Spinal anesthesia with two different dosages of 0.75% glucose-free ropivacaine: a comparison of efficacy and safety in Chinese parturients undergoing cesarean section.

J. O. Wong, T. D. Tan, P. Leung, K. Tseng, Ning-Wei Cheu
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引用次数: 14

Abstract

BACKGROUND We compared the clinical efficacy and safety between 2 doses of 2.5 ml (18.75 mg) and 3 ml (22.5 mg) of 0.75% glucose free spinal ropivacaine in Chinese parturients undergoing Cesarean section. METHODS In this randomized, open-label study, 40 parturients enrolled were divided into two groups: Group A received a 2.5 ml 0.75% ropivacaine as opposed to 3 ml in Group B. Sensory and motor blocks were assessed during and after surgery until complete recovery. Eight standard measurements were taken: time at onset of sensory block; maximum cephalic sensory spread; maximum number of blocked segments; time to maximum sensory block; duration of sensory block at L3; time at onset of complete motor block and duration until complete recovery. Vital signs and any adverse effects related to spinal anesthesia were also recorded. RESULTS Five of the 6 variables showed no significant difference between groups A and B: onset time of sensory block at L3 was 1.8 +/- 6.7 min vs. 2.3 +/- 9.8 min; maximum cephalic spread was T3-4 (C3-T7) vs. T3 (C2-T8); maximum number of blocked segments was 20.7 +/- 3.5 vs. 20.2 +/- 3.4; time to maximum sensory block 15.4 +/- 5.5 min vs. 20.3 +/- 15.1 min; time for regression to L3 was 200.8 +/- 59.5 min vs. 215.0 +/- 37.6 min and time for complete recovery of motor block 208.5 +/- 55.5 min vs. 226.5 +/- 461. min. Group B had a significantly faster onset time for complete motor block (P < 0.05) 15.4 +/- 5.6 min vs. 10.4 +/- 4.7 min. Moreover, there were no significant differences in global hemodynamic changes during and after the operation. Transient hypotension attacks were more frequent in group A at the beginning of anesthesia, perhaps due to inadequate prehydration. Otherwise, there were no differences in adverse effects during or after surgery. CONCLUSIONS We conclude that for Cesarean section in Chinese parturients either 18.75 mg (2.5 ml) or 22.5 mg (3 ml) 0.75% glucose-free ropivacaine can provide a spinal anesthesia of the same efficacy and safety.
0.75%无糖罗哌卡因两种不同剂量腰麻在剖宫产术中的疗效和安全性比较
背景:我们比较了2剂2.5 ml (18.75 mg)和3 ml (22.5 mg) 0.75%无糖脊髓性罗哌卡因在剖宫产术中的临床疗效和安全性。方法在这项随机、开放标签的研究中,40名孕妇被分为两组:A组接受2.5 ml 0.75%罗哌卡因治疗,b组接受3 ml罗哌卡因治疗,在手术期间和手术后评估感觉和运动阻滞,直到完全恢复。采用八项标准测量:感觉阻滞发生时间;最大的头侧感觉扩散;最大阻塞段数;达到最大感觉阻塞的时间;L3感觉阻滞持续时间;完全运动阻滞的开始时间和完全恢复的持续时间。同时记录生命体征和与脊髓麻醉相关的任何不良反应。结果A组和B组在6个变量中有5个变量差异无统计学意义:L3感觉阻滞发生时间分别为1.8 +/- 6.7 min和2.3 +/- 9.8 min;最大的头侧扩散为T3-4 (C3-T7)和T3 (C2-T8);最大阻滞片段数为20.7 +/- 3.5 vs. 20.2 +/- 3.4;最大感觉阻滞时间15.4 +/- 5.5 min vs. 20.3 +/- 15.1 min;L3恢复时间分别为200.8 +/- 59.5 min和215.0 +/- 37.6 min,运动块完全恢复时间分别为208.5 +/- 55.5 min和226.5 +/- 461 min。B组完全运动阻滞的起效时间(15.4 +/- 5.6 min)明显高于10.4 +/- 4.7 min (P < 0.05)。此外,术中和术后整体血流动力学变化无显著差异。A组在麻醉开始时短暂性低血压发作更为频繁,可能是由于预水合不足。除此之外,手术期间和术后的不良反应没有差异。结论:18.75 mg (2.5 ml)或22.5 mg (3 ml) 0.75%无糖罗哌卡因均可为剖宫产术患者提供相同疗效和安全性的脊髓麻醉。
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