Janata Andreas, Holzer Michael, Bayegan Keywan, Frossard Martin, Sterz Fritz, Losert Udo M, Laggner Anton N, Behringer Wilhelm
Department of Emergency Medicine and Core Center of Biomedical Research , Medical University of Vienna, Austria.
Crit Care Med. 2006 Jun;34(6):1769-74. doi: 10.1097/01.CCM.0000218816.30297.A2.
Induction of deep cerebral hypothermia before reperfusion might improve neurologic outcome after cardiac arrest. We hypothesized that an aortic flush with cold saline during cardiac arrest is able to induce deep cerebral hypothermia and that the cooling efficiency can be enhanced by a) increasing the arteriovenous pressure gradient during the flush with vasopressin; b) improving the cerebral microcirculation during the flush with the thrombolytic agent alteplase; and c) increasing the arteriovenous pressure gradient further with venting the right heart by draining blood during the flush.
Prospective randomized experimental study.
University research laboratory.
Twenty-four pigs Large White breed (31-42 kg).
After 10 mins of ventricular fibrillation, pigs received an aortic flush (100 mL/kg, 4 degrees C, flow rate 35 mL/kg/min) into the descending aorta via a balloon catheter. The animals were subjected randomly to either an aortic flush with saline, saline plus vasopressin 1.2 IU/kg, saline plus alteplase 1 mg/kg, saline plus a combination of vasopressin 1.2 IU/kg and alteplase 1 mg/kg, or saline plus vasopressin 1.2 IU/kg and venting the right heart. Arterial and venous pressures and brain temperatures were recorded for an observation time of 10 mins after flush.
A sufficient arteriovenous pressure gradient and deep cerebral hypothermia were only achieved with a flush containing vasopressin (brain temperature 16.1+/-1.3 degrees C in the vasopressin group vs. 35.4+/-1.5 degrees C in the saline group, p<.001); combining vasopressin with alteplase, or venting the right heart, did not further enhance the cooling efficiency of the flush.
A cold saline aortic flush with vasopressin rapidly decreases brain temperature during prolonged normovolemic cardiac arrest in pigs. Whether deep cerebral hypothermia induced before reperfusion can improve neurologic outcome after cardiac arrest needs further investigation in large animal outcome studies.
在再灌注前诱导深度脑低温可能会改善心脏骤停后的神经功能结局。我们假设在心脏骤停期间用冷盐水进行主动脉冲洗能够诱导深度脑低温,并且可以通过以下方式提高冷却效率:a)在冲洗时使用血管加压素增加动静脉压力梯度;b)在冲洗时使用溶栓剂阿替普酶改善脑微循环;c)在冲洗时通过引流血液使右心排气进一步增加动静脉压力梯度。
前瞻性随机实验研究。
大学研究实验室。
24只大白猪(体重31 - 42千克)。
在室颤10分钟后,猪通过球囊导管接受向降主动脉的主动脉冲洗(100毫升/千克,4℃,流速35毫升/千克/分钟)。动物被随机分为接受单纯盐水主动脉冲洗、盐水加1.2国际单位/千克血管加压素、盐水加1毫克/千克阿替普酶、盐水加1.2国际单位/千克血管加压素与1毫克/千克阿替普酶联合使用,或盐水加1.2国际单位/千克血管加压素并使右心排气。冲洗后记录10分钟观察期内的动脉和静脉压力以及脑温。
仅在含有血管加压素的冲洗中实现了足够的动静脉压力梯度和深度脑低温(血管加压素组脑温为16.1±1.3℃,盐水组为35.4±1.5℃,p<0.001);将血管加压素与阿替普酶联合使用或使右心排气并未进一步提高冲洗的冷却效率。
在猪长时间正常血容量心脏骤停期间,用血管加压素进行冷盐水主动脉冲洗可迅速降低脑温。再灌注前诱导的深度脑低温是否能改善心脏骤停后的神经功能结局,需要在大型动物结局研究中进一步探究。