The renal epidemiology and information network (REIN): a new registry for end-stage renal disease in France

The French Renal Epidemiology and Information Network (REIN) registry began in 2002 to provide a tool for public health decision support, evaluation and research related to renal replacement therapies (RRT) for end-stage renal disease (ESRD). It relies on a network of nephrologists, epidemiologists,...

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Veröffentlicht in:	Nephrology, dialysis, transplantation dialysis, transplantation, 2006-02, Vol.21 (2), p.411-418
Hauptverfasser:	Couchoud, Cécile, Stengel, Bénédicte, Landais, Paul, Aldigier, Jean-Claude, de Cornelissen, François, Dabot, Christian, Maheut, Hervé, Joyeux, Véronique, Kessler, Michèle, Labeeuw, Michel, Isnard, Hubert, Jacquelinet, Christian
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Aged, 80 and over Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Child Child, Preschool Emergency and intensive care: renal failure. Dialysis management end-stage renal disease registry epidemiology Female France France - epidemiology Humans Immunology Intensive care medicine Kidney Failure, Chronic Kidney Failure, Chronic - epidemiology Life Sciences Male Medical sciences Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure network public health decisional support systems quality control Registries Renal failure renal replacement therapy Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system
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