TY - JOUR
T1 - Phosphate Kinetic Models in Hemodialysis
T2 - A Systematic Review
AU - Laursen, Sisse Heiden
AU - Hejlesen, Ole
AU - Vestergaard, Peter
N1 - Publisher Copyright: © 2017 National Kidney Foundation, Inc.
PY - 2018
Y1 - 2018
N2 - Background Understanding phosphate kinetics in dialysis patients is important for the prevention of hyperphosphatemia and related complications. One approach to gain new insights into phosphate behavior is physiologic modeling. Various models that describe and quantify intra- and/or interdialytic phosphate kinetics have been proposed, but there is a dearth of comprehensive comparisons of the available models. The objective of this analysis was to provide a systematic review of existing published models of phosphate metabolism in the setting of maintenance hemodialysis therapy. Study Design Systematic review. Setting & Population Hemodialysis patients. Selection Criteria for Studies Studies published in peer-reviewed journals in English about phosphate kinetic modeling in the setting of hemodialysis therapy. Predictor Modeling equations from specific reviewed studies. Outcomes Changes in plasma phosphate or serum phosphate concentrations. Results Of 1,964 nonduplicate studies evaluated, 11 were included, comprising 9 different phosphate models with 1-, 2-, 3-, or 4-compartment assumptions. Between 2 and 11 model parameters were included in the models studied. Quality scores of the studies using the Newcastle-Ottawa Scale ranged from 2 to 11 (scale, 0-14). 2 studies were considered low quality, 6 were considered medium quality, and 3 were considered high quality. Limitations Only English-language studies were included. Conclusions Many parameters known to influence phosphate balance are not included in existing phosphate models that do not fully reflect the physiology of phosphate metabolism in the setting of hemodialysis. Moreover, models have not been sufficiently validated for their use as a tool to simulate phosphate kinetics in hemodialysis therapy.
AB - Background Understanding phosphate kinetics in dialysis patients is important for the prevention of hyperphosphatemia and related complications. One approach to gain new insights into phosphate behavior is physiologic modeling. Various models that describe and quantify intra- and/or interdialytic phosphate kinetics have been proposed, but there is a dearth of comprehensive comparisons of the available models. The objective of this analysis was to provide a systematic review of existing published models of phosphate metabolism in the setting of maintenance hemodialysis therapy. Study Design Systematic review. Setting & Population Hemodialysis patients. Selection Criteria for Studies Studies published in peer-reviewed journals in English about phosphate kinetic modeling in the setting of hemodialysis therapy. Predictor Modeling equations from specific reviewed studies. Outcomes Changes in plasma phosphate or serum phosphate concentrations. Results Of 1,964 nonduplicate studies evaluated, 11 were included, comprising 9 different phosphate models with 1-, 2-, 3-, or 4-compartment assumptions. Between 2 and 11 model parameters were included in the models studied. Quality scores of the studies using the Newcastle-Ottawa Scale ranged from 2 to 11 (scale, 0-14). 2 studies were considered low quality, 6 were considered medium quality, and 3 were considered high quality. Limitations Only English-language studies were included. Conclusions Many parameters known to influence phosphate balance are not included in existing phosphate models that do not fully reflect the physiology of phosphate metabolism in the setting of hemodialysis. Moreover, models have not been sufficiently validated for their use as a tool to simulate phosphate kinetics in hemodialysis therapy.
KW - disease, health science and nursing
UR - http://www.scopus.com/inward/record.url?scp=85035203890&partnerID=8YFLogxK
U2 - 10.1053/j.ajkd.2017.07.016
DO - 10.1053/j.ajkd.2017.07.016
M3 - Review article
SN - 0272-6386
VL - 71
SP - 75
EP - 90
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 1
ER -