The treatment with cardiovascular medical devices enhances survival for many patients with otherwise hopeless medical conditions. Unfortunately, in many cases these devices cause dangerous pathological complications, in particular thrombosis and thromboembolism, which are directly related to non-physiological conditions acting on the blood flowing through these devices. One of the most important design and analysis tools used by bioengineers is computational fluid dynamics (CFD) aided simulation and analysis. With CFD analysis, the fluid induced mechanical stresses through these devices can be computed and assessed. The regions of non-physiologic mechanical shear stresses and stagnant flow in blood flow paths can be precisely identified. The objective of this proposal is to build the link between the dynamics of the shear-induced blood damage and CFD modeling. We propose to examine foundational aspects of flow-induced blood damage hemolysis, platelet activation, cell lysis, and associated byproducts (LDH, aggregates, fragments, coagulation cascade). We will conduct a series of coordinated multi-scale biologic and engineering experiments and link the outcome measures of the blood damage to their mechanistic origins through CFD-based modeling.
The specific aims of the proposed project are to: (1) Identify the correlation between CFD-derived fluid-dynamic variables (shear stress, exposure time, flow pattern) and blood damage data (platelet activation, thrombosis, and hemolysis) obtained from human patients and animals implanted with ventricular assist devices (VADs). (2) Develop multi-scale in-vitro experimental platforms to investigate the influence of specific fluid dynamic characteristics on blood cell damage. Using these platforms, generate comprehensive databases of flow-induced blood damage. (3) Based on the collective databases of blood damage, develop and implement a validated CFD model of flow-induced blood damage in a biomedical device. The long-term goal of these studies is to develop accurate, robust, and physiologically realistic numerical models capable of predicting the functional characteristics and bio/hemo-compatibility of cardiovascular devices. The models can aid in the development of new designs in order to improve the functional characteristics and bio/hemo-compatibility of the devices.

Public Health Relevance

Blood contacting biomedical devices have played and will continue to play a major role in health care and clinical practice. Continued improvement of these devices relies on multidisciplinary knowledge of medicine, science, and engineering, as well as our persistence in pursuing better technologies. The objective of this proposal is to establish a link between the design and development tool, CFD modeling, and the dynamics of flow-induced blood damage, specifically, hemolysis, platelet activation, cell lysis, and associated byproducts. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL088100-01A2
Application #
7526707
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Sarkar, Rita
Project Start
2008-09-01
Project End
2012-05-31
Budget Start
2008-09-01
Budget End
2009-05-31
Support Year
1
Fiscal Year
2008
Total Cost
$359,000
Indirect Cost
Name
University of Maryland Baltimore
Department
Surgery
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Chen, Zengsheng; Jena, Sofen K; Giridharan, Guruprasad A et al. (2018) Flow features and device-induced blood trauma in CF-VADs under a pulsatile blood flow condition: A CFD comparative study. Int J Numer Method Biomed Eng 34:
Chen, Zengsheng; Mondal, Nandan K; Ding, Jun et al. (2016) Paradoxical Effect of Nonphysiological Shear Stress on Platelets and von Willebrand Factor. Artif Organs 40:659-68
Mondal, Nandan K; Sorensen, Erik N; Pham, Si M et al. (2016) Systemic Inflammatory Response Syndrome in End-Stage Heart Failure Patients Following Continuous-Flow Left Ventricular Assist Device Implantation: Differences in Plasma Redox Status and Leukocyte Activation. Artif Organs 40:434-43
Wei, Xufeng; Sanchez, Pablo G; Liu, Yang et al. (2016) Extracorporeal Respiratory Support With a Miniature Integrated Pediatric Pump-Lung Device in an Acute Ovine Respiratory Failure Model. Artif Organs 40:1046-1053
Ding, Jun; Niu, Shuqiong; Chen, Zengsheng et al. (2015) Shear-Induced Hemolysis: Species Differences. Artif Organs 39:795-802
Ding, Jun; Chen, Zengsheng; Niu, Shuqiong et al. (2015) Quantification of Shear-Induced Platelet Activation: High Shear Stresses for Short Exposure Time. Artif Organs 39:576-83
Chen, Zengsheng; Mondal, Nandan K; Ding, Jun et al. (2015) Shear-induced platelet receptor shedding by non-physiological high shear stress with short exposure time: glycoprotein Ib? and glycoprotein VI. Thromb Res 135:692-8
Chen, Zengsheng; Mondal, Nandan K; Ding, Jun et al. (2015) Activation and shedding of platelet glycoprotein IIb/IIIa under non-physiological shear stress. Mol Cell Biochem 409:93-101
Liu, Yang; Sanchez, Pablo G; Wei, Xufeng et al. (2015) Effects of Cardiopulmonary Support With a Novel Pediatric Pump-Lung in a 30-Day Ovine Animal Model. Artif Organs 39:989-97
Mondal, Nandan K; Sorensen, Erik N; Feller, Erika D et al. (2015) Comparison of intraplatelet reactive oxygen species, mitochondrial damage, and platelet apoptosis after implantation of three continuous flow left ventricular assist devices: HeartMate II, Jarvik 2000, and HeartWare. ASAIO J 61:244-52

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