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

Authors :
Dennis, Martin
Forbes, John
Graham, Catriona
Hackett, Maree
Hankey, Graeme J.
House, Allan
Lewis, Stephanie
Lundström, Erik
Sandercock, Peter
Mead, Gillian
Anderson, Rosemary
Buchanan, David
Deary, Ann
Drever, Jonathan
Fraser, Ruth
Innes, Karen
McGill, Connor
McGrath, Aileen
Perry, David
Walker, Pauli
Williams, Carol
Chun, Yvonne
Dinsmore, Lynn
Maschauer, Emma
Fraser, Greig
Lawrence, Katherine
Shaw, Alison
Barugh, Amanda
Mikhail, Shadia
Blair, Gordon
Hoeritzauer, Ingrid
Scott, Maggie
Lewis, Steff
Williamson, Judith
Murray, Veronica
French, Ray
Stott, David
Burgess, David
Emberson, Jonathan
Ellis, Graham
Tyrrell, Pippa
Brady, Marian
MacLeod, Malcolm
Milligan, Hazel
Sullivan, Frank
van Wijck, Frederike
Watkins, Caroline
Anderson, Craig
Morales, D.
Langhorne, Peter
Reid, Fiona
Rodgers, Helen
Dennis, Martin
Forbes, John
Graham, Catriona
Hackett, Maree
Hankey, Graeme J.
House, Allan
Lewis, Stephanie
Lundström, Erik
Sandercock, Peter
Mead, Gillian
Anderson, Rosemary
Buchanan, David
Deary, Ann
Drever, Jonathan
Fraser, Ruth
Innes, Karen
McGill, Connor
McGrath, Aileen
Perry, David
Walker, Pauli
Williams, Carol
Chun, Yvonne
Dinsmore, Lynn
Maschauer, Emma
Fraser, Greig
Lawrence, Katherine
Shaw, Alison
Barugh, Amanda
Mikhail, Shadia
Blair, Gordon
Hoeritzauer, Ingrid
Scott, Maggie
Lewis, Steff
Williamson, Judith
Murray, Veronica
French, Ray
Stott, David
Burgess, David
Emberson, Jonathan
Ellis, Graham
Tyrrell, Pippa
Brady, Marian
MacLeod, Malcolm
Milligan, Hazel
Sullivan, Frank
van Wijck, Frederike
Watkins, Caroline
Anderson, Craig
Morales, D.
Langhorne, Peter
Reid, Fiona
Rodgers, Helen
Publication Year :
2019

Abstract

Background Results of small trials indicate that fluoxetine might improve functional outcomes after stroke. The FOCUS trial aimed to provide a precise estimate of these effects. Methods FOCUS 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. Findings Between 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. Interpretation Fluoxetine 20 mg given daily for 6 months after acute stroke does not se

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235204383
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.S0140-6736(18)32823-X