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[关于终末期肾功能不全病例管理的数据收集。可行性研究。肾脏病流行病学与信息网络(REIN)]

[Data collection about the case management of end-stage renal insufficiency. Feasibility study. Nephrology Epidemiologic and information Network (REIN)].

作者信息

Stengel B, Landais P

机构信息

INSERM U 170, Villejuif.

出版信息

Nephrologie. 1999;20(1):29-40.

Abstract

End-stage renal failure (ESRD) is an important public health issue, because of both the increasing number of patients requiring renal replacement therapy and the cost of treatment. The need for a reliable data system, capable of describing the patient care network as a whole, including dialysis or transplantation, has often been reiterated. The Direction Générale de la Santé (the French Department of Health) commissioned INSERM (the National Institute of Health and Medical Research) to "study the feasibility of different scenarios of data collection about ESRD patient care in order to meet the priority needs of health care administration, physicians, and researchers". Analysis of these needs allowed the goals to be defined: to provide an accurate picture of ESRD patient care in order to guide and evaluate health care policy, to inform clinicians, and to provide a tool for more focused special studies in renal research issues. Three scenarios were studied: the first would use data systems of both the government and the National Health Insurance system for planning health care services, upon EfG (The French Transplant Agency) network to evaluate transplantation, and upon a few regional registries for epidemiology and research; the second is based on repeated cross-sectional surveys; the third would rely upon the organization of an information system, the Renal Epidemiology and Information Network (REIN). Regional centers and a national coordinating office would register and follow-up ESRD patients, principally to evaluate health care supply and quality. The REIN database would also be a resource for research. The advantage of the first scenario is its low cost; its principal drawback is that evaluations will not be possible in the regions without registries. The second suggestion is inadequate. The last project would fulfil the goals that were defined. The REIN data system would be a true public health project of interest to all the participants and institutions in this field.

摘要

终末期肾衰竭(ESRD)是一个重要的公共卫生问题,这是由于需要肾脏替代治疗的患者数量不断增加以及治疗费用所致。人们经常重申需要一个可靠的数据系统,该系统能够描述包括透析或移植在内的整个患者护理网络。法国卫生部委托法国国家健康与医学研究院(INSERM)“研究收集ESRD患者护理不同数据方案的可行性,以满足医疗保健管理部门、医生和研究人员的优先需求”。对这些需求的分析使目标得以确定:提供ESRD患者护理的准确情况,以指导和评估医疗保健政策,为临床医生提供信息,并为肾脏研究问题的更有针对性的专项研究提供工具。研究了三种方案:第一种方案将使用政府和国家健康保险系统的数据系统来规划医疗服务,利用法国移植机构(EfG)网络评估移植情况,并利用一些地区登记处进行流行病学研究和科研;第二种方案基于重复的横断面调查;第三种方案将依赖于一个信息系统——肾脏流行病学和信息网络(REIN)的组织。地区中心和一个国家协调办公室将对ESRD患者进行登记和随访,主要目的是评估医疗服务的提供情况和质量。REIN数据库也将成为科研资源。第一种方案的优点是成本低;其主要缺点是在没有登记处的地区无法进行评估。第二种方案不合适。最后一个项目将实现所确定的目标。REIN数据系统将是一个真正的公共卫生项目,对该领域的所有参与者和机构都具有重要意义。

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