Narasimhamurthy Girish Chikkanayakanahalli, Patel Muralidhara Danappa, Menezes Yvonne, Gurushanth Kavyashree Nagenahalli
Assistant Professor, Department of Anaesthesiology, Shridevi Institute of Medical sciences and Research Hospital , Tumkur, Karnataka, India .
Associate Professor, Department of Anaesthesiology, Goa Medical College , Goa-India .
J Clin Diagn Res. 2016 Apr;10(4):UC14-7. doi: 10.7860/JCDR/2016/18946.7665. Epub 2016 Apr 1.
Ropivacaine is amide local anaesthetic pure S(-)enantiomer of bupivacaine. Its duration of analgesia is similar to that of Bupivacaine (in equivalent doses) but the motor block is slower in onset, less intense, shorter in duration for a given level of sensory block with lesser cardiac side effects but addition of an adjuvant like clonidine which is an imidazoline derivative has been studied for its sedative, anxiolytic and analgesic properties.
This study was aimed to show the optimum concentrations of Ropivacaine and Clonidine to maximize analgesia without side effects by evaluating its safety and efficacy.
Sixty children aged 2-10 years of ASA grade 1, scheduled to undergo infraumbilical surgeries were randomly allocated to Group A & Group B of 30 each. Group A received 0.2% Ropivacaine with normal saline and Group B received 0.2% Ropivacaine and preservative free Clonidine 1μg/kg, the total volume of solution being 1ml/kg haemodynamic changes were monitored intraoperatively and haemodynamic parameters along with motor blockade, pain score and sedation score were assessed postoperatively.
Done with unpaired student t and Mann-Whitney test.
The groups were comparable regarding demographic characterstics. The mean duration of analgesia was prolonged in group B (12+2.22 hours) than in group A (6.53+1.16 hours) with p-value <0.001 leading to less rescue analgesia in former group. None of the children in the groups had a pain score of ≥ 4 at the end of 2 hours. A 6.6% and 60% of group A children had score of ≥ 4 at the end of 4(th) & 6(th) hour respectively. None in Group B had a score of ≥ 4. At the end of 8(th) hour, only 6.6% of the children in Group B had a pain score of ≥ 4 whereas it was 33.33% in Group A which is statistically significant. No bradycardia or hypotension and no significant sedation.
Combination of Ropivacaine and Clonidine in the concentration used (0.2% ropivacaine and 1μg/kg of clonidine) can be optimal for postoperative analgesia in paediatric population.
罗哌卡因是一种酰胺类局部麻醉药,是布比卡因的纯S(-)对映体。其镇痛持续时间与布比卡因(同等剂量)相似,但运动阻滞起效较慢,在给定感觉阻滞水平下强度较小、持续时间较短,心脏副作用较小,但已对添加如可乐定(一种咪唑啉衍生物)等佐剂的镇静、抗焦虑和镇痛特性进行了研究。
本研究旨在通过评估其安全性和有效性,显示罗哌卡因和可乐定的最佳浓度,以在无副作用的情况下使镇痛效果最大化。
60名年龄在2至10岁、ASA分级为1级、计划接受脐下手术的儿童被随机分为A组和B组,每组30名。A组接受0.2%罗哌卡因加生理盐水,B组接受0.2%罗哌卡因和不含防腐剂的可乐定1μg/kg,溶液总体积为1ml/kg。术中监测血流动力学变化,术后评估血流动力学参数以及运动阻滞、疼痛评分和镇静评分。
采用非配对学生t检验和曼-惠特尼检验。
两组在人口统计学特征方面具有可比性。B组的平均镇痛持续时间(12+2.22小时)比A组(6.53+1.16小时)延长,p值<0.001,导致前一组的补救性镇痛较少。两组儿童在2小时结束时均无疼痛评分≥4分。A组分别有6.6%和60%的儿童在第4小时和第6小时结束时疼痛评分≥4分。B组无一人评分≥4分。在第8小时结束时,B组只有6.6%的儿童疼痛评分≥4分,而A组为33.33%,具有统计学意义。未出现心动过缓或低血压,也无明显镇静作用。
所用浓度(0.2%罗哌卡因和1μg/kg可乐定)的罗哌卡因和可乐定联合应用对小儿群体术后镇痛可能是最佳的。