Lignocaine-based opioid-free anesthesia increases sevoflurane need in head-and-neck cancer surgery
This randomized trial compared a lignocaine-based opioid-free anesthesia (OFA) regimen with a morphine-based regimen in 30 patients undergoing wide excision and reconstruction for head-and-neck cancer. The lignocaine group received a bolus of 1.5 mg/kg and infusion of 1 mg/kg/h, while the morphine group received a bolus of 0.2 mg/kg and infusion of 2 mg/h. The primary outcome was the end-tidal sevoflurane concentration needed to maintain bispectral index (BIS) values of 40-60.
The study found that the lignocaine-based OFA group required significantly higher end-tidal sevoflurane concentrations and had higher sevoflurane consumption compared to the morphine group. Additionally, hypertension was significantly more frequent in the lignocaine group, and more patients required additional analgesics. Heart rate was higher immediately after induction and at 1 minute postintubation in the lignocaine group, but lower at 60 minutes postintubation. No intraoperative awareness was reported in either group.
Safety data were limited; hypertension was noted as an adverse event, but serious adverse events, discontinuations, and tolerability were not reported. The small sample size and lack of blinding or detailed methodology limit the strength of these findings. Clinicians should interpret these results cautiously, as the study suggests that lignocaine-based OFA may not reduce anesthetic requirements and could increase hemodynamic instability in this surgical population.