Key result
Intraoperative injection of liposomal bupivacaine during pediatric palatoplasty yielded average inpatient FLACC pain scores of 3.8/10 and 8.5 mg hydrocodone equivalents used over a 2.1-day stay.
Why the study?
Does intraoperative liposomal bupivacaine provide safe and effective postoperative pain control in pediatric patients undergoing palatoplasty?
Observational (n=27)
No
Does intraoperative liposomal bupivacaine provide safe and effective postoperative pain control in pediatric patients undergoing palatoplasty?
Intraoperative liposomal bupivacaine appears safe and may provide adequate pain control with low opioid use in pediatric patients undergoing palatoplasty.
LB may improve pediatric palatoplasty pain control; hypothesis-generating and requires prospective trials before practice change.
Introduction: Liposomal bupivacaine (LB) is a long-acting local anesthetic reported to decrease postoperative pain in adults. The authors demonstrate the safe use of LB in pediatric patients with improved pain control following palatoplasty. Materials and Methods: Retrospective patient series of all single-surgeon palatoplasty patients treated at a tertiary craniofacial center from August 2014 to December 2015 were included. All patients received 1.3% LB intraoperatively as greater palatal nerve and surgical field blocks in 2-flap V–Y pushback palatoplasty. Postoperative oral intake, opioids administered, duration of hospitalization, and FLACC (face, legs, activity, cry, consolability) pain scores were measured. Results: Twenty-seven patients (16 males and 11 females, average age of 10.8 months, weight 8.8 kg) received 2.9 ± 0.9 mL (2.6 ± 1.9 mg/kg) 1.3% LB. Average FLACC scores were 2.4 ± 2.2/10 in the postanesthesia care unit and 3.8 ± 1.8/10 while inpatients. Oral intake was first tolerated 10.3 ± 11.5 hours postoperatively and tolerated 496.4 ± 354.2 mL orally in the first 24 hours postoperatively. Patients received 8.5 ± 8.4 mg hydrocodone equivalents (0.46 ± 0.45 mg/kg per d hydrocodone equivalents) and were discharged 2.1 ± 1.3 days postoperatively. Opioid-related adverse events included emesis in 7.4% and pruritis in 3.7% of patients. Conclusions: The LB may be used safely in pediatric patients. Intraoperative injection of LB during palatoplasty can yield low postoperative opioid use and an early and adequate volume of oral intake over an average hospital stay. Further cost-efficacy studies of LB are needed to assess its value in pediatric plastic surgery.
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Day et al. (2018) conducted an observational in Postoperative pain following palatoplasty (n=27). Liposomal bupivacaine (LB) was evaluated on Postoperative oral intake, opioids administered, duration of hospitalization, and FLACC pain scores. Intraoperative injection of liposomal bupivacaine during pediatric palatoplasty yielded average inpatient FLACC pain scores of 3.8/10 and 8.5 mg hydrocodone equivalents used over a 2.1-day stay.
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