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首页> 外文期刊>Journal of bone and mineral metabolism >Beneficial effects of intravenous pamidronate treatment in children with osteogenesis imperfecta under 24 months of age
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Beneficial effects of intravenous pamidronate treatment in children with osteogenesis imperfecta under 24 months of age

机译:静脉注射帕米膦酸治疗24岁以下成骨不全患儿的有益效果

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Osteogenesis imperfecta (OI) is an inherited disorder characterized by bone fragility and low bone mass. Low bone density and fracture is a cause of morbidity. Limited data exists on bisphosphonate treatment in patients under 24 months of age. The objective of the study was to examine the safety and efficacy of pamidronate in children under 24 months with OI. To do so, we carried out a retrospective chart review and analysis of OI patients started on intravenous pamidronate under 24 months of age. Pamidronate was administered in three-day cycles. Growth, the number of fractures, and lumbar bone mineral densities were recorded both prior to and after treatment initiation. A total of 18 patients were reviewed. Five were classified as OI type I, seven were type III, and six were type IV. The mean age at treatment initiation was 12 months (range 11 days to 23 months). The mean lumbar z score at baseline was -3.63, which improved to -1.53 at one year (P < 0.01) and 0.79 (P < 0.01) at the end of the study. The fracture rate improved from 68 fractures in 209 months (0.32 fractures/patient-month) before treatment to 41 fractures in 1,248 months (0.03 fractures/patient-month) post-treatment (P < 0.05). Height standard deviation score (SDS) was conserved from baseline to end of study (-2.12 +/- A 2.45 vs. -2.45 +/- A 2.73) (P = 0.05) with an average follow-up of 73 months. The only adverse effect recorded in six infants was fever during the initial pamidronate infusion. Treatment with intravenous pamidronate is safe, significantly improves lumbar bone mineral density (L-BMD), and reduces fracture rates in young infants with OI while preserving linear growth.
机译:成骨不全症(OI)是一种遗传性疾病,以骨脆性和低骨量为特征。低骨密度和骨折是发病的原因。在24个月以下的患者中,有关双膦酸盐治疗的数据有限。这项研究的目的是检查帕米膦酸在24个月以下OI患儿中的安全性和有效性。为此,我们进行了回顾性图表审查,并分析了24个月以下开始接受静脉注射帕米膦酸治疗的OI患者。帕米膦酸以三天的周期给药。在治疗开始之前和之后都记录了生长,骨折数量和腰椎骨密度。总共对18例患者进行了检查。五类被归为I型OI,七类为III型,六类为IV型。治疗开始时的平均年龄为12个月(11天至23个月不等)。基线时平均腰椎z评分为-3.63,一年后提高至-1.53​​(P <0.01),研究结束时提高至0.79(P <0.01)。骨折率由治疗前的209个月内的68例骨折(0.32例/患者/月)提高到治疗后1,248个月中的41例(0.03例/患者/月)(P <0.05)。从基线到研究结束,身高标准偏差评分(SDS)保持不变(-2.12 +/- A 2.45对-2.45 +/- A 2.73)(P = 0.05),平均随访73个月。记录的6名婴儿中唯一的不良反应是初次帕米膦酸盐输注时发烧。静脉注射帕米膦酸治疗是安全的,可显着提高OI婴儿的腰骨矿物质密度(L-BMD),并降低骨折率,同时保持线性增长。

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