Reysner Malgorzata, Reysner Tomasz, Janusz Piotr, Kowalski Grzegorz, Shadi Milud, Daroszewski Przemysław, Wieczorowska-Tobis Katarzyna, Kotwicki Tomasz
Palliative Medicine, Poznan University of Medical Sciences, Poznan, Poland
Palliative Medicine, Poznan University of Medical Sciences, Poznan, Poland.
Reg Anesth Pain Med. 2024 Aug 29. doi: 10.1136/rapm-2024-105694.
This study assessed the effect of perineural dexamethasone on block duration, opioid requirement, blood glucose levels, and stress response to surgery as measured by the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR), following pediatric foot and ankle surgery.
In this parallel, double-blinded randomized controlled trial, 90 children (ages 2-5 years, >5 kg) scheduled for foot or ankle surgery under spinal anesthesia with ultrasound-guided single-shot popliteal sciatic nerve block were randomized into 3 groups: 0.5% ropivacaine with saline (control), 0.5% ropivacaine plus dexamethasone 0.1 mg/kg (DEX0.1), and 0.5% ropivacaine plus dexamethasone 0.05 mg/kg (DEX0.05). Primary outcome was the time to first rescue opioid analgesia. Secondary outcomes included motor block duration, pain scores, NLR, PLR, and blood glucose levels.
Time to first rescue opioid analgesia was significantly longer in the DEX0.1 group compared with the DEX0.05 group (18.4 hours, SD 2.6 hours vs 16 hours, SD 2.8 hours), with a mean difference of 2.2 hours (95% CI 0.7 to 3.6), p<0.01; and the control group (8.5 hours, SD 1.5 hours), with a mean difference of -9.9 (95% CI -11.4 to -8.4), p<0.001. Motor block was significantly longer in the DEX0.1 group (17.3 hours, SD 2.5 hours) compared with the DEX0.05 (15.2 hours, SD 2.7 hours; p<0.01) and control groups (7.8±1.1, p<0.001). Total opioid consumption was significantly lower in the DEX0.1 group compared with the control group (p=0.01). NLR, PLR, and glucose levels did not differ significantly between the groups at baseline, 24 hours, and 48 hours post surgery.
Perineural dexamethasone significantly prolonged postoperative motor block duration and did not influence blood glucose, NLR, or PLR levels.
NCT06086418.
本研究评估了小儿足踝手术后,经神经周围注射地塞米松对阻滞持续时间、阿片类药物需求量、血糖水平以及通过中性粒细胞与淋巴细胞比值(NLR)和血小板与淋巴细胞比值(PLR)衡量的手术应激反应的影响。
在这项平行、双盲随机对照试验中,90名计划在脊髓麻醉下接受足踝手术并采用超声引导单次腘窝坐骨神经阻滞的儿童(年龄2至5岁,体重>5千克)被随机分为3组:0.5%罗哌卡因加生理盐水(对照组)、0.5%罗哌卡因加地塞米松0.1毫克/千克(DEX0.1组)和0.5%罗哌卡因加地塞米松0.05毫克/千克(DEX0.05组)。主要结局是首次使用补救性阿片类镇痛药物的时间。次要结局包括运动阻滞持续时间、疼痛评分、NLR、PLR和血糖水平。
DEX0.1组首次使用补救性阿片类镇痛药物的时间显著长于DEX0.05组(18.4小时,标准差2.6小时 vs 16小时,标准差2.8小时),平均差异为2.2小时(95%置信区间0.7至3.6),p<0.01;也显著长于对照组(8.5小时,标准差1.5小时),平均差异为 -9.9(95%置信区间 -11.4至 -8.4),p<(此处原文有误,应为p<0.001)。DEX0.1组的运动阻滞时间显著长于DEX0.05组(17.3小时,标准差2.5小时)(15.2小时,标准差2.7小时;p<0.01)和对照组(7.8±1.1,p<0.001)。DEX0.1组的阿片类药物总消耗量显著低于对照组(p = 0.01)。在基线、术后24小时和48小时时,各组之间的NLR、PLR和血糖水平无显著差异。
经神经周围注射地塞米松显著延长了术后运动阻滞持续时间,且不影响血糖、NLR或PLR水平。
NCT06086418 。