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法国肾脏流行病学与信息网络二十年。

Twenty years of the French Renal Epidemiology and Information Network.

作者信息

Kazes Isabelle, Solignac Justine, Lassalle Mathilde, Mercadal Lucile, Couchoud Cécile

机构信息

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

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

出版信息

Clin Kidney J. 2023 Nov 13;17(1):sfad240. doi: 10.1093/ckj/sfad240. eCollection 2024 Jan.

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.

摘要

背景

法国肾脏流行病学与信息网络(REIN)已成立20周年。它不仅是一个国家数据登记处,更是一个为慢性肾脏病患者、肾脏病团队及医疗服务机构提供服务的流行病学和信息网络。

方法

本文呈现了过去10年中通过透析或肾移植进行肾脏替代治疗的发病率、患病率以及等待名单活动的趋势。为检测2012年至2021年期间趋势的潜在显著变化,使用了Joinpoint回归模型。

结果

2021年,接受治疗的终末期肾病(ESKD)总体发病率为每百万人口169例(pmp)。尽管糖尿病发病率有所上升,但总体发病率保持稳定。我们发现急诊开始透析的患者比例呈下降趋势,而使用临时导管开始血液透析(HD)的患者比例有所增加。腹膜透析每年下降1.7%,而家庭血液透析尽管仅占透析患者的1%,但每年增长10%。对于不在家接受治疗的患者,从患者家到透析单位的驾车中位时间为17分钟。透析开始时在移植等待名单上的患者比例从7%增至12%。在2012年至2021年的111263例新ESKD患者中,8%在1年时接受了首次移植,20%在5年时接受了移植。在肾移植受者中,等待名单上的平均时间从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%。

结论

REIN登记处的数据有助于评估需求,并为法国当局提供规划工具。逐步实现从透析信息图表中自动检索数据可能会减轻数据收集的负担。此外,REIN开展的研究活动使卫生当局对法国肾脏病学的活力重新产生信心,这为REIN带来了乐观的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac73/10768769/b42408cecafe/sfad240fig1g.jpg

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