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Published on: November 6, 2019
Parecoxib sodium reduces the need for opioids after tonsillectomy in children: a double-blind placebo-controlled
Xiuze Li1, Mengjun Zhou2, Qing Xia3
1Department of Anesthesiology, Mianyang Central Hospital, 12 Changjia Lane, Mianyang, 621000, Sichuan, China. lxz123@126.com.
Insights
Intravenous parecoxib sodium effectively manages pediatric tonsillectomy pain, reducing the need for morphine and lowering the incidence of postoperative nausea and vomiting (PONV). This treatment offers significant pain relief for children undergoing the procedure.
Area of Science:
- Pediatric Anesthesiology
- Pain Management
- Pharmacology
Background:
- Postoperative pain is a significant concern following pediatric tonsillectomy.
- Effective pain management strategies are crucial for patient recovery and well-being.
Purpose of the Study:
- To evaluate the analgesic efficacy of intravenous parecoxib sodium in children undergoing tonsillectomy.
- To compare parecoxib sodium with placebo in terms of pain control and adverse effects.
Main Methods:
- A prospective randomized double-blind placebo-controlled trial involving 60 children aged 3-7 years.
- Participants received either intravenous parecoxib sodium (1 mg·kg⁻¹) or saline post-anesthesia induction.
- Outcomes measured included rescue morphine requirements, time to first analgesic, pain scores, and adverse events like PONV.
Main Results:
- Fewer children receiving parecoxib sodium required rescue morphine (57% vs. 83% for placebo).
- The time to the first rescue analgesic was significantly longer in the parecoxib group (193 min vs. 132 min).
- Parecoxib sodium reduced pain scores and the incidence of postoperative nausea and vomiting (PONV).
Conclusions:
- Intravenous parecoxib sodium (1 mg·kg⁻¹) is an effective analgesic for pediatric tonsillectomy.
- It demonstrates a morphine-sparing effect and reduces PONV.
- This intervention improves postoperative pain control in pediatric patients.
Objective:
Postoperative pain is a common phenomenon after pediatric tonsillectomy. This prospective randomized double-blind placebo-controlled clinical trial was performed to evaluate the analgesic efficacy of intravenous parecoxib sodium in children undergoing tonsillectomy.
Methods:
Sixty children (American Society of Anesthesiologists physical status I-III, aged three to seven years, and scheduled to undergo elective tonsillectomy under general anesthesia) were randomly allocated into one of two groups to receive intravenous parecoxib sodium 1 mg·kg(-1) (Group P, n = 30) or the same volume of saline (Group S, n = 30) just after induction of general anesthesia. Between-group comparisons were made for the number of patients requiring rescue morphine, total number of doses of postoperative rescue morphine, time to first rescue analgesic, postoperative pain and sedation scores, and adverse effects.
Results:
Rescue morphine was given to more children in Group S (25/30, 83%) than in Group P (17/30, 57%) [relative risk (RR), 1.5; 95% confidence interval (CI), 1.0 to 2.1; P = 0.024]. The mean (SD) time to first rescue analgesic was shorter in Group S than in Group P [132 (54) min vs 193 (78) min, respectively; mean difference, 61; 95% CI, 26.6 to 96.1; P = 0.001]. The median (interquartile range [IQR]) Children's Hospital of Eastern Ontario Pain Scale scores in the postanesthesia care unit were lower in Group P than in Group S (7 [5-8] vs 9 [8-11], respectively; P = 0.001). The incidence of postoperative nausea and vomiting (PONV) was higher in Group S than in Group P [11/30 (37%) vs 4/30 (13%), respectively; RR, 2.8; 95% CI, 1.0 to 7.7; P = 0.037].
Conclusions:
A single intravenous injection of parecoxib sodium 1 mg·kg(-1) after anesthesia induction is an effective method for the control of postoperative pain. It provides a morphine-sparing effect, prolongs the time to first rescue analgesic, and reduces PONV in children undergoing tonsillectomy.
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