Height-adjusted dose of intrathecal bupivacaine on surgical anesthesia for the cesarean section

IF 0.2 Q4 ANESTHESIOLOGY
Noyomi Saring, Tomar Basar, R. Sanyal, Mihin Nania
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Abstract

Background: In the spinal anesthetic technique, local anesthetic dose (concentration and volume) is the main determinant of its adequacy and success of block to be achieved. The lack of pain during surgical intervention rather than on dermatome sensory block level is considered to be an appropriate indicator of surgical anesthesia. Spinal anesthesia is the most common anesthetic technique to provide anesthesia for the elective or emergent cesarean section (CS). However, spinal block-induced maternal hypotension is the most common adverse effect during single-shot spinal anesthesia. In our study, we aim to study the height-adjusted dose of 0.5% Bupivacaine Heavy (BH) in achieving surgical anesthesia and its effect on maternal hypotension. Participants and Method: One hundred parturients scheduled for elective CS were enrolled and were compared to the parallel arms of parturients receiving conventional BH. Fifty parturients in each group were included. In the conventional group (B), participants received spinal block with 12 mg of 0.5% BH, and in the height adjusted-dose group (H), participants received a dose of 0.5% BH in 0.06 mg per centimetre height. A sensory block level of T6 dermatome or higher was consider adequate to start surgery. The adequate surgical anesthesia is considered to be achieved if cesarean delivery can be performed without supplementary analgesia. The need of supplementary analgesia, conversion to general anesthesia, or no block till 15 min of intrathecal BH is considered spinal failure. Results: 4% of the height-adjusted dose group have a low block level. Two cases complained of pain, and of them, one received supplementary analgesia and one was converted to general anesthesia. Systolic hypotension of a maternal blood pressure of less than 90 mm Hg was found in 19 (38%) and 10 (20%) in the conventional group and HAD group, respectively, which was highly significant statistically (p value 0.001%). Conclusion: Intrathecal hyperbaric bupivacaine in height adjusted 0.06 mg per cm height of patient can achieve surgical anesthesia with maintainance of systolic blood pressure. However, low dosing of intrathecal BH has higher cases of block failure in comparison to the conventional fixed dose regime of spinal anesthesia.
高度调节剂量布比卡因对剖宫产术麻醉的影响
背景:在脊髓麻醉技术中,局部麻醉剂量(浓度和体积)是决定阻滞是否充分和成功的主要因素。在手术干预过程中没有疼痛,而不是皮肤感觉阻滞水平,被认为是手术麻醉的适当指标。脊髓麻醉是为择期或紧急剖宫产术(CS)提供麻醉的最常用麻醉技术。然而,脊髓阻滞引起的母体低血压是单次脊髓麻醉中最常见的不良反应。在我们的研究中,我们的目的是研究高度调整剂量0.5%布比卡因重(BH)实现手术麻醉及其对产妇低血压的影响。参与者和方法:入选了100名选择CS的产妇,并与接受常规BH的产妇的平行臂进行了比较。每组50例产妇。在常规组(B)中,参与者接受12毫克0.5% BH的脊髓阻滞,在高度调整剂量组(H)中,参与者接受0.5% BH的剂量,每厘米高度0.06毫克。T6或更高的感觉阻滞水平被认为足以开始手术。如果剖宫产可以在没有辅助镇痛的情况下进行,则认为达到了充分的手术麻醉。需要补充镇痛、转全麻或鞘内BH 15分钟前不进行阻滞均被认为是脊柱衰竭。结果:调高剂量组有4%出现低阻滞。2例患者主诉疼痛,其中1例给予辅助镇痛,1例转为全身麻醉。常规组和HAD组分别有19例(38%)和10例(20%)产妇出现收缩期低血压< 90 mm Hg,差异有高度统计学意义(p值0.001%)。结论:布比卡因鞘内高压调节高度0.06 mg / cm,可在维持收缩压的情况下实现手术麻醉。然而,与传统的固定剂量脊髓麻醉相比,低剂量鞘内BH有更高的阻滞失败病例。
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37
审稿时长
29 weeks
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