Evidence map›Paper›PMID 30852791›Full record

ArticleLa Radiologia medica2019

Value of structured reporting in neuromuscular disorders.

Francesco Alessandrino, Lara Cristiano, Claudia Maria Cinnante, Tommaso Tartaglione, Simonetta Gerevini, Tommaso Verdolotti, Giovanna Stefania Colafati, Emanuele Ghione, Raimondo Vitale, Lorenzo Peverelli and 5 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in La Radiologia medica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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

15 authors at 7 institutions in 3 countries.

Francesco AlessandrinoNeuroradiology Department, IRCCS C. Mondino Foundation, Pavia, Italy. falessandrino@bwh.harvard.edu.ORCID http://orcid.org/0000-0002-1681-1284
Lara CristianoDepartment of Radiology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
Claudia Maria CinnanteNeuroradiology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Tommaso TartaglioneDepartment of Radiology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
Simonetta GereviniUnit of Neuroradiology, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Tommaso VerdolottiDepartment of Radiology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
Giovanna Stefania ColafatiNeuroradiology Unit, Department of Imaging, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
Emanuele GhioneNeuroradiology Department, IRCCS C. Mondino Foundation, Pavia, Italy.
Raimondo VitaleNeuroradiology Department, IRCCS C. Mondino Foundation, Pavia, Italy.
Lorenzo PeverelliNeuromuscular and Rare Diseases Unit, Department of Neuroscience, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Claudia BrognaPediatric Neurology and Nemo Clinical Centre, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
Angela BerardinelliChild and Adolescent Unit, IRCCS C. Mondino Foundation, Pavia, Italy.
Maurizio MoggioNeuromuscular and Rare Diseases Unit, Department of Neuroscience, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Eugenio M MercuriPediatric Neurology and Nemo Clinical Centre, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
Anna PichiecchioNeuroradiology Department, IRCCS C. Mondino Foundation, Pavia, Italy.
Università Cattolica del Sacro Cuore · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITFondazione Istituto Neurologico Nazionale Casimiro Mondino · ITBambino Gesù Children's Hospital · ITBrigham and Women's Hospital · USUniversity of Pavia · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess whether structured reports (SRs) of MRI in patients with inherited neuromuscular disorders (IND) provide more clinically relevant information than non-structured reports (NSRs) and whether neuroradiologists' expertise affects completeness of reports. MATERIAL AND

methodsLower limbs' MRI reports of patients with IND produced by neuroradiologists with different level of expertise (> 15 years vs. < 15 years of experience in reading IND-MRI) before and after implementation of a SR template were included. Reports were assessed for the presence of 9 key features relevant for IND management. Reports and images were evaluated by neurologists who assessed: disease-specific muscular involvement pattern; presence of sufficient information to order the appropriate genetic/diagnostic tests; presence of sufficient information to make therapeutic decision/perform biopsy and necessity to review MRI images. Mann-Whitney and Fisher's exact tests were used to compare the number of key features for NSR and SR and neurologists' answers for reports produced by neuroradiologists with different experience.

resultsThirty-one SRs and 101 NSRs were reviewed. A median of 8 and 6 key features was present in SR and NSR, respectively (p value < 0.0001). When reports were produced by less expert neuroradiologists, neurologists recognized muscular involvement pattern, had sufficient information for clinical decision-making/perform biopsy more often with SR than NSR (p values: < 0.0001), and needed to evaluate images less often with SR (p value: 0.0001). When reports produced by expert neuroradiologists were evaluated, no significant difference in neurologists' answers was observed.

conclusionSR of IND-MRI contained more often clinically relevant information considered important for disease management than NSR. Radiologist's expertise affects completeness of NSR reports.

Indexed as

Lower ExtremityAdolescentAdultAgedFemaleHumansMagnetic Resonance ImagingMaleMedical RecordsMiddle AgedNeuromuscular DiseasesRetrospective StudiesLimb-girdle muscular dystrophiesMagnetic resonance imagingNeuromuscular diseasesSarcoglycanopathiesStructured reporting

Identifiers

PMID30852791
OpenAlexW2921766583

What OpenQuestion holds

Textmetadata
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.