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严重容量控制性失血性休克的新型猴模型

New monkey model of severe-volume controlled hemorrhagic shock.

作者信息

Bar-Joseph G, Safar P, Stezoski S W, Alexander H, Levine G

机构信息

Department of Anaesthesiology, Presbyterian-University Hospital, University of Pittsburgh, PA 15260.

出版信息

Resuscitation. 1989 Feb;17(1):11-32. doi: 10.1016/0300-9572(89)90076-2.

Abstract

Three series of experiments were conducted to develop a model of volume-controlled severe hemorrhagic shock in the unanesthetized analgesic cynomolgus monkey. This report concerns the insult without resuscitation. In Series I, seven monkeys were sedated with 75% N2O/25% O2, bled 40% of their measured blood volume over 20 min and observed until death. Mean arterial pressure (MAP) decreased to 21 +/- 6 mmHg, spontaneously increased to 46 +/- 5 mmHg, then gradually decreased to pulselessness at 146 +/- 42 min (range 101-213). Hemodynamic variables, lactate, base excess, electroencephalogram and sagittal sinus PO2 followed the same biphasic pattern. In Series II, eight monkeys were bled 27 ml/kg (43% of estimated blood volume) over 20 min under the same N2O analgesia and with similar responses as in Series I. In Series III 26 monkeys were bled 27 ml/kg over 20 min (time zero) as in Series II. Three developed apnea and pulselessness at end of hemorrhage. In 23 the shock period was prolonged for testing resuscitation therapies. Starting at 0 + 30 min, MAP was controlled with minute blood volume adjustments at 30 mmHg until 0 + 2 h. Three died due to inaccurate (preventable) MAP adjustments. At MAP 30 mmHg, all animals lost consciousness, EEG activity decreased, and brain stem reflexes disappeared. The "volume-pressure controlled" hemorrhagic shock model of Series III retains the initial natural response to bleeding, simulates the clinical picture of severe prolonged shock without anesthesia, and represents a more controllable insult than volume controlled hemorrhage alone.

摘要

进行了三组实验,以建立未麻醉镇痛食蟹猴容量控制的严重失血性休克模型。本报告涉及未进行复苏的损伤情况。在第一组实验中,七只猴子用75% N₂O/25% O₂进行镇静,在20分钟内放血40%的测量血容量,并观察至死亡。平均动脉压(MAP)降至21±6 mmHg,随后自发升至46±5 mmHg,然后在146±42分钟(范围101 - 213分钟)逐渐降至无脉状态。血流动力学变量、乳酸、碱剩余、脑电图和矢状窦PO₂遵循相同的双相模式。在第二组实验中,八只猴子在相同的N₂O镇痛下于20分钟内放血27 ml/kg(估计血容量的43%),反应与第一组相似。在第三组实验中,26只猴子如第二组一样在20分钟(时间零点)内放血27 ml/kg。三只猴子在出血结束时出现呼吸暂停和无脉状态。23只猴子的休克期被延长以测试复苏治疗。从0 + 30分钟开始,通过调整每分钟血容量将MAP控制在30 mmHg,直至0 + 2小时。三只猴子因MAP调整不准确(可预防)而死亡。在MAP为30 mmHg时,所有动物失去意识,脑电图活动减弱,脑干反射消失。第三组的“容量 - 压力控制”失血性休克模型保留了对出血的初始自然反应,模拟了无麻醉情况下严重长时间休克的临床表现,并且比单纯的容量控制出血代表了一种更可控的损伤情况。

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