Effectiveness and safety of pamidronate treatment in nonambulatory children with low bone mineral density

Purpose Nonambulatory pediatric patients may have low bone mineral density (BMD) and increased risk of pathologic fractures. Though bisphosphonate therapy is the mainstream medical intervention in these children, clinical data regarding this treatment are limited. Therefore, this study aimed to eval...

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Glavni autori: Myeongseob Lee (Autor), Ahreum Kwon (Autor), Kyungchul Song (Autor), Hae In Lee (Autor), Han Saem Choi (Autor), Junghwan Suh (Autor), Hyun Wook Chae (Autor), Ho-Seong Kim (Autor)
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Izdano: Korean Society of Pediatric Endocrinology, 2024-02-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Myeongseob Lee  |e author 
700 1 0 |a Ahreum Kwon  |e author 
700 1 0 |a Kyungchul Song  |e author 
700 1 0 |a Hae In Lee  |e author 
700 1 0 |a Han Saem Choi  |e author 
700 1 0 |a Junghwan Suh  |e author 
700 1 0 |a Hyun Wook Chae  |e author 
700 1 0 |a Ho-Seong Kim  |e author 
245 0 0 |a Effectiveness and safety of pamidronate treatment in nonambulatory children with low bone mineral density 
260 |b Korean Society of Pediatric Endocrinology,   |c 2024-02-01T00:00:00Z. 
500 |a 2287-1012 
500 |a 2287-1292 
500 |a 10.6065/apem.2346028.014 
520 |a Purpose Nonambulatory pediatric patients may have low bone mineral density (BMD) and increased risk of pathologic fractures. Though bisphosphonate therapy is the mainstream medical intervention in these children, clinical data regarding this treatment are limited. Therefore, this study aimed to evaluate the effectiveness and safety of bisphosphonate therapy in such children. Methods We conducted a retrospective study of 21 nonambulatory children (Gross Motor Function Classification System level V) with BMD z-score ≤ -2.0 who were treated with intravenous pamidronate for at least 1 year. These patients received pamidronate every 4 months at a dose of 1.0 to 3.0 mg/kg for each cycle and had regular follow-ups for at least 1 year. The main outcome measures were changes in BMD, risk rate of fracture, biochemical data, and adverse events. Results The average duration of pamidronate treatment was 2.0±0.9 years, and the mean cumulative dose of pamidronate according to body weight was 7.7±2.5 mg/kg/yr. After treatment, the mean lumbar spine bone mineral content, BMD, and height-for-age-z-score-adjusted BMD z-score (BMDhazZ) significantly improved. The relative risk of fracture after treatment was 0.21 (p=0.0032), suggesting that pamidronate treatment reduced fracture incidence significantly. The increase in the average dose per body weight in each cycle significantly increased the changes in BMDhazZ. Conclusions Pamidronate treatment improved the bone health of nonambulatory children with low bone density without any significant adverse events. Independent of cumulative dosage and duration of treatment, the effectiveness of pamidronate increased significantly with an increase in the average dose per body weight in subsequent cycles. 
546 |a EN 
690 |a osteoporosis 
690 |a bone density 
690 |a diphosphonates 
690 |a pamidronate 
690 |a immobilization 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 1, Pp 46-53 (2024) 
787 0 |n http://e-apem.org/upload/pdf/apem-2346028-014.pdf 
787 0 |n https://doaj.org/toc/2287-1012 
787 0 |n https://doaj.org/toc/2287-1292 
856 4 1 |u https://doaj.org/article/c725358358bc40f4befd2bc3f4f64a85  |z Connect to this object online.