By W. Van Biesen
In view of the young age of the patient, and the absence of any co-morbidity, a living related donation is put forward as a first option and both parents are screened as potential donors. The father, a heavy smoker, is found to have severe hypertension, with proteinuria and a shrunken kidney on the right side. It is obvious that he cannot be considered as a potential donor. The mother, who has a minor form of osteogenesis imperfecta, is found to have microalbuminuria. Her creatinine clearance is measured to be 65 ml/min. No clear explanation for this mild renal dysfunction is found, as she refuses further investigations as her daughter makes it clear that, under these circumstances, she is not willing to accept a donation from her mother.
The patient is listed on the cadaveric donor waiting lis,t and meanwhile, the option is taken to place her on peritoneal dialysis.
A peritoneal dialysis catheter is inserted under local anesthaesia, and after 10 days, peritoneal dialysis is started, and the temporary haemodialysis catheter is removed.
A peritoneal equilibration test (PET) was was performed after 2 weeks. The patient is found to be a low average transporter with a D/P creatinine of 0.65 after 4 hours. She has minimal residual renal function with a creatinine clearance of 1.5ml/min and a diuresis of about 500ml/day. Her body weight is 65 kg.