Gaseous Micro-Embolic Activity and Goal-Directed Perfusion Management in a Closed System for Cardiopulmonary Bypass and Minimally Invasive Extracorporeal Circulation during Coronary Artery Bypass Grafting.
Ignazio Condello, Giuseppe Nasso, Kurt Staessens, Giuseppe Speziale
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引用次数: 0
Abstract
Background: Cardiopulmonary bypass (CPB) techniques are becoming minimally invasive in clinical practice. The literature describes various extracorporeal techniques which seek to eliminate air-blood contact and reduce both hemodilution and the contact surface such as in Minimally invasive Extracorporeal Circulation (MiECC) and closed systems for CPB. However, the delivery of micro-embolic activity in the circuit and metabolic activity in terms of oxygen delivery for Goal-Directed Perfusion (GDP) management, in relation to the patient's blood volume and central venous pressure, have never been related and correlated. In this report, we present a cohort study that investigated these aspects between the closed SVR2000 System and modular MiECC (both from Eurosets SRL, Medolla, Italy).
Materials and methods: Data were collected retrospectively and used to compare 60 consecutive patients who underwent isolated coronary artery bypass grafting (CABG) surgery by two surgeons using an SVR2000 oxygenator in 30 procedures, with a matched cohort of patients from the same period who underwent isolated CABG surgery by two other surgeons using a modular MiECC in 30 procedures. The primary endpoints collected were data on micro-embolic activity, including the number of gaseous micro-emboli in the circuit during the procedure, the mean maintenance value of oxygen delivery (DO2) and data relating to venous return volume and central venous pressure (CVP).
Results: During the CPB procedures, the following values were recorded for the closed SVR2000 and MiECC groups, respectively: the average number of gaseous micro-emboli (GME) in the venous line, 833 ± 23 vs 1221 ± 45 (p = 0.028); GME in the outlet of the pump, 375 ± 45 vs 429 ± 76 (p = 0.89; GME in the arterial line, 189 ± 36 vs 205 ± 27 (p = 0.92), and the volume of GME in the arterial line (mL), 0.32± 12 vs 0.49± 17 (p = 0.93). The mean Indexed Oxygen Delivery (DO2i) during cross-clamp (ml/min/m2) was 319 ±12 vs 278 ±9 (p = 0.0019), respectively. The maximum mean volume of venous return in the soft-shell venous reservoir (ml) was 1801 ±128 vs 824 ±192 (p = 0.038). The mean central venous pressure (CVP) during cross-clamp (mmHg) was 0 ± 2 vs 6 ± 2 (p = 0.019).
Conclusions: In this study, the results in the closed SVR2000 group were not statistically inferior to those in the modular MiECC group in terms of gaseous micro-embolic activity during CPB. Our analysis showed an important reduction of GME delivery in both systems. The closed SVR2000 group showed better management for GDP in terms of DO2i, associated with the flexibility of dynamic volume management and the absence of cavitation and regulation of the rate per minute and pump flow, which were reported in the MiECC group. The SVR2000 and modular MiECC systems were both safe and effective in perioperative practice without iatrogenic problems.
背景:体外循环(CPB)技术在临床实践中正成为微创技术。文献描述了各种体外技术,这些技术旨在消除空气-血液接触,减少血液稀释和接触表面,例如微创体外循环(MiECC)和CPB的封闭系统。然而,在目标导向灌注(GDP)管理中,回路中微栓塞活性的输送和氧气输送方面的代谢活性与患者的血容量和中心静脉压之间从未有过相关性。在本报告中,我们提出了一项队列研究,调查了封闭式SVR2000系统和模块化MiECC(均来自意大利梅多拉的Eurosets SRL)之间的这些方面。材料和方法:回顾性收集数据,并用于比较连续60名患者,这些患者由两名外科医生在30次手术中使用SVR2000氧合器进行了单独的冠状动脉旁路移植(CABG)手术,来自同一时期的匹配患者队列,他们在30次手术中由另外两名外科医生使用模块化MiECC进行了单独的CABG手术。收集的主要终点是微栓子活性数据,包括手术过程中回路中气态微栓子的数量、氧气输送的平均维持值(DO2)以及与静脉回流量和中心静脉压(CVP)相关的数据,静脉中气体微栓子(GME)的平均数量分别为833±23和1221±45(p=0.028);泵出口的GME为375±45 vs 429±76(p=0.89;动脉线中的GME分别为189±36 vs 205±27(p=0.92),动脉线中GME的体积(mL)为0.32±12 vs 0.49±17(p=0.9 3)。交叉夹持期间的平均指数氧输送(DO2i)(mL/min/m2)分别为319±12 vs 278±9(p=0.0019)。软壳静脉储器中的最大平均静脉回流量(ml)为1801±128 vs 824±192(p=0.038)。交叉夹持期间的平均中心静脉压(CVP)为0±2 vs 6±2(p=0.019)。结论:在本研究中,就CPB期间的气体微栓塞活性而言,封闭SVR2000组的结果在统计学上并不劣于模块化MiECC组。我们的分析显示,在这两个系统中,GME的输送都显著减少。封闭式SVR2000组在DO2i方面表现出更好的GDP管理,这与MiECC组报告的动态容量管理的灵活性以及每分钟速率和泵流量的无空化和调节有关。SVR2000和模块化MiECC系统在围手术期实践中既安全又有效,没有医源性问题。