Evidence map›Paper›PMID 34805206›Full record

ArticleFrontiers in medicine2021

A Clinically-Compatible Workflow for Computer-Aided Assessment of Brain Disease Activity in Multiple Sclerosis Patients.

Benoit Combès, Anne Kerbrat, Guillaume Pasquier, Olivier Commowick, Brandon Le Bon, Francesca Galassi, Philippe L'Hostis, Nora El Graoui, Raphael Chouteau, Emmanuel Cordonnier and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Benoit CombèsUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Anne KerbratUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Guillaume PasquierIRT bcom, Rennes, France.
Olivier CommowickUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Brandon Le BonUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Francesca GalassiUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Philippe L'HostisBiotrial, Rennes, France.
Nora El GraouiUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Raphael ChouteauNeurology Department, Rennes University Hospital, Rennes, France.
Emmanuel CordonnierIRT bcom, Rennes, France.
Gilles EdanUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Jean-Christophe FerréUniv Rennes, Inria, CNRS, Inserm IRISA UMR 6074, Empenn ERL U 1228, Rennes, France.
Centre Hospitalier Universitaire de Rennes · FRInserm · FRUniversité de Rennes · FRCentre National de la Recherche Scientifique · FRInstitut de Recherche en Informatique et Systèmes Aléatoires · FRStructure Fédérative de Recherche en Biologie et Santé de Rennes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last 10 years, the number of approved disease modifying drugs acting on the focal inflammatory process in Multiple Sclerosis (MS) has increased from 3 to 10. This wide choice offers the opportunity of a personalized medicine with the objective of no clinical and radiological activity for each patient. This new paradigm requires the optimization of the detection of new FLAIR lesions on longitudinal MRI. In this paper, we describe a complete workflow-that we developed, implemented, deployed, and evaluated-to facilitate the monitoring of new FLAIR lesions on longitudinal MRI of MS patients. This workflow has been designed to be usable by both hospital and private neurologists and radiologists in France. It consists of three main components: (i) a software component that allows for automated and secured anonymization and transfer of MRI data from the clinical Picture Archive and Communication System (PACS) to a processing server (and vice-versa); (ii) a fully automated segmentation core that enables detection of focal longitudinal changes in patients from T1-weighted, T2-weighted and FLAIR brain MRI scans, and (iii) a dedicated web viewer that provides an intuitive visualization of new lesions to radiologists and neurologists. We first present these different components. Then, we evaluate the workflow on 54 pairs of longitudinal MRI scans that were analyzed by 3 experts (1 neuroradiologist, 1 radiologist, and 1 neurologist) with and without the proposed workflow. We show that our workflow provided a valuable aid to clinicians in detecting new MS lesions both in terms of accuracy (mean number of detected lesions per patient and per expert 1.8 without the workflow vs. 2.3 with the workflow,

Indexed as

computer aided diagnosislesion activityMRIMultiple Sclerosisradiology

Identifiers

PMID34805206
PMCPMC8595265
OpenAlexW3208044348

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.