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Clinical Trial
. 1996 Mar;122(3):261-3.
doi: 10.1001/archotol.1996.01890150039007.

Preincisional infiltration with bupivacaine in tonsillectomy

Affiliations
Clinical Trial

Preincisional infiltration with bupivacaine in tonsillectomy

M Johansen et al. Arch Otolaryngol Head Neck Surg. 1996 Mar.

Abstract

Objective: To investigate the value of preincisional peritonsillar infiltration of bupivacaine hydrochloride before tonsillectomy under general anesthesia.

Design: Double-blind trial with two groups comparing 0.25% bupivacaine with placebo (normal saline). The patients were followed up for 10 days after surgery.

Setting: Department of Otolaryngology, University Hospital of Aarhus (Denmark).

Patients: Men and women 18 to 40 years of age referred to our department for bilateral tonsillectomy, but with no sign of acute infection or suspected malignant neoplasm. Twenty-six patients entered the study; five were excluded for failure to complete the postoperative data; and two, one from each group, had postoperative bleeding. Data from 19 patients were analyzed, nine in the bupivacaine group and 10 in the placebo group.

Intervention: One group had 5 mL of 0.25% bupivacaine hydrochloride (Marcaine) infiltrated around each tonsil, the other an identical placebo (normal saline) infiltration.

Outcome measures: A visual analogue scale was used as the primary efficacy measure. The daily intake of analgesics and a possible weight loss were registered.

Results: A notably lower score on the visual analogue scale was found in the bupivacaine group.

Conclusions: Preoperative blocking of nociceptive impulses reduces prolonged postoperative pain, but no reduction in the intake of analgesics was found. Medication was insufficient for the first postoperative days.

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