Literature DB >> 8281718

Diffusion kinetics of urea, creatinine and uric acid in blood during hemodialysis. Clinical implications.

E Descombes1, F Perriard, G Fellay.   

Abstract

In order to elucidate some conflicting data reported in the literature the diffusion kinetics between red blood cells (RBC) and plasma during dialysis were studied for urea, creatinine and uric acid. Several complementary studies were performed. According to our results urea diffuses very rapidly from RBC to plasma and is almost at equilibrium at the dialyser outlet; thus the extraction of urea during dialysis is from both plasma and RBC. On the other hand creatinine and uric acid hardly diffuse at all from RBC to plasma during blood transit through the hemodialyser and these solutes are thus extracted mainly from plasma. As a consequence an important in-vitro equilibration process occurs for both solutes in blood drawn at the dialyser outlet; the equilibration rate is greatly temperature-dependent and to achieve complete equilibrium at room temperature, up to 6 to 12 hours were needed for creatinine and 2 to 3 hours for uric acid. Moreover, in the case of creatinine, but not for uric acid, a RBC/plasma disequilibrium was also found in blood drawn at the dialyser inlet; this finding is in contrast with previous reports and suggests that with high-efficiency dialysis modalities the interval between two successive RBC transits through the dialyser may be insufficient for complete equilibration of slowly equilibrating solutes. The clinical implications of these findings with respect to the in-vivo dialyser performance and clearance determinations are discussed.

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Year:  1993        PMID: 8281718

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN: 0301-0430            Impact factor:   0.975


  8 in total

1.  A wearable artificial kidney for patients with end-stage renal disease.

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Journal:  JCI Insight       Date:  2016-06-02

2.  Interdialytic creatinine change versus predialysis creatinine as indicators of nutritional status in maintenance hemodialysis.

Authors:  Carl P Walther; Caitlin Wise Carter; Chai L Low; Peter Williams; Dena E Rifkin; Robert W Steiner; Joachim H Ix
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3.  Methylamine clearance by haemodialysis is low.

Authors:  Manish P Ponda; Zhe Quan; Michal L Melamed; Amanda Raff; Timothy W Meyer; Thomas H Hostetter
Journal:  Nephrol Dial Transplant       Date:  2009-12-17       Impact factor: 5.992

4.  Uric acid is the major determinant of absorbance in spent dialysate allowing spectrophotometric evaluation of dialysis dose.

Authors:  Carlo Donadio; Dario Calia; Silvia Ghimenti; Massimo Onor; Elisa Colombini; Roger Fuoco; Fabio Di Francesco
Journal:  J Nephrol       Date:  2013-12-07       Impact factor: 3.902

5.  Removal of urea by electro-oxidation in a miniature dialysis device: a study in awake goats.

Authors:  Maarten Wester; Maaike K van Gelder; Jaap A Joles; Frank Simonis; Diënty H M Hazenbrink; Theo W M van Berkel; Koen R D Vaessen; Walther H Boer; Marianne C Verhaar; Karin G F Gerritsen
Journal:  Am J Physiol Renal Physiol       Date:  2018-07-11

6.  Mechanism of Prominent Trimethylamine Oxide (TMAO) Accumulation in Hemodialysis Patients.

Authors:  Xin Hai; Veeda Landeras; Mirela A Dobre; Peter DeOreo; Timothy W Meyer; Thomas H Hostetter
Journal:  PLoS One       Date:  2015-12-09       Impact factor: 3.240

7.  Selective Transport of Protein-Bound Uremic Toxins in Erythrocytes.

Authors:  Olivier Deltombe; Griet Glorieux; Sami Marzouki; Rosalinde Masereeuw; Daniel Schneditz; Sunny Eloot
Journal:  Toxins (Basel)       Date:  2019-07-01       Impact factor: 4.546

8.  Creatinine generation from kinetic modeling with or without postdialysis serum creatinine measurement: results from the HEMO study.

Authors:  John T Daugirdas; Thomas A Depner
Journal:  Nephrol Dial Transplant       Date:  2017-11-01       Impact factor: 5.992

  8 in total

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