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风湿病学中比较疗效研究的格局。

The landscape of comparative effectiveness research in rheumatology.

机构信息

Department of Pediatrics and The James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Centre, Division of Rheumatology, MLC 4010, 3333 Burnet Avenue, Cincinnati, OH 45229-3026, USA.

出版信息

Nat Rev Rheumatol. 2014 Jan;10(1):57-62. doi: 10.1038/nrrheum.2013.140. Epub 2013 Sep 24.

DOI:10.1038/nrrheum.2013.140
PMID:24061502
Abstract

Comparative effectiveness research (CER) is a growing area of investigation aimed at determining the most beneficial treatments for patients in view of their clinical characteristics. CER provides personalized treatment information that cannot be obtained from traditional clinical trials. However, many analytical challenges to performing CER remain, particularly in nonexperimental settings. The main obstacles to CER include bias from variation in use of treatments, and heterogeneity in types and quality of data across registries. Increasing standardization of care and consensus among stakeholders regarding CER methodology will strengthen the validity of CER from observational data. Innovations in outcomes measurement, and the ability to repurpose electronic health record data for research will increase the capability to assess treatment effects by CER in clinical practice. Investment in infrastructure, informatics, and data management to sustain high-quality registries, along with engagement of stakeholders to maintain a co-ordinated research agenda, are essential for successful CER in rheumatology.

摘要

比较疗效研究(CER)是一个日益发展的研究领域,旨在根据患者的临床特征确定最有益于患者的治疗方法。CER 提供了无法从传统临床试验中获得的个性化治疗信息。然而,在非实验环境中,进行 CER 仍然存在许多分析挑战。CER 的主要障碍包括治疗方法使用的变化带来的偏差,以及注册中心之间数据类型和质量的异质性。增加对 CER 方法学的护理标准化和利益相关者之间的共识将增强从观察性数据中得出 CER 的有效性。结果测量的创新,以及重新利用电子健康记录数据进行研究的能力,将提高 CER 在临床实践中评估治疗效果的能力。投资于基础设施、信息学和数据管理,以维持高质量的注册中心,以及让利益相关者参与,以保持协调一致的研究议程,对于风湿病学中的 CER 成功至关重要。

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本文引用的文献

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Will comparative effectiveness research finally succeed?比较效果研究最终会成功吗?
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Canadian Rheumatology Association recommendations for the pharmacological management of rheumatoid arthritis with traditional and biologic disease-modifying antirheumatic drugs: part II safety.加拿大风湿病学会关于传统和生物改善病情抗风湿药物治疗类风湿关节炎的药物治疗建议:第二部分安全性。
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Summary of AHRQ's comparative effectiveness review of drug therapy for rheumatoid arthritis (RA) in adults--an update.美国医疗保健研究与质量局(AHRQ)对成人类风湿关节炎(RA)药物治疗的比较效果评估综述——最新情况
J Manag Care Pharm. 2012 May;18(4 Supp C):S1-18. doi: 10.18553/jmcp.2012.18.s4-c.1.
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The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS).风湿病中测量患者报告结局的未来:患者报告结局测量信息系统(PROMIS)。
Arthritis Care Res (Hoboken). 2011 Nov;63 Suppl 11(Suppl 11):S486-90. doi: 10.1002/acr.20581.
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The Patient-Centered Outcomes Research Institute (PCORI) national priorities for research and initial research agenda.以患者为中心的结果研究协会(PCORI)的国家研究重点及初步研究议程。
JAMA. 2012 Apr 18;307(15):1583-4. doi: 10.1001/jama.2012.500.
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Arthritis Care Res (Hoboken). 2012 May;64(5):625-39. doi: 10.1002/acr.21641.