Evidence map›Paper›PMID 37474665›Full record

ArticleLa Radiologia medica2023

Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities.

Tamarisk du Plessis, Gopika Ramkilawon, William Ian Duncombe Rae, Tanita Botha, Neil Alexander Martinson, Sarah Alice Parry Dixon, Andre Kyme, Mike Michael Sathekge

Abstract read
In one paragraph

Article in La Radiologia medica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

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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.

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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

8 authors.

Tamarisk du PlessisDepartment of Nuclear Medicine, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa. tamarisk.duplessis@gmail.com.ORCID http://orcid.org/0000-0002-3955-1833
Gopika RamkilawonDepartment of Statistics, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0002-2919-1918
William Ian Duncombe RaeMedical Imaging Department, Prince of Wales Hospital, Sydney, Australia.ORCID http://orcid.org/0000-0002-3866-8562
Tanita BothaDepartment of Statistics, Faculty of Natural and Agricultural Sciences, University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0002-8861-4466
Neil Alexander MartinsonPerinatal HIV Research Unit (PHRU), University of the Witwatersrand, Johannesburg, South Africa.ORCID http://orcid.org/0000-0002-0184-5705
Sarah Alice Parry DixonSchool of Biomedical Engineering, University of Sydney, Sydney, Australia.ORCID http://orcid.org/0000-0003-4626-7782
Andre KymeSchool of Biomedical Engineering, University of Sydney, Sydney, Australia.ORCID http://orcid.org/0000-0003-3297-5390
Mike Michael SathekgeDepartment of Nuclear Medicine, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0002-2806-0625

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccurate segmentation (separating diseased portions of the lung from normal appearing lung) is a challenge in radiomic studies of non-neoplastic diseases, such as pulmonary tuberculosis (PTB). In this study, we developed a segmentation method, applicable to chest X-rays (CXR), that can eliminate the need for precise disease delineation, and that is effective for constructing radiomic models for automatic PTB cavity classification.

methodsThis retrospective study used a dataset of 266 posteroanterior CXR of patients diagnosed with laboratory confirmed PTB. The lungs were segmented using a U-net-based in-house automatic segmentation model. A secondary segmentation was developed using a sliding window, superimposed on the primary lung segmentation. Pyradiomics was used for feature extraction from every window which increased the dimensionality of the data, but this allowed us to accurately capture the spread of the features across the lung. Two separate measures (standard-deviation and variance) were used to consolidate the features. Pearson's correlation analysis (with a 0.8 cut-off value) was then applied for dimensionality reduction followed by the construction of Random Forest radiomic models.

resultsTwo almost identical radiomic signatures consisting of 10 texture features each (9 were the same plus 1 other feature) were identified using the two separate consolidation measures. Two well performing random forest models were constructed from these signatures. The standard-deviation model (AUC = 0.9444 (95% CI, 0.8762; 0.9814)) performed marginally better than the variance model (AUC = 0.9288 (95% CI, 0.9046; 0.9843)).

conclusionThe introduction of the secondary sliding window segmentation on CXR could eliminate the need for disease delineation in pulmonary radiomic studies, and it could improve the accuracy of CXR reporting currently regaining prominence as a high-volume screening tool as the developed radiomic models correctly classify cavities from normal CXR.

Indexed as

Lung DiseasesTuberculosis, PulmonaryHumansLungRadiographyRetrospective StudiesPulmonary tuberculosisRadiomicsSegmentationSliding window

Identifiers

PMID37474665
PMCPMC10474191

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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.