Evidence map›Paper›PMID 31201526›Full record

ArticleEuropean radiology2019

Follow-up MRI in multiple sclerosis patients: automated co-registration and lesion color-coding improves diagnostic accuracy and reduces reading time.

David Zopfs, Kai R Laukamp, Stefanie Paquet, Simon Lennartz, Daniel Pinto Dos Santos, Christoph Kabbasch, Alexander Bunck, Marc Schlamann, Jan Borggrefe

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In one paragraph

Article in European radiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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

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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

9 authors.

David ZopfsFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany. david.zopfs@uk-koeln.de.ORCID http://orcid.org/0000-0001-9978-7453
Kai R LaukampFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Stefanie PaquetFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Simon LennartzFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Daniel Pinto Dos SantosFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Christoph KabbaschFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Alexander BunckFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Marc SchlamannFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.
Jan BorggrefeFaculty of Medicine and University Hospital Cologne, Institute for Diagnostic and Interventional Radiology, University of Cologne, Cologne, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn multiple sclerosis (MS), the heterogeneous and numerous appearances of lesions may impair diagnostic accuracy. This study investigates if a combined automated co-registration and lesion color-coding method (AC) improves assessment of MS follow-up MRI compared with conventional reading (CR).

methodsWe retrospectively assessed 70 follow-up MRI of 53 patients. Heterogeneous datasets of diverse scanners and institutions were used. Two readers determined presence of (a) progression, (b) regression, (c) mixed change, or (d) stable disease between the two examinations using corresponding FLAIR sequences in CR and AC-assisted reading. Consensus reference reading was provided by two blinded radiologists. Kappa statistics tested interrater agreement, McNemar's test dichotomous variables, and Wilcoxon's test continuous variables (statistical significance p ≤ 0.05).

resultsThe cohort comprised 41 female and 12 male patients with a mean age of 40 (± 14) years. Average rating time was reduced from 78 (± 36) to 44 (±22) s with the AC approach (p < 0.001). The time needed to start and match datasets with AC was 14 (± 1) s. Compared with CR, AC improved interrater agreement, both between raters (0.52 vs. 0.67) and between raters and consensus reference reading (0.47/0.5 vs. 0.83/0.78). Compared with CR, the diagnostic accuracy increased from 67 to 90% (reader 1, p < 0.01) and from 70 to 87% (reader 2, p < 0.05) in the AC-assisted reading.

conclusionsCompared with CR, automated co-registration and lesion color-coding of MS-associated FLAIR-lesions in follow-up MRI increased diagnostic accuracy and reduced the time required for follow-up evaluation significantly. The AC algorithm therefore appears to be helpful to improve MS follow-up assessments in clinical routine. KEY POINTS: • Automated co-registration and lesion color-coding increases diagnostic accuracy in the assessment of MRI follow-up examinations in patients with multiple sclerosis. • Automated co-registration and lesion color-coding reduces reading time of MRI follow-up examinations in patients with multiple sclerosis. • Automated co-registration and lesion color-coding improved interrater agreement in the assessment of MRI follow-up examinations in patients with multiple sclerosis.

Indexed as

AdolescentAdultAgedBrainDisease ProgressionFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedMultiple SclerosisReproducibility of ResultsRetrospective StudiesYoung AdultBrainDisease progressionImage processing, computer-assistedMagnetic resonance imagingMultiple sclerosis

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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.