Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions

Abstract In‐depth understanding of intra‐ and postdialytic phosphate kinetics is important to adjust treatment regimens in hemodialysis. We aimed to modify and validate a three‐compartment phosphate kinetic model to individual patient data and assess the temporal robustness. Intradialytic phosphate...

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Main Authors: Sisse H. Laursen, Lise Boel, Lisbet Brandi, Jeppe H. Christensen, Peter Vestergaard, Ole Kristian Hejlesen
Format: Article
Language:English
Published: Wiley 2023-12-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.15899
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author Sisse H. Laursen
Lise Boel
Lisbet Brandi
Jeppe H. Christensen
Peter Vestergaard
Ole Kristian Hejlesen
author_facet Sisse H. Laursen
Lise Boel
Lisbet Brandi
Jeppe H. Christensen
Peter Vestergaard
Ole Kristian Hejlesen
author_sort Sisse H. Laursen
collection DOAJ
description Abstract In‐depth understanding of intra‐ and postdialytic phosphate kinetics is important to adjust treatment regimens in hemodialysis. We aimed to modify and validate a three‐compartment phosphate kinetic model to individual patient data and assess the temporal robustness. Intradialytic phosphate samples were collected from the plasma and dialysate of 12 patients during two treatments (HD1 and HD2). 2‐h postdialytic plasma samples were collected in four of the patients. First, the model was fitted to HD1 samples from each patient to estimate the mass transfer coefficients. Second, the best fitted model in each patient case was validated on HD2 samples. The best model fits were determined from the coefficient of determination (R2) values. When fitted to intradialytic samples only, the median (interquartile range) R2 values were 0.985 (0.959–0.997) and 0.992 (0.984–0.994) for HD1 and HD2, respectively. When fitted to both intra‐ and postdialytic samples, the results were 0.882 (0.838–0.929) and 0.963 (0.951–0.976) for HD1 and HD2, respectively. Eight patients demonstrated a higher R2 value for HD2 than for HD1. The model seems promising to predict individual plasma phosphate in hemodialysis patients. The results also show good temporal robustness of the model. Further modifications and validation on a larger sample are needed.
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spelling doaj.art-16dddb707bcb4671a901c659870c95b22023-12-27T03:58:32ZengWileyPhysiological Reports2051-817X2023-12-011124n/an/a10.14814/phy2.15899Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictionsSisse H. Laursen0Lise Boel1Lisbet Brandi2Jeppe H. Christensen3Peter Vestergaard4Ole Kristian Hejlesen5The Danish Diabetes Academy Odense University Hospital Odense DenmarkDepartment of Clinical Medicine Aalborg University Aalborg DenmarkDepartment of Cardiology, Nephrology, and Endocrinology, Nordsjællands Hospital Hillerød DenmarkDepartment of Nephrology Aalborg University Hospital Aalborg DenmarkSteno Diabetes Center North Jutland Aalborg University Hospital Aalborg DenmarkDepartment of Health Science and Technology Aalborg University Aalborg DenmarkAbstract In‐depth understanding of intra‐ and postdialytic phosphate kinetics is important to adjust treatment regimens in hemodialysis. We aimed to modify and validate a three‐compartment phosphate kinetic model to individual patient data and assess the temporal robustness. Intradialytic phosphate samples were collected from the plasma and dialysate of 12 patients during two treatments (HD1 and HD2). 2‐h postdialytic plasma samples were collected in four of the patients. First, the model was fitted to HD1 samples from each patient to estimate the mass transfer coefficients. Second, the best fitted model in each patient case was validated on HD2 samples. The best model fits were determined from the coefficient of determination (R2) values. When fitted to intradialytic samples only, the median (interquartile range) R2 values were 0.985 (0.959–0.997) and 0.992 (0.984–0.994) for HD1 and HD2, respectively. When fitted to both intra‐ and postdialytic samples, the results were 0.882 (0.838–0.929) and 0.963 (0.951–0.976) for HD1 and HD2, respectively. Eight patients demonstrated a higher R2 value for HD2 than for HD1. The model seems promising to predict individual plasma phosphate in hemodialysis patients. The results also show good temporal robustness of the model. Further modifications and validation on a larger sample are needed.https://doi.org/10.14814/phy2.15899compartment modelingdialysishyperphosphatemiakineticsphosphate
spellingShingle Sisse H. Laursen
Lise Boel
Lisbet Brandi
Jeppe H. Christensen
Peter Vestergaard
Ole Kristian Hejlesen
Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
Physiological Reports
compartment modeling
dialysis
hyperphosphatemia
kinetics
phosphate
title Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
title_full Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
title_fullStr Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
title_full_unstemmed Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
title_short Evaluation of a phosphate kinetics model in hemodialysis therapy—Assessment of the temporal robustness of model predictions
title_sort evaluation of a phosphate kinetics model in hemodialysis therapy assessment of the temporal robustness of model predictions
topic compartment modeling
dialysis
hyperphosphatemia
kinetics
phosphate
url https://doi.org/10.14814/phy2.15899
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