This paper is written by four authors from four European Registries that serve the treatment of endstage renal failure (ESRF). Each of these Registries is introduced by a short historical note. We enjoy informal professional links and are developing patient linkage to facilitate checking and interchange of data.The purpose of this paper is to give a “glimpse behind the scenes” into the methodologies evolving within and between the Registries. Some developments have been necessitated by the particular problems of maintaining patient files which are as accurate and comprehensive as possible; others are required to optimize research into the large data bases which have now been accumulated. We report methods under development by our four Regis...
In 1964 the ERA-EDTA Registry was started as one of the first renal registries in the world. This me...
International audienceThe French Renal Epidemiology and Information Network (REIN) registry began in...
Background: Kidney biopsy registries all over the world benefit research, teaching and health policy...
This paper is written by four authors from four European Registries that serve the treatment of ends...
International audienceBackgroundRecord linkage is increasingly used in health research worldwide. Co...
Background. Data collected from registries provide a useful source of information for clinical pract...
Clinical decisions rely on expert knowledge that draws on quality patient phenotypic and physiologic...
BACKGROUND Traditionally, renal registries collect and report population-based epidemiological data...
International audienceChronic kidney disease is a chronic non-transmittable disease of increasing in...
A European patient registry to track the outcomes of organ transplant recipients does not exist. As ...
Registries will enable cohort studies to be performed, which are usually considered to be the best q...
Population-based registries implement the comprehensive collection of all disease events that occur ...
Large scale collection and analysis of data on patients’ experiences and outcomes have become staple...
BACKGROUND: In June 2000 a new ERA-EDTA Registry Office was opened in Amsterdam. This Registry will ...
A Multi-Source Information System (MSIS), has been designed for the Renal Epidemiology and Informati...
In 1964 the ERA-EDTA Registry was started as one of the first renal registries in the world. This me...
International audienceThe French Renal Epidemiology and Information Network (REIN) registry began in...
Background: Kidney biopsy registries all over the world benefit research, teaching and health policy...
This paper is written by four authors from four European Registries that serve the treatment of ends...
International audienceBackgroundRecord linkage is increasingly used in health research worldwide. Co...
Background. Data collected from registries provide a useful source of information for clinical pract...
Clinical decisions rely on expert knowledge that draws on quality patient phenotypic and physiologic...
BACKGROUND Traditionally, renal registries collect and report population-based epidemiological data...
International audienceChronic kidney disease is a chronic non-transmittable disease of increasing in...
A European patient registry to track the outcomes of organ transplant recipients does not exist. As ...
Registries will enable cohort studies to be performed, which are usually considered to be the best q...
Population-based registries implement the comprehensive collection of all disease events that occur ...
Large scale collection and analysis of data on patients’ experiences and outcomes have become staple...
BACKGROUND: In June 2000 a new ERA-EDTA Registry Office was opened in Amsterdam. This Registry will ...
A Multi-Source Information System (MSIS), has been designed for the Renal Epidemiology and Informati...
In 1964 the ERA-EDTA Registry was started as one of the first renal registries in the world. This me...
International audienceThe French Renal Epidemiology and Information Network (REIN) registry began in...
Background: Kidney biopsy registries all over the world benefit research, teaching and health policy...