A. Ciandrini, S. Severi, S. Cavalcanti, F. Grandi, S. Santoro
{"title":"Model-based analysis of Na-K+ pump influence on potassium depuration during Acetate Free Biofiltration (AFB)","authors":"A. Ciandrini, S. Severi, S. Cavalcanti, F. Grandi, S. Santoro","doi":"10.1109/CIC.2008.4749181","DOIUrl":null,"url":null,"abstract":"Potassium ion (K<sup>+</sup>) kinetics in intra and extracellular compartments during hemodialysis was studied by means of a double-pool computer model which included potassium-dependent active transport (Na-K-ATPase pump) in thirty-four patients (21M/13F; aged 66 plusmn 22 years old, dry weight 68 plusmn 18 kg, height 160 plusmn 15 cm) on renal replacement therapy with thrice weekly 4 hour double-needle hemodialysis. Each patient was studied during acetate free biofiltration (AFB) with a constant K<sup>+</sup> dialysate concentration (K<sub>CONST</sub> therapy) and with a time-varying (profiled) K<sup>+</sup> dialysate concentration (K<sub>PROF</sub> therapy). The two therapies induced different levels of K<sup>+</sup> plasma concentration (K<sub>CONST</sub>: 3.6plusmn0.8 vs. K<sub>PROF</sub>: 4.0plusmn0.7 mmol/L, time-averaged values, p<0.01). The computer model was tuned to accurately fit plasmatic K<sup>+</sup> measured in the course of K<sub>CONST</sub> and K<sub>PROF</sub> therapies and was then used to simulate the kinetics of intra and extracellular K<sup>+</sup>. Model-based analysis showed that almost all the K<sup>+</sup> removal in the first 90 minutes of dialysis was mainly derived from the extracellular compartment. The different K<sup>+</sup> time course in the dialysate and the consequently different Na-K pump activity resulted in a different sharing of removed potassium mass at the end of dialysis: 55+17% from the extracellular compartment in K<sup>+</sup> <sub>PROF</sub> vs. 41plusmn14% in K<sup>+</sup> <sub>CONST</sub>. These results suggest that the Na-K pump plays a major role in K<sup>+</sup> apportionment between extracellular and intracellular compartments, and potassium dialysate concentration strongly influences pump activity. For this reason the computer-model here presented may represent a useful tool to quantitatively assess the impact of dialysate potassium on K<sup>+</sup> kinetics in intra and extracellular compartments and to design dialysate potassium content tailored to the patient's needs.","PeriodicalId":194782,"journal":{"name":"2008 Computers in Cardiology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2008-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2008 Computers in Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CIC.2008.4749181","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Potassium ion (K+) kinetics in intra and extracellular compartments during hemodialysis was studied by means of a double-pool computer model which included potassium-dependent active transport (Na-K-ATPase pump) in thirty-four patients (21M/13F; aged 66 plusmn 22 years old, dry weight 68 plusmn 18 kg, height 160 plusmn 15 cm) on renal replacement therapy with thrice weekly 4 hour double-needle hemodialysis. Each patient was studied during acetate free biofiltration (AFB) with a constant K+ dialysate concentration (KCONST therapy) and with a time-varying (profiled) K+ dialysate concentration (KPROF therapy). The two therapies induced different levels of K+ plasma concentration (KCONST: 3.6plusmn0.8 vs. KPROF: 4.0plusmn0.7 mmol/L, time-averaged values, p<0.01). The computer model was tuned to accurately fit plasmatic K+ measured in the course of KCONST and KPROF therapies and was then used to simulate the kinetics of intra and extracellular K+. Model-based analysis showed that almost all the K+ removal in the first 90 minutes of dialysis was mainly derived from the extracellular compartment. The different K+ time course in the dialysate and the consequently different Na-K pump activity resulted in a different sharing of removed potassium mass at the end of dialysis: 55+17% from the extracellular compartment in K+PROF vs. 41plusmn14% in K+CONST. These results suggest that the Na-K pump plays a major role in K+ apportionment between extracellular and intracellular compartments, and potassium dialysate concentration strongly influences pump activity. For this reason the computer-model here presented may represent a useful tool to quantitatively assess the impact of dialysate potassium on K+ kinetics in intra and extracellular compartments and to design dialysate potassium content tailored to the patient's needs.