A Regional Blood Flow Model for Glucose and Insulin Kinetics During Hemodialysis

Autor: Jacek Waniewski, Magda Galach, Karl Thomaseth, Daniel Schneditz
Rok vydání: 2013
Předmět:
Blood Glucose
medicine.medical_treatment
insulin blood level
Bolus (medicine)
Blood flow modeling
diabetic patient
Fluid management
blood flow
insulin release
glucose
systemic circulation
clinical article
hemodialysis
Chemistry
Insulin secretion
adult
Models
Cardiovascular

Model parameters
article
General Medicine
insulin clearance
Insulin kinetics
aged
glucose utilization
female
priority journal
ultrafiltration
Hemodialysis
insulin
extracorporeal circulation
medicine.medical_specialty
brain
Biomedical Engineering
Biophysics
Bioengineering
Hemodialyzers
liver
insulin dependent diabetes mellitus
Extracorporeal
fluid therapy
Biomaterials
Glucose concentration
male
Renal Dialysis
Internal medicine
Mole
medicine
Humans
controlled study
human
distribution volume
Distribution Volume
parameters
Insulin
Hemodynamics
glucose transport
hemodialysis patient
Blood flow
Extracorporeal systems
Kinetics
Lakes
glucose blood level
Endocrinology
Regional Blood Flow
Dialysis
Zdroj: ASAIO journal (1992) 59 (2013): 627–635. doi:10.1097/MAT.0000436714.72752.13
info:cnr-pdr/source/autori:Schneditz D., Galach M., Thomaseth K., Waniewski J./titolo:A regional blood flow model for glucose and insulin kinetics during hemodialysis/doi:10.1097%2FMAT.0000436714.72752.13/rivista:ASAIO journal (1992)/anno:2013/pagina_da:627/pagina_a:635/intervallo_pagine:627–635/volume:59
ISSN: 1058-2916
DOI: 10.1097/mat.0000436714.72752.13
Popis: The distribution and elimination of a bolus of glucose injected during hemodialysis (HD) was examined using a distributed double-pool regional blood flow model. Intracorporeal glucose disposal was assumed as insulin-independent (λ) in the central high-flow compartment comprising blood, brain, and internal organs, including pancreatic insulin secretion (a, C1) and hepatic insulin clearance (α). Insulin-dependent (γ) glucose utilization was allocated to the low-flow system comprising muscle, skin, and bone. This model was compared with a compact single-pool model using the same model parameters except for the distribution volume (V). Six parameters (C1, a, α, λ, γ, and V) were identified from data obtained in seven nondiabetic patients (59-115 kg). The fraction Fd of glucose removed by HD significantly (p < 0.05) correlated with baseline glucose concentration Cg,0 (5.561 ± 0.646 mmol/L; r = 0.535), extracorporeal clearance Kg (0.137 ± 0.024 L/min; r = 0.537), a (0.278 ± 0.095 L/mmol, r = -0.586), and λ (0.099 ± 0.078 L/min, r = -0.587). V was much larger in the double-compartment (17.8 ± 5.1 L) than in the single-compartment model (10.0 ± 3.0 L). The modeled glucose compartment volumes could be of interest for fluid management in HD patients. The use of extracorporeal glucose disposal to detect impaired glucose utilization (a, λ) remains to be validated in diabetic HD patients.
Databáze: OpenAIRE