Accuracy of clinical diagnosis of behavioural variant frontotemporal dementia: a protocol for a systematic review and meta-analysis.

BMJ Open

Center for Neurodegenerative Diseases and the Aging Brain, Department of Clinical Research in Neurology, University of Bari Aldo Moro, Pia Fondazione Cardinale G. Panico, Tricase, Puglia, Italy.

Published: July 2024

AI Article Synopsis

  • The systematic review aims to assess the accuracy of clinical diagnostic criteria for behavioural variant frontotemporal dementia (bvFTD) by comparing them to pathological diagnoses and evaluating improvements over time.
  • The review will follow established guidelines, searching multiple databases for peer-reviewed articles that report on diagnostic parameters for bvFTD, with selection performed by independent reviewers.
  • The study will collect data on various diagnostic metrics and quality assessments, and findings will be shared through publications and scientific conferences upon completion.

Article Abstract

Introduction: Behavioural variant frontotemporal dementia (bvFTD) characterisation has evolved, but diagnosis remains challenging, relying on clinical diagnostic criteria that have undergone revisions over time. In this systematic review, our aims are to evaluate the accuracy of clinical diagnostic criteria for bvFTD by comparing them against pathological diagnoses and determine potential improvement in performance over the years.

Methods And Analysis: This systematic review protocol follows the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols 2015 guidelines and is registered on PROSPERO. We will search four databases (MEDLINE-PubMed, Web of Science, Embase and LILACS) using tailored search terms on May 1st 2024. Inclusion criteria encompass peer-reviewed articles reporting diagnostic parameters or raw data regarding bvFTD clinical diagnosis based on well-defined criteria. Screening and selection of relevant articles will be independently performed by two reviewers using the Covidence systematic review manager. Discrepancies will be resolved by a third researcher. Pathologic and genetic diagnosis will be the main gold standard, but we will also consider refined diagnoses after a follow-up period. Data will be collected on study design, baseline demographics and sensitivity, specificity, positive predictive value, negative predictive value and diagnostic accuracy. Study quality will be assessed with Quality Assessment of Diagnostic Accuracy Studies-2. If possible, we will conduct a meta-analysis using bivariate random-effect models. Subgroup analyses will consider study settings, gold standards, disease stages and bias.

Ethics And Dissemination: Ethics approval will not be needed because the data used in this systematic review will be extracted from published studies. Findings will be disseminated through peer-reviewed publications and presentations at relevant scientific conferences, potentially enhancing our understanding of bvFTD clinical diagnosis reliability and guiding future criteria refinements.

Prospero Registration Number: CRD42023389063.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11256028PMC
http://dx.doi.org/10.1136/bmjopen-2023-081935DOI Listing

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