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Lignocaine-based opioid-free anesthesia increases sevoflurane need in head-and-neck cancer surgery

Lignocaine-based opioid-free anesthesia increases sevoflurane need in head-and-neck cancer surgery
Photo by Cht Gsml / Unsplash
Key Takeaway
Consider that lignocaine-based opioid-free anesthesia may increase sevoflurane requirements and hypertension risk compared to morphine-based anesthesia 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.

Study Details

Study typeRct
Sample sizen = 30
EvidenceLevel 2
PublishedMay 2026
View Original Abstract ↓
BACKGROUND AND AIMS: In opioid-free anesthesia (OFA) protocol, intravenous lignocaine can offer perioperative analgesic benefits. However, maintaining adequate anesthetic depth during OFA, particularly with neuromuscular blockade, poses a challenge due to the unreliable nature of hemodynamic parameters as indicators of anesthetic depth. We aimed to compare the end-tidal sevoflurane concentration needed to maintain bispectral index (BIS) values of 40-60 in patients undergoing major head-and-neck cancer surgery using lignocaine-based OFA versus a morphine-based regimen. METHODS: This prospective, randomized, double-blind study enrolled 30 patients undergoing wide excision and reconstruction for head-and-neck cancer. Group L received a lignocaine bolus (1.5 mg/kg) and infusion (1 mg/kg/h), while Group B received a morphine bolus (0.2 mg/kg) and 2 mg/h infusion. Propofol was used to induce anesthesia, and nasal intubation was carried out. Sevoflurane in a 1:1 air-oxygen mixture was used for maintenance, titrated to maintain BIS values between 40 and 60. Additional analgesics were added if indicated. RESULTS: End-tidal sevoflurane concentration and sevoflurane consumption were significantly higher in Group L. Hypertension was significantly more frequent in Group L and required significantly more additional analgesics ( P < 0.001). Mean heart rate was higher in Group L immediately after induction and at 1 min postintubation, while it was lower at 60 min postintubation. Neither group reported any incidence of intraoperative awareness. CONCLUSION: Lignocaine-based OFA required a significantly higher end-tidal sevoflurane to maintain sufficient anesthetic depth compared to morphine-based anesthesia. In addition, sevoflurane use, intraoperative hypertension, and the need for supplemental analgesics were notably greater in the OFA group.
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