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Updated: Jun 20, 2026

Pseudofracture: An Acute Peripheral Tissue Trauma Model
Published on: April 18, 2011
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.
Aim:
To describe and compare the characteristics of acute fracture and chronic non-fracture pain in children with osteogenesis imperfecta (OI).
Methods:
A questionnaire about fracture-related pain and prospective 7-d diary about non-fracture-related pain was completed by a random sample of 35 children aged 5-18 from a UK national OI service. Main outcome measures included pain intensity, location, frequency, quality, coping strategies and analgesia use.
Results:
Most children reported moderate to severe pain associated with fractures and less intense non-fracture pain (p<0.001). Pain intensity was significantly higher in the children who used analgesics (p<0.001). The quality of fracture and non-fracture pain differed only for affective words, which were less frequently used to describe non-fracture pain (p=0.002). More activities of daily living (ADLs) were affected by fracture pain than by non-fracture pain (p<0.001). Children reported more frequent use of approach coping strategies with fracture pain and more frequent use of distraction for non-fracture pain (p<0.01). There were no differences in non-fracture pain intensity, duration, quality, effect on ADLs or coping between children who did or did not take bisphosphonates.
Conclusions:
Pain is a common occurrence for children with OI and is both acute and chronic in nature, interfering with children's daily living activities. OI pain may not be optimally treated because many children experienced moderate to severe pain despite use of analgesics and/or coping strategies.
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