Evidence map›Paper›PMID 37611423›Full record

ArticleComputers in biology and medicine2023

Fully automated construction of three-dimensional finite element simulations from Optical Coherence Tomography.

Ross Straughan, Karim Kadry, Sahil A Parikh, Elazer R Edelman, Farhad R Nezami

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Current progress of digital twin construction using medical imaging.Journal of applied clinical medical physics · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Systematic characterization and automated alignment of coronary tree geometries.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference · 2024
    Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Ross StraughanCardiac Surgery Division, Brigham and Women's Hospital, Harvard Medical School, Boston, 02115, MA, USA; Department of Mechanical and Process Engineering, ETH Zurich, Leonhardstrasse 21, 8092 Zurich, Switzerland. Electronic address: ross.straughan@hest.ethz.ch.
Karim KadryInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, 77 Massachusetts Ave, Cambridge, 02139, MA, USA. Electronic address: kkadry@mit.edu.
Sahil A ParikhDivision of Cardiology, Columbia University Irving Medical Center, New York, 10032, NY, USA. Electronic address: sap2196@cumc.columbia.edu.
Elazer R EdelmanInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, 77 Massachusetts Ave, Cambridge, 02139, MA, USA; Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, 02115, MA, USA. Electronic address: ere@mit.edu.
Farhad R NezamiCardiac Surgery Division, Brigham and Women's Hospital, Harvard Medical School, Boston, 02115, MA, USA. Electronic address: frikhtegarnezami@bwh.harvard.edu.

Funding

Personalized lesion modification optimizes atherosclerosis interventionR01HL161069 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI EDELMAN, ELAZER R · 2022 to 2025
$2.8M
NHLBI NIH HHS R01 HL161069
6 · The paper itself

Abstract

Despite recent advances in diagnosis and treatment, atherosclerotic coronary artery diseases remain a leading cause of death worldwide. Various imaging modalities and metrics can detect lesions and predict patients at risk; however, identifying unstable lesions is still difficult. Current techniques cannot fully capture the complex morphology-modulated mechanical responses that affect plaque stability, leading to catastrophic failure and mute the benefit of device and drug interventions. Finite Element (FE) simulations utilizing intravascular imaging OCT (Optical Coherence Tomography) are effective in defining physiological stress distributions. However, creating 3D FE simulations of coronary arteries from OCT images is challenging to fully automate given OCT frame sparsity, limited material contrast, and restricted penetration depth. To address such limitations, we developed an algorithmic approach to automatically produce 3D FE-ready digital twins from labeled OCT images. The 3D models are anatomically faithful and recapitulate mechanically relevant tissue lesion components, automatically producing morphologies structurally similar to manually constructed models whilst including more minute details. A mesh convergence study highlighted the ability to reach stress and strain convergence with average errors of just 5.9% and 1.6% respectively in comparison to FE models with approximately twice the number of elements in areas of refinement. Such an automated procedure will enable analysis of large clinical cohorts at a previously unattainable scale and opens the possibility for in-silico methods for patient specific diagnoses and treatment planning for coronary artery disease.

Indexed as

Coronary Artery DiseasePlaque, AtheroscleroticCoronary VesselsFinite Element AnalysisHumansTomography, Optical CoherenceAtherosclerosisDigital twinOptical Coherence TomographyStructural mechanicsThree-dimensional reconstruction

Identifiers

PMID37611423
PMCPMC10528179

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.