Detection of Echinocyte during Perfusion with Oxygenator Based on Continuous Blood Viscosity Monitoring

We applied our proposed continuous blood viscosity monitoring system for cardiopulmonary bypass to an experimental model that introduced echinocytes, and we confirm the viscosity change detection due to red blood cell (RBC) deformability decline. For the in vitro experiment, a test circuit including an oxygenator and a controlled bovine blood sample with excessive alkalemia to induce the echinocyte were prepared, and a perfusion experiment was performed. During the experiment, the anticoagulated bovine blood sample maintained a hematocrit of approximately 22%, temperature of 37°C, and more than 800 s of the activated clotting time. The estimated viscosity obtained from the proposed system was 2.10 mPas at the beginning of the experiment and 3.58 mPas at the end of the experiment, and it increased 1.48 mPas during the experiment. According to the scanning electron micrographs of blood samples, the echinocytes with multiple spicules at the beginning of the experiment and distorted spherical RBCs including the echinocytes with multiple spicules at the end of experiment were observed. We conclude that the system may be helpful for clinical perfusion management, because it detected the presence of echinocytes as the blood viscosity in an oxygenator flow pass increased.

[1]  T. Sueda,et al.  Hydrodynamic characteristics of a membrane oxygenator: modeling of pressure-flow characteristics and their influence on apparent viscosity , 2015, Perfusion.

[2]  S. Chien,et al.  Red cell rheology in stomatocyte-echinocyte transformation: roles of cell geometry and cell shape. , 1986, Blood.

[3]  D. Birnbaum,et al.  Heparin-coated equipment reduces the risk of oxygenator failure. , 1998, The Annals of thoracic surgery.

[4]  M. Whitehorne,et al.  Normal and abnormal trans-oxygenator pressure gradients during cardiopulmonary bypass , 2003, Perfusion.

[5]  F. Rohner,et al.  The influence of extracorporeal circulation on erythrocytes and flow properties of blood. , 1990, The Journal of thoracic and cardiovascular surgery.

[6]  R. Groom,et al.  Parallel replacement of the oxygenator that is not transferring oxygen: the PRONTO procedure , 2002, Perfusion.

[7]  A R Fisher,et al.  The incidence and cause of emergency oxygenator changeovers , 1999, Perfusion.

[8]  M. Blombäck,et al.  Pathologic fibrin formation and cold-induced clotting of membrane oxygenators during cardiopulmonary bypass. , 1995, Journal of cardiothoracic and vascular anesthesia.

[9]  W H Reinhart,et al.  Echinocytosis induced by haemodialysis. , 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[10]  Valter Travagli,et al.  Comparison of blood viscosity using a torsional oscillation viscometer and a rheometer. , 2008, Clinical hemorheology and microcirculation.

[11]  Satoshi Miyamoto,et al.  Continuous Blood Viscosity Monitoring System for Cardiopulmonary Bypass Applications , 2017, IEEE Transactions on Biomedical Engineering.

[12]  J E Ferrell,et al.  Phosphoinositide metabolism and the morphology of human erythrocytes , 1984, The Journal of cell biology.

[13]  Toshio Tsuji,et al.  A Novel Blood Viscosity Estimation Method Based on Pressure‐Flow Characteristics of an Oxygenator During Cardiopulmonary Bypass , 2017, Artificial organs.