Evidence map›Paper›PMID 36517850›Full record

ArticleJournal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance2022

3D black blood cardiovascular magnetic resonance atlases of congenital aortic arch anomalies and the normal fetal heart: application to automated multi-label segmentation.

Alena U Uus, Milou P M van Poppel, Johannes K Steinweg, Irina Grigorescu, Paula Ramirez Gilliland, Thomas A Roberts, Alexia Egloff Collado, Mary A Rutherford, Joseph V Hajnal, David F A Lloyd and 2 more

Abstract read
In one paragraph

Article in Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

12 authors.

Alena U UusSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK. alena.uus@kcl.co.uk.
Milou P M van PoppelSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Johannes K SteinwegSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Irina GrigorescuSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Paula Ramirez GillilandSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Thomas A RobertsSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Alexia Egloff ColladoCentre for the Developing Brain, King's College London, London, UK.
Mary A RutherfordCentre for the Developing Brain, King's College London, London, UK.
Joseph V HajnalSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
David F A LloydSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Kuberan PushparajahSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Maria DeprezSchool of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.

Funding

Department of HealthMedical Research Council MR/K006355/1Rosetrees Trust A2725Wellcome Trust 102431Wellcome Trust 203148/Z/16/ZWellcome Trust WT 203148/Z/16/Z
6 · The paper itself

Abstract

backgroundImage-domain motion correction of black-blood contrast T2-weighted fetal cardiovascular magnetic resonance imaging (CMR) using slice-to-volume registration (SVR) provides high-resolution three-dimensional (3D) images of the fetal heart providing excellent 3D visualisation of vascular anomalies [1]. However, 3D segmentation of these datasets, important for both clinical reporting and the application of advanced analysis techniques is currently a time-consuming process requiring manual input with potential for inter-user variability.

methodsIn this work, we present novel 3D fetal CMR population-averaged atlases of normal and abnormal fetal cardiovascular anatomy. The atlases are created using motion-corrected 3D reconstructed volumes of 86 third trimester fetuses (gestational age range 29-34 weeks) including: 28 healthy controls, 20 cases with postnatally confirmed neonatal coarctation of the aorta (CoA) and 38 vascular rings (21 right aortic arch (RAA), 17 double aortic arch (DAA)). We used only high image quality datasets with isolated anomalies and without any other deviations in the cardiovascular anatomy.In addition, we implemented and evaluated atlas-guided registration and deep learning (UNETR) methods for automated 3D multi-label segmentation of fetal cardiac vessels. We used images from CoA, RAA and DAA cohorts including: 42 cases for training (14 from each cohort), 3 for validation and 6 for testing. In addition, the potential limitations of the network were investigated on unseen datasets including 3 early gestational age (22 weeks) and 3 low SNR cases.

resultsWe created four atlases representing the average anatomy of the normal fetal heart, postnatally confirmed neonatal CoA, RAA and DAA. Visual inspection was undertaken to verify expected anatomy per subgroup. The results of the multi-label cardiac vessel UNETR segmentation showed 100[Formula: see text] per-vessel detection rate for both normal and abnormal aortic arch anatomy.

conclusionsThis work introduces the first set of 3D black-blood T2-weighted CMR atlases of normal and abnormal fetal cardiovascular anatomy including detailed segmentation of the major cardiovascular structures. Additionally, we demonstrated the general feasibility of using deep learning for multi-label vessel segmentation of 3D fetal CMR images.

Indexed as

Aortic CoarctationHeart Defects, CongenitalAorta, ThoracicFetal HeartHumansInfantInfant, NewbornMagnetic Resonance ImagingMagnetic Resonance SpectroscopyPredictive Value of Tests3D fetal MRICongenital aortic arch anomaliesHeart atlasVessel segmentation

Identifiers

PMID36517850
PMCPMC9753334

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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.