Paul Amreesh, Borkar Anjali, Bhalerao Nikhil, Wanjari Dnyanshree
Anaesthesiology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Cureus. 2023 Aug 23;15(8):e43956. doi: 10.7759/cureus.43956. eCollection 2023 Aug.
Background The study was done to determine the duration of postoperative analgesia brought on by incorporating intra-articular Bupivacaine with Dexmedetomidine as an adjuvant following knee arthroscopies. Methods A prospective randomized control study was conducted on 60 patients of ASA classes I and II, between the ages of 20 and 60 years, undergoing arthroscopic surgeries of the knee under spinal anaesthesia. The patients were divided into group B and group D, each containing 30 patients. The participants in group B were administered Inj. Bupivacaine 0.5% 19 mL + 1 mL of normal saline intra-articularly and the participants in group D were administered Inj. Bupivacaine 0.5% 19 mL, Inj. Dexmedetomidine 1 μg/kg and normal saline post-surgery. The number of analgesics used in the first 24 hours, pain levels using the visual analogue scale and the timing of administration of the first analgesic dose between the two study groups were evaluated. Results In comparison to the Bupivacaine group, the Dexmedetomidine group required fewer rescue analgesics. The visual analogue visual scale score in group B at four hours and six hours was 2.7 ± 1.39 and 2.9 ± 1.03, respectively, and in group D at four hours and six hours was 1.9 ± 1.09 and 1.83 ± 0.91. The visual analogue scale scores at these times were statistically significant. The visual analogue scale scores at 12 hours and 24 hours were statistically not significant. Conclusion Dexmedetomidine added to Intra-articular Bupivacaine provides an increased duration of postoperative analgesia in patients undergoing arthroscopic surgeries of the knee. The combination offers improved analgesia and reduces the overall dosage of rescue analgesics needed without causing substantial side effects.
本研究旨在确定在膝关节镜检查后,关节腔内注射布比卡因并联合右美托咪定作为辅助药物所带来的术后镇痛持续时间。
对60例年龄在20至60岁之间、ASA分级为I级和II级、在脊髓麻醉下接受膝关节镜手术的患者进行了一项前瞻性随机对照研究。患者被分为B组和D组,每组30例。B组患者关节腔内注射0.5%布比卡因19 mL + 1 mL生理盐水,D组患者术后注射0.5%布比卡因19 mL、右美托咪定1 μg/kg及生理盐水。评估了两组在前24小时内使用的镇痛药物数量、使用视觉模拟量表评估的疼痛程度以及首次使用镇痛药物剂量的时间。
与布比卡因组相比,右美托咪定组所需的补救性镇痛药物更少。B组在4小时和6小时时的视觉模拟量表评分分别为2.7±1.39和2.9±1.03,D组在4小时和6小时时的视觉模拟量表评分分别为1.9±1.09和1.83±0.91。这些时间点的视觉模拟量表评分具有统计学意义。12小时和24小时时的视觉模拟量表评分无统计学意义。
关节腔内注射布比卡因时添加右美托咪定可延长接受膝关节镜手术患者的术后镇痛时间。该联合用药可提供更好的镇痛效果,减少所需补救性镇痛药物的总体剂量,且不会引起明显的副作用。