Evidence map›Paper›PMID 36781953›Full record

ArticleScientific reports2023

How scan parameter choice affects deep learning-based coronary artery disease assessment from computed tomography.

Felix Denzinger, Michael Wels, Katharina Breininger, Oliver Taubmann, Alexander Mühlberg, Thomas Allmendinger, Mehmet A Gülsün, Max Schöbinger, Florian André, Sebastian J Buss and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

5 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

13 authors.

Felix DenzingerPattern Recognition Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany. felix.denzinger@fau.de.
Michael WelsComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Katharina BreiningerDepartment Artificial Intelligence in Biomedical Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Oliver TaubmannComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Alexander MühlbergComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Thomas AllmendingerComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Mehmet A GülsünComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Max SchöbingerComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Florian AndréDas Radiologische Zentrum-Radiology Center, Sinsheim-Eberbach-Erbach-Walldorf-Heidelberg, Germany.
Sebastian J BussDas Radiologische Zentrum-Radiology Center, Sinsheim-Eberbach-Erbach-Walldorf-Heidelberg, Germany.
Johannes GörichDas Radiologische Zentrum-Radiology Center, Sinsheim-Eberbach-Erbach-Walldorf-Heidelberg, Germany.
Michael SühlingComputed Tomography, Siemens Healthcare GmbH, Forchheim, Germany.
Andreas MaierPattern Recognition Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, algorithms capable of assessing the severity of Coronary Artery Disease (CAD) in form of the Coronary Artery Disease-Reporting and Data System (CAD-RADS) grade from Coronary Computed Tomography Angiography (CCTA) scans using Deep Learning (DL) were proposed. Before considering to apply these algorithms in clinical practice, their robustness regarding different commonly used Computed Tomography (CT)-specific image formation parameters-including denoising strength, slab combination, and reconstruction kernel-needs to be evaluated. For this study, we reconstructed a data set of 500 patient CCTA scans under seven image formation parameter configurations. We select one default configuration and evaluate how varying individual parameters impacts the performance and stability of a typical algorithm for automated CAD assessment from CCTA. This algorithm consists of multiple preprocessing and a DL prediction step. We evaluate the influence of the parameter changes on the entire pipeline and additionally on only the DL step by propagating the centerline extraction results of the default configuration to all others. We consider the standard deviation of the CAD severity prediction grade difference between the default and variation configurations to assess the stability w.r.t. parameter changes. For the full pipeline we observe slight instability (± 0.226 CAD-RADS) for all variations. Predictions are more stable with centerlines propagated from the default to the variation configurations (± 0.122 CAD-RADS), especially for differing denoising strengths (± 0.046 CAD-RADS). However, stacking slabs with sharp boundaries instead of mixing slabs in overlapping regions (called true stack ± 0.313 CAD-RADS) and increasing the sharpness of the reconstruction kernel (± 0.150 CAD-RADS) leads to unstable predictions. Regarding the clinically relevant tasks of excluding CAD (called rule-out; AUC default 0.957, min 0.937) and excluding obstructive CAD (called hold-out; AUC default 0.971, min 0.964) the performance remains on a high level for all variations. Concluding, an influence of reconstruction parameters on the predictions is observed. Especially, scans reconstructed with the true stack parameter need to be treated with caution when using a DL-based method. Also, reconstruction kernels which are underrepresented in the training data increase the prediction uncertainty.

Indexed as

Coronary Artery DiseaseDeep LearningCoronary AngiographyHeartHumansPredictive Value of TestsTomography, X-Ray Computed

Identifiers

PMID36781953
PMCPMC9925789

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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.