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全滚动无泵体外循环系统的临床研究

Clinical study of totally roller pumpless cardiopulmonary bypass system.

作者信息

Murakami F, Usui A, Hiroura M, Kawamura M, Koyama T, Murase M

机构信息

Division of Cardiovascular Surgery, Owari Aichi Prefectural Hospital, Aichi, Japan.

出版信息

Artif Organs. 1997 Jul;21(7):803-7. doi: 10.1111/j.1525-1594.1997.tb03747.x.

Abstract

We have developed a low negative pressure vacuum suction system in which cardiotomy suction is performed by the negative pressure of the venous reservoir controlled by a vacuum controller. We have employed this vacuum suction system with a centrifugal pump as a totally roller pumpless cardiopulmonary bypass (CPB) system. In this study, the clinical availability and hemocompatibility of our totally roller pumpless CPB system were evaluated by a randomized prospective study. Thirty patients undergoing aortocoronary bypass grafting were assigned to the study. Data from seventeen patients treated with a totally roller pumpless CPB system were compared with data from 13 treated with a conventional roller pump CPB system. Totally roller pumpless CPB reduces hemolysis, showing lower plasma free hemoglobin levels (81.8 +/- 25.0 versus 42.0 +/- 16.3 at 30 min after CPB initiation, p < 0.05), higher plasma haptoglobin levels (37.8 +/- 36.6 versus 77.2 +/- 31.3 at 120 min after CPB, p < 0.05), and lower blood lactate dehydrogenase (LDH) levels (1391 +/- 497 versus 972 +/- 187, p < 0.01) than those of CPB with a roller pump suction with no significant difference between platelet counts. Arterial blood oxygen tension after using a totally roller pumpless CPB system was slightly better than that with a roller pump (396 +/- 48 versus 437 +/- 43, p = 0.069); however, there was no significant difference in intubation times between groups. A totally roller pumpless CPB system provides sufficient biocompatibility for the blood to reduce hemolysis significantly and simplifies and miniaturizes the entire CPB system to achieve good visuality and handling for control as well.

摘要

我们开发了一种低负压真空吸引系统,其中心脏手术吸引通过由真空控制器控制的静脉储血器的负压来进行。我们已将这种带有离心泵的真空吸引系统用作全滚轴无泵体外循环(CPB)系统。在本研究中,通过随机前瞻性研究评估了我们的全滚轴无泵CPB系统的临床可用性和血液相容性。30例行主动脉冠状动脉旁路移植术的患者被纳入研究。将17例接受全滚轴无泵CPB系统治疗的患者的数据与13例接受传统滚轴泵CPB系统治疗的患者的数据进行比较。全滚轴无泵CPB减少了溶血,显示出较低的血浆游离血红蛋白水平(CPB开始后30分钟时为81.8±25.0对42.0±16.3,p<0.05)、较高的血浆触珠蛋白水平(CPB后120分钟时为37.8±36.6对77.2±31.3,p<0.05)以及较低的血液乳酸脱氢酶(LDH)水平(1391±497对972±187,p<0.01),与滚轴泵吸引的CPB相比,血小板计数无显著差异。使用全滚轴无泵CPB系统后的动脉血氧张力略优于滚轴泵(396±48对437±43,p=0.069);然而,两组之间的插管时间无显著差异。全滚轴无泵CPB系统为血液提供了足够的生物相容性,以显著减少溶血,并简化和小型化整个CPB系统,从而实现良好的可视性和易于控制。

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