不同几何形状的儿童动脉插管在儿童体外循环模型中的性能评估。

Gabriela B de O Carvalho, Luiz Fernando Caneo, Gregory Matte, Caio Henrique de A Cruz, Everton Neri da Silva, Luciana P Carletto, Ana Vitória C X de Castro, Betina G Madueño Silva, Valéria C Policarpo, Idágene A Cestari, Fabio B Jatene, Marcelo Biscegli Jatene
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引用次数: 0

摘要

目的:定义一个参考图,比较目前在儿科手术体外循环条件下使用的一套动脉插管产生的压降与流量。方法:选择两个制造商的套管,考虑其设计以及外径和内径。根据模拟体外循环条件下的压降与流量来评估插管性能。实验回路由Jostra HL-20滚轴泵、Quadrox-i儿童氧合器(Maquet Cardiopulous AG,Rastatt,Germany)和定制的儿童导管组组成。仅用乳酸林格溶液(第一种条件)和添加人填充红细胞(第二种条件)对回路进行预处理,以实现30%的红细胞压积。使用“Y”连接器将尺寸为8-16Fr的套管插入体外循环回路。在每个套管的典型流量范围内以100毫升/分钟的增量调节流量。测量插管前和插管后的压力以计算压降。结果:使用100 mmHg的压降限值,我们的结果表明,对于大小为8、10、12、14和16Fr的Braile动脉插管,建议的流量限值分别为500、900、1400、2600和3100 mL/min。对于尺寸为8、10、12、14和16Fr的美敦力DLP动脉插管,建议的流量限制分别为600、1100、1700、2700和3300 mL/min。结论:本研究强调了不同制造商提供的相同直径套管之间压降的差异,以及独立转化研究对评估组件性能的重要性。
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Performance Evaluation of Geometrically Different Pediatric Arterial Cannulae in a Pediatric Cardiopulmonary Bypass Model.

Objective: To define a reference chart comparing pressure drop vs. flow generated by a set of arterial cannulae currently utilized in cardiopulmonary bypass conditions in pediatric surgery.

Methods: Cannulae from two manufacturers were selected considering their design and outer and inner diameters. Cannula performance was evaluated in terms of pressure drop vs. flow during simulated cardiopulmonary bypass conditions. The experimental circuits consisted of a Jostra HL-20 roller pump, a Quadrox-i pediatric oxygenator (Maquet Cardiopulmonary AG, Rastatt, Germany), and a custom pediatric tubing set. The circuit was primed with lactated Ringer's solution only (first condition) and with human packed red blood cells added (second condition) to achieve a hematocrit of 30%. Cannula sizes 8 to 16 Fr were inserted into the cardiopulmonary bypass circuit with a "Y" connector. The flow was adjusted in 100 ml/min increments within typical flow ranges for each cannula. Pre-cannula and post-cannula pressures were measured to calculate the pressure drop.

Results: Utilizing a pressure drop limit of 100 mmHg, our results suggest a recommended flow limit of 500, 900, 1400, 2600, and 3100 mL/min for Braile arterial cannulae sizes 8, 10, 12, 14, and 16 Fr, respectively. For Medtronic DLP arterial cannulae sizes 8, 10, 12, 14, and 16 Fr, the recommended flow limit is 600, 1100, 1700, 2700, and 3300 mL/min, respectively.

Conclusion: This study reinforces discrepancies in pressure drop between cannulae of the same diameter supplied by different manufacturers and the importance of independent translational research to evaluate components' performance.

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