Kidney Failure, Chronic Clinical Trial
Official title:
Characteristics and Treatment Course of Patients Older Than 75 Years Old Reaching ESRD. Development of a Prognosis Tools for Early Mortality
Elderly (i.e.>75 yrs) represent about 40% of incident dialysis patients in the French REIN
Registry and are growing population in high income countries. Those elderly patients with
CKD have a high risk of dying within the first months of dialysis start or could have a good
long-term prognosis suggesting kidney transplantation access. Elderly patients with CKD also
have a higher risk of dying than reaching ESRD. Therefore, outcomes of elderly patients with
advanced CKD need to be better described and understood to be able to give accurate
information to the patients and their relatives and help decision making concerning the
treatment strategy including several options (i.e preemptive kidney transplantation, in
center or home dialysis and conservative care). In France we have information about patients
who started dialysis with French dialysis registry (REIN) but not about elderly patient
treated with conservative care. Then we don't have information about description of the
therapeutic project in this population and their evolution in a prospective cohort design.
Finally we need to identify patients with high risk of early mortality to help shared
decision making for better care organisation.
The project of the study is the development of a French multicenter prospective cohort
including elderly patients more than 75 years old reaching ESRD. Objectives are as follow:
Description of the characteristics of the population such as, clinical and social
conditions, medicine treatment, therapeutic project declared by nephrologist and laboratory
value at inclusion.
Description of the evolution of therapeuic project, kidney function and the outcomes defined
as death or dialysis or kidney transplantation.
Development of a mortality prognosis tools to help decision making in this population.
At inclusion for each patient data were collected on demographic and clinical conditions
(comorbidities and disabilities), mobility (walk without help, need assistance and totally
dependent for transfers), way of living (home living or institutionalized), biological data
(blood and urine), therapeutic projects about the option for dialysis and the medicals
reason to start dialysis. As it is an observational study of current practices, no
additional tests or additional visits were mandatory either at inclusion or during the
follow-up.
Data on dialysis start and outcomes were extracted from the French National ESRD registry
REIN. This linkage was approved by the French Advisory Committee on Information Processing
in Material Research in the Field of Health (CCTIRS), the National Commission for
Information Technology and Privacy (Commission Nationale de l'Informatique et des Libertes)
and ethic committee. The starting dialysis condition included patient's clinical
characteristics, the use of a central vascular catheter (CVC), the unplanned condition of
dialysis start and the first modality of dialysis (peritoneal or hemodialysis). After
dialysis start, patient survival and information about dialysis withdrawal before death was
collected.
The number of patients to include was fixed to more than 500 to study at least 15 prognosis
factors with estimation of more than 30% of death during follow-up.
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Observational Model: Cohort, Time Perspective: Prospective
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