Twenty years of the French Renal Epidemiology and Information Network

NDT Plus Pub Date : 2023-11-13 DOI:10.1093/ckj/sfad240
Isabelle Kazes, Justine Solignac, Mathilde Lassalle, Lucile Mercadal, Cécile Couchoud
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Abstract

Abstract Background The French 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 the increase in 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 months to 22.6 months. Living donor transplants increased in frequency, representing 15% of kidney transplants. Conclusions Data from the REIN registry allow for evaluating needs and provide a planning tool for French authorities. The progressive implementation of automatic data retrievals from dialysis informatics charts might alleviate the burden of data collection. Furthermore, the research activity REIN engenders, resulting in renewed confidence by health authorities in the dynamism of French nephrology, allows for an optimistic outlook for REIN.
二十年的法国肾脏流行病学和信息网络
背景法国REIN已有20年的历史。它不仅仅是一个国家数据登记,而是一个流行病学和信息网络,为慢性肾病患者、肾脏病小组和卫生服务机构提供服务。方法回顾近10年来透析或肾移植肾替代治疗的发生率和流行趋势,并分析肾移植患者的等待名单。为了检测2012年和2021年的潜在显著趋势变化,使用了Joinpoint回归模型。结果2021年,接受治疗的终末期肾病(ESKD)的总发病率为169 /百万人(pmp)。尽管糖尿病的发病率有所增加,但这一数据保持稳定。我们发现在紧急情况下开始透析的患者比例呈下降趋势,但在开始血液透析(HD)时使用临时导管的患者比例有所增加。腹膜透析每年减少1.7%,而家庭透析虽然只涉及1%的透析患者,但每年增加10%。对于不在家中接受治疗的患者,从患者家中开车到透析室的中位时间为17分钟。透析开始时移植等待名单上的患者比例从7%增加到12%。在2012年至2021年的11263例ESKD新患者中,8%在1年接受了首次移植,20%在5年接受了首次移植。在肾移植受者中,平均等待时间从13.8个月增加到22.6个月。活体供体移植的频率增加,占肾移植的15%。REIN登记处的数据可用于评估需求,并为法国当局提供规划工具。从透析信息学图表中逐步实现自动数据检索可能减轻数据收集的负担。此外,REIN开展的研究活动使卫生当局重新对法国肾脏病学的活力充满信心,使REIN的前景更加乐观。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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