greater in the fluoxetine group (adjusted mean 34·0 points [95% CI 29·7-38·4]) than in the placebo group (24·3 points [19·9-28·7]; p=0·003). The main adverse events in the fluoxetine and placebo groups were hyponatraemia (two [4%] vs two [4%]), transient digestive disorders including nausea, diarrhoea, and abdominal pain (14 [25%] vs six [11%]), hepatic enzyme disorders (five [9%] vs ten [18%]), psychiatric disorders (three [5%] vs four [7%]), insomnia (19 [33%] vs 20 [36%]), and partial seizure (one [<1%] vs 0).
Interpretation: In patients with ischaemic stroke and moderate to severe motor deficit, the early prescription of fluoxetine with physiotherapy enhanced motor recovery after 3 months. Modulation of spontaneous brain plasticity by drugs is a promising pathway for treatment of patients with ischaemic stroke and moderate to severe motor deficit.
Funding: Public French National Programme for Clinical Research.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Comment in
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Selective serotonin-reuptake inhibitors and recovery after stroke.Lancet Neurol. 2011 Feb;10(2):110-1. doi: 10.1016/S1474-4422(10)70326-4. Epub 2011 Jan 7. Lancet Neurol. 2011. PMID: 21216671 No abstract available.
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Stroke: fluoxetine improves motor function after acute ischemic stroke.Nat Rev Neurol. 2011 Mar;7(3):123. doi: 10.1038/nrneurol.2011.7. Nat Rev Neurol. 2011. PMID: 21509995 No abstract available.
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Fluoxetine and motor recovery after ischaemic stroke.Lancet Neurol. 2011 Jun;10(6):499; author reply 500-1. doi: 10.1016/S1474-4422(11)70111-9. Lancet Neurol. 2011. PMID: 21601157 No abstract available.
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Fluoxetine and motor recovery after ischaemic stroke.Lancet Neurol. 2011 Jun;10(6):499-500; author reply 500-1. doi: 10.1016/S1474-4422(11)70112-0. Lancet Neurol. 2011. PMID: 21601158 No abstract available.
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