Joshi Kiranjit K, Siafarikas Aris, Prince Richard
University of Western Australia Perth WA Australia.
Perth Children's Hospital Department of Endocrinology and Diabetes Perth WA Australia.
JBMR Plus. 2023 Jun 21;7(9):e10782. doi: 10.1002/jbm4.10782. eCollection 2023 Sep.
The fracture experience of children and adolescents with osteogenesis imperfecta (OI) type 1 is not well described in the literature. We present data on symptomatic long bones and axial skeleton fractures of all patients aged 0 to 18 years with OI type 1 seen at a specialized bone clinic in Western Australia in the period 2008 to 2020 using a retrospective chart review method. The cohort consisted of 44 patients (21 males, 23 females). Median (interquartile range [IQR]) age was 11.3 (6.2 to 17) years, giving a total of 520 patient-years in the study during which 197 fractures were experienced. The mean fracture rate was 379 fractures per 1000 patient-years (95% confidence interval [CI]: 310 to 440); however, the experience for fractures varied from ≤1 fracture in 23% ( = 10) to two to 20 in 77% ( = 34) of the cohort. Twenty-one patients (48.5%) received bisphosphonates during the study period. In logistic regression, age, but not sex or family history of OI, was a significant predictor of fracture risk. The highest total fracture rate was observed in the age group 0 to <3 years at 469 fractures/1000 patient-years, which declined to 140 fractures/1000 patient-years in the age group 15 to 18 years. The lower limbs were the site of 49.7% of all fractures. The highest rate for lower limb fracture was in the age group 0 to <3 years at 331 fractures/1000 patient-years, decreasing to 0 fractures/1000 patient-years in the age group 15 to 18 years. Upper limb fracture rates increased from 100 fractures/1000 patient-years in the 0 to <3 years age group to 307 fractures/1000 patient-years in the 9 to <12 years age group and then declining to 70 fractures/1000 years in the 15 to 18 years age group. In pediatric patients with OI type 1, fracture risk is highest in early life, especially in the lower limbs. Multidisciplinary care of children with OI should have a particular focus on strategies to prevent these fractures. © 2023 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
关于1型成骨不全症(OI)儿童和青少年的骨折经历,文献中描述得并不充分。我们采用回顾性病历审查方法,呈现了2008年至2020年期间在西澳大利亚一家专业骨病诊所就诊的所有0至18岁1型OI患者的有症状长骨和轴向骨骼骨折的数据。该队列由44名患者组成(21名男性,23名女性)。中位(四分位间距[IQR])年龄为11.3(6.2至17)岁,研究期间共有520患者年,在此期间共发生197次骨折。平均骨折率为每1000患者年379次骨折(95%置信区间[CI]:310至440);然而,该队列中23%(n = 10)的患者骨折次数≤1次,77%(n = 34)的患者骨折次数为2至20次。21名患者(48.5%)在研究期间接受了双膦酸盐治疗。在逻辑回归分析中,年龄是骨折风险的显著预测因素,而性别或OI家族史则不是。在0至<3岁年龄组中观察到的总骨折率最高,为469次骨折/1000患者年,在15至18岁年龄组中降至140次骨折/1000患者年。下肢是所有骨折部位的49.7%。下肢骨折率最高的是0至<3岁年龄组,为331次骨折/1000患者年,在15至18岁年龄组中降至0次骨折/1000患者年。上肢骨折率从0至<3岁年龄组的100次骨折/1000患者年增加到9至<12岁年龄组的307次骨折/1000患者年,然后在15至18岁年龄组中降至70次骨折/1000患者年。在1型OI的儿科患者中,骨折风险在生命早期最高,尤其是在下肢。对OI患儿的多学科护理应特别关注预防这些骨折的策略。© 2023作者。由Wiley Periodicals LLC代表美国骨与矿物质研究学会出版。