Children and the risk of fractures caused by oral corticosteroids
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Published on: March 29, 2018
T P van Staa1, C Cooper, H G M Leufkens
1MRC Environmental Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton, United Kingdom.
Insights
Frequent oral corticosteroid use in children increases fracture risk, particularly for humerus fractures. Stopping medication normalized risk, suggesting treatment patterns are key. This highlights a need for careful monitoring in pediatric patients.
Area of Science:
- Pediatric Endocrinology
- Pediatric Orthopedics
- Pharmacovigilance
Background:
- Oral corticosteroids (OCS) are widely used in children but their association with fracture risk is not well-established.
- Existing data primarily focuses on adult populations, leaving a knowledge gap in pediatric OCS use and bone health.
Purpose of the Study:
- To investigate the association between oral corticosteroid use and fracture incidence in children aged 4-17 years.
- To identify specific OCS treatment patterns linked to increased fracture risk in pediatric patients.
Main Methods:
- Retrospective cohort study utilizing UK General Practice Research Database.
- Matched case-control analysis comparing children with fractures to those without, analyzing OCS exposure (frequency, dosage).
Main Results:
- Children receiving four or more courses of OCS had a 32% increased odds of fracture (OR 1.32).
- Humerus fracture risk was doubled in children with frequent OCS use (OR 2.17).
- Daily prednisolone doses of 30 mg or more also correlated with elevated fracture risk (OR 1.24).
Conclusions:
- Frequent OCS use in children is associated with a significantly increased risk of fracture.
- The underlying disease severity cannot be fully disentangled from OCS effects, but frequent OCS users require closer fracture risk monitoring.
- Discontinuation of OCS returned fracture risk to baseline levels, suggesting a direct treatment effect or consequence of disease activity.
Abstract:
Oral corticosteroids are known to increase the risk of fracture in adults, but their effects in children remain uncertain. The medical records of general practitioners in the United Kingdom (from the General Practice Research Database) were used to estimate the incidence rates of fracture of children ages 4-17 years taking oral corticosteroids (n = 37,562) and of control children taking nonsystemic corticosteroids (n = 345,748). Each child with a fracture (n = 22,846) was subsequently matched by age, sex, practice, and calendar time to one child without a fracture. The average duration of treatment was 6.4 days (median, 5 days). The risk of fracture was increased in children with a history of frequent use of oral corticosteroids; children who received four or more courses of oral corticosteroids had an adjusted odds ratio (OR) for fracture of 1.32 (95% CI, 1.03-1.69). Of the various fracture types, the risk of humerus fracture was doubled in children who received four or more courses of oral corticosteroids (adjusted OR, 2.17 [1.01-4.67]). Fracture risk was also increased among children using 30 mg prednisolone or more each day (adjusted OR for fracture, 1.24 [1.00-1.52]) and among those receiving four or more courses of oral corticosteroids (OR, 1.32 [1.03-1.69]). Children who stopped taking oral corticosteroids had a comparable risk of fracture to those in the control group. Our findings suggest that children who require more than four courses of oral corticosteroid as treatment for underlying disease are at increased risk of fracture. It is not entirely clear whether this relates directly to oral corticosteroid use or the underlying disease and its severity. Irrespective of these issues, this group of children is at increased risk of fracture.
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