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Review
. 2009 Aug;24(8):1453-64.
doi: 10.1007/s00467-008-0848-4. Epub 2008 Jun 3.

Selection of modalities, prescription, and technical issues in children on peritoneal dialysis

Affiliations
Review

Selection of modalities, prescription, and technical issues in children on peritoneal dialysis

Enrico Verrina et al. Pediatr Nephrol. 2009 Aug.

Abstract

Peritoneal dialysis (PD) is widely employed as a dialytic therapy for uraemic children, especially in its automated form (APD), that is associated with less burden of care on patient and family than continuous ambulatory PD. Since APD offers a wide range of treatment options, based on intermittent and continuous regimens, prescription can be individualized according to patient's age, body size, residual renal function, nutritional intake, and growth-related metabolic needs. Transport capacity of the peritoneal membrane of each individual patient should be assessed, and regularly monitored, by means of standardized peritoneal function tests validated in pediatric patients. To ensure maximum recruitment of peritoneal exchange area, fill volume should be scaled to body surface area and adapted to each patient, according to clinical tolerance and intraperitoneal pressure. PD solutions should be employed according to their biocompatibility and potential ultrafiltration capacity; new pH-neutral, glucose-free solutions can be used in an integrated way in separate dwells, or by appropriately mixing during the same dialytic session. Kinetic modelling software programs may help in the tailoring of PD prescription to individual patients' characteristics and needs. Owing to advances in the technology of new APD machines, greater programming flexibility, memorized delivery control, and tele-dialysis are currently possible.

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Figures

Fig. 1
Fig. 1
Factors that should be accurately evaluated for each individual patient in the process of peritoneal dialysis (PD) prescription, and PD regimen parameters that have to be defined to achieve the final treatment schedule (PRD primary renal disease, RRF residual renal function)

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