Undar A, Masai T, Inman R, Beyer E A, Mueller M A, McGarry M C, Frazier O H, Fraser C D
Congenital Heart Surgery Service, Texas Children's Hospital, Houston 77030-2399, USA.
ASAIO J. 1999 Jan-Feb;45(1):53-8. doi: 10.1097/00002480-199901000-00013.
An alternate physiologic pulsatile pump (PPP) system was designed and evaluated to produce sufficient pulsatility during neonate-infant open heart surgery. This hydraulically driven pump system has a unique "dual" pumping chamber mechanism. The first chamber is placed between the venous reservoir and oxygenator and the second chamber between the oxygenator and patient. Each chamber has two unidirectional tricuspid valves. Stroke volume (0.2-10 ml), upstroke rise time (10-350 msec), and pump rate (2-250 beats per minute [bpm]) can be adjusted independently to produce adequate pulsatility. This system has been tested in 3-kg piglets (n = 6), with a pump flow of 150 ml/kg/min, a pump rate of 150 bpm, and a pump ejection time of 110 msec. After initiation of cardiopulmonary bypass (CPB), all animals were subjected to 25 minutes of hypothermia to reduce the rectal temperatures to 18 degrees C, 60 minutes of deep hypothermic circulatory arrest (DHCA), then 10 minutes of cold perfusion with a full pump flow, and 40 minutes of rewarming. During CPB, mean arterial pressures were kept at less than 50 mm Hg. Mean extracorporeal circuit pressure (ECCP), the pressure drop of a 10 French aortic cannula, and the pulse pressure were 67+/-9, 21+/-6, and 16+/-2 mm Hg, respectively. All values are represented as mean+/-SD. No regurgitation or abnormal hemolysis has been detected during these experiments. The oxygenator had no damping effect on the quality of the pulsatility because of the dual chamber pumping mechanism. The ECCP was also significantly lower than any other known pulsatile system. We conclude that this system, with a 10 French aortic cannula and arterial filter, produces adequate pulsatility in 3 kg piglets.
设计并评估了一种替代生理搏动泵(PPP)系统,以在新生儿和婴儿心脏直视手术期间产生足够的搏动性。这种液压驱动的泵系统具有独特的“双”泵腔机制。第一个腔室置于静脉储液器和氧合器之间,第二个腔室置于氧合器和患者之间。每个腔室都有两个单向三尖瓣。每搏输出量(0.2 - 10毫升)、上升时间(10 - 350毫秒)和泵速(每分钟2 - 250次搏动[bpm])可独立调节,以产生足够的搏动性。该系统已在3千克的仔猪(n = 6)身上进行测试,泵流量为150毫升/千克/分钟,泵速为150 bpm,泵射血时间为110毫秒。开始体外循环(CPB)后,所有动物均经历25分钟的低温,将直肠温度降至18摄氏度,60分钟的深度低温循环停搏(DHCA),然后以全泵流量进行10分钟的冷灌注,以及40分钟的复温。在CPB期间,平均动脉压保持在50毫米汞柱以下。平均体外循环压力(ECCP)、10号法国主动脉插管的压力降和脉压分别为67±9、21±6和16±2毫米汞柱。所有值均表示为平均值±标准差。在这些实验中未检测到反流或异常溶血。由于双腔泵机制,氧合器对搏动质量没有阻尼作用。ECCP也显著低于任何其他已知的搏动系统。我们得出结论,该系统搭配10号法国主动脉插管和动脉过滤器,能在3千克的仔猪中产生足够的搏动性。