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Comparing Computational Peritoneal Dialysis Models in Pigs and Patients

  • Sangita Swapnasrita
  • , Joost C de Vries
  • , Joanna Stachowska-Piętka
  • , Carl M Öberg
  • , Karin G F Gerritsen*
  • , Aurélie Carlier*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Computational models of peritoneal dialysis (PD) are increasingly useful for optimizing treatment in patients with kidney disease requiring dialysis (KDRD). However, although several mathematical models have been developed in the past few decades, a direct comparison of the models' accuracy with respect to predicting in vivo data is needed to further create robust personalized models. Here, we used a dataset obtained in a previous in vivo experimental model of PD in pigs (23 sessions of 4 h 2 L dwells in four pigs) and humans (20 sessions in 20 patients) to compare six computational models of PD: the Graff model (UGM), the three-pore model (TPM), the Garred model (GM), and the Waniewski model (WM), as well as two variations of these (UGM-18, SWM). We conducted this comparison to predict the dialysate concentrations of key uremic toxins and electrolytes (four in humans) throughout a 4 h dwell. The model predictions can provide insight into inter-individual differences in ultrafiltration, which are critical for tailoring PD regimens in KDRD. While TPM offered improved physiological reality, its computational cost suggests a trade-off between model complexity and clinical applicability for real-time or portable kidney support systems. In future applications, such models could provide adaptive PD regimens for tailored care based on patient-specific toxin kinetics and fluid dynamics.

Original languageEnglish
Article number329
JournalToxins
Volume17
Issue number7
DOIs
Publication statusPublished - 28 Jun 2025

Keywords

  • Aged
  • Animals
  • Computer Simulation
  • Dialysis Solutions
  • Female
  • Humans
  • Male
  • Middle Aged
  • Models, Biological
  • Peritoneal Dialysis
  • Swine
  • Uremic Toxins

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