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Electrophysiological Measurements and Analysis of Nociception in Human Infants
Published on: December 20, 2011
Preemptive analgesic effectiveness of single dose intravenous ibuprofen in infants undergoing cleft palate repair: a
Zhe Zhe Peng1, Yan Ting Wang1, Ma Zhong Zhang1
1Department of Anesthesiology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Insights
Preoperative intravenous ibuprofen effectively reduced opioid use in infants after cleft palate surgery. This approach offers a safe and effective strategy for managing postoperative pain, minimizing the need for potentially risky opioid analgesics.
Area of Science:
- Pediatric Anesthesiology
- Pain Management
- Surgical Recovery
Background:
- Cleft palate repair (palatoplasty) is typically performed in infants aged 9-18 months.
- Postoperative pain is a significant concern following palatoplasty.
- Opioid use for analgesia is limited due to risks of respiratory adverse events in infants.
Purpose of the Study:
- To evaluate the efficacy of preemptive intravenous ibuprofen in reducing postoperative opioid requirements in infants undergoing palatoplasty.
- To assess the safety profile of intravenous ibuprofen in this patient population.
Main Methods:
- A prospective randomized clinical trial involving 40 infants (9-24 months) undergoing palatoplasty.
- Participants received either intravenous ibuprofen (10 mg/kg) or normal saline before surgery.
- Postoperative pain was assessed using the Children and Infants Postoperative Pain Scale (CHIPPS), with fentanyl used for rescue analgesia.
Main Results:
- The intravenous ibuprofen group required significantly less postoperative fentanyl for pain management compared to the placebo group (p<0.001).
- No significant differences were observed in the time to first rescue analgesia or surgical blood loss between groups.
- No significant adverse events were reported within 24 hours post-surgery in either group.
Conclusions:
- Preemptive intravenous administration of ibuprofen at induction provides an opioid-sparing effect in the early postoperative period for infants undergoing palatoplasty.
- This method appears to be safe, with no significant adverse effects observed.
Background:
Correction surgery for cleft palate is recommended between 9 and 18 months of age. Patients suffer from acute pain after palatoplasty. Clinicians are hesitant to use opioids for analgesia concerning the potential high risk of respiratory adverse events. Intravenous ibuprofen perhaps be a suitable adjuvant to pain relief. We try to assess whether preoperative administration of intravenous ibuprofen can decrease opioid requirements following cleft palate repair in infants.
Methods:
This single center prospective randomized clinical trial was performed from February to April 2021 at Department of Anesthesiology in Shanghai Children's Medical Center. Forty patients ASA I-II, aged 9-24 months with isolated cleft palate and undergoing palatoplasty were randomized in a 1:1 ratio to receive either a single dose of 10 mg/kg ibuprofen intravenously or normal saline at induction. Children and infants postoperative pain scale (CHIPPS) was used for pain assessment. Those patients CHIPPS pain score equal or higher than 4 received analgesic rescue with titrating intravenous fentanyl 0.5 μg/kg and repeated in 10 min if required. The primary outcome was the amount of postoperative fentanyl used for rescue analgesia in postanesthesia care unit (PACU).
Results:
Patients (n = 20 in each group) in IV-Ibuprofen group required less postoperative fentanyl than those in placebo group (p<0.001). There was no significant difference between two groups in first rescue analgesia time (p = 0.079) and surgical blood loss (p = 0.194). No incidence of obvious adverse events had been found within the first 24 h after surgery in both groups.
Conclusions:
Preemptive intravenous administration ibuprofen 10 mg/kg at induction had a significant opioid sparing effect in early postoperative period without obvious adverse effects in infants undergoing palatoplasty.
Trial Registration:
CHICTR, CTR2100043718, 27/02/2021 http://www.chictr.org.cn/showproj.aspx?proj=122187.
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