Kalappa Sandhya, Sridhar Raghavendra Biligiri, Nagappa Saraswathi
Department of Anaesthesia, Bangalore Medical College and Research Institute, Bengaluru, Karnataka, India.
Anesth Essays Res. 2017 Apr-Jun;11(2):416-420. doi: 10.4103/0259-1162.194581.
The challenge in providing analgesia for spine surgeries is to provide extended postoperative pain relief and simultaneously allow early neurological assessment and mobilization. Our study aimed to evaluate the analgesic efficacy of intravenous versus caudal dexamethasone in lumbosacral spine surgeries.
In this prospective double-blind study, a total of 96 patients undergoing lumbosacral spine surgery were randomized into three groups to receive 25 ml of preemptive caudal epidural injection of either injection ropivacaine 0.2% (Group A, = 32), a 25 ml of injection ropivacaine 0.2%, and intravenous injection dexamethasone 8 mg (Group B, = 32) or 25 ml mixture of injection ropivacaine 0.2% with injection dexamethasone 8 mg (Group C, = 32) under general anesthesia. Visual analog scale (VAS), heart rate, blood pressures, blood sugar levels, and time to rescue analgesia were recorded at regular intervals for the first 24 h. Time to discharge was noted. Analysis of variance has been used to find the significance of study parameters between the groups of patients. Statistical software, namely, SAS 9.2 and SPSS 15.0, have been used for the analysis of the data.
The mean VAS was significantly lower in the Group C for up to 24 h following the caudal block. No significant hemodynamic changes were noted in any of the groups. The intravenous dexamethasone group showed higher blood glucose levels at 24 h but was not clinically relevant.
These results suggest that injection dexamethasone is a safe adjunct to caudal ropivacaine in lumbosacral spine surgeries.
为脊柱手术提供镇痛的挑战在于提供术后长期疼痛缓解,同时允许早期神经功能评估和活动。我们的研究旨在评估静脉注射与骶管注射地塞米松在腰骶部脊柱手术中的镇痛效果。
在这项前瞻性双盲研究中,总共96例行腰骶部脊柱手术的患者被随机分为三组,在全身麻醉下接受25ml的预防性骶管硬膜外注射,分别为0.2%罗哌卡因注射液(A组,n = 32)、25ml 0.2%罗哌卡因注射液加静脉注射8mg地塞米松(B组,n = 32)或25ml 0.2%罗哌卡因注射液与8mg地塞米松注射液的混合液(C组,n = 32)。在最初24小时内定期记录视觉模拟评分(VAS)、心率、血压、血糖水平和补救镇痛时间。记录出院时间。采用方差分析来确定患者组间研究参数的显著性。使用统计软件SAS 9.2和SPSS 15.0进行数据分析。
骶管阻滞术后24小时内,C组的平均VAS显著更低。各组均未观察到明显的血流动力学变化。静脉注射地塞米松组在24小时时血糖水平较高,但无临床相关性。
这些结果表明,在腰骶部脊柱手术中,地塞米松注射液是骶管罗哌卡因的安全辅助用药。