What is the per kilogram dose of dialysate (peritoneal dialysis solution) for pediatric patients?

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Peritoneal Dialysis Fill Volume for Pediatric Patients

The recommended per kilogram dose of peritoneal dialysis solution for pediatric patients is approximately 30-40 mL/kg, with an instilled volume of at least 1,100 mL/m² body surface area (BSA) being the preferred normalization method. 1

Primary Dosing Recommendation

  • The initial fill volume should start at 10-20 mL/kg to minimize dialysate leakage risk, with gradual increases to approximately 30-40 mL/kg (800-1,100 mL/m²) as tolerated by the patient. 2

  • Body surface area (BSA) normalization is strongly preferred over weight-based dosing because peritoneal surface area correlates closely with BSA in an age-independent manner. 1

  • Individual tolerance must be carefully assessed, as not all patients can accommodate the target volume without complications. 1

Optimal Fill Volume Targets

  • For children ≥2 years of age, a peak fill volume of 1,400-1,500 mL/m² can be prescribed when considering tolerance, efficiency, and peritoneal membrane recruitment. 3

  • The minimum recommended instilled volume is at least 1,100 mL/m² for most pediatric patients. 1

  • Smaller fill volumes (below 1,000-1,100 mL/m²) result in artificially rapid equilibration and the false appearance of increased membrane transport capacity, which can lead to suboptimal prescriptions. 1

Acute Peritoneal Dialysis Considerations

  • In acute kidney injury settings, the initial fill volume should be limited to 10-20 mL/kg, with gradual increases as tolerated. 2

  • In neonates and small infants, cycle duration may need reduction to achieve adequate ultrafiltration due to smaller volumes. 2

  • Close monitoring of total fluid intake and output is mandatory to achieve and maintain normotension and euvolemia. 2

Critical Pitfalls to Avoid

  • Using weight-based dosing (mL/kg) alone without BSA normalization can result in inadequate dialysis in larger children and excessive volumes in smaller children. 1

  • Prescribing fill volumes below 1,000 mL/m² during peritoneal equilibration testing (PET) will artificially suggest the patient is a high transporter, leading to inappropriate prescription modifications. 1

  • Failing to gradually increase fill volume from the initial conservative dose can result in chronically inadequate dialysis delivery. 2

  • Ignoring individual tolerance factors (intraperitoneal pressure, patient comfort, leak risk) when pushing toward optimal volumes can cause treatment complications. 1, 3

Monitoring and Adjustment Strategy

  • Intraperitoneal pressure measurement in centimeters of H₂O provides the best clinical control for determining maximum tolerable fill volume. 3

  • The peritoneal equilibration test (PET) should be performed approximately 1 month following initiation using the standardized exchange volume of 1,000-1,100 mL/m² BSA. 1

  • Delivered dose should be measured 2-4 weeks following initiation through 24-hour dialysate and urine collection for Kt/Vurea and creatinine clearance calculations. 1

  • Target delivered PD dose should be a total Kt/Vurea of at least 2.0 per week for CAPD, with creatinine clearance targets of at least 60 L/wk/1.73 m² for high transporters and 50 L/wk/1.73 m² for low transporters. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

ISPD guidelines for peritoneal dialysis in acute kidney injury: 2020 Update (paediatrics).

Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis, 2021

Research

Adequacy of peritoneal dialysis in children: consider the membrane for optimal prescription.

Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis, 2007

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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