医学
骨质疏松症
糖皮质激素
重症监护医学
内科学
作者
Michael Heffernan,Kenneth G. Saag,June K. Robinson,Jeffrey P. Callen
出处
期刊:JAMA
[American Medical Association]
日期:2006-03-14
卷期号:295 (11): 1300-1300
被引量:27
标识
DOI:10.1001/jama.295.11.1300
摘要
Brett T. Summey, MD; Gil Yosipovitch, MDObjective: To raise awareness of the new treatment options and current recommendations among dermatologists treating patients with systemic corticosteroids.Data Sources: MEDLINE peer-reviewed publications.Study Selection: English language and clinical pertinence to corticosteroid-induced osteoporosis.Data Extraction: Pertinent information on pathophysiologic, epidemiologic, clinical trial, cost-effectiveness, and treatment option data regarding corticosteroid-induced osteoporosis.Data Synthesis: Comprehensive summary of published data on the pathophysiologic, epidemiologic, clinical, and treatment data and current practice guidelines regarding corticosteroid-induced osteoporosis; creation of an algorithmic management approach for patients treated with long-term oral corticosteroids.Conclusions: Glucocorticoid-induced bone loss is the most predictable and debilitating complication of prolonged administration of systemic corticosteroids. Every dermatologist prescribing systemic corticosteroids must be aware of corticosteroid-induced osteoporosis and ensure that every patient is receiving general measures to prevent it. Despite efficacious preventive and therapeutic options, actual implementation of these strategies remains unacceptably low. Based on currently available evidence, the first choice for prevention and treatment of glucocorticoid-induced osteoporosis should be a potent oral bisphosphonate such as alendronate (70 mg/wk) or risedronate sodium (35 mg/wk). For patients with severe osteoporosis or patients with active osteoporotic fractures, the anabolic agent teriparatide (recombinant fragmented parathyroid hormone) should be considered as a first-line option for up to 2 years.
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