Related Experiment Video
Updated: Mar 2, 2026

Hemocompatibility Testing of Blood-Contacting Implants in a Flow Loop Model Mimicking Human Blood Flow
Published on: March 5, 2020
Blood Stasis on Transcatheter Valve Leaflets and Implications for Valve-in-Valve Leaflet Thrombosis
Koohyar Vahidkhah1, Shahnaz Javani1, Mostafa Abbasi1
1The DU Cardiovascular Biomechanics Laboratory, University of Denver, Denver, Colorado.
Insights
Transcatheter aortic valve (TAV) thrombosis after valve-in-valve (ViV) procedures is linked to increased blood residence time (BRT) on leaflets compared to surgical aortic valves (SAV). This prolonged BRT, especially on TAV leaflets, may promote leaflet thrombosis.
Area of Science:
- Cardiovascular research
- Biomedical engineering
- Fluid dynamics
Background:
- Leaflet thrombosis is a growing concern following valve-in-valve (ViV) procedures.
- Understanding the hemodynamic factors contributing to thrombosis is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the role of blood flow dynamics in leaflet thrombosis after ViV procedures.
- To compare blood stasis on surgical aortic valve (SAV) and transcatheter aortic valve (TAV) leaflets in a ViV setting.
Main Methods:
- Developed patient-specific computational models for SAV and TAV in ViV configurations.
- Utilized fluid-solid interaction modeling to simulate 3D flow fields.
- Quantified blood residence time (BRT) on coronary and noncoronary leaflets.
Main Results:
- Transcatheter aortic valve (TAV) leaflets exhibited significantly longer blood residence time (BRT) compared to surgical aortic valves (SAV), particularly near leaflet fixation points.
- Areas of high BRT (≥1.2 seconds) on TAV leaflets were four times larger than on SAV leaflets at end-diastole.
- SAV models showed high BRT predominantly on noncoronary leaflets, while TAV models displayed a more uniform distribution across all leaflets.
Conclusions:
- Increased BRT on TAV leaflets, caused by geometric confinement within the degenerated bioprosthesis, is a potential factor promoting leaflet thrombosis after ViV.
- The uniform BRT distribution on TAV leaflets may explain the similar thrombosis rates observed across all three leaflets.
Background:
Leaflet thrombosis after valve-in-valve (ViV) procedure has been increasingly recognized. This study aimed to investigate the flow dynamics aspect of leaflet thrombosis by quantifying the blood stasis on the noncoronary and coronary leaflets of a surgical aortic valve (SAV) and a transcatheter aortic valve (TAV) in a ViV setting.
Methods:
Two computational models, representing a SAV and a TAV in ViV setting, were developed in a patient-specific geometry. Three-dimensional flow fields were obtained through a fluid-solid interaction modeling approach to study the difference in blood residence time (BRT) on the coronary and noncoronary leaflets.
Results:
Longer BRT was observed on the TAV leaflets compared with the SAV, specifically near the leaflet fixed boundary. Particularly, at the end of diastole, the areas of high BRT (≥1.2 seconds) on the surface of the TAV model leaflets were four times larger than those of the SAV model. The distribution of BRT on the three leaflets exhibited a similar pattern in the model for the TAV in ViV setting. That was in contrast to the SAV model where large areas of high BRT were observed on the noncoronary leaflet.
Conclusions:
Geometric confinement of the TAV by the leaflets and the frame of the degenerated bioprosthesis that circumferentially surround the TAV stent increases the BRT on the leaflets, which may act as a permissive factor in the TAV leaflet thrombosis after ViV procedure. A similar distribution pattern of BRT observed on the TAV leaflets may explain the similar rate of occurrence of thrombosis on the three leaflets.
More Related Videos
Related Concept Videos
Venous Thrombosis I: Introduction
Venous Thrombosis II: Clinical Manifestations and Diagnostic Studies
Venous Thrombosis III: Interprofessional Care
Disorders of Hemostasis
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Mitral Stenosis III: Medical Management

