Hiroki Tadanao, Suzuki Hideo, Fujita Nao, Suto Takashi, Tsukamoto Noboru, Iriyama Wataru, Hoshina Mayu, Obata Hideaki
Department of Anesthesiology, Isesaki Municipal Hospital, 12-1 Tsunatorihon-Machi, Isesaki Gunma, 372-0817, Japan.
Department of Anesthesiology, Keiyu Orthopedic Hospital, 2267-1 Akoda-Cho, Tatebayashi Gunma, 374-0013, Japan.
J Anesth. 2025 Jun 15. doi: 10.1007/s00540-025-03530-w.
Nitrous oxide (NO) reportedly lessens postoperative pain and neuropathic pain by counteracting N-methyl-D-aspartate (NMDA) receptors. Surgeries such as postoperative lumbar posterior intervertebral fusion (PLIF) can induce severe pain, including neuropathic pain-like symptoms. Here, we investigated the impact of intraoperatively administered NO on postoperative pain and other symptoms following PLIF.
During PLIF surgery, the patients received either N2O 60% or air, with the inhaled oxygen concentration set at 0.4. For postoperative pain management, patients were administered fentanyl (4 µg/kg), acetaminophen, and flurbiprofen during surgery. Additionally, an intravenous patient-controlled analgesia device delivering fentanyl was connected. Postsurgical pain and other symptoms were evaluated based on the numerical rating scale (NRS), amount of fentanyl used, rate of adjuvant analgesic use, and numbness.
Eighty patients were randomly assigned to either the control (air) group (n = 34) or the NO group (n = 39). No differences in patient background, postoperative low back pain NRS (air: 3.5 (2-6.25) vs NO: 4 (2-6) at 24 h, median (interquartile range), P = 0.655), or pain and numbness in the lower limbs were detected between groups. No differences in fentanyl use at 48 h (air: 330 (165-525) µg, NO: 225 (120-390) µg; P = 0.15). At 1 month after surgery, the two groups exhibited similar low back pain, lower limb pain, and numbness symptoms.
Intraoperative administration of NO did not improve acute or subacute postoperative nociceptive or neuropathic pain after PLIF and did not decrease the use of postoperative analgesics.
据报道,一氧化二氮(NO)可通过拮抗N-甲基-D-天冬氨酸(NMDA)受体减轻术后疼痛和神经性疼痛。诸如术后腰椎后路椎间融合术(PLIF)等手术可引发严重疼痛,包括类似神经性疼痛的症状。在此,我们研究了术中给予NO对PLIF术后疼痛及其他症状的影响。
在PLIF手术期间,患者吸入60%的N2O或空气,吸入氧浓度设定为0.4。对于术后疼痛管理,患者在手术期间接受芬太尼(4μg/kg)、对乙酰氨基酚和氟比洛芬治疗。此外,连接了一个静脉自控镇痛装置,用于输送芬太尼。术后疼痛及其他症状通过数字评分量表(NRS)、芬太尼使用量、辅助镇痛药使用率和麻木感进行评估。
80例患者被随机分为对照组(空气组,n = 34)或NO组(n = 39)。两组患者的背景、术后24小时下腰痛NRS(空气组:3.5(2 - 6.25),NO组:4(2 - 6),中位数(四分位间距),P = 0.655)或下肢疼痛和麻木感无差异。48小时时芬太尼使用量无差异(空气组:330(165 - 525)μg,NO组:225(120 - 390)μg;P = 0.15)。术后1个月,两组的下腰痛、下肢疼痛和麻木症状相似。
术中给予NO并不能改善PLIF术后的急性或亚急性伤害性或神经性疼痛,也不能减少术后镇痛药的使用。