Nazareth Marilyn, Ghoshal Pabitra, Namshikar Viraj, Gaude Yogesh
Department of Anaesthesiology, Goa Medical College, Bambolim, Goa, India.
Anesth Essays Res. 2013 Jan-Apr;7(1):76-82. doi: 10.4103/0259-1162.114003.
This study was undertaken in 100 patients scheduled for lower limb orthopaedic surgeries.
The objective of this study was to study the effect of addition of intrathecal fentanyl to bupivacaine clonidine mixture on the quality of subarachnoid block and compare it with intrathecal bupivacaine clonidine mixture without fentanyl.
In this prospective and double blind randomized controlled study, one hundred patients, between 20-40 years of age, of either sex, weighing between 40-65 Kg, measuring more than 150 cm in height, of ASA Grade I and II who were undergoing orthopaedic lower limb surgeries were selected in order to study the quality of subarachnoid block and post-operative analgesia produced by a combination of bupivacaine clonidine and fentanyl in comparison with bupivacaine clonidine.
The patients were randomly divided in two groups of 50 each: Group BC: 2.4 ml of 0.5% hyperbaric bupivacaine (12 mg) + 0.2 ml (30 μg) clonidine + 0.4 ml of 0.9% NaCl. Group BCF: 2.4 ml of 0.5% hyperbaric bupivacaine (12 mg) + 0.2 ml (30 μg) clonidine + 0.4 ml (20 μg) of fentanyl. The total volume of solution in both the groups was 3.0 ml. The quality of subarachnoid block and post-operative analgesia were studied.
The data thus obtained was statistically analysed using the following tests: Unpaired student's t-test. Average % change in data over baseline values to detect trends. A 'P' value of <0.05 was considered to be statistically significant.
There was no significant difference in duration of sensory and motor blockade in group BCF compared to BC. The duration of analgesia as assessed by, either VAS score of >5 or demand of additional analgesia was > 524.6 ± 32.21 mins in group BC and > 774.4 ± 59.59 mins in group BCF. This prolongation of duration of analgesia in group BCF compared to group BC has statistical significance. Blood pressure and heart rate changes were not significantly different among groups, whereas sedation and pruritus were significantly more frequent in Group BCF.
In conclusion, this study has demonstrated that addition of 20 μg fentanyl to intrathecal 30 μg clonidine and 12 mg bupivacaine enhanced the duration of post-operative analgesia with moderately increased sedation and was not associated with hemodynamic instability or other complications.
本研究纳入了100例计划接受下肢骨科手术的患者。
本研究的目的是探讨在布比卡因可乐定混合液中加入鞘内注射芬太尼对蛛网膜下腔阻滞质量的影响,并将其与不含芬太尼的布比卡因可乐定混合液进行比较。
在这项前瞻性双盲随机对照研究中,选择了100例年龄在20 - 40岁之间、性别不限、体重在40 - 65千克、身高超过150厘米、ASA分级为I级和II级且正在接受下肢骨科手术的患者,以研究布比卡因可乐定与芬太尼联合使用与布比卡因可乐定相比产生的蛛网膜下腔阻滞质量和术后镇痛效果。
患者被随机分为两组,每组50例:BC组:2.4毫升0.5%的高压布比卡因(12毫克) + 0.2毫升(30微克)可乐定 + 0.4毫升0.9%氯化钠溶液。BCF组:2.4毫升0.5%的高压布比卡因(12毫克) + 0.2毫升(30微克)可乐定 + 0.4毫升(20微克)芬太尼。两组溶液的总体积均为3.0毫升。研究了蛛网膜下腔阻滞质量和术后镇痛效果。
对所获得的数据进行以下统计分析:非配对学生t检验。计算数据相对于基线值的平均百分比变化以检测趋势。P值<0.05被认为具有统计学意义。
与BC组相比,BCF组感觉和运动阻滞持续时间无显著差异。以VAS评分>5或需要额外镇痛评估的镇痛持续时间,BC组为>524.6±32.21分钟,BCF组为>774.4±59.59分钟。与BC组相比,BCF组镇痛持续时间的延长具有统计学意义。各组间血压和心率变化无显著差异,而BCF组镇静和瘙痒更为常见。
总之,本研究表明,在鞘内注射30微克可乐定和12毫克布比卡因中加入20微克芬太尼可延长术后镇痛持续时间,镇静适度增加,且与血流动力学不稳定或其他并发症无关。