Sakota Daisuke, Fujiwara Tatsuki, Ouchi Katsuhiro, Kuwana Katsuyuki, Yamazaki Hiroyuki, Maruyama Osamu
National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.
Department of Cardiovascular Surgery, Tokyo Medical and Dental University, Tokyo, Japan.
Artif Organs. 2016 Sep;40(9):834-41. doi: 10.1111/aor.12819.
Continuous optical monitoring of thrombus formation in extracorporeal mechanical circulatory support (EMCS) devices will contribute to safe, long-term EMCS. A clinically applicable optical detector must be able to distinguish among the optical characteristics of oxygen saturation (SaO2 ), hematocrit (Hct), and thrombus formation. In vitro studies of spectral changes at wavelengths from 400 to 900 nm associated with SaO2 , Hct, and thrombus formed around the top pivot bearing of a Gyro C1E3 pump were conducted. Fresh porcine blood anticoagulated with sodium citrate was circulated in a mock circuit using the pump. The SaO2 , Hct, and anticoagulation activity were altered using an oxygenator, autologous plasma, and calcium chlorite injection, respectively. Light from a xenon lamp was guided by an incident fiber perpendicularly fixed on the top bearing. This light was scattered by blood pooled between the male and female pivots. The detection fiber was perpendicularly fixed against the incident fiber, and the side-scattered light was detected and guided to a spectrophotometer. As a result, light at two different wavelengths, 420 and 810 nm, was identified as suitable for thrombus detection because it was negligibly influenced by SaO2 and was able to detect the optical characteristics of fibrin. The light at these two wavelengths responded more quickly to thrombus formation than the inlet or outlet pressure, and flow rate change. The optical changes showed the changes in Hct around the top pivot bearing, which is caused by the reduction in density of fibrin-trapped red blood cells (RBCs) due to the RBCs being swept away by the surrounding blood flow. The proposed method was also able to detect fibrin production by extracting subtle differences in the optical characteristics between the Hct and thrombus formation.
对体外机械循环支持(EMCS)设备中的血栓形成进行连续光学监测将有助于实现安全、长期的EMCS。一种临床适用的光学探测器必须能够区分血氧饱和度(SaO2)、血细胞比容(Hct)和血栓形成的光学特征。我们对与SaO2、Hct以及在Gyro C1E3泵顶部枢轴轴承周围形成的血栓相关的400至900nm波长的光谱变化进行了体外研究。用柠檬酸钠抗凝的新鲜猪血通过该泵在模拟回路中循环。分别使用氧合器、自体血浆和亚氯酸钙注射液改变SaO2、Hct和抗凝活性。来自氙灯的光由垂直固定在顶部轴承上的入射光纤引导。该光被汇集在公母枢轴之间的血液散射。检测光纤垂直于入射光纤固定,侧向散射光被检测并引导至分光光度计。结果,420和810nm这两个不同波长的光被确定适合用于血栓检测,因为它受SaO2的影响可忽略不计,并且能够检测纤维蛋白的光学特征。这两个波长的光对血栓形成的反应比入口或出口压力以及流速变化更快。光学变化显示了顶部枢轴轴承周围Hct的变化,这是由于被困在纤维蛋白中的红细胞(RBC)被周围血流冲走,导致纤维蛋白捕获的红细胞密度降低所致。所提出的方法还能够通过提取Hct和血栓形成之间光学特征的细微差异来检测纤维蛋白的产生。