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Peritoneal dialysis in children: consider the membrane for optimal prescription
M Fischbach1, C Dheu, A C Michallat
1Pediatry 1, University Hospital, Avenue Moliere, 67098 Strasbourg Cedex, France.
Insights
Individualizing peritoneal dialysis (PD) prescriptions, particularly fill volume and dwell times, optimizes treatment for patients. New PD fluids enhance membrane function and preserve vascular health.
Area of Science:
- Nephrology
- Biomedical Engineering
Background:
- Peritoneal dialysis (PD) prescriptions were historically empirical, especially for continuous ambulatory peritoneal dialysis (CAPD).
- Advancements in understanding the peritoneal membrane enable personalized PD prescriptions, particularly for automated peritoneal dialysis (APD) in children.
Purpose of the Study:
- To establish evidence-based guidelines for optimizing peritoneal dialysis prescription parameters.
- To explore the impact of fill volume, dwell times, and new PD fluid formulations on treatment efficacy and patient outcomes.
Main Methods:
- Prescribing fill volume based on body surface area (mL/m(2)).
- Utilizing intraperitoneal pressure measurement (IPP; cm H2O) for safe fill volume optimization.
- Individualizing dwell times based on solute clearance and ultrafiltration needs.
- Evaluating new peritoneal dialysis fluids free of GPDs, with neutral pH, and non-exclusively lactate buffering.
Main Results:
- A peak fill volume of 1400-1500 mL/m(2) is suggested for optimal tolerance and efficiency.
- Balancing dwell times is crucial: shorter times for solute clearance and ultrafiltration, longer times for phosphate clearance.
- New PD fluid formulations support peritoneal membrane recruitment and preserve peritoneal vascular hyperperfusion.
Conclusions:
- Individualized peritoneal dialysis prescriptions, considering fill volume and dwell times, improve treatment.
- Optimized fill volumes and tailored dwell times enhance solute clearance and ultrafiltration.
- Novel PD fluids offer benefits for peritoneal membrane health and vascular function.
Abstract:
The peritoneal dialysis prescription was, for a long time, based on clinical experience and very empirical, especially for patients on continuous ambulatory peritoneal dialysis (CAPD). Better comprehension of the peritoneal membrane as a dynamic dialysis surface allows an individualized prescription, especially for children on automated peritoneal dialysis (APD). Fill volume prescription should be scaled for body surface area (mL/m(2)) and not in a too low amount to avoid a hyperpermeable exchange. Fill volume enhancement should be done under clinical control and is best secured by intraperitoneal pressure measurement (IPP; cm H2O). A peak fill volume of 1400-1500 mL/m(2) could be prescribed both in terms of tolerance and of efficiency. The dwell times should be determined individually with respect to two opposite parameters namely: short dwell times which provide adequate small solute clearance and maintain ultrafiltration capacity and long dwell times which enhance phosphate clearance but can contribute to dialysate reabsorption. The new peritoneal dialysis fluids which are free of GPD's, have neutral pH and are not exclusively lactate buffered, appear as the best choice in the context of peritoneal exchange membrane recruitment and of peritoneal vascular hyperperfusion preservation.
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