Oral Analgesics Utilization for Children With Musculoskeletal Injury (OUCH Trial): An RCT

Author:

Le May Sylvie12,Ali Samina34,Plint Amy C.56,Mâsse Benoit2,Neto Gina7,Auclair Marie-Christine2,Drendel Amy L.58,Ballard Ariane123,Khadra Christelle123,Villeneuve Edith9,Parent Stefan10,McGrath Patrick J.11,Leclair Grégoire12,Gouin Serge13,

Affiliation:

1. Faculties of Nursing and

2. CHU Sainte-Justine Research Center, Montreal, Quebec, Canada;

3. Women and Children’s Health Research Institute, Edmonton, Alberta, Canada;

4. Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada;

5. Departments of Pediatrics and

6. Emergency Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada;

7. Emergency Department, Children’s Hospital of Eastern Ontario, Ottawa, Ontario, Canada;

8. Emergency Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin;

9. Departments of Anesthesia and

10. Surgery, and

11. IWK Health Centre, Nova Scotia Health Authority and Dalhousie University, Halifax, Nova Scotia, Canada

12. Pharmacy, University of Montreal, Montreal, Quebec, Canada;

13. Division of Emergency Medicine, Department of Pediatrics, CHU Sainte-Justine, Montreal, Quebec, Canada; and

Abstract

BACKGROUND: Musculoskeletal injuries (MSK-Is) are a common and painful condition among children that remains poorly treated in the emergency department (ED). We aimed to test the efficacy of a combination of an anti-inflammatory drug with an opioid for pain management of MSK-I in children presenting to the ED. METHODS: In this randomized, double-blinded, placebo-controlled trial, we enrolled children between 6 and 17 years presenting to the ED with an MSK-I and a pain score >29 mm on the visual analog scale (VAS). Participants were randomly assigned to oral morphine (0.2 mg/kg) + ibuprofen (10 mg/kg) (morphine + ibuprofen) or morphine (0.2 mg/kg) + placebo of ibuprofen or ibuprofen (10 mg/kg) + placebo of morphine. Primary outcome was children with VAS pain score <30 mm at 60 minutes postmedication administration. RESULTS: A total of 501 participants were enrolled and 456 were included in primary analyses (morphine + ibuprofen = 177; morphine = 188; ibuprofen = 91). Only 29.9% (morphine + ibuprofen), 29.3% (morphine), and 33.0% (ibuprofen) of participants achieved the primary outcome (P = .81). Mean VAS pain reduction at 60 minutes were −18.7 (95% confidence interval [CI]: −21.9 to −16.6) (morphine + ibuprofen), −17.0 (95% CI: −20.0 to −13.9) (morphine), −18.6 (95% CI: −22.9 to −14.2) (ibuprofen) (P = .69). Children in the morphine + ibuprofen group (P < .001) and in the morphine group (P < .001) experienced more side effects than those in the ibuprofen group. No serious adverse event was reported. CONCLUSIONS: Combination of morphine with ibuprofen did not provide adequate pain relief for children with MSK-I in the ED. None of the study medication provided an optimal pain management because most of children did not reach a mild pain score (NCT02064894).

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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