2005
DOI: 10.1093/ndt/gfi198
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The renal epidemiology and information network (REIN): a new registry for end-stage renal disease in France

Abstract: 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, patients and public health representatives, coordinated regionally and nationally. Continuous registration covers all dialysis and transplanted patients. In 2003, 2070 patients started RRT, 7854 were on dialysis an… Show more

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Cited by 237 publications
(174 citation statements)
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“…The percentage of diabetic nephropathy in our study was low, 13%. This is likely to reflect a combination of low prevalence of the disease in the Paris area (18% of the prevalent ESRD population has diabetic nephropathy) 42 and the later referral to nephrologists, commonly at stage 5, of patients with diabetes compared with other patients with CKD, as well as recruitment bias from university hospitals. This may result in underestimating the prevalence of anemia, given its link with diabetic kidney disease.…”
Section: Discussionmentioning
confidence: 99%
“…The percentage of diabetic nephropathy in our study was low, 13%. This is likely to reflect a combination of low prevalence of the disease in the Paris area (18% of the prevalent ESRD population has diabetic nephropathy) 42 and the later referral to nephrologists, commonly at stage 5, of patients with diabetes compared with other patients with CKD, as well as recruitment bias from university hospitals. This may result in underestimating the prevalence of anemia, given its link with diabetic kidney disease.…”
Section: Discussionmentioning
confidence: 99%
“…The REIN was founded in 2001 as a tool to provide public health decision support, evaluation, and research related to RRT for ESRD (15). Data are collected at the initiation of RRT (i.e., hemodialysis [HD], peritoneal dialysis, or kidney transplantation [KTR]) for all patients in France and updated annually.…”
Section: Materials and Methods Patient Population Data Collection Amentioning
confidence: 99%
“…REIN is used as a decision support system for public health policy-making, evaluation, and epidemiological research related to ESRD in France. In 2002, it began recording data about ESRD patients treated by dialysis or KTx (36,37) in each administrative region where all hospitals and dialysis centers treating ESRD agreed to participate. As agreements increased, the registry progressively included more regions and finally reached complete national coverage (France and overseas) in 2011 ( Figure 1): 26 administrative regions and 64 million inhabitants.…”
Section: Rein Registrymentioning
confidence: 99%