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透析和移植登记在临床实践中的应用:伦巴第登记处

Application of dialysis and transplant registries to clinical practice: the Lombardy Registry.

作者信息

Locatelli Francesco, Tentori Francesca, Del Vecchio Lucia, Pontoriero Giuseppe

机构信息

Divisione di Nefrologia e Dialisi, Ospedale A. Manzoni, Via Dell'Eremo 11, 23900 Lecco, Italy.

出版信息

Nephrol Dial Transplant. 2004 Jun;19 Suppl 3:iii2-4. doi: 10.1093/ndt/gfh1005.

Abstract

BACKGROUND

Data collected from registries provide a useful source of information for clinical practice. Therefore, several regional and national registries of end-stage renal disease (ESRD) patients have been established. The Lombardy Registry of Dialysis and Transplantation (RLDT) was established in 1982, with participation of all 44 dialysis units that were present at that time within the region.

METHODS

Demographic and clinical data on ESRD patients are collected yearly. We present here the results of some of the analyses that have been performed on RLDT data since it was started.

RESULTS

Briefly, data on epidemiology of ESRD, cardiovascular disease, patterns of care and patients' outcomes have been considered. Comparisons with international registries have also been performed.

CONCLUSIONS

This analysis shows how data collected from a homogeneous patient population receiving similar patterns of care provide precise information on that population. A clear example is provided by the similar results obtained in the comparison of high-flux vs low-flux membranes in a randomized control trial, the HEMO study, and in an analysis of RLDT data. Therefore, analysis of data collected by registries represents an important tool to improve clinical practice and possibly patients' outcomes.

摘要

背景

从登记处收集的数据为临床实践提供了有用的信息来源。因此,已经建立了几个地区和国家的终末期肾病(ESRD)患者登记处。伦巴第透析与移植登记处(RLDT)成立于1982年,当时该地区所有44个透析单位均参与其中。

方法

每年收集ESRD患者的人口统计学和临床数据。我们在此展示自RLDT启动以来对其数据进行的一些分析结果。

结果

简而言之,已经考虑了ESRD的流行病学、心血管疾病、护理模式和患者结局的数据。还与国际登记处进行了比较。

结论

该分析表明,从接受相似护理模式的同质患者群体中收集的数据如何为该群体提供精确信息。在一项随机对照试验(HEMO研究)中比较高通量与低通量膜以及对RLDT数据进行分析时获得的相似结果就是一个明显的例子。因此,对登记处收集的数据进行分析是改善临床实践并可能改善患者结局的重要工具。

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