Evidence map›Paper›PMID 36704465›Full record

ArticleFrontiers in cardiovascular medicine2022

MITEA: A dataset for machine learning segmentation of the left ventricle in 3D echocardiography using subject-specific labels from cardiac magnetic resonance imaging.

Debbie Zhao, Edward Ferdian, Gonzalo D Maso Talou, Gina M Quill, Kathleen Gilbert, Vicky Y Wang, Thiranja P Babarenda Gamage, João Pedrosa, Jan D'hooge, Timothy M Sutton and 7 more

Abstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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

7 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

17 authors.

Debbie ZhaoAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Edward FerdianDepartment of Anatomy and Medical Imaging, University of Auckland, Auckland, New Zealand.
Gonzalo D Maso TalouAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Gina M QuillAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Kathleen GilbertAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Vicky Y WangAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Thiranja P Babarenda GamageAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
João PedrosaInstitute for Systems and Computer Engineering, Technology and Science (INESC TEC), Porto, Portugal.
Jan D'hoogeDepartment of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.
Timothy M SuttonCounties Manukau Health Cardiology, Middlemore Hospital, Auckland, New Zealand.
Boris S LoweGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Malcolm E LeggetDepartment of Medicine, University of Auckland, Auckland, New Zealand.
Peter N RuygrokGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Robert N DoughtyGreen Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Oscar CamaraDepartment of Information and Communication Technologies, Universitat Pompeu Fabra, Barcelona, Spain.
Alistair A YoungDepartment of Anatomy and Medical Imaging, University of Auckland, Auckland, New Zealand.
Martyn P NashAuckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.

Funding

The Cardiac Atlas ProjectR01HL121754 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MCCULLOCH, ANDREW D., OMENS, JEFFREY H. · 2014 to 2023
$5.0M
NHLBI NIH HHS R01 HL121754
6 · The paper itself

Abstract

Segmentation of the left ventricle (LV) in echocardiography is an important task for the quantification of volume and mass in heart disease. Continuing advances in echocardiography have extended imaging capabilities into the 3D domain, subsequently overcoming the geometric assumptions associated with conventional 2D acquisitions. Nevertheless, the analysis of 3D echocardiography (3DE) poses several challenges associated with limited spatial resolution, poor contrast-to-noise ratio, complex noise characteristics, and image anisotropy. To develop automated methods for 3DE analysis, a sufficiently large, labeled dataset is typically required. However, ground truth segmentations have historically been difficult to obtain due to the high inter-observer variability associated with manual analysis. We address this lack of expert consensus by registering labels derived from higher-resolution subject-specific cardiac magnetic resonance (CMR) images, producing 536 annotated 3DE images from 143 human subjects (10 of which were excluded). This heterogeneous population consists of healthy controls and patients with cardiac disease, across a range of demographics. To demonstrate the utility of such a dataset, a state-of-the-art, self-configuring deep learning network for semantic segmentation was employed for automated 3DE analysis. Using the proposed dataset for training, the network produced measurement biases of -9 ± 16 ml, -1 ± 10 ml, -2 ± 5 %, and 5 ± 23 g, for end-diastolic volume, end-systolic volume, ejection fraction, and mass, respectively, outperforming an expert human observer in terms of accuracy as well as scan-rescan reproducibility. As part of the Cardiac Atlas Project, we present here a large, publicly available 3DE dataset with ground truth labels that leverage the higher resolution and contrast of CMR, to provide a new benchmark for automated 3DE analysis. Such an approach not only reduces the effect of observer-specific bias present in manual 3DE annotations, but also enables the development of analysis techniques which exhibit better agreement with CMR compared to conventional methods. This represents an important step for enabling more efficient and accurate diagnostic and prognostic information to be obtained from echocardiography.

Indexed as

3D echocardiography (3DE)Cardiac Atlas Projectcardiac magnetic resonance (CMR) imagingdomain adaptationleft ventricle (LV)machine learning (ML)multimodal imagingsegmentation (image processing)

Identifiers

PMID36704465
PMCPMC9871929

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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.