Evidence map›Paper›PMID 39143242›Full record

ArticleNPJ digital medicine2024

Robust automated calcification meshing for personalized cardiovascular biomechanics.

Daniel H Pak, Minliang Liu, Theodore Kim, Caglar Ozturk, Raymond McKay, Ellen T Roche, Rudolph Gleason, James S Duncan

Abstract read
In one paragraph

Article in NPJ digital medicine, 2024. 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

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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. AI-Powered Multimodal Modeling of Personalized Hemodynamics in Aortic Stenosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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.

Daniel H PakYale University, 300 Cedar St, New Haven, CT, 06511, USA. daniel.pak@yale.edu.ORCID http://orcid.org/0000-0003-3425-428X
Minliang LiuTexas Tech University, 805 Boston Avenue, Lubbock, TX, 79409, USA.
Theodore KimYale University, 300 Cedar St, New Haven, CT, 06511, USA.
Caglar OzturkMassachusetts Institute of Technology, 45 Carleton St, Cambridge, MA, 02142, USA.ORCID http://orcid.org/0000-0002-3688-0148
Raymond McKayHartford Hospital, 85 Seymour St, Hartford, CT, 06106, USA.
Ellen T RocheMassachusetts Institute of Technology, 45 Carleton St, Cambridge, MA, 02142, USA.
Rudolph GleasonGeorgia Institute of Technology, 315 Ferst Dr NW, Atlanta, GA, 30332, USA.
James S DuncanYale University, 300 Cedar St, New Haven, CT, 06511, USA.

Funding

q4DE: A Biomarker for Image-Guided, Post-MI Hydrogel TherapyR01HL121226 · NHLBI · YALE UNIVERSITY · PI DUNCAN, JAMES S, O'DONNELL, MATTHEW · 2014 to 2022
$6.3M
Training In Multi-modality Molecular & Translational Cardiovascular ImagingT32HL098069 · NHLBI · YALE UNIVERSITY · PI JAMES S DUNCAN, Georges El Fakhri · 2010 to 2026
$5.2M
Data-Driven Automation of Patient-Specific Finite Element Modeling for TAVRF31HL162505 · NHLBI · YALE UNIVERSITY · PI PAK, DANIEL · 2022 to 2023
$64k
NHLBI NIH HHS F31 HL162505NHLBI NIH HHS R01 HL121226NHLBI NIH HHS T32 HL098069
6 · The paper itself

Abstract

Calcification has significant influence over cardiovascular diseases and interventions. Detailed characterization of calcification is thus desired for predictive modeling, but calcium deposits on cardiovascular structures are still often manually reconstructed for physics-driven simulations. This poses a major bottleneck for large-scale adoption of computational simulations for research or clinical use. To address this, we propose an end-to-end automated image-to-mesh algorithm that enables robust incorporation of patient-specific calcification onto a given cardiovascular tissue mesh. The algorithm provides a substantial speed-up from several hours of manual meshing to ~1 min of automated computation, and it solves an important problem that cannot be addressed with recent template-based meshing techniques. We validated our final calcified tissue meshes with extensive simulations, demonstrating our ability to accurately model patient-specific aortic stenosis and Transcatheter Aortic Valve Replacement. Our method may serve as an important tool for accelerating the development and usage of personalized cardiovascular biomechanics.

Identifiers

PMID39143242
PMCPMC11324740

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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.