Evidence map›Paper›PMID 37961745›Full record

ArticleArXiv2023

SDF4CHD: Generative Modeling of Cardiac Anatomies with Congenital Heart Defects.

Fanwei Kong, Sascha Stocker, Perry S Choi, Michael Ma, Daniel B Ennis, Alison Marsden

Abstract readPreprint
In one paragraph

Article in ArXiv, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Fanwei KongDepartment of Pediatrics, Cardiovascular Institute, Stanford University, Stanford.
Sascha StockerDepartment of Radiology, Stanford University, Stanford.
Perry S ChoiDepartment of Cardiothoracic Surgery, Stanford University, Stanford.
Michael MaDepartment of Cardiothoracic Surgery, Stanford University, Stanford.
Daniel B EnnisDepartment of Radiology, Cardiovascular Institute, Stanford University, Stanford.
Alison MarsdenDepartment of Bioengineering, Department of Mechanical Engineering, Department of Pediatrics, Stanford University, Stanford.

Funding

Stanford Integrated Cardiovascular/Pulmonary Residency Research Training ProgramR38HL143615 · NHLBI · STANFORD UNIVERSITY · PI Michael Peter Fischbein, Marlene Rabinovitch · 2020 to 2026
$2.2M
SCH: INT: A Virtual Surgery Simulator to Accelerate Medical Training in Cardiovascular Disease R01EB029362 · NIBIB · STANFORD UNIVERSITY · PI MARSDEN, ALISON L · 2019 to 2022
$1.4M
Automated data curation to ensure model credibility in the Vascular Model RepositoryR01LM013120 · NLM · STANFORD UNIVERSITY · PI MARSDEN, ALISON L · 2019 to 2021
$1.0M
NHLBI NIH HHS R38 HL143615NIBIB NIH HHS R01 EB029362NLM NIH HHS R01 LM013120
6 · The paper itself

Abstract

Congenital heart disease (CHD) encompasses a spectrum of cardiovascular structural abnormalities, often requiring customized treatment plans for individual patients. Computational modeling and analysis of these unique cardiac anatomies can improve diagnosis and treatment planning and may ultimately lead to improved outcomes. Deep learning (DL) methods have demonstrated the potential to enable efficient treatment planning by automating cardiac segmentation and mesh construction for patients with normal cardiac anatomies. However, CHDs are often rare, making it challenging to acquire sufficiently large patient cohorts for training such DL models. Generative modeling of cardiac anatomies has the potential to fill this gap via the generation of virtual cohorts; however, prior approaches were largely designed for normal anatomies and cannot readily capture the significant topological variations seen in CHD patients. Therefore, we propose a type- and shape-disentangled generative approach suitable to capture the wide spectrum of cardiac anatomies observed in different CHD types and synthesize differently shaped cardiac anatomies that preserve the unique topology for specific CHD types. Our DL approach represents generic whole heart anatomies with CHD type-specific abnormalities implicitly using signed distance fields (SDF) based on CHD type diagnosis, which conveniently captures divergent anatomical variations across different types and represents meaningful intermediate CHD states. To capture the shape-specific variations, we then learn invertible deformations to morph the learned CHD type-specific anatomies and reconstruct patient-specific shapes. Our approach has the potential to augment the image-segmentation pairs for rarer CHD types for cardiac segmentation and generate cohorts of CHD cardiac meshes for computational simulation.

Indexed as

Congenital Cardiac DefectsGenerative Shape ModelingImplicit Neural Representations

Identifiers

PMID37961745
PMCPMC10635288

What OpenQuestion holds

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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.