Evidence map›Paper›PMID 36777636›Full record

SynthesisFrontiers in neuroscience2023

Assessing MR-compatibility of somatosensory stimulation devices: A systematic review on testing methodologies.

Carolina Travassos, Alexandre Sayal, Bruno Direito, João Pereira, Teresa Sousa, Miguel Castelo-Branco

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in Frontiers in neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Carolina TravassosCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.
Alexandre SayalCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.
Bruno DireitoCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.
João PereiraCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.
Teresa SousaCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.
Miguel Castelo-BrancoCoimbra Institute for Biomedical Imaging and Translational Research (CIBIT), University of Coimbra (UC), Coimbra, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional magnetic resonance imaging (fMRI) has been extensively used as a tool to map the brain processes related to somatosensory stimulation. This mapping includes the localization of task-related brain activation and the characterization of brain activity dynamics and neural circuitries related to the processing of somatosensory information. However, the magnetic resonance (MR) environment presents unique challenges regarding participant and equipment safety and compatibility. This study aims to systematically review and analyze the state-of-the-art methodologies to assess the safety and compatibility of somatosensory stimulation devices in the MR environment. A literature search, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement guidelines, was performed in PubMed, Scopus, and Web of Science to find original research on the development and testing of devices for somatosensory stimulation in the MR environment. Nineteen records that complied with the inclusion and eligibility criteria were considered. The findings are discussed in the context of the existing international standards available for the safety and compatibility assessment of devices intended to be used in the MR environment. In sum, the results provided evidence for a lack of uniformity in the applied testing methodologies, as well as an in-depth presentation of the testing methodologies and results. Lastly, we suggest an assessment methodology (safety, compatibility, performance, and user acceptability) that can be applied to devices intended to be used in the MR environment. Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42021257838.

Indexed as

compatibilityfunctional MRI (fMRI)magnetic resonance imaging (MRI)MR-compatibleMR-safesafetysomatosensory stimulation devices

Identifiers

PMID36777636
PMCPMC9909190

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.