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高渗盐复合液对急性颅内高压伴失血性休克犬的治疗作用
引用本文:肖华平,古妙宁,肖金仿,徐翔,赵振龙.高渗盐复合液对急性颅内高压伴失血性休克犬的治疗作用[J].南方医科大学学报,2008,28(3):385-388.
作者姓名:肖华平  古妙宁  肖金仿  徐翔  赵振龙
作者单位:南方医科大学南方医院麻醉科,广东,广州,510515
摘    要:目的 探讨高渗氯化钠羟乙基淀粉40注射液(HSH)对急性颅内高压伴失血性休克犬的治疗作用及机制.方法 20条犬随机分为4组,分别为7.5%氯化钠组(HS组)、林格氏液组(RL组)、羟乙基淀粉组(HES组)和HSH组,每组5只.采用硬膜外球囊注水和动脉放血的方法复制急性颅内高压伴失血性休克模型,各组分别在休克1 h后按上述分组顺序输入6ml/kgHS、3倍失血量RL、1倍失血量HES、8ml/kgHSH,观测复苏后颅内压(ICP)、平均动脉压(MAP)、脑灌注压(CPP)的变化,并检测实验前和休克后,复苏后30min、1 h、4h的血钠(Na )和血浆渗透压(OSM)水平.结果 (1)复苏前各组MAP、CPP、ICP无统计学差异(P0.05).(2)与复苏前相比,复苏后各组均能显著提高MAP(P<0.01),各组间无统计学差异(P0.05),但HSH组反应速度最快,除HS组2 h后显著下降外(P<0.01),其余各组均能维持4 h.(3)与复苏前相比,复苏后各组均能显著提高CPP(P<0.01),2 h后HS组CPP显著下降(P<0.01),4 h后HSH组仍能维持较高CPP.(4)与复苏前相比,复苏后RL组与HES组的ICP显著上升(P<0.01),分别在1 h和3 h达到高峰,HS组和HSH组ICP显著降低(P<0.01),均在1 h内下降至最低值,两组降低ICP无统计学意义(P0.05),且均能维持4h.(5)复苏后HS组、HSH组血Na 浓度和血浆OSM较复苏前明显升高(P<0.05).结论 对于急性颅内高压伴失血性休克的犬模型,HSH能有效纠正休克和降低颅内压.且维持时间较HS长.

关 键 词:脑水肿  颅内压  失血性休克  高渗氯化钠羟乙基淀粉40注射液  高渗盐  复合液  急性颅内高压  失血性休克  治疗  作用  dogs  hemorrhagic  shock  complicated  hypertension  acute  treatment  injection  hydroxyethyl  starch  sodium  chloride  维持时间  降低颅内压  犬模型  血浆渗透压  浓度
文章编号:1673-4254(2008)03-0385-04
修稿时间:2007年10月27

Effects of hypertonic sodium chloride hydroxyethyl starch 40 injection in treatment of acute intracranial hypertension complicated by hemorrhagic shock in dogs
XIAO Hua-ping,GU Miao-ning,XIAO Jin-fang,XU Xiang,ZHAO Zhen-long.Effects of hypertonic sodium chloride hydroxyethyl starch 40 injection in treatment of acute intracranial hypertension complicated by hemorrhagic shock in dogs[J].Journal of Southern Medical University,2008,28(3):385-388.
Authors:XIAO Hua-ping  GU Miao-ning  XIAO Jin-fang  XU Xiang  ZHAO Zhen-long
Institution:Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. creasevase@126.com
Abstract:OBJECTIVE: To observe the effect of hypertonic sodium chloride hydroxyethyl starch 40 injection (HSH) in treatment of acute intracranial hypertension complicated by hemorrhagic shock in dogs, and explore the mechanism of the effects of HSH. METHODS: Twenty dogs were randomized into 4 equal groups, namely the 7.5% NaCl (HS) group, Ringer-Lactates solution (RL) group, hydroxyethyl strarch (HES) group, and HSH group. Canine models of acute intracranial hypertension complicated by hemorrhagic shock were established by epidural balloon inflation with saline and rapid discharge of the arterial blood. One hour after the induced shock, the dogs were given HS (6 ml/kg), RL of 3-fold volume of blood loss, HES of equivalent volume of blood loss, and HSH 8 ml/kg in the 4 groups, respectively. During the shock and resuscitationperiod, the intracranial pressure (ICP), mean arterial pressure (MAP) and cerebral perfusion pressure (CPP) of the dogs were monitored, and the serum sodium level and plasma osmolality were measured at 30 min, 1 h and 4 h after the resuscitation. RESULTS: All dogs had similar MAP, CPP, and ICP before resuscitation (P>0.05). After resuscitation, the MAP was significantly improved (P<0.01), but the dogs in HSH group exhibited the fastest response; with the exception of the dogs in HS group to have significantly decreased MAP 2 h after resuscitation (P<0.01), all the other dogs maintained the MAP for 4 h. The CPP was also significantly increased after resuscitation (P<0.01), and in HS group, CPP decreased significantly after 2 h (P<0.01), and HSH group maintained the high CPP after 4 h. The ICP was increased significantly in RL and HES groups after resuscitation (P<0.01), reaching the peak level at 1 and 3 h, respectively, but in HS and HSH groups, the ICP decreased significantly to the lowest level at 1 h (P<0.01) which was maintained for 4 h. After resuscitation, the plasma sodium and plasma osmolality were significantly increased in HSH and HS groups. CONCLUSION: In dogs with acute intracranial hypertension and hemorrhagic shock, HSH can effectively resuscitate hemorrhagic shock and decrease ICP, and the effect is longer-lasting than that of HS.
Keywords:brain edema  intracranial pressure  hemorrhagic shock  hypertonic sodium chloride hydroxyethl starch 40 injection  
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