2022
DOI: 10.1016/j.nephro.2022.01.004
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Which data in the French registry for advanced chronic kidney disease for public health and patient care?

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Cited by 16 publications
(13 citation statements)
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“…To better investigate the kidney transplantation access potential disparities between women and men in France, this research used a mixed methods approach that combines a quantitative study and a qualitative study [ 51 ]. The quantitative study describes and objectifies the factors associated with access to renal transplantation by analyzing data from the French national Renal Epidemiology and Information Network (REIN) [ 52 , 53 ] registry. The qualitative study will focus on the questions that cannot be assessed with a quantitative study (e.g., actors’ behaviors, action rationale, sense given to these actions) [ 51 , 54 , 55 ].…”
Section: Methodsmentioning
confidence: 99%
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“…To better investigate the kidney transplantation access potential disparities between women and men in France, this research used a mixed methods approach that combines a quantitative study and a qualitative study [ 51 ]. The quantitative study describes and objectifies the factors associated with access to renal transplantation by analyzing data from the French national Renal Epidemiology and Information Network (REIN) [ 52 , 53 ] registry. The qualitative study will focus on the questions that cannot be assessed with a quantitative study (e.g., actors’ behaviors, action rationale, sense given to these actions) [ 51 , 54 , 55 ].…”
Section: Methodsmentioning
confidence: 99%
“…Data will be extracted from the REIN registry. This registry was started in 2002 and includes all patients with ESKD treated by RRT in France [ 52 , 53 , 59 ]. Since 2012, all mainland regions and overseas territories are included.…”
Section: Methodsmentioning
confidence: 99%
“…This study was based on the French Renal Epidemiology and Information Network (REIN), 28,29 the French national health insurance information system (Système National des Données de Santé: SNDS) and the histocompatibility laboratory of Nancy. Patients with KAF were identified by REIN as having graft failure requiring dialysis for more than 2 months.…”
Section: Study Populationmentioning
confidence: 99%
“…Details on methods and quality control have been described elsewhere. 24 The REIN registry and its utilization for research purposes have been approved by the relevant French ethics committees, specifically, the Comité consultatif sur le traitement de l'information en matière de recherche (CCTIRS) and the Commission nationale de l'informatique et des libertés (CNIL N° 903188). French regulations do not require participants' written or verbal informed consent for their inclusion in population-based registries requiring exhaustiveness.…”
Section: Study Sample and Data Collectionmentioning
confidence: 99%