EFFECT OF ADDING DIFFERENT DOSES OF DEXAMETHASONE TO BUPIVACAINE ON INTRATHECAL ANESTHESIA IN CESAREAN SECTION

A. Mohammad
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Abstract

Background: The cost-effectiveness and facility in the administration have been made the spinal anesthesia as the most used technique in cesarean section. However, the short-term duration of local anesthetic drugs’ action has created a matter of concern for anesthesiologists. The purpose of this investigation was to evaluate the effect of different doses of dexamethasone conjugated with bupivacaine on the duration of spinal anesthesia as the primary outcome, and their adverse effects were examined among patients underwent cesarean section as well. Subject and Methods: In the current double-blind clinical trial, 90 pregnant women scheduled for cesarean section were randomly assigned into three groups after taking written consent. Patients assigned to the group A (n=30) received intrathecal bupivacaine 12.5mg (2.5 ml) of 0.5% hyperbaric bupivacaine diluted in preservative free normal saline (1 ml), group B (n=30): received 12.5 mg (2.5 ml) of 0.5% intrathecal hyperbaric bupivacaine and 2 mg (0.5 ml) preservative free dexamethasone, diluted in preservative free normal saline (0.5 ml), overall 3.5 ml volume intrathecally, and group C (n=30): received 12.5 mg (2.5 ml) of 0.5% hyperbaric bupivacaine and 4 mg (1 ml) preservative free dexamethasone, overall 3.5 ml volume intrathecally. Results: In the present study the crude mean age of the patients was 26.49±5.49 (range: 1840 years) and the patients’ age, weight, and body mass index were comparable among three groups (p>0.05). The study showed the sensory block (min) in patients was significantly higher in groups 2 and 4 mg dexamethasone; 284.63±64.85 and 313.37±70.53, respectively compared to the control or group control, 165.33±44.95 minutes. Similarly, the motor block (min) in patients assigned groups 2 and 4 mg dexamethasone was substantially higher; 223.43±52.67 and 227.20±47.17, respectively in comparison with it’s in group control, 126.33±34.62 minutes. However, the difference between groups 2 and 4 mg dexamethasone not substantial for both sensory and motor blocks (p>0.05). The patients of three groups had not substantial difference in frequency of post-operative adverse effects, including postopetaive nausea & vomiting, hypotension, bradycardia, shivering, post-dural-puncture headache. Conclusions: administration of 2 or 4 mg dexamethasone intrathecally prolongs the duration of sensory and motor block of bubivacaine substantially in patients underwent cesarean section under spinal anesthesia and the effect of adding 2 mg on the duration of sensory and motor blocks is same like adding 4 mg. Duhok Med J 2018; 12 (1): 73-83.
布比卡因中加入不同剂量地塞米松对剖宫产术鞘内麻醉的影响
背景:腰麻因其成本效益和给药方便而成为剖宫产术中最常用的麻醉方法。然而,局部麻醉药物作用的短期持续时间引起了麻醉医生的关注。本研究的目的是评价不同剂量地塞米松联合布比卡因对脊髓麻醉持续时间的影响,并在剖宫产患者中观察其不良反应。对象与方法:本双盲临床试验选取90例拟行剖宫产术的孕妇,经书面同意后随机分为三组。A组(n=30)患者接受鞘内布比卡因12.5mg (2.5 ml) 0.5%高压布比卡因用无防腐剂生理盐水(1 ml)稀释,B组(n=30)患者接受0.5%鞘内高压布比卡因12.5mg (2.5 ml)和无防腐剂地塞米松2 mg (0.5 ml),用无防腐剂生理盐水(0.5 ml)稀释,鞘内总容量为3.5 ml, C组(n=30):给予12.5 mg (2.5 ml) 0.5%高压布比卡因和4 mg (1 ml)无防腐剂地塞米松,总容量为3.5 ml。结果:本组患者的粗平均年龄为26.49±5.49(范围1840岁),三组患者的年龄、体重、体质指数具有可比性(p>0.05)。研究显示,2、4 mg地塞米松组患者感觉阻滞(min)明显增高;与对照组相比,分别为284.63±64.85和313.37±70.53分钟,分别为165.33±44.95分钟。同样,分配给2和4 mg地塞米松组的患者的运动阻滞(min)明显更高;与对照组的126.33±34.62分钟相比,分别为223.43±52.67分钟和227.20±47.17分钟。然而,2和4 mg地塞米松组在感觉和运动阻滞方面的差异不显著(p>0.05)。三组患者术后不良反应发生率无显著差异,包括术后恶心呕吐、低血压、心动过缓、寒战、硬膜穿刺后头痛。结论:腰麻剖宫产术患者鞘内给予2、4 mg地塞米松可显著延长布比卡因感觉阻滞和运动阻滞持续时间,且添加2 mg与添加4 mg对布比卡因感觉阻滞和运动阻滞持续时间的影响相同。杜霍克医学杂志2018;12(1): 73-83。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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