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Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Bone densitometry in pediatric patients treated with pamidronate
Leslie E Grissom1, Heidi H Kecskemethy, Steven J Bachrach
1Department of Medical Imaging, Alfred I. duPont Hospital for Children, Nemours Children's Clinic, P.O. Box 269, Wilmington, DE 19899, USA. lgrissom@nemours.org
Insights
Intravenous pamidronate effectively increased bone mineral density in children with osteogenesis imperfecta and cerebral palsy. While bone density improved, children with osteogenesis imperfecta continued to experience fractures at a reduced rate.
Area of Science:
- Pediatric Endocrinology
- Pediatric Orthopedics
- Pediatric Rheumatology
Background:
- Bisphosphonate therapy, specifically pamidronate, is increasingly used for pediatric low bone mineral density.
- Children at high risk for fractures due to bone disorders or limited mobility are primary candidates for this treatment.
Purpose of the Study:
- To evaluate the efficacy of intravenous pamidronate in enhancing bone mineral density (BMD) in pediatric patients.
- Specifically assessed outcomes in children diagnosed with osteogenesis imperfecta (OI) and spastic quadriplegic cerebral palsy (CP).
Main Methods:
- Retrospective chart review of 38 children (20 with OI, 18 with CP) treated with pamidronate.
- Patients selected based on prior fractures or significantly low BMD.
- Treatment involved intravenous pamidronate administered every 2-8 months, with BMD assessed via dual-energy X-ray absorptiometry (DXA).
Main Results:
- Significant BMD improvements were observed in 31 of 32 patients.
- Average BMD increase was 78% in OI and 47.4% in CP patients at the lumbar spine.
- Femur BMD increased by 96% in OI and 65.7% in CP patients, exceeding age-expected growth.
- Children with CP ceased fracturing after treatment initiation; OI patients had a reduced fracture rate.
Conclusions:
- Intravenous pamidronate is effective for increasing BMD in pediatric patients with OI and CP.
- While both groups showed BMD gains, OI patients continued to fracture less frequently.
- Children with CP experienced significant BMD increases and fracture cessation.
Background:
Increasing numbers of children are being treated with the bisphosphonate pamidronate for low bone mineral density, particularly children with increased risk of fractures caused by bone disorders or low/non-weight bearing.
Objective:
To determine the effect of intravenous pamidronate on the bone mineral density of children with osteogenesis imperfecta and spastic quadriplegic cerebral palsy.
Materials And Methods:
Charts of 38 children with osteogenesis imperfecta (n=20) and spastic quadriplegic cerebral palsy (n=18) treated with pamidronate were retrospectively reviewed. Patients were selected for treatment because of prior fracture and/or abnormally low bone mineral density. All received intravenous pamidronate at two-month to eight-month intervals and were periodically examined using dual energy X-ray absorptiometry.
Results:
All patients had abnormally low bone mineral density prior to treatment. Lumbar spine bone mineral density and z-scores showed serial improvement in 31 of 32 patients. Spine bone mineral density increased 78+/-38.1% in OI and 47.4+/-39.0% in children with cerebral palsy. The area of greatest lateral distal femur bone mineral density improvement was in the metaphysis adjacent to the growth plate, with a 96+/-87.8% improvement in the osteogenesis imperfecta group and 65.7+/-55.2% improvement in the cerebral palsy group. Increases in bone mineral density exceeded that expected for age-specific growth. This was demonstrated by improvement in both spine and femur z-scores for both groups. No children with spastic quadriplegic cerebral palsy experienced fractures after the first week of treatment, whereas patients with osteogenesis imperfecta continued to have fractures but at a decreased rate.
Conclusions:
Intravenous pamidronate given at 3- to 4-month intervals proved to be effective in increasing bone mineral density in patients with osteogenesis imperfecta and spastic quadriplegic cerebral palsy. The greatest gains in bone mineral density were observed in the children with osteogenesis imperfecta, but they did continue to fracture, albeit at a decreased rate. Children with cerebral palsy gained bone mineral density and did not continue to fracture.
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