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Identifying stroke therapeutics from preclinical models: A protocol for a novel application of network meta-analysis.

  • Manoj M. Lalu*
  • , Dean A. Fergusson
  • , Wei Cheng
  • , Marc T. Avey
  • , Dale Corbett
  • , Dar Dowlatshahi
  • , Malcolm R. Macleod
  • , Emily S. Sena
  • , David Moher
  • , Risa Shorr
  • , Sarah K. McCann
  • , Laura J. Gray
  • , Michael D. Hill
  • , Annette O'Connor
  • , Kristina Thayer
  • , Fatima Haggar
  • , Aditi Dobriyal
  • , Hee Sahng Chung
  • , Nicky J. Welton
  • , Brian Hutton
  • *Corresponding author for this work
  • University of Ottawa
  • Edinburgh Medical School
  • University of Leicester
  • University of Calgary
  • Iowa State University
  • National Institutes of Health
  • University of Bristol

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Introduction: Globally, stroke is the second leading cause of death. Despite the burden of illness and death, few acute interventions are available to patients with ischemic stroke. Over 1,000 potential neuroprotective therapeutics have been evaluated in preclinical models. It is important to use robust evidence synthesis methods to appropriately assess which therapies should be translated to the clinical setting for evaluation in human studies. This protocol details planned methods to conduct a systematic review to identify and appraise eligible studies and to use a network meta-analysis to synthesize available evidence to answer the following questions: in preclinical in vivo models of focal ischemic stroke, what are the relative benefits of competing therapies tested in combination with the gold standard treatment alteplase in (i) reducing cerebral infarction size, and (ii) improving neurobehavioural outcomes? Methods: We will search Ovid Medline and Embase for articles on the effects of combination therapies with alteplase. Controlled comparison studies of preclinical in vivo models of experimentally induced focal ischemia testing the efficacy of therapies with alteplase versus alteplase alone will be identified. Outcomes to be extracted include infarct size (primary outcome) and neurobehavioural measures. Risk of bias and construct validity will be assessed using tools appropriate for preclinical studies. Here we describe steps undertaken to perform preclinical network meta-analysis to synthesise all evidence for each outcome and obtain a comprehensive ranking of all treatments. This will be a novel use of this evidence synthesis approach in stroke medicine to assess pre-clinical therapeutics. Combining all evidence to simultaneously compare mutliple therapuetics tested preclinically may provide a rationale for the clinical translation of therapeutics for patients with ischemic stroke.  Dissemination: Review findings will be submitted to a peer-reviewed journal and presented at relevant scientific meetings to promote knowledge transfer. Registration: PROSPERO number to be submitted following peer review.

Original languageEnglish
Article number8
JournalF1000Research
Volume8
DOIs
StatePublished - 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Network meta-analysis
  • Network metaanalysis
  • Preclinical
  • Stroke
  • Systematic review

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