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Safety and efficacy of denosumab in osteoporotic patients previously treated with other medications: a systematic review and meta-analysis

机译:Denosumab在骨质疏松患者用其他药物治疗的骨质疏松患者的安全性和有效性:系统审查和荟萃分析

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Introduction: Denosumab is a monoclonal antibody that received approval by the FDA for the treatment of osteoporosis in 2010. Available higher level research evidence concerns the treatment of patients that have not received any anti-osteoporotic medication in the past. Further investigation is warranted, since clinicians often face the challenge of administering the most efficacious drug in patients, pretreated with other medications. Areas covered: We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of denosumab compared to other active anti-osteoporotic agents in patients formerly receiving other treatments. We searched MEDLINE, EMBASE, CENTRAL, the metaRegister of Controlled Trials (mRCT) and clinicaltrials.gov up to April 2017 to identify eligible trials in patients with primary osteoporosis. Expert opinion: Our meta-analysis included 6 Randomised Controlled Trials encompassing 2968 patients formerly treated with anti-osteoporotic medications. Quantitative data synthesis demonstrated superiority of denosumab in augmenting Bone Mineral Density in all skeletal sites studied compared to controls [treatment difference in total hip: 1.59% (95% CI 1.01, 2.17)], whereas the overall incidence of serious adverse events was not increased (OR 1.12, 95% CI 0.85 to 1.47, p = 0.42). Future research geared towards the fracture incidence, quality of life and patient reported outcomes is warranted. ? 2018 Informa UK Limited, trading as Taylor & Francis Group.
机译:介绍:Denosumab是一种单克隆抗体,由FDA获得FDA在2010年治疗骨质疏松症的批准。可用的更高水平的研究证据涉及过去患有过去任何抗骨质化药物的患者。有必要进一步调查,因为临床医生常常面临患者患者最有效的药物的挑战,以其他药物预处理。所涵盖的区域:我们进行了系统审查和荟萃分析,以评估Denosumab的疗效和安全性与以前接受其他治疗的患者的其他活性抗骨科药物相比。我们搜索了Medline,Embase,Central,Metaregister(MRCT)和Clinicaltrials.gov至2017年4月,以确定原发性骨质疏松症患者的符合条件的试验。专家意见:我们的META分析包括6例随机对照试验,包括以前用抗骨质疏松药物治疗的2968名患者。定量数据合成在研究与对照组相比,在研究的所有骨骼部位中的增强骨矿物密度的优越性[总髋关节治疗差异:1.59%(95%CI 1.01,2.17)],而严重不良事件的总发生率没有增加(或1.12,95%CI 0.85至1.47,p = 0.42)。未来的研究旨在朝骨折发病率,生活质量和患者报告的结果是有保证的。还2018年Informa UK Limited,贸易为泰勒&弗朗西斯集团。

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