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剖宫产孕妇硬膜外给局麻药的药代动力学 被引量:3

Pharmacokinetics of epidural local anesthetics in parturient women undergoing cesareau sections.
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摘要 为了解孕妇硬膜外给局麻药的药代动力学,选择20名实施剖宫产手术的健康临产妇,随机分成硬膜外腔给予了哌卡因组(B1组)和给予利多卡因组(L组)。另外, 6例非妊娠患者硬膜外腔给予了哌卡因(B2组)。B1和B2组均给予0.75%丁哌卡因1~1.5mg·kg-1,L组给予2%利多卡因4~4.5mg·kg-1。采用高效液相色谱(HPLC)测定硬膜外给药后血浆药物浓度。结果表明三组病例血药浓度均在安全范围内。B1组的血药浓度达高峰时间(Tpeak)和脐静脉与母体血药浓度比(UV/MV)值均小于L组,表明丁哌卡因在硬膜外腔的吸收比利多卡因快,且透过胎盘屏障的药量小于利多卡因,新生儿Apgar评分在娩出后5分钟均为10分。B1组的药代动力学参数与B2组基本相似。结论:剖宫产手术硬膜外腔给予临床剂量的局麻药是安全的。 To evaluate the variations in pharmacokinetics of epidural local anesthetics in pregnant women, twenty healthy parturient women,scheduled to undergo cesarean sections,were randomly allocated to receiving epidural 0. 75'% bupivacaine 1. 2mg.kg-1 (B1 group)or 2%lidocaine 4. 5mg .kg-1 (L group)respectively,and six non-pregnant female patients were elected to receive epidural 0. 75 % bupivacaine 1. 5mg .kg-1 (B2 group). High performance liquid chromatography(HPLC) was used to measure the plasma concentrations of local anesthetics following epidural administration. The results showed that the plasma concentrations were all within safty ranges in these three groups. Tpeak and UV/MV value in B1 group were less than those in L groap,indicating that the absorption following epidural bupivacaine was more rapid and its placental transfer dosage was lower as compared with those of lidocaine. Neonatal Apgar scores were equally ten at five minutes after delivery. The pharmacokinetic parameters in B1 group were all basically similar to those in B2 group. it's concluded that the clinical routine dosages of epidural local anesthetics for cesarean section are safe.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 1995年第8期341-344,共4页 Chinese Journal of Anesthesiology
关键词 药代动力学 丁哌卡因 硬膜外给药 剖腹产 Pharmacokinetics Bupivacaine Lidocaine Cesarean section Epidural administration
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参考文献2

  • 1张沂,中国药学杂志,1991年,26卷,213页
  • 2张菁,中华妇产科杂志,1988年,23卷,258页

同被引文献17

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