Soybilgic Arzu, Tesher Melissa, Wagner-Weiner Linda, Onel Karen B
University of Illinois at Chicago, Chicago, IL, USA.
Pediatr Rheumatol Online J. 2014 Jul 9;12:24. doi: 10.1186/1546-0096-12-24. eCollection 2014.
The purpose of our study is to assess practices of North American pediatric rheumatologists regarding monitoring, prevention, and treatment of low bone mineral density (BMD) in children on long-term glucocorticoid treatment. Long-term glucocorticoid therapy is associated with accelerated bone loss. Children with JIA and lupus have low baseline BMD and incident vertebral fractures commonly occur in these groups of patients even after a relatively short period of time being on systemic glucocorticoids. There are no established guidelines for identification, prevention, and treatment of glucocorticoid-induced bone loss in children.
A cross-sectional online survey was conducted with 199 physicians who were listed in the ACR database as practicing pediatric rheumatology in North America.
86 physicians (43%) responded; 87% were board-certified in pediatric rheumatology. 95% used dual energy X-ray absorptiometry as their primary modality for assessing BMD. 79% "rarely" or "never" obtained a baseline BMD measurement prior to initiation of glucocorticoid therapy. 42% of respondents followed BMD annually. 93% "frequently" or "always" prescribed calcium for patients on long-term corticosteroid therapy; 81% "frequently" or "always" prescribed vitamin D. In patients diagnosed with osteoporosis, 35%-50 % of the practitioners "sometimes", "frequently" or "always" prescribed bisphosphonates. Bisphosphonates are prescribed at similar rates for male and female patients, and slightly more frequently for pubertal than for pre-pubertal patients. 96% of respondents "rarely" or "never" prescribed calcitonin for patients on long-term glucocorticoid therapy; 92% "rarely" or "never" prescribe this medication for patients with known osteopenia or osteoporosis.
Utilization of DXA in children on long-term corticosteroid therapy varies greatly among North American pediatric rheumatologists. Most respondents do not screen for low BMD on a regular basis despite acknowledging the risks of bone loss in this population. Broad consensus appears to be present among practitioners favoring the prescription of calcium and vitamin D for patients receiving long-term corticosteroid therapy. Relatively few respondents consistently recommend bisphosphonate therapy, even for patients with known low bone density; calcitonin is rarely used. These data underscore the need for studies to acquire specific data on bone loss, and its prevention and treatment in young patients on long-term glucocorticoid therapy.
我们研究的目的是评估北美儿科风湿病学家对长期接受糖皮质激素治疗的儿童低骨密度(BMD)进行监测、预防和治疗的实践情况。长期糖皮质激素治疗与骨质流失加速有关。幼年特发性关节炎(JIA)和狼疮患儿的基线骨密度较低,即使在接受全身性糖皮质激素治疗相对较短的时间后,这些患者群体中也常发生椎体骨折。目前尚无针对儿童糖皮质激素诱导性骨质流失的识别、预防和治疗的既定指南。
对199名在ACR数据库中列为在北美从事儿科风湿病学工作的医生进行了横断面在线调查。
86名医生(43%)回复;87%获得了儿科风湿病学委员会认证。95%使用双能X线吸收法作为评估骨密度的主要方法。79%在开始糖皮质激素治疗前“很少”或 “从不”进行基线骨密度测量。42%的受访者每年跟踪骨密度。93%“经常”或“总是”为长期接受皮质类固醇治疗的患者开钙;81%“经常”或“总是”开维生素D。在被诊断为骨质疏松症的患者中,35%-50%的从业者“有时”、“经常”或“总是”开双膦酸盐。双膦酸盐在男性和女性患者中的处方率相似,在青春期患者中的处方频率略高于青春期前患者。96%的受访者在长期接受糖皮质激素治疗的患者中“很少”或“从不”开降钙素;92%在已知骨质减少或骨质疏松的患者中“很少”或“从不”开这种药物。
北美儿科风湿病学家对长期接受皮质类固醇治疗的儿童使用双能X线吸收法(DXA)的情况差异很大。尽管认识到该人群存在骨质流失风险,但大多数受访者并未定期筛查低骨密度。从业者之间似乎普遍达成共识,赞成给长期接受皮质类固醇治疗的患者开钙和维生素D。相对较少的受访者始终推荐双膦酸盐治疗,即使是已知骨密度低的患者;降钙素很少使用。这些数据强调需要开展研究,以获取长期接受糖皮质激素治疗的年轻患者骨质流失及其预防和治疗的具体数据。