Journal of anesthesia · 2025
Randomized active-controlled study of the effect of intraoperative nitrous oxide on postoperative pain and numbness after posterior lumbar interbody fusion surgery.
СтатьяРандомизированное исследованиеНазвание и аннотация: Перевод в очереди
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Hiroki Tadanao, Suzuki Hideo, Fujita Nao, Suto Takashi, Tsukamoto Noboru, Iriyama Wataru, Hoshina Mayu, Obata Hideaki
Аннотация
PURPOSE: Nitrous oxide (N2O) 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 N2O on postoperative pain and other symptoms following PLIF.
METHODS: 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.
RESULTS: Eighty patients were randomly assigned to either the control (air) group (n = 34) or the N2O group (n = 39). No differences in patient background, postoperative low back pain NRS (air: 3.5 (2-6.25) vs N2O: 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, N2O: 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.
CONCLUSIONS: Intraoperative administration of N2O did not improve acute or subacute postoperative nociceptive or neuropathic pain after PLIF and did not decrease the use of postoperative analgesics.
METHODS: 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.
RESULTS: Eighty patients were randomly assigned to either the control (air) group (n = 34) or the N2O group (n = 39). No differences in patient background, postoperative low back pain NRS (air: 3.5 (2-6.25) vs N2O: 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, N2O: 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.
CONCLUSIONS: Intraoperative administration of N2O did not improve acute or subacute postoperative nociceptive or neuropathic pain after PLIF and did not decrease the use of postoperative analgesics.