ESRD Databases, Public Policy, and Quality of Care: Translational Medicine and Nephrology

终末期肾病数据库、公共政策和医疗质量:转化医学与肾脏病学

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Abstract

Efforts to improve care of patients with ESRD and the policies that guide those activities depend on evidence-based best practices derived from clinical trials and carefully conducted observational studies. Our review describes this process in the context of the translational research model (bench to bedside to populations), with a particular emphasis on bedside care. We illustrate some of its accomplishments and describe the limitations of the data and evidence supporting policy and practice.

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