• Arch Otolaryngol · Feb 2002

    Randomized Controlled Trial Clinical Trial

    Preincisional bupivacaine in posttonsillectomy pain relief: a randomized prospective study.

    • Nilesh Raman Vasan, Scott Stevenson, and Mark Ward.
    • Department of Otolaryngology-Head and Neck Surgery, Glasgow Royal Infirmary, 84 Castle St, Glasgow G4 0SF, Scotland, UK. nileshvasan@aol.com
    • Arch Otolaryngol. 2002 Feb 1;128(2):145-9.

    ObjectiveTo determine the effect of preincisional bupivacaine hydrochloride infiltration on postoperative pain after tonsillectomy.DesignProspective, randomized, double-blind clinical trial.SettingA secondary/tertiary referral center in Christchurch, New Zealand.PatientsA volunteer sample of 70 patients, aged 16 to 42 years, with recurrent tonsillitis. Seven patients were excluded.InterventionsAfter randomization, one group received 5 mL of 0.5% bupivacaine hydrochloride in the peritonsillar space, with the patient under general anesthesia. The other group received 5 mL of isotonic sodium chloride solution, with the patient under general anesthesia. Both groups underwent surgery with a standardized surgical and anesthetic technique.Main Outcome MeasuresPostoperative pain was assessed with a visual analog scale at 15 minutes and 1, 4, 12, 16, and 24 hours after the procedure. Postoperative analgesic requirement, length of admission, and antiemetic requirement were also assessed.ResultsNo statistical difference was found between the 2 groups for postoperative pain by means of the visual analog scale at any time interval, nor was any statistical difference found for the other variables measured. A trend toward less pain in the immediate postoperative period in the group receiving bupivacaine was noted.ConclusionNo statistically significant benefit is found for use of preincisional bupivacaine in tonsillectomy.

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