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帕米膦酸盐与钙及骨化三醇补充剂治疗儿童和青少年类固醇诱导性骨质疏松症的随机对照试验尝试

Attempted randomized controlled trial of pamidronate versus calcium and calcitriol supplements for management of steroid-induced osteoporosis in children and adolescents.

作者信息

Brown J J, Zacharin M R

机构信息

Department of Endocrinology and Diabetes, Royal Children's Hospital, Parkville, Victoria, Australia.

出版信息

J Paediatr Child Health. 2005 Nov;41(11):580-2. doi: 10.1111/j.1440-1754.2005.00720.x.

Abstract

OBJECTIVES

To describe an attempted interventional trial for glucocorticoid-induced osteoporosis in children and adolescents and to discuss the reasons for trial failure to inform future interventional studies in this important group of patients.

METHODS

Prospective randomized controlled trial comparing the effect of bisphosphonate therapy with calcium and vitamin D supplementation on bone mineral accrual is described. For non-trial patients, retrospective analysis of the effect of calcium and vitamin D supplementation combined with bisphosphonate treatment on bone mineral accrual.

RESULTS

Only 12 patients were enrolled in the trial over 4 years. Bisphosphonate recipients (n = 5) had a mean annual percentage increase in lumbar spine bone mineral density of 8.76 +/- 5.2% compared to 6.6 +/- 4.0% in the calcium/vitamin-treated group (difference not significant). Mean annual change in lumbar spine areal bone mineral density in non-trial patients (n = 11) was 3.72 +/- 2.5%.

CONCLUSION

Conducting a randomized controlled trial in this group of corticosteroid users is difficult, given the unpredictable nature of the underlying disease and intermittent need for steroid treatment. The trial failed through inadequate recruitment combined with discontinued interventions.

摘要

目的

描述一项针对儿童和青少年糖皮质激素诱导性骨质疏松症的介入性试验,并讨论试验失败的原因,以便为这一重要患者群体未来的介入性研究提供参考。

方法

描述一项前瞻性随机对照试验,比较双膦酸盐疗法与补充钙和维生素D对骨矿物质积累的影响。对于非试验患者,回顾性分析补充钙和维生素D联合双膦酸盐治疗对骨矿物质积累的影响。

结果

4年期间仅有12名患者入组该试验。接受双膦酸盐治疗的患者(n = 5)腰椎骨矿物质密度的年平均百分比增加为8.76±5.2%,而钙/维生素治疗组为6.6±4.0%(差异不显著)。非试验患者(n = 11)腰椎面积骨矿物质密度的年平均变化为3.72±2.5%。

结论

鉴于潜在疾病的不可预测性以及对类固醇治疗的间歇性需求,在这组使用皮质类固醇的患者中进行随机对照试验很困难。该试验因招募不足以及干预措施中断而失败。

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