Twenty years of the French Renal Epidemiology and Information Network

Author:

Kazes Isabelle1,Solignac Justine2ORCID,Lassalle Mathilde3,Mercadal Lucile4,Couchoud Cécile3ORCID

Affiliation:

1. Service de Néphrologie, Centre Hospitalo-Universitaire de Reims , Reims , France

2. Service de Néphrologie, Assistance Publique Hôpitaux de Marseille , Marseille , France

3. Registre REIN, Agence de la biomédecine , Saint Denis La Plaine , France

4. Service de Néphrologie, Hôpital de la Pitié Salpêtrière, APHP , Paris , France

Abstract

ABSTRACT Background The French Renal Epidemiology and Information Network (REIN) is 20 years old. It is not just a national data registry, but rather an epidemiological and informational network serving patients with chronic kidney disease, nephrology teams and health services. Methods The past 10-year trends of the incidence and prevalence of renal replacement therapy by dialysis or kidney transplantation and waitlist activity are presented. To detect potential significant changes in trends from 2012 and 2021, a Joinpoint regression model was used. Results The overall incidence of treated end-stage kidney disease (ESKD) was 169 per million population (pmp) in 2021. It was stable despite an increase in the incidence of diabetes. We found a decreasing trend in the proportion of patients starting dialysis in an emergency but an increase in those starting haemodialysis (HD) with a temporary catheter. Peritoneal dialysis decreased by 1.7% each year, whereas home HD, although involving only 1% of dialysis patients, increased by 10% each year. For patients not treated at home, the median time to drive from the patient's home to the dialysis unit was 17 min. The proportion of patients on the transplantation waitlist at the start of dialysis increased from 7% to 12%. Among the 111 263 new ESKD patients from 2012 to 2021, 8% received a first transplant at 1 year and 20% at 5 years. Among kidney transplant recipients, the mean time on the waitlist increased from 13.8 to 22.6 months. Living donor transplants increased in frequency, representing 15% of kidney transplants. Conclusions Data from the REIN registry allow for the evaluation of needs and provide a planning tool for French authorities. The progressive implementation of automatic data retrieval from dialysis informatics charts might alleviate the burden of data collection. Furthermore, the research activity the REIN engenders, resulting in renewed confidence by health authorities in the dynamism of French nephrology, allows for an optimistic outlook for the REIN.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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