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Current practices in studies applying the target trial emulation framework: a protocol for a systematic review.
Bigirumurame, Theophile; Hiu, Shaun Kuan Wei; Teare, M Dawn; Wason, James M S; Bryant, Andrew; Breckons, Matthew.
Afiliação
  • Bigirumurame T; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK theophile.bigirumurame@newcastle.ac.uk.
  • Hiu SKW; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Teare MD; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Wason JMS; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Bryant A; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Breckons M; Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
BMJ Open ; 13(6): e070963, 2023 06 27.
Article em En | MEDLINE | ID: mdl-37369393
ABSTRACT

INTRODUCTION:

Observational studies represent an alternative to estimate real-world causal effects in the absence of available randomised controlled trials (RCTs). Target trial emulation is a framework for the application of RCT design principles to emulate a hypothetical open-label RCT (the hypothetical target trial) using existing observational data as the primary data source as opposed to the prospective recruitment and measurement of randomised units. The aim of this systematic review is to investigate the practices of studies applying the target trial emulation framework to evaluate the effectiveness of interventions. METHODS AND

ANALYSIS:

We will systematically search in Medline (via Ovid), Embase (via Ovid, entries from medRxiv are included), PsycINFO (via Ovid), SCOPUS, Web of Science, Cochrane Library, the ISRCTN registry and ClinicalTrials.gov for all study reports and protocols which used the trial emulation framework (without time restriction). We will extract information concerning study design, data source, analysis, results, interpretation and dissemination. Two reviewers will perform study selection, data extraction and quality assessment. Disagreements between reviewers will be resolved by a third reviewer. A narrative approach will be used to synthesise and report qualitative and quantitative data. Reporting of the review will be informed by Preferred Reporting Items for Systematic Review and Meta-Analysis guidance (PRISMA). ETHICS AND DISSEMINATION Ethical approval is not required as it is a protocol for a systematic review. Findings will be disseminated through peer-reviewed publications and conference presentations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Narração Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Narração Idioma: En Ano de publicação: 2023 Tipo de documento: Article