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The Use of Fluid Mechanics to Predict Regions of Microscopic Thrombus Formation in Pulsatile VADs.
Topper, Stephen R; Navitsky, Michael A; Medvitz, Richard B; Paterson, Eric G; Siedlecki, Christopher A; Slattery, Margaret J; Deutsch, Steven; Rosenberg, Gerson; Manning, Keefe B.
Afiliação
  • Topper SR; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA.
  • Navitsky MA; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA.
  • Medvitz RB; Applied Research Laboratory, The Pennsylvania State University, University Park, PA 16802, USA.
  • Paterson EG; Applied Research Laboratory, The Pennsylvania State University, University Park, PA 16802, USA.
  • Siedlecki CA; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA ; Department of Surgery, Penn State Hershey Medical Center, The Pennsylvania State University, Hershey, PA 17033, USA.
  • Slattery MJ; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA.
  • Deutsch S; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA.
  • Rosenberg G; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA ; Department of Surgery, Penn State Hershey Medical Center, The Pennsylvania State University, Hershey, PA 17033, USA.
  • Manning KB; Department of Bioengineering, The Pennsylvania State University, 205 Hallowell Building, University Park, PA 16802, USA ; Department of Surgery, Penn State Hershey Medical Center, The Pennsylvania State University, Hershey, PA 17033, USA.
Cardiovasc Eng Technol ; 5(1): 54-69, 2014 Mar 01.
Article em En | MEDLINE | ID: mdl-24634700
We compare the velocity and shear obtained from particle image velocimetry (PIV) and computational fluid dynamics (CFD) in a pulsatile ventricular assist device (VAD) to further test our thrombus predictive methodology using microscopy data from an explanted VAD. To mimic physiological conditions in vitro, a mock circulatory loop is used with a blood analog that matched blood's viscoelastic behavior at 40% hematocrit. Under normal physiologic pressures and for a heart rate of 75 bpm, PIV data is acquired and wall shear maps are produced. The resolution of the PIV shear rate calculations are tested using the CFD and found to be in the same range. A bovine study, using a model of the 50 cc Penn State V-2 VAD, for 30 days at a constant beat rate of 75 beats per minute (bpm) provides the microscopic data whereby after the 30 days, the device is explanted and the sac surface analyzed using scanning electron microscopy (SEM) and, after immunofluorescent labeling for platelets and fibrin, confocal microscopy. Areas are examined based on PIV measurements and CFD, with special attention to low shear regions where platelet and fibrin deposition are most likely to occur. Data collected within the outlet port in a direction normal to the front wall of the VAD shows that some regions experience wall shear rates less than 500 s-1, which increases the likelihood of platelet and fibrin deposition. Despite only one animal study, correlations between PIV, CFD, and in vivo data show promise. Deposition probability is quantified by the thrombus susceptibility potential, a calculation to correlate low shear and time of shear with deposition.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cardiovasc Eng Technol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cardiovasc Eng Technol Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos