Evidence map›Paper›PMID 30528472›Full record

Trial reportLancet (London, England)2019

Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial.

FOCUS Trial Collaboration

2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyPragmatic Clinical Trial
In one paragraph

Trial report in Lancet (London, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 116 papers, 19 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 19 pooled it
27.6field-weighted citation impact, top 1% of its field
1 · What the graph read from 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.

2 · The registry

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.

NCT03843463 phase2recruitingnot on this mapstarted 2021, after this paper: background citation

Escitalopram and Language Intervention for Subacute Aphasia (ELISA)

TypeinterventionalSponsorJohns Hopkins UniversityRan2021 to 2027Enrolled88ConditionsAphasia, StrokeArmsEscitalopram 10mg, Placebo, Computer-delivered naming treatment
NCT05426304 phase4unknown statusnot on this mapstarted 2022, after this paper: background citation

A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Efficacy and Safety of Agomelatine in the Prevention of Poststroke Depression

TypeinterventionalSponsorFirst Affiliated Hospital, Sun Yat-Sen UniversityRan2022 to 2024Enrolled420ConditionsDepression, Acute Ischemic StrokeArmsAgomelatine, Placebo Tablets
3 · Its place in the literature

Who cites it

116 citing papers in PubMed, 19 syntheses or guidelines pooled it, 280 citations in OpenAlex.

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  5. Individual patient data meta-analysis of the effects of fluoxetine on functional outcomes after acute stroke.International journal of stroke : official journal of the International Stroke Society · 2024
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  11. Selective serotonin reuptake inhibitors (SSRIs) for stroke recovery.The Cochrane database of systematic reviews · 2021
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  17. Selective serotonin reuptake inhibitors (SSRIs) for stroke recovery.The Cochrane database of systematic reviews · 2019
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56 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 2 institutions in 2 countries.

FOCUS Trial Collaboration
University of Edinburgh · GBInstitute of Technology Assessment · AT

Funding

Department of Health HTA/13/04/30Medical Research Council MR/R005923/1
6 · The paper itself

Abstract

backgroundResults of small trials indicate that fluoxetine might improve functional outcomes after stroke. The FOCUS trial aimed to provide a precise estimate of these effects.

methodsFOCUS was a pragmatic, multicentre, parallel group, double-blind, randomised, placebo-controlled trial done at 103 hospitals in the UK. Patients were eligible if they were aged 18 years or older, had a clinical stroke diagnosis, were enrolled and randomly assigned between 2 days and 15 days after onset, and had focal neurological deficits. Patients were randomly allocated fluoxetine 20 mg or matching placebo orally once daily for 6 months via a web-based system by use of a minimisation algorithm. The primary outcome was functional status, measured with the modified Rankin Scale (mRS), at 6 months. Patients, carers, health-care staff, and the trial team were masked to treatment allocation. Functional status was assessed at 6 months and 12 months after randomisation. Patients were analysed according to their treatment allocation. This trial is registered with the ISRCTN registry, number ISRCTN83290762.

findingsBetween Sept 10, 2012, and March 31, 2017, 3127 patients were recruited. 1564 patients were allocated fluoxetine and 1563 allocated placebo. mRS data at 6 months were available for 1553 (99·3%) patients in each treatment group. The distribution across mRS categories at 6 months was similar in the fluoxetine and placebo groups (common odds ratio adjusted for minimisation variables 0·951 [95% CI 0·839-1·079]; p=0·439). Patients allocated fluoxetine were less likely than those allocated placebo to develop new depression by 6 months (210 [13·43%] patients vs 269 [17·21%]; difference 3·78% [95% CI 1·26-6·30]; p=0·0033), but they had more bone fractures (45 [2·88%] vs 23 [1·47%]; difference 1·41% [95% CI 0·38-2·43]; p=0·0070). There were no significant differences in any other event at 6 or 12 months.

interpretationFluoxetine 20 mg given daily for 6 months after acute stroke does not seem to improve functional outcomes. Although the treatment reduced the occurrence of depression, it increased the frequency of bone fractures. These results do not support the routine use of fluoxetine either for the prevention of post-stroke depression or to promote recovery of function.

fundingUK Stroke Association and NIHR Health Technology Assessment Programme.

Indexed as

Administration, OralAgedAntidepressive Agents, Second-GenerationDepressionDouble-Blind MethodFemaleFluoxetineFractures, BoneHumansMaleMiddle AgedRecovery of FunctionStroke RehabilitationSurveys and QuestionnairesAntidepressive Agents, Second-GenerationFluoxetine

Identifiers

PMID30528472
PMCPMC6336936
OpenAlexW2902979281

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.