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Which data in the French registry for advanced chronic kidney disease for public health and patient care? Volume 18, issue 4, Juillet 2022

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Authors

1 IntroductionThe frequency, complications, treatment burden and cost of chronic kidney disease (CKD) require the development of registry tools to improve patient management and care arrangements. Several European countries have a registry with grouped data forming the European registry [1]. In France, a registry was set up with public funding in 2002 (REIN, i.e. Renal Epidemiology and Information Network) to ensure the evaluation of care policies, the development of tools to aid medical decision-making [...]