Innovative experimental animal models for real‐time comparison of antithrombogenicity between two oxygenators using dual extracorporeal circulation circuits and indocyanine green fluorescence imaging

氧合器 吲哚青绿 生物医学工程 脉动流 血栓 医学 体外膜肺氧合 体外循环 体外 体外循环 外科 麻醉 心脏病学
作者
Hironobu Sakurai,Tatsuki Fujiwara,Katsuhiro Ohuchi,Wataru Hijikata,Yusuke Inoue,Osamu Maruyama,Tomoki Tahara,Sachie Yokota,Y. Tanaka,Yoshiaki Takewa,Tomohiro Mizuno,Hirokuni Arai
出处
期刊:Artificial Organs [Wiley]
卷期号:47 (1): 77-87 被引量:3
标识
DOI:10.1111/aor.14380
摘要

Abstract Background Antithrombogenicity of extracorporeal membrane oxygenation (ECMO) devices, particularly oxygenators, is a current problem, with numerous studies and developments underway. However, there has been limited progress in developing methods to accurately compare the antithrombogenicity of oxygenators. Animal experiments are commonly conducted to evaluate the antithrombogenicity of devices; however, it is challenging to maintain a steady experimental environment. We propose an innovative experimental animal model to evaluate different devices in a constant experimental environment in real‐time. Methods This model uses two venous–arterial ECMO circuits attached to one animal (one by jugular vein and carotid artery, one by femoral vein and artery) and real‐time assessment of thrombus formation in the oxygenator by indocyanine green (ICG) fluorescence imaging. Comparison studies were conducted using three pigs: one to compare different oxygenators (MERA vs. CAPIOX) (Case 1), and two to compare antithrombotic properties of the oxygenator (QUADROX) when used under different hydrodynamic conditions (continuous flow vs. pulsatile flow) (Cases 2 and 3). Results Thrombi, visualized using ICG imaging, appeared as black dots on a white background in each oxygenator. In Case 1, differences in the site of thrombus formation and rate of thrombus growth were observed in real‐time in two oxygenators. In Case 2 and 3, the thrombus region was smaller in pulsatile than in continuous conditions. Conclusions We devised an innovative experimental animal model for comparison of antithrombogenicity in ECMO circuits. This model enabled simultaneous evaluation of two different ECMO circuits under the same biological conditions and reduced the number of sacrificed experimental animals.
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