Repeated Measures of Modified Rankin Scale Scores to Assess Functional Recovery From Stroke: AFFINITY Study Findings.

cerebrovascular disease functional outcomes modified Rankin Scale partial proportional odds repeated measures stroke

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
16 08 2022
Historique:
pubmed: 6 8 2022
medline: 19 8 2022
entrez: 5 8 2022
Statut: ppublish

Résumé

Background Function after acute stroke using the modified Rankin Scale (mRS) is usually assessed at a point in time. The analytical implications of serial mRS measurements to evaluate functional recovery over time is not completely understood. We compare repeated-measures and single-measure analyses of the mRS from a randomized clinical trial. Methods and Results Serial mRS data from AFFINITY (Assessment of Fluoxetine in Stroke Recovery), a double-blind placebo randomized clinical trial of fluoxetine following stroke (n=1280) were analyzed to identify demographic and clinical associations with functional recovery (reduction in mRS) over 12 months. Associations were identified using single-measure (day 365) and repeated-measures (days 28, 90, 180, and 365) partial proportional odds logistic regression. Ninety-five percent of participants experienced a reduction in mRS after 12 months. Functional recovery was associated with age at stroke <70 years; no prestroke history of diabetes, coronary heart disease, or ischemic stroke; prestroke history of depression, a relationship partner, living with others, independence, or paid employment; no fluoxetine intervention; ischemic stroke (compared with hemorrhagic); stroke treatment in Vietnam (compared with Australia or New Zealand); longer time since current stroke; and lower baseline National Institutes of Health Stroke Scale & Patient Health Questionnaire-9 scores. Direction of associations was largely concordant between single-measure and repeated-measures models. Association strength and variance was generally smaller in the repeated-measures model compared with the single-measure model. Conclusions Repeated-measures may improve trial precision in identifying trial associations and effects. Further repeated-measures stroke analyses are required to prove methodological value. Registration URL: http://www.anzctr.org.au; Unique identifier: ACTRN12611000774921.

Identifiants

pubmed: 35929466
doi: 10.1161/JAHA.121.025425
pmc: PMC9496315
doi:

Substances chimiques

Fluoxetine 01K63SUP8D

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e025425

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Auteurs

Alexander Chye (A)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.

Maree L Hackett (ML)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.
The University of Central Lancashire Preston Lancashire United Kingdom.

Graeme J Hankey (GJ)

Medical School Faculty of Health and Medical Sciences, The University of Western Australia Perth Western Australia Australia.
Department of Neurology Sir Charles Gairdner Hospital Perth Western Australia Australia.

Erik Lundström (E)

Department of Neuroscience Neurology, Uppsala University Uppsala Sweden.

Osvaldo P Almeida (OP)

Medical School University of Western Australia Perth Western Australia Australia.

John Gommans (J)

Hawke's Bay Hospital, Hastings Hawke's Bay New Zealand.

Martin Dennis (M)

Centre for Clinical Brain Sciences University of Edinburgh Edinburgh Scotland United Kingdom.

Stephen Jan (S)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.

Gillian E Mead (GE)

Usher Institute University of Edinburgh Edinburgh Scotland United Kingdom.

Andrew H Ford (AH)

Medical School University of Western Australia Perth Western Australia Australia.

Christopher Etherton Beer (CE)

Medical School University of Western Australia Perth Western Australia Australia.

Leon Flicker (L)

Medical School University of Western Australia Perth Western Australia Australia.

Candice Delcourt (C)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.
Faculty of Medicine University of New South Wales Sydney New South Wales Australia.
Department of Clinical Medicine, Faculty of Medicine Health and Human Sciences, Macquarie University Macquarie Park New South Wales Australia.

Laurent Billot (L)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.

Craig S Anderson (CS)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.
Faculty of Medicine University of New South Wales Sydney New South Wales Australia.
Neurology Department Royal Prince Alfred Hospital Sydney New South Wales Australia.
The George Institute for Global Health at Peking University Health Science Center Beijing People's Republic of China.

Katharina Stibrant Sunnerhagen (K)

Institute of Neuroscience and Physiology-Clinical Neuroscience The Sahlgrenska Academy, University of Gothenburg Gothenburg Sweden.

Qilong Yi (Q)

Canadian Blood Services and University of Toronto Toronto Canada.

Severine Bompoint (S)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.

Thang Huy Nguyen (TH)

Cerebrovascular Disease Department The People's Hospital 115 Ho Chi Min City Vietnam.

Thomas Lung (T)

The George Institute for Global Health University of New South Wales Sydney New South Wales Australia.
Faculty of Medicine and Health The University of Sydney Sydney Australia.

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Classifications MeSH