首页 | 本学科首页   官方微博 | 高级检索  
检索        


2017 Annual Report Digest of the Renal Epidemiology Information Network (REIN) registry
Authors:Mathilde Lassalle  Elisabeth Monnet  Carole Ayav  Julien Hogan  Olivier Moranne  Ccile Couchoud
Institution:Mathilde Lassalle,Elisabeth Monnet,Carole Ayav,Julien Hogan,Olivier Moranne,Cécile Couchoud,
Abstract:The French Renal Epidemiology and Information Network (REIN) registry started in 2002 with the goal to provide a tool to evaluate renal replacement therapy (RRT) practices and outcomes, to provide data for research and to support public health decisions related to end‐stage renal disease ESRD. This summary presents the incidence and prevalence of RRT including kidney transplantation and wait‐listing activity in 2017, and patients’ survival and trends over 5 years. In 2017, 11 543 patients started RRT for ESRD, that is, incidence of 172 pmp. Between 2012 and 2017, the incidence of RRT increased by 1% per year CI 95% (0.0; +2.0)]. On 31 December 2017, 87 275 patients were receiving RRT, that is, prevalence of 1294 pmp, 55% on dialysis, 45% with a functioning transplant. In 2017, 3782 kidney transplantations have been performed including 16% from a living donor, 13% being retransplantations and 15% pre‐emptive transplantations. The median time on the waiting list was 19.7 months when only taking into account active waiting periods on the list. In 2017, 5280 new patients were registered on the renal transplant waiting list (i.e. 78.7 pmp). The number of patients considered as ‘inactive’ represented 45% of the patients on the list.
Keywords:end‐stage renal disease  incidence  prevalence  registry  survival  transplantation
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号