混合0.3%利多卡因对丙泊酚注射痛的影响
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  • 英文篇名:Effect of the mixture of 0.3% lidocaine and propofol on propofol injection pain
  • 作者:王恒 ; 汤为香 ; 汤黎黎 ; 陈立建
  • 英文作者:WANG Heng;TANG Wei-xiang;TANG Li-li;CHEN Li-jian;Department of Anesthesiology,The First Affiliated Hospital of Anhui Medical University;
  • 关键词:注射痛 ; 丙泊酚 ; 利多卡因 ; 预处理
  • 英文关键词:injection pain;;propofol;;lidocaine;;pretreatment
  • 中文刊名:BANG
  • 英文刊名:Journal of Bengbu Medical College
  • 机构:安徽医科大学第一附属医院麻醉科;
  • 出版日期:2019-02-15
  • 出版单位:蚌埠医学院学报
  • 年:2019
  • 期:v.44;No.278
  • 语种:中文;
  • 页:BANG201902021
  • 页数:4
  • CN:02
  • ISSN:34-1067/R
  • 分类号:71-74
摘要
目的:探讨混合利多卡因抑制丙泊酚注射痛的最佳浓度,并对其有效性及安全性进行评价。方法:收集无痛人工流产手术病人(ASAⅠ~Ⅱ级)809例,采用阶梯式递增、递减模式,滴定混合利多卡因的最佳浓度。病人静注舒芬太尼后随机分为3组,空白组(A组)静注1%丙泊酚;对照组(B组)预注利多卡因40 mg后,静注1%丙泊酚;试验组(C组)注射0.3%利多卡因及0.83%丙泊酚的混合液。注射期间对注射痛评分,同时观察记录注药前后血压、心率(HR)及氧饱和度(SpO_2)、清醒时间及呼吸、循环抑制、恶心呕吐等不良反应,术后调查病人满意度。结果:3组病人用药前舒张压差异无统计学意义(P>0.05),B组、C组收缩压均高于A组(P<0.01),用药后1 min、3 min 3组收缩压、舒张压均较术前明显降低(P<0.01),组间比较差异无统计学意义(P>0.05);3组病人HR用药前无差别,用药后1 min均下降(P<0.05~P<0.01),用药后3 min A组HR仍低于用药前(P<0.05),B组、C组HR均低于用药前,但差异无统计学意义(P>0.05);用药后C组HR高于B组(P<0.05);SpO_2用药后均明显降低(P<0.01),但组间差异无统计学意义(P>0.05),3组用药后3 min SpO_2较用药后1min明显升高(P<0.01),且B组、C组明显高于A组(P<0.01)。3组疼痛发生率比较:C组B组>A组(P<0.05)。3组病人低SpO_2、低血压、低心率、恶心呕吐及体动等不良反应发生率差异均无统计学意义(P>0.05)。结论:混合0.3%利多卡因的丙泊酚可以安全、有效消除注射痛。
        Objective:To investigate the optimal concentration of lidocaine in inhibiting the propofol injection pain,and evaluate its efficacy and safety.Methods:The optimal concentration of lidocaine in painless artifical abortion patients(ASA Ⅰ to Ⅱ)was detected using step by step increasing or decreasing mode.The patients injected with sufentanil were randomly divided into the blank group(group A injected with 1% propofol),control group(group B injected with 1% propofol after 40 mg of lidocain preinjection) and experimental group(group C injected with the mixture of 0.3% lidocaine and 0.83% propofol).The pain scores in three groups were evaluated during injection period.The blood pressure before and after injection,heart rate(HR) and SpO_2,waking time,respiratory or circulatory inhibition,nausea or vomiting and satisfaction degree in three groups were analyzed.Results:Before medication,the differences of diastolic pressure among three groups were not statistically significant(P>0.05),and the levels of systolic pressure in group B and group C were higher than that in group C(P<0.01).After 1 min and 3 min of medication,the levels of diastolic pressure and systolic pressure in three groups significantly decreased compared with before medication(P<0.01),and the differences of those among three groups were not statistically significant(P>0.05).There was no difference in HR among three groups before medication,the HR in three groups after 1 min of medication significantly decreased(P<0.05 to P<0.01).After 3 min of medication,the HR in group A was lower than before medication(P<0.05).After 3 min of medication,the HR in group B and group C were lower than before medication,and the difference of which was not statistically significant(P>0.05).After medication,the HR in group C was significantly higher than that in group B(P<0.05).After medication,the SpO_2 levels in three groups significantly decreased(P<0.01),but the differences of which among three groups were not statistically significant(P>0.05).After 3 min of medication,the SpO_2 levels in three groups significantly increased compared with after 1 min of medication(P<0.01),and which in group B and group C were higher than that in group A(P<0.01).The incidence rates of severe pain and satisfaction degree in group C,group B and group A gradually increased in turn,respectively(P<0.05).The differences of the incidence rates of low SpO_2,blood pressure and heart rate,nausea,vomiting and movement among three groups were not statistically significant(P>0.05).Conclusions:The mixture of 0.3% lidocaine and 0.83% propofol can safely and effectively eliminate the injection pain of propofol.
引文
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