Role of sodium in hemodialysis
- PMID: 10936802
- DOI: 10.1046/j.1523-1755.2000.07609.x
Role of sodium in hemodialysis
Abstract
Sodium chloride is the most abundant salt in extracellular fluid. In normal individuals, the tonicity exerted by dissolved sodium chloride determines plasma osmolality and indirectly determines intracellular tonicity and cell volume. Uremic patients retain nitrogenous wastes and have an elevated plasma osmolality. While urea exhibits osmotic activity in serum, no sustained gradient can be established across cell boundaries because it readily diffuses through cell membranes. Thus, sodium remains the major indicator of body tonicity and determines the distribution of water across the intracellular-extracellular boundary, subsequent cell volume, thirst, and, among patients with renal insufficiency, systemic blood pressure. As a result of highly conserved plasma tonicity control systems, uremic subjects demonstrate remarkable stability of their serum sodium. Dialysate is a synthetic interstitial fluid capable of reconstituting extracellular fluid composition through urea extraction and extremely efficient solute and solvent (salt and water) transfer to the patient. Subtle transdialyzer gradients deliver and remove large quantities of trace elements, solvent, and solute to patients, creating a variety of dialysis "disequilibrium" syndromes manifest as cellular and systemic distress. Every dialysis patient uses dialysate, and the most abundant chemicals in dialysate are salt and water. Despite its universal use, no consensus on dialysate composition or tonicity exists. This can only be explained if we believe that dialysate composition is best determined by matching unique dialysis delivery system characteristics to specific patient requirements. Such a paradigm treats dialysate as a drug and the dialysis system as a delivery device. Understanding the therapeutic and toxic profiles of this drug (dialysate) and its delivery device (the dialyzer) is important to safe, effective, goal-directed modifications of therapy. This article explores some of the historical rationale behind choosing specific dialysate tonicities.
Similar articles
-
Technology in clinical practice.ASAIO J. 2005 Nov-Dec;51(6):xxxii-xxxv. doi: 10.1097/01.mat.0000187397.85551.0b. ASAIO J. 2005. PMID: 16340347
-
Sodium balance in maintenance hemodialysis.Semin Dial. 2010 Nov-Dec;23(6):549-55. doi: 10.1111/j.1525-139X.2010.00794.x. Semin Dial. 2010. PMID: 21175831 Review.
-
Fluid dynamics during hemodialysis in relationship to sodium gradient between dialysate and plasma.ASAIO J. 2007 May-Jun;53(3):339-42. doi: 10.1097/MAT.0b013e318033cba7. ASAIO J. 2007. PMID: 17515726
-
Optimal composition of the dialysate, with emphasis on its influence on blood pressure.Nephrol Dial Transplant. 2004 Apr;19(4):785-96. doi: 10.1093/ndt/gfh102. Nephrol Dial Transplant. 2004. PMID: 15031331 Review.
-
[Use of dialysate conductivity to obtain neutral sodium balance in chronic hemodialysis patients].G Ital Nefrol. 2005 Jul-Aug;22(4):321-8. G Ital Nefrol. 2005. PMID: 16267792 Review. Italian.
Cited by
-
Preservation of blood pressure stability with hypertonic mannitol during hemodialysis initiation.Am J Nephrol. 2012;36(2):168-74. doi: 10.1159/000341273. Epub 2012 Jul 26. Am J Nephrol. 2012. PMID: 22846598 Free PMC article.
-
The Dialysis Sodium Gradient: A Modifiable Risk Factor for Fluid Overload.Nephron Extra. 2017 Feb 9;7(1):10-17. doi: 10.1159/000453674. eCollection 2017 Jan-Apr. Nephron Extra. 2017. PMID: 28413417 Free PMC article.
-
Dyselectrolytemia-management and implications in hemodialysis (Review).Exp Ther Med. 2021 Jan;21(1):102. doi: 10.3892/etm.2020.9534. Epub 2020 Nov 26. Exp Ther Med. 2021. PMID: 33363613 Free PMC article. Review.
-
The growing problem of intradialytic hypertension.Nat Rev Nephrol. 2010 Jan;6(1):41-8. doi: 10.1038/nrneph.2009.200. Epub 2009 Nov 24. Nat Rev Nephrol. 2010. PMID: 19935745 Review.
-
Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis.Artif Organs. 2019 Oct;43(10):1002-1013. doi: 10.1111/aor.13463. Epub 2019 Apr 29. Artif Organs. 2019. PMID: 30939213 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials