Nollert G, Sperling J, Sakamoto T, Jaeger B R, Jonas R A
Department of Cardiac Surgery, Children's Hospital Boston, Harvard Medical School, MA 02115, USA.
Thorac Cardiovasc Surg. 2001 Aug;49(4):226-30. doi: 10.1055/s-2001-16115.
Hemodilution has been applied conventionally during cardiopulmonary bypass (CPB) and deep hypothermic circulatory arrest (DHCA) to counteract the increase in viscosity and deleterious rheological effects caused by hypothermia. However, liver dysfunction after low-flow bypass and DHCA is common, and little is known about the effects of hematocrit (Hct). The purpose of the present study is to evaluate the impact of two hemodilution priming protocols used clinically on liver perfusion and metabolism.
Ten piglets were randomized into 2 groups. One group (n = 5) had a crystalloid prime resulting in an Hct of about 15 % (low hematocrit; group L), the other (n = 5) a total-blood prime (Hct = 25 %; high hematocrit; group H). All animals underwent 70 min cooling at full flow (150 ml/kg/min), 30 min of low flow (50 ml/kg/min) at 15 degrees C followed by 45 min of DHCA and 75 min of rewarming at full flow. Liver blood flow (LBF) was assessed at the beginning of CPB at 34 degrees C, at the end of cooling at 15 degrees C, at the end of low flow, 5 min after the start of warming, and at the end of rewarming at 34 degrees C by injections of radioactive microspheres. Liver function was evaluated at the same time using the MEGX test, which measures the metabolism of lidocaine.
LBF was insignificantly reduced during cooling, decreased during low flow (p = 0.001), and increased again after DHCA with the highest flow at the end of rewarming. LBF tended to be lower at all times in group L (p = 0.096). The liver lidocaine metabolic rate did not significantly decrease during cooling and low flow, but was increased at the end of rewarming (p = 0.01); the metabolism was higher in group H (p = 0.025). Multiregression analysis revealed liver blood flow (p = 0.003) and hematocrit (p < 0.001) as independent determinants of the liver lidocaine metabolism; arterial blood pressure and temperature did not have significant influence in this model.
Hemodilution results in a tendency towards reduced liver blood flow during CPB; much worse is the resulting impaired liver metabolism, independent of reduced blood flow and pressure. Avoidance of low hematocrit during CPB may be a useful adjunct to preserve liver function in patients undergoing cardiac surgery with long duration CPB and DHCA.
在体外循环(CPB)和深低温停循环(DHCA)期间,传统上采用血液稀释来抵消低温引起的粘度增加和有害的流变学效应。然而,低流量旁路和DHCA后的肝功能障碍很常见,而关于血细胞比容(Hct)的影响知之甚少。本研究的目的是评估临床上使用的两种血液稀释预充方案对肝脏灌注和代谢的影响。
将10只仔猪随机分为2组。一组(n = 5)采用晶体预充,使Hct约为15%(低血细胞比容;L组),另一组(n = 5)采用全血预充(Hct = 25%;高血细胞比容;H组)。所有动物先以全流量(150 ml/kg/min)进行70分钟降温,然后在15℃下以低流量(50 ml/kg/min)进行30分钟,接着进行45分钟的DHCA,最后以全流量进行75分钟复温。在CPB开始时(34℃)、降温结束时(15℃)、低流量结束时、复温开始后5分钟以及复温结束时(34℃),通过注射放射性微球评估肝脏血流量(LBF)。同时使用MEGX试验评估肝功能,该试验用于测量利多卡因的代谢。
LBF在降温期间略有下降,在低流量期间降低(p = 0.001),在DHCA后再次增加,在复温结束时流量最高。L组在所有时间点的LBF均有降低趋势(p = 0.096)。肝脏利多卡因代谢率在降温及低流量期间无显著下降,但在复温结束时升高(p = 0.01);H组的代谢更高(p = 0.025)。多元回归分析显示肝脏血流量(p = 0.003)和血细胞比容(p < 0.001)是肝脏利多卡因代谢的独立决定因素;在该模型中,动脉血压和温度无显著影响。
血液稀释导致CPB期间肝脏血流量有降低趋势;更糟糕的是由此导致的肝脏代谢受损,这与血流量和压力降低无关。在进行长时间CPB和DHCA的心脏手术患者中,避免CPB期间低血细胞比容可能是保护肝功能的有益辅助措施。