Polycystic Kidney Diseases
Conditions
Brief summary
Pathological features of Autosomal Dominant Polycystic Kidney disease (ADPKD) include enlarged kidney volume, a higher frequency of digestive diverticulitis and abdominal wall hernias. Therefore, many nephrologists have concerns about the use of peritoneal dialysis (PD) in ADPKD patients. We aimed to analyze survival and technique failure in ADPKD patients treated with PD.
Detailed description
Pathological features of Autosomal Dominant Polycystic Kidney disease (ADPKD) include enlarged kidney volume, a higher frequency of digestive diverticulitis and abdominal wall hernias. Therefore, many nephrologists have concerns about the use of peritoneal dialysis (PD) in ADPKD patients. We aimed to analyze survival and technique failure in ADPKD patients treated with PD. We conducted two retrospective studies on patients starting dialysis between 2000 and 2010, and based on two French registries: The French Renal Epidemiology and Information Network (REIN) and The French Language Peritoneal Dialysis Registry (RDPLF).
Interventions
OTHERDialysis
Sponsors
CHU de Reims
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
Iinclusion criteria : * Patients starting dialysis * Patients included from the French Renal Epidemiology and Information Network (REIN) and The French Language Peritoneal Dialysis Registry (RDPLF)
Exclusion criteria
* patients without diagnosis of nephropathy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival | 15 years | the time from the start of dialysis to death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| technique survival | 15 years | the time from the start of dialysis to change of dialysis technique (death and transplantation were considered as competing risk) |
Countries
France
Outcome results
None listed