An evaluation of the safety and efficacy of administering rofecoxib for postoperative pain management.

Author(s): Joshi W, Connelly NR, Reuben SS, Wolckenhaar M, Thakkar N

Affiliation(s): Department of Anesthesiology, Baystate Medical Center, Springfield, Massachusetts 01199, USA.

Publication date & source: 2003-07, Anesth Analg., 97(1):35-8, table of contents.

Publication type: Clinical Trial; Randomized Controlled Trial

The goal of our study was to evaluate the analgesic efficacy and safety of administering rofecoxib (1 mg/kg), a cyclo-oxygenase (COX)-2 selective nonsteroidal antiinflammatory drug, before pediatric tonsillectomy. Sixty-six patients, aged 3-11 yr, scheduled to undergo tonsillectomy received either placebo or rofecoxib (1 mg/kg). There were no significant differences between the two study groups with respect to demographics and blood loss. We found that the pain scores were significantly lower in the rofecoxib group compared with the control group at 2 h (P < 0.05) and 24 h (P < 0.006). The incidence of nausea (P < 0.03) and vomiting (P < 0.004) at home was more frequent in the control group than in the rofecoxib group. We conclude that a single preoperative dose of rofecoxib resulted in less vomiting and lower 24-h pain scores in pediatric patients undergoing an elective tonsillectomy. IMPLICATIONS: In children undergoing tonsillectomy, a single preoperative dose of rofecoxib decreases 2- and 24-h pain and decreases nausea and vomiting at home.