Kościelniak-Merak Barbara, Batko Ilona, Kobylarz Krzysztof, Sztefko Krystyna, Tomasik Przemysław J
Department of Clinical Biochemistry, Pediatrics Institute, Jagiellonian University Medical College, Cracow, Poland.
Intensive Care Unit, University Children's Hospital, Cracow, Poland.
Pain Med. 2020 Nov 7;21(7):1464-1473. doi: 10.1093/pm/pnz212.
We analyzed the influence of perioperative, intravenous (i.v.) lidocaine infusion as a part of multimodal anesthesia on concentrations of selected pain modulators.
An observational study.
University Children's Hospital in Cracow, Poland, from May 2015 to May 2018.
Forty-four children undergoing extensive spinal surgery, divided into two groups after surgery: the study group (N = 23), anesthetized generally with lidocaine as a co-analgesic, and the control group (N = 22), anesthetized generally without lidocaine.
We assessed proinflammatory mediators like neuron growth factor (NGF), high mobility group box 1 (HMGB1), interleukin 6 (IL-6), and FOS protein before, immediately after, six hours and 12-15 hours after surgery. We evaluated pain intensity at corresponding time points using a 10-point numerical/graphical scale.
We observed that children in the lidocaine group had reduced pain intensity in the resting state and during movement until six hours after surgery when compared with controls. We found lower NGF concentrations in the lidocaine group vs controls only at six hours after surgery. Mean HMGB1 concentrations during the postoperative period in the study group were relatively stable, whereas we observed significant increases at six hours after surgery and a slight decrease at 12-15 hours after surgery in the control group. IL-6 concentrations at six hours were lower in lidocaine patients when compared with controls. We noted a negative correlation between HMGB1, NGF, Il-6, and lidocaine concentrations after surgery. We did not find any differences in FOS protein concentrations between the groups.
Our findings suggest that intraoperative and postoperative i.v. lidocaine administration as a part of multimodal anesthesia may reduce inflammatory-dependent postoperative pain intensity.
我们分析了围手术期静脉输注利多卡因作为多模式麻醉一部分对所选疼痛调节因子浓度的影响。
一项观察性研究。
2015年5月至2018年5月期间,波兰克拉科夫的大学儿童医院。
44例接受广泛脊柱手术的儿童,术后分为两组:研究组(N = 23),采用利多卡因作为辅助镇痛药进行全身麻醉;对照组(N = 22),未使用利多卡因进行全身麻醉。
我们在手术前、术后即刻、术后6小时以及术后12 - 15小时评估促炎介质,如神经生长因子(NGF)、高迁移率族蛋白B1(HMGB1)、白细胞介素6(IL - 6)和FOS蛋白。我们使用10分数字/图形量表在相应时间点评估疼痛强度。
我们观察到,与对照组相比,利多卡因组儿童在术后6小时内静息状态和活动时的疼痛强度降低。我们发现仅在术后6小时,利多卡因组的NGF浓度低于对照组。研究组术后期间的平均HMGB1浓度相对稳定,而对照组在术后6小时显著升高,在术后12 - 15小时略有下降。与对照组相比,利多卡因组患者术后6小时的IL - 6浓度较低。我们注意到术后HMGB1、NGF、Il - 6与利多卡因浓度之间呈负相关。两组之间的FOS蛋白浓度未发现差异。
我们的研究结果表明,术中及术后静脉注射利多卡因作为多模式麻醉的一部分,可能会降低炎症相关的术后疼痛强度。