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每周使用双膦酸盐的长期疗效。

Long-term outcome of weekly bisphosphonates.

作者信息

Rizzoli René

机构信息

Division of Bone Diseases [WHO Collaborating Center for Osteoporosis Prevention], Department of Rehabilitation and Geriatrics, University Hospital, Geneva, Switzerland.

出版信息

Clin Orthop Relat Res. 2006 Feb;443:61-5. doi: 10.1097/01.blo.0000200249.12006.6e.

Abstract

UNLABELLED

Bisphosphonates currently are the preferred therapy for treating osteoporosis. Treatment with potent bisphosphonates such as alendronate or risedronate decreases biochemical markers of bone turnover and increases bone mineral density. These changes are associated with significant reductions in vertebral and nonvertebral fracture risk. Clinical trial data with up to 10 years of followup shows these agents are effective and well tolerated for long-term periods. Daily administration is effective and generally well tolerated. However, once weekly doses are more convenient, which may enhance long-term compliance and lead to more successful outcomes. The pharmacokinetics and mechanism of action predict the short-term and long-term skeletal effects and safety profile of once-weekly doses of bisphosphonates are similar to daily doses. These predictions are supported by authors of trials of up to 2 years who report once-weekly doses are therapeutically equivalent to daily doses in terms of BMD and biochemical markers of bone remodeling. Once-weekly bisphosphonate doses have safety and tolerability profiles as good as daily doses and are comparable with the placebo.

LEVEL OF EVIDENCE

Therapeutic study, Level V (expert opinion). See the Guidelines for Authors for a complete description of the levels of evidence.

摘要

未标注

双膦酸盐目前是治疗骨质疏松症的首选疗法。使用阿仑膦酸钠或利塞膦酸钠等强效双膦酸盐进行治疗可降低骨转换的生化指标,并增加骨矿物质密度。这些变化与椎体和非椎体骨折风险的显著降低相关。长达10年随访的临床试验数据表明,这些药物长期有效且耐受性良好。每日给药有效且通常耐受性良好。然而,每周一次给药更方便,这可能会提高长期依从性并带来更成功的结果。药代动力学和作用机制可预测双膦酸盐每周一次给药的短期和长期骨骼效应,且其安全性与每日给药相似。长达2年的试验作者支持这些预测,他们报告称,就骨密度和骨重塑的生化指标而言,每周一次给药在治疗上等同于每日给药。双膦酸盐每周一次给药的安全性和耐受性与每日给药一样好,且与安慰剂相当。

证据水平

治疗性研究,V级(专家意见)。有关证据水平的完整描述,请参见作者指南。

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