Evaluation of extra-corporeal membrane oxygenator cannulae in pulsatile and non-pulsatile pediatric mock circuits.

IF 2.2 3区 医学 Q3 ENGINEERING, BIOMEDICAL Artificial organs Pub Date : 2024-10-28 DOI:10.1111/aor.14897
Lorenzo Ferrari, Maris Bartkevics, Hansjörg Jenni, Alexander Kadner, Matthias Siepe, Dominik Obrist
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Abstract

Background: This study evaluated the hemodynamic performance of arterial and venous cannulae in a compliant pediatric extracorporeal membrane oxygenation (ECMO) mock circuit in pulsatile and non-pulsatile flow conditions.

Methods: The ECMO setup consisted of an oxygenator, diagonal pump, and standardized-length arterial/venous tubing with pressure transducers. A validated left-heart mock loop was adapted to simulate pediatric conditions. The pulsatile flow was driven by a computer-controlled piston pump set at 120 bpm. A roller pump was used for non-pulsatile conditions. The circuit was primed with 40% glycerol-based solution. The cardiac output was set to 1 L/min and the aortic pressure to 40-50 mmHg. Four arterial cannulae (8Fr, 10Fr, 12Fr, 14Fr) and five venous cannulae (12Fr, 14Fr, 16Fr, 18Fr, 20Fr) (Medtronic, Inc., Minneapolis, MN, USA) were tested at increasing flow rate in 12 combinations.

Results: The pulsatile condition required lower ECMO pump speeds for all cannulae combinations at a given flow rate, inducing a significantly smaller increase of flow in the mock loop. Under non-pulsatile conditions, the aortic and arterial pressures in the cannulae were higher (p < 0.01) while no significant differences in pressure drop and pressure-flow characteristics (M-number) were observed. The total hemodynamic energy was higher in case of non-pulsatile flow (p < 0.01).

Conclusion: Under non-pulsatile conditions, the system was characterized by overall higher pressures, resulting in higher support to the patient. The consequent increase of potential energy compensates for increases of kinetic energy, leading to a higher total hemodynamic energy. Pressure gradients and M number are independent of the testing conditions. Pulsatile testing conditions led to more physiological testing conditions, and it is recommended for ECMO testing.

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评估体外膜氧合器插管在脉动和非脉动儿科模拟回路中的应用。
背景:这项研究评估了顺应性儿科体外膜肺氧合(ECMO)模拟回路中的动静脉插管在脉动和非脉动流量条件下的血液动力学性能:ECMO 装置包括氧合器、对角泵、标准化长度的动/静脉管道和压力传感器。经过验证的左心模拟环路经调整后可模拟儿科情况。脉动流量由计算机控制的活塞泵驱动,设定为 120 bpm。滚筒泵用于非脉冲条件。回路由 40% 的甘油溶液填满。心输出量设定为 1 L/min,主动脉压设定为 40-50 mmHg。以 12 种组合测试了四个动脉插管(8Fr、10Fr、12Fr、14Fr)和五个静脉插管(12Fr、14Fr、16Fr、18Fr、20Fr)(美敦力公司,美国明尼苏达州明尼阿波利斯市)在流量增加时的情况:结果:在给定流速下,脉动条件下所有插管组合所需的 ECMO 泵速度都较低,导致模拟环路中的流量增幅明显较小。在非搏动条件下,插管中的主动脉压和动脉压较高 (p 结论:在非搏动条件下,ECMO 系统的主动脉压和动脉压较低:在非搏动条件下,系统的总体压力较高,从而为患者提供了更大的支持。随之而来的势能增加补偿了动能的增加,导致血液动力学总能量增加。压力梯度和 M 数与测试条件无关。脉动测试条件更符合生理测试条件,建议用于 ECMO 测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Artificial organs
Artificial organs 工程技术-工程:生物医学
CiteScore
4.30
自引率
12.50%
发文量
303
审稿时长
4-8 weeks
期刊介绍: Artificial Organs is the official peer reviewed journal of The International Federation for Artificial Organs (Members of the Federation are: The American Society for Artificial Internal Organs, The European Society for Artificial Organs, and The Japanese Society for Artificial Organs), The International Faculty for Artificial Organs, the International Society for Rotary Blood Pumps, The International Society for Pediatric Mechanical Cardiopulmonary Support, and the Vienna International Workshop on Functional Electrical Stimulation. Artificial Organs publishes original research articles dealing with developments in artificial organs applications and treatment modalities and their clinical applications worldwide. Membership in the Societies listed above is not a prerequisite for publication. Articles are published without charge to the author except for color figures and excess page charges as noted.
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