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Intravenous nalbuphine 50 microg x kg(-1) is ineffective for opioid-induced pruritus in pediatrics
Nao Nakatsuka1, Sean C Minogue, Joanne Lim
1Department of Anesthesia, Pharmacology and Therapeutics, BC Children's Hospital, University of British Columbia; Vancouver, British Columbia, Canada.
Insights
Nalbuphine did not effectively treat itching in pediatric patients after surgery. Further research is needed on the modified color analogue scale and pruritus intensity difference measures.
Area of Science:
- Anesthesiology
- Pharmacology
- Pediatric Medicine
Background:
- Postoperative pruritus (Pr) is a common side effect of opioid analgesia in pediatric patients.
- Effective management of opioid-induced pruritus is crucial for patient comfort and recovery.
- Nalbuphine is an opioid agonist-antagonist with potential anti-pruritic properties.
Purpose of the Study:
- To evaluate the efficacy of nalbuphine in treating postoperative opioid-induced pruritus in pediatric patients.
- To assess the effectiveness of a 50 microg x kg(-1) intravenous dose of nalbuphine compared to placebo.
Main Methods:
- A dual-site, tertiary care teaching center study enrolled 212 pediatric patients (age >= 7 years) receiving postoperative opioid analgesia.
- Pruritus intensity (PrI) was measured using a modified self-report color analogue scale (CAS).
- Patients with PrI score >= 5/10 were randomized to receive intravenous nalbuphine (50 microg x kg(-1)) or saline placebo.
Main Results:
- Of 212 subjects, 37 (20.1%) experienced pruritus intensity >= 5/10.
- Intravenous morphine, particularly patient-controlled analgesia (PCA), was associated with a high incidence of pruritus (68%).
- Nalbuphine (55.6%) and saline placebo (57.9%) showed similar efficacy in achieving a >= 50% pruritus intensity difference.
Conclusions:
- Nalbuphine 50 microg x kg(-1) intravenous administration is not effective in treating postoperative opioid-induced pruritus in pediatric patients.
- The modified CAS and pruritus intensity difference (PrID) metrics require further investigation for their utility.
- This preliminary report highlights the need for alternative strategies to manage pruritus in pediatric surgical patients.
Purpose:
This investigation evaluated the efficacy of nalbuphine in treating postoperative opioid-induced pruritus (Pr) in pediatric patients.
Methods:
After Ethics Board approval, the dual site, tertiary care teaching centre study recruited 212 subjects, age > or = seven years, who received opioid analgesia postoperatively. A modified, self-report colour analogue scale (CAS) scored pruritus intensity (PrI). Subjects who reported PrI score > or = 5/10 were randomized to treatment with nalbuphine 50 microg x kg(-1) iv (max 5 mg) or saline placebo. A pruritus intensity difference (PrID) > or = 50% was considered a positive outcome.
Results:
Of 260 subjects approached, 212 consented and 184 received opioids. Median age was 13 yr (range 7-19) and median weight was 51 kg (range 19.6-134.8 kg). Pruritus intensity > or = 5/10 occurred in 37 (20.1%) subjects. Intravenous morphine [patient-controlled analgesia (PCA)/continuous infusion] was associated with Pr in 68% of subjects over a wide dose range (9.4-63.2 mug.kg(-1).hr(-1)). Pruritus occurred in 36% of patients in the PCA group compared to continuous opioid infusion (27%) and epidural administration (27%). Pruritus intensity difference > or = 50% was achieved in 55.6% of nalbuphine and 57.9% of saline-treated subjects.
Conclusion:
This preliminary report suggests that nalbuphine 50 microg x kg(-1) iv is not effective in treating postoperative opioid-induced pruritus in pediatric patients. The modified CAS score and PrID warrant further investigation.
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