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机构地区:[1]广东省深圳市第九人民医院,广东深圳518116
出 处:《中国医学创新》2016年第27期17-19,共3页Medical Innovation of China
基 金:广东省深圳市卫生局科技计划项目(201202191)
摘 要:目的:观察罗哌卡因的急性毒性作用,并计算其致死剂量。方法:根据药理实验方法学改良寇氏(Karber)法,给大鼠尾静脉注射不同剂量罗哌卡因原液,观察并记录给药后大鼠的中毒表现及死亡情况;根据各组半数致死剂量(LD_(50)),计算半数致死量及95%可信区间(CI)。结果:罗哌卡因入血剂量在2.6 mg/kg时实验鼠可出现惊厥性收缩(抽搐)、翻正反射消失和自主活动减弱、呼吸抑制等,但无死亡;随着入血剂量增加,实验鼠可发生死亡,剂量增大至13.2 mg/kg,全部死亡。本研究资料测得致死剂量范围在2.6~12.6 mg/kg,其LD_(50)=7.29 mg/kg,95%CI(5.88,8.70)。解剖死亡大鼠,肉眼观察心、肝、脾、肺、肾及肠胃等主要脏器病理改变。结论:罗哌卡因小剂量入血后中枢神经系统中毒是可逆的,大剂量将引起不可逆的死亡。Objective: To observe the acute toxic effect of Ropivacaine and its lethal dose. Method: According to the pharmacology experiment of improved Karber's method, poisoning manifestations and deaths of rats given different dose of ropivacaine were observed and recorded.LD50 and 95% confidence interval were calculated according to LD50 of different groups.Result: When inserted Ropivacaine with blood dose of 2.6 mg/kg, the rats showed symptoms of convulsive induced contraction ( convulsion ), a loss of righting reflex, weakness of autonomic activities and respiratory depression without deaths.As the blood dose increased, the rats might die.When the blood dose reached 13.2 mg/kg, all the rats died.According to this research, lethal dose was between 2.6-12.6 mg/kg, whose LD50=7.29 mg/kg and 95%CI ( 5.88, 8.70 ) .After anatomy, the pathologic changes of the heart, liver, spleen, lung, kidney, intestines and stomach of the dead rats were given visual inspection.Conclusions: After a small dose of Ropivacaine into blood, the poisoning of central nervous system is reversible.A great dose of Ropivacaine causes reversible death.
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