Evidence map›Paper›PMID 30132090›Full record

ArticleClinical neuroradiology2019

MDCT-based Finite Element Analysis of Vertebral Fracture Risk: What Dose is Needed?

D Anitha, Kai Mei, Michael Dieckmeyer, Felix K Kopp, Nico Sollmann, Claus Zimmer, Jan S Kirschke, Peter B Noel, Thomas Baum, Karupppasamy Subburaj

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Article in Clinical neuroradiology, 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.

  1. Pooled it
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  9. X-ray-based quantitative osteoporosis imaging at the spine.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2020
    Review
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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

10 authors.

D AnithaEngineering Product Development (EPD) Pillar, Singapore University of Technology and Design (SUTD), 8 Somapah Road, 487372, Singapore, Singapore.
Kai MeiDepartment of Radiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Michael DieckmeyerDepartment of Radiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Felix K KoppDepartment of Radiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Nico SollmannDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Claus ZimmerDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Jan S KirschkeDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Peter B NoelDepartment of Radiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Thomas BaumDepartment of Neuroradiology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Karupppasamy SubburajEngineering Product Development (EPD) Pillar, Singapore University of Technology and Design (SUTD), 8 Somapah Road, 487372, Singapore, Singapore. subburaj@sutd.edu.sg.ORCID http://orcid.org/0000-0003-0723-2405

Funding

Deutsche Forschungsgemeinschaft BA 4906/2-1Fakultät für Medizin, Technische Universität München KKF grant H01
6 · The paper itself

Abstract

purposeThe aim of this study was to compare vertebral failure loads, predicted from finite element (FE) analysis of patients with and without osteoporotic vertebral fractures (OVF) at virtually reduced dose levels, compared to standard-dose exposure from multidetector computed tomography (MDCT) imaging and evaluate whether ultra-low dose derived FE analysis can still differentiate patient groups. MATERIALS AND

methodsAn institutional review board (IRB) approval was obtained for this retrospective study. A total of 16 patients were evaluated at standard-dose MDCT; eight with and eight without OVF. Images were reconstructed at virtually reduced dose levels (i. e. half, quarter and tenth of the standard dose). Failure load was determined at L1-3 from FE analysis and compared between standard, half, quarter, and tenth doses and used to differentiate between fracture and control groups.

resultsFailure load derived at standard dose (3254 ± 909 N and 3794 ± 984 N) did not significantly differ from half (3390 ± 890 N and 3860 ± 1063 N) and quarter dose (3375 ± 915 N and 3925 ± 990 N) but was significantly higher for one tenth dose (4513 ± 1762 N and 4766 ± 1628 N) for fracture and control groups, respectively. Failure load differed significantly between the two groups at standard, half and quarter doses, but not at tenth dose. Receiver operating characteristic (ROC) curve analysis also demonstrated that standard, half, and quarter doses can significantly differentiate the fracture from the control group.

conclusionThe use of MDCT enables a dose reduction of at least 75% compared to standard-dose for an adequate prediction of vertebral failure load based on non-invasive FE analysis.

Indexed as

Biomechanical PhenomenaCase-Control StudiesFemaleFinite Element AnalysisHumansLumbar VertebraeMaleMultidetector Computed TomographyOsteoporotic FracturesPredictive Value of TestsRadiation DosageRadiographic Image Interpretation, Computer-AssistedRetrospective StudiesRisk AssessmentROC CurveSpinal FracturesFinite element analysisMultidetector computed tomographyOsteoporosisRadiation dosageSpinal fractures

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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.