Fracture and non-fracture pain in children with osteogenesis imperfecta

Philip Zack1, Linda Franck, Catherine Devile

  • 1North West Thames Regional Genetics Service, Harrow, United Kingdom. p.zack@virgin.net

Insights

Children with osteogenesis imperfecta (OI) experience significant acute fracture pain and chronic non-fracture pain, impacting daily activities. Current pain management strategies may be insufficient, as many children report moderate to severe pain despite treatment.

Area of Science:

  • Pediatric Rheumatology
  • Pain Management
  • Genetics

Background:

  • Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by brittle bones.
  • Chronic pain is a significant challenge for children with OI, affecting their quality of life.

Purpose of the Study:

  • To characterize and compare acute fracture pain with chronic non-fracture pain in pediatric patients with OI.
  • To identify differences in pain intensity, quality, coping mechanisms, and treatment efficacy.

Main Methods:

  • A prospective study involving 35 children (aged 5-18) with OI from a UK national service.
  • Utilized questionnaires for fracture pain and 7-day diaries for non-fracture pain, assessing pain intensity, location, quality, coping, and analgesia use.

Main Results:

  • Fracture pain was more intense and affected daily activities more than non-fracture pain (p<0.001).
  • Affective descriptors were less common for non-fracture pain (p=0.002).
  • Children used different coping strategies for fracture (approach) versus non-fracture (distraction) pain (p<0.01).

Conclusions:

  • Pain is prevalent in children with OI, manifesting as both acute and chronic conditions that impair daily functioning.
  • Existing pain management, including analgesics and coping strategies, appears suboptimal for many children with OI.
  • Bisphosphonate treatment did not significantly alter non-fracture pain characteristics.
Abstract

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