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Efficacy and Safety of Naldemedine for Opioid-Induced Constipation in Children
Rina Miura1, Tomoyuki Utano1, Yoriko Miura1
1Department of Pharmaceuticals, National Center for Child Health and Development, Tokyo, Japan.
Insights
Naldemedine effectively treated opioid-induced constipation (OIC) in pediatric patients, increasing bowel movements. However, diarrhea occurred in half of patients, sometimes requiring discontinuation, so caution is advised.
Area of Science:
- Pharmacology
- Pediatric Gastroenterology
Background:
- Opioid-induced constipation (OIC) is a common side effect of opioid therapy.
- Naldemedine is a peripherally acting opioid antagonist approved for OIC in adults.
- Limited data exists on naldemedine's efficacy and safety in pediatric populations.
Purpose of the Study:
- To evaluate the efficacy of naldemedine in treating OIC in pediatric patients.
- To assess the safety profile of naldemedine in this patient group.
Main Methods:
- Retrospective analysis of 32 pediatric patients with OIC treated with naldemedine.
- Efficacy assessed by bowel movement (BM) response (≥3 BMs in 7 days, +1 BM from baseline).
- Safety evaluated via adverse events (AEs) using Common Terminology Criteria for AEs v5.0.
Main Results:
- A BM response was observed in 11 of 13 evaluable patients (85%).
- Daily BM frequency significantly increased from 0.43 to 1.00 (p=0.025).
- Diarrhea was the most common AE (50%), with 3 patients discontinuing due to worsening symptoms (grade 1-2).
Conclusions:
- Naldemedine demonstrated efficacy in improving bowel function for pediatric OIC.
- Naldemedine is generally safe in pediatric patients, but diarrhea necessitates cautious use and monitoring.
- Further research is needed to establish optimal dosing for pediatric patients.
Abstract:
Background: Naldemedine, a peripherally acting opioid μ receptor antagonist, is effective for prevention of opioid-induced constipation (OIC); however, evidence on its use in children is limited. Objective: To evaluate the efficacy and safety of naldemedine in pediatric patients with OIC. Design, Setting/Subjects: Retrospective analysis of 32 pediatric patients with OIC treated with naldemedine in a single institution in Japan from June 2017 to March 2021. Measurements: Efficacy was evaluated in 13 evaluable patients with bowel movement (BM) response, defined as those with at least three BMs in the first 7 days after naldemedine initiation and an increase of at least one BM from baseline. Safety was evaluated by examining adverse events (AEs) based on the Common Terminology Criteria for AEs (v5.0). Results: BM response was recorded in 11 of the 13 patients (85%), and the number BMs per day significantly increased from 0.43 before naldemedine to 1.00 after naldemedine (p = 0.025). The most common AE was diarrhea, observed in 16 of the 32 patients (50%), and all instances were grade 1 or 2. In three of the 16 patients, naldemedine was discontinued owing to worsening diarrhea. Conclusions: In pediatric patients, naldemedine resulted in a high rate of BM response and increased the BM frequency, indicating its efficacy. In some patients, grade 2 diarrhea required naldemedine discontinuation, suggesting that it should be used with caution in pediatric patients. Further studies are warranted to determine the optimal naldemedine dose in pediatric patients.
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