Burns John W, Baer Lisa A, Darlington Daniel N, Dubick Michael A, Wade Charles E
U.S. Army Institute of Surgical Research Ft. Sam Houston, TX, USA.
Int J Burns Trauma. 2012;2(1):59-67. Epub 2012 Mar 15.
Small volumes of resuscitation products to sustain survival until definitive care are desired in extreme environments due to limited resources. A severe controlled hemorrhage model in sedated, sexually mature miniature swine has been developed to evaluate these products. Valproic Acid (VPA) and Pentoxifylline (PTX) have been suggested as potential products for small volume resuscitation following hemorrhage predominately in anesthetized small animal models. We evaluated the survival time of VPA and PTX in the swine model.
Fifteen male miniature swine weighing 41.1 ± 2.9 kg were sedated and hemorrhaged 60% of estimated blood volume over 1 hr and treated with one of the following: 1) VPA at 400 mg/kg in a volume of 1.33 ml/kg over 2 min (n=4); 2) VPA at 300 mg/kg in a volume of 2 ml/kg over 30 min (n=3); 3) PTX at 50 mg/kg in a volume of 2 ml/kg over 2 min (n=4); 4) saline vehicle at 2 ml/kg over 2 min (n=4). Survival times were compared to non-resuscitated historic controls (n=16). Survival was determined from the end of hemorrhage/initiation of treatment.
Median (95% CI) survival times were: Control 55.7 (17.5 - 86) min; VPA (400 mg/kg) 6 (4 - 8) min; VPA (300 mg/kg) 17.5 (12 - 24.5) min; PTX 60.8 (21 - 75) min; and vehicle 92 (15 - 180) min. No treatment increased survival time compared to controls and there were no significant differences in percent survival among groups.
In this sedated severe hemorrhage model VPA and PTX were unacceptable as small volume resuscitation products at the concentrations and delivery rates used because of early deaths. Considering that these drugs are FDA approved for other indications at lower doses the present data suggest that further investigation of mechanisms involved are warranted.
由于资源有限,在极端环境中需要少量复苏产品来维持生命直至获得确定性治疗。已建立一种用于评估这些产品的、在镇静的性成熟小型猪身上的严重控制性出血模型。丙戊酸(VPA)和己酮可可碱(PTX)已被建议作为主要在麻醉的小动物模型中出血后进行小容量复苏的潜在产品。我们评估了VPA和PTX在猪模型中的存活时间。
15只体重41.1±2.9千克的雄性小型猪被镇静,在1小时内出血至估计血容量的60%,并接受以下治疗之一:1)400毫克/千克的VPA,以1.33毫升/千克的体积在2分钟内给药(n = 4);2)300毫克/千克的VPA,以2毫升/千克的体积在30分钟内给药(n = 3);3)50毫克/千克的PTX,以2毫升/千克的体积在2分钟内给药(n = 4);4)2毫升/千克的生理盐水载体在2分钟内给药(n = 4)。将存活时间与未复苏的历史对照(n = 16)进行比较。存活时间从出血结束/治疗开始时确定。
中位(95%CI)存活时间为:对照组55.7(17.5 - 86)分钟;VPA(400毫克/千克)6(4 - 8)分钟;VPA(300毫克/千克)17.5(12 - 24.5)分钟;PTX 60.8(21 - 75)分钟;载体组92(15 - 180)分钟。与对照组相比,没有治疗能增加存活时间,且各组之间的存活率没有显著差异。
在这个镇静的严重出血模型中,由于早期死亡,VPA和PTX在所用的浓度和给药速率下作为小容量复苏产品是不可接受的。鉴于这些药物在较低剂量下已获美国食品药品监督管理局批准用于其他适应症,目前的数据表明有必要对相关机制进行进一步研究。