Larabee Todd M, Paradis Norman A, Bartsch Jason, Cheng Lisa, Little Charles
Department of Surgery, Division of Emergency Medicine, University of Colorado at Denver and Health Sciences Center, 12401 East 17th Avenue B215, Aurora, CO 80045, United States.
Resuscitation. 2008 Aug;78(2):196-9. doi: 10.1016/j.resuscitation.2008.03.011. Epub 2008 May 27.
The incidence of pulseless electrical activity (PEA) as a presenting rhythm during cardiac arrest is increasing. The current animal models of PEA arrest, post-countershock or total asphyxiation, unreliably generate PEA for a specific time period. Neither of these models predictably generate pseudo-PEA. The purpose of this study was to create an animal model of pseudo-PEA that will allow for a prolonged time period in this arrest state for future research.
In a laboratory setting, five ventilated swine on inhaled anesthesia and 100% oxygen with continuous EKG recordings were instrumented with central aortic and venous pressure-transducing catheters. Animals were then switched to intravenous anesthesia while being ventilated with a 16% oxygen/84% nitrogen mix. Continuous EKG, aortic and venous pressures were recorded to a computerized data collection program. Arterial blood gas samples were taken every 10min. Time until onset of pseudo-PEA, duration of pseudo-PEA, and cardiac rhythm during pseudo-PEA were recorded.
Mean time to onset of pseudo-PEA was 80.6+/-47.3min. Mean duration of pseudo-PEA was 18.6+/-6.2min. Mean arterial pH at pseudo-PEA onset was 7.20+/-0.05 with a mean associated base excess of -11.4+/--5.94. No significant differences were noted in other recorded variables.
Partial asphyxiation using a 16% oxygen/84% nitrogen mix is a reliable laboratory method to create a prolonged state of pseudo-PEA in a swine model. The mechanism generating pseudo-PEA is hypoxemia-induced systemic acidosis. This model will allow sufficient time in this low-flow cardiac state for future research to be conducted.
心脏骤停时无脉电活动(PEA)作为初始节律的发生率正在上升。目前PEA骤停的动物模型,无论是电击后还是完全窒息模型,都无法在特定时间段内可靠地产生PEA。这些模型都无法可预测地产生假性PEA。本研究的目的是创建一种假性PEA动物模型,以便在这种骤停状态下维持较长时间,供未来研究使用。
在实验室环境中,对五只吸入麻醉并吸入100%氧气且持续记录心电图的猪,插入中心主动脉和静脉压力传感导管。然后在动物用16%氧气/84%氮气混合气体通气的同时转换为静脉麻醉。将连续的心电图、主动脉和静脉压力记录到计算机化数据收集程序中。每10分钟采集一次动脉血气样本。记录假性PEA开始的时间、假性PEA的持续时间以及假性PEA期间的心律。
假性PEA开始的平均时间为80.6±47.3分钟。假性PEA的平均持续时间为18.6±6.2分钟。假性PEA开始时的平均动脉pH值为7.20±0.05,平均碱剩余为-11.4±5.94。在其他记录变量中未发现显著差异。
使用16%氧气/84%氮气混合气体进行部分窒息是在猪模型中创建假性PEA长期状态的可靠实验室方法。产生假性PEA的机制是低氧血症诱导的全身酸中毒。该模型将在这种低流量心脏状态下提供足够的时间用于未来的研究。