Evidence map›Paper›PMID 41542166›Full record

ArticleArXiv2026

Biomechanically Informed Image Registration for Patient-Specific Aortic Valve Strain Analysis.

Mohsen Nakhaei, Alison M Pouch, Silvani Amin, Matthew Daemer, Christian Herz, Natalie Yushkevich, Lourdes Al Ghofaily, Nimesh Desai, Joseph Bavaria, Matthew A Jolley and 1 more

Abstract readPreprint
In one paragraph

Article in ArXiv, 2026. 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

11 authors.

Mohsen NakhaeiDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Alison M PouchDepartment of Radiology and Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Silvani AminDepartment of Radiology and Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Matthew DaemerDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Christian HerzDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Natalie YushkevichDepartment of Radiology and Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Lourdes Al GhofailyDepartment of Anesthesiology, University of Pennsylvania, Philadelphia, PA, USA.
Nimesh DesaiDepartment of Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Joseph BavariaDepartment of Cardiac Surgery, Jefferson Health, Philadelphia, PA, USA.
Matthew A JolleyDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Wensi WuDepartment of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Funding

Computer Modeling of the Tricuspid Valve in Hypoplastic Left Heart SyndromeR01HL153166 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI JOLLEY, MATTHEW · 2020 to 2024
$3.7M
4D Multimodal Image-Based Modeling for Bicuspid Aortic Valve Repair SurgeryR01HL163202 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI Alison Marie Pouch · 2022 to 2026
$3.5M
Toward Patient-Specific Computational Modeling of Tricuspid Valve Repair in Hypoplastic Left Heart SyndromeK25HL168235 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Wensi Wu · 2023 to 2026
$580k
NHLBI NIH HHS K25 HL168235NHLBI NIH HHS R01 HL153166NHLBI NIH HHS R01 HL163202
6 · The paper itself

Abstract

Purpose: Aortic valve (AV) biomechanics play a critical role in maintaining normal cardiac function. Pathological variations, particularly in bicuspid aortic valves, alter leaflet loading, increase strain, and accelerate disease progression. Accurate patient-specific characterization of valve geometry and deformation is therefore essential for predicting disease progression and guiding durable repair. However, existing imaging and computational methods often fail to capture rapid valve motion and complex patient-specific features, limiting precise biomechanical assessment. Methods: To address these limitations, we developed an image registration framework coupled with the finite element method (FEM) to improve AV tracking and biomechanical evaluation. Patient-specific valve geometries derived from 4D echocardiography and CT were used to simulate AV closure and generate intermediate deformation states. These FEM-generated states facilitated leaflet tracking, while image registration corrected misalignment between simulations and imaging data. Results: In 20 patients, FEM-augmented registration improved tracking accuracy by 40% compared with direct registration. This improvement enabled more reliable strain estimation by measuring leaflet deformation directly from imaging and reducing uncertainties associated with boundary conditions and material assumptions. Using the improved tracking results, areal, Green-Lagrange, and deviatoric strains were quantified in adult trileaflet and bicuspid valves, as well as pediatric patients, revealing distinct deformation patterns across valve groups. Convergence in mean deviatoric strain between adult trileaflet and pediatric valves suggests volumetric deformation underlies age- and size-related differences in AV mechanics. Conclusion: Overall, this FEM-augmented registration framework enhances geometric tracking and biomechanical evaluation accuracy, providing clinically relevant insights into patient-specific AV deformation to support individualized medical and intervention planning.

Indexed as

Aortic valve biomechanicsComputational biomechanicsFinite element simulationImage registration

Identifiers

PMID41542166
PMCPMC12803325

What Socratic holds

Textmetadata
LicenceCC BY
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.