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Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis

INTRODUCTION: The kidneys play a crucial role in the regulation of electrolytes and acid-base homeostasis. Urinary Strong Ion Difference (SIDu = NaU + KU—ClU) represents an important aspect of renal acid-base regulation. We evaluated the role of SIDu as a marker of renal dysfunction in critically il...

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Autores principales: Balsorano, Paolo, Romagnoli, Stefano, Evans, Samuel Kagan, Ricci, Zaccaria, De Gaudio, Angelo Raffaele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892615/
https://www.ncbi.nlm.nih.gov/pubmed/27258049
http://dx.doi.org/10.1371/journal.pone.0156941
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author Balsorano, Paolo
Romagnoli, Stefano
Evans, Samuel Kagan
Ricci, Zaccaria
De Gaudio, Angelo Raffaele
author_facet Balsorano, Paolo
Romagnoli, Stefano
Evans, Samuel Kagan
Ricci, Zaccaria
De Gaudio, Angelo Raffaele
author_sort Balsorano, Paolo
collection PubMed
description INTRODUCTION: The kidneys play a crucial role in the regulation of electrolytes and acid-base homeostasis. Urinary Strong Ion Difference (SIDu = NaU + KU—ClU) represents an important aspect of renal acid-base regulation. We evaluated the role of SIDu as a marker of renal dysfunction in critically ill patients. MATERIALS AND METHODS: Patients admitted to the Medical Intensive Care Unit with a diagnosis of AKI for whom concomitant urinary samples available for SIDu calculation were retrospectively reviewed and staged according to KDIGO criteria for 3 days from inclusion. Patients were classified as Recovered (R-AKI) or Persistent-AKI (P-AKI) whether they exited KDIGO criteria within the 3-day observation period or not. A control group with normal renal function and normal serum acid-base and electrolytes was prospectively recruited in order to identify reference SIDu values. RESULTS: One-hundred-and-forty-three patients with a diagnosis of AKI were included: 77 with R-AKI, and 66 with P-AKI. Thirty-six controls were recruited. Patients with P-AKI had more severe renal dysfunction and higher mortality than patients with R-AKI (SCr 2.23(IQR:1.68–3.45) and 1.81(IQR1.5–2.5) mg/dl respectively, p<0.001; 24-h UO 1297(950) and 2100(1094) ml respectively, p = 0.003); 30-d mortality, 39% and 13% respectively; p<0.001). SIDu significantly differed between groups, with rising values from controls to P-AKI groups (16.4(12), 30(24) and 47.3(21.5) mEq/l respectively, p<0.001). DISCUSSION: SIDu may be a simple and inexpensive tool in AKI patients’ evaluation. Further research is needed to evaluate the ability of SIDu to identify patients with renal dysfunction before derangements in serum creatinine or urine output are observed.
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spelling pubmed-48926152016-06-16 Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis Balsorano, Paolo Romagnoli, Stefano Evans, Samuel Kagan Ricci, Zaccaria De Gaudio, Angelo Raffaele PLoS One Research Article INTRODUCTION: The kidneys play a crucial role in the regulation of electrolytes and acid-base homeostasis. Urinary Strong Ion Difference (SIDu = NaU + KU—ClU) represents an important aspect of renal acid-base regulation. We evaluated the role of SIDu as a marker of renal dysfunction in critically ill patients. MATERIALS AND METHODS: Patients admitted to the Medical Intensive Care Unit with a diagnosis of AKI for whom concomitant urinary samples available for SIDu calculation were retrospectively reviewed and staged according to KDIGO criteria for 3 days from inclusion. Patients were classified as Recovered (R-AKI) or Persistent-AKI (P-AKI) whether they exited KDIGO criteria within the 3-day observation period or not. A control group with normal renal function and normal serum acid-base and electrolytes was prospectively recruited in order to identify reference SIDu values. RESULTS: One-hundred-and-forty-three patients with a diagnosis of AKI were included: 77 with R-AKI, and 66 with P-AKI. Thirty-six controls were recruited. Patients with P-AKI had more severe renal dysfunction and higher mortality than patients with R-AKI (SCr 2.23(IQR:1.68–3.45) and 1.81(IQR1.5–2.5) mg/dl respectively, p<0.001; 24-h UO 1297(950) and 2100(1094) ml respectively, p = 0.003); 30-d mortality, 39% and 13% respectively; p<0.001). SIDu significantly differed between groups, with rising values from controls to P-AKI groups (16.4(12), 30(24) and 47.3(21.5) mEq/l respectively, p<0.001). DISCUSSION: SIDu may be a simple and inexpensive tool in AKI patients’ evaluation. Further research is needed to evaluate the ability of SIDu to identify patients with renal dysfunction before derangements in serum creatinine or urine output are observed. Public Library of Science 2016-06-03 /pmc/articles/PMC4892615/ /pubmed/27258049 http://dx.doi.org/10.1371/journal.pone.0156941 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Balsorano, Paolo
Romagnoli, Stefano
Evans, Samuel Kagan
Ricci, Zaccaria
De Gaudio, Angelo Raffaele
Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title_full Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title_fullStr Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title_full_unstemmed Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title_short Urinary Strong Ion Difference as a Marker of Renal Dysfunction. A Retrospective Analysis
title_sort urinary strong ion difference as a marker of renal dysfunction. a retrospective analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892615/
https://www.ncbi.nlm.nih.gov/pubmed/27258049
http://dx.doi.org/10.1371/journal.pone.0156941
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