Ledan C, Collet D, Vincelot A, Debord J, Lachatre G, Feiss P
Département d'Anesthésie-Réanimation Chirurgicale, CHU Dupuytren, Limoges.
Ann Fr Anesth Reanim. 1993;12(6):552-9. doi: 10.1016/s0750-7658(05)80621-5.
Twenty ASA 1 pregnant women at term, undergoing elective Caesarean section were included in this study. They were randomly assigned to one of two groups, receiving either a spinal or an epidural anaesthesia. Before induction, in order to prevent hypotension, all patients were given an i.v. infusion of 1000 ml of Ringer-lactate and a subcutaneous injection of ephedrine 30 mg. They were positioned on the operating table with a 15 degrees left lateral tilt. Spinal anaesthesia was performed with hyperbaric bupivacaine 0.5 p. cent (0.08 mg.cm-1 of height). Epidural anaesthesia was obtained with a bolus dose of 0.5 p. cent plain bupivacaine, followed by a continuous infusion through the epidural catheter until the level of surgical block reached T6 bilaterally. Bupivacaine was assayed in plasma by high performance liquid chromatography (HPLC). Following pharmacokinetic parameters of bupivacaine were determined: Cmax (maximal concentration), Tmax (time to reach maximum), AUC (area under curve), Cl (total plasma clearance), Vz (volume of distribution during the elimination phase), T1/2 (elimination half-life). Bupivacaine concentration was also measured in samples obtained at birth from umbilical vein and umbilical artery. The mean dose of bupivacaine used was 12.8 +/- 0.6 mg in the spinal group and 118.6 +/- 17.8 mg in the epidural group. The time of onset of surgical anaesthesia was significantly shorter with spinal anaesthesia (7.6 +/- 4.4 vs 31 +/- 11.1 min; p < 0.01). The sensory block had a longer duration in epidural group (223.2 +/- 15 vs 291 +/- 13.8; p < 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究纳入了20名足月行择期剖宫产的美国麻醉医师协会(ASA)1级孕妇。她们被随机分为两组,分别接受脊髓麻醉或硬膜外麻醉。诱导前,为预防低血压,所有患者均静脉输注1000 ml乳酸林格液,并皮下注射30 mg麻黄碱。她们以左侧倾斜15度的姿势躺在手术台上。脊髓麻醉采用0.5%的重比重布比卡因(每厘米身高0.08 mg)。硬膜外麻醉通过单次推注0.5%的普通布比卡因获得,随后通过硬膜外导管持续输注,直至双侧手术阻滞平面达到T6。采用高效液相色谱法(HPLC)测定血浆中的布比卡因。测定了布比卡因的以下药代动力学参数:Cmax(最大浓度)、Tmax(达到最大值的时间)、AUC(曲线下面积)、Cl(总血浆清除率)、Vz(消除相分布容积)、T1/2(消除半衰期)。还测定了出生时脐静脉和脐动脉样本中的布比卡因浓度。脊髓组使用的布比卡因平均剂量为12.8±0.6 mg,硬膜外组为118.6±17.8 mg。脊髓麻醉的手术麻醉起效时间明显更短(7.6±4.4 vs 31±11.1分钟;p<0.01)。硬膜外组的感觉阻滞持续时间更长(223.2±15 vs 29l±13.8;p<0.001)。(摘要截断于250字)