Abstract

BackgroundEven with abundant evidence for osmotic demyelination in patients with hyponatremia, the risk factors for overcorrection have not been fully investigated. Therefore the purpose of this study is to clarify the risks for overcorrection during the treatment of chronic profound hyponatremia.MethodsThis is a single-center retrospective observational study. We enrolled 56 adult patients with a serum sodium (SNa) concentration of ≤125 mEq/L who were treated in an intensive care unit by nephrologists using a locally developed, fixed treatment algorithm between February 2012 and April 2014. The impact of patient parameters on the incidence of overcorrection was estimated using univariable and multivariable logistic regression models. Overcorrection was defined as an increase of SNa by >10 mEq/L and >18 mEq/L during the first 24 and 48 h, respectively.ResultsThe median age was 78 years, 48.2% were male, and 94.6% of the patients presented with symptoms associated with hyponatremia. The initial median SNa was 115 mEq/L (quartile, 111–119 mEq/L). A total of 11 (19.6%) patients met the criteria for overcorrection with 9 (16.0%) occurring at 24 h, 6 (10.7%) at 48 h, and 4 (7.1%) at both 24 and 48 h. However, none of these patients developed osmotic demyelination. Primary polydipsia, initial SNa, and early urine output were the significant risk factors for overcorrection on univariable analysis. Multivariable analysis revealed that the initial SNa had a statistically significant impact on the incidence of overcorrection with an adjusted odds ratio of 0.84 (95% confidence interval, 0.70–0.98; p = 0.037) for every 1 mEq/L increase. Additionaly, the increase in SNa during the first 4 h and early urine output were significantly higher in patients with overcorrection than in those without (p = 0.001 and 0.005, respectively).ConclusionsAn initial low level of SNa was associated with an increased risk of overcorrection in patients with profound hyponatremia. In this regard, the rapid increase in SNa during the first 4 h may play an important role.

Highlights

  • Even with abundant evidence for osmotic demyelination in patients with hyponatremia, the risk factors for overcorrection have not been fully investigated

  • There is a paucity of literature on the risk factors for overcorrection [14], especially in “Chronic” profound hyponatremia, which carries a greater risk of neurologic complications from overcorrection, even though several risk factors for Osmotic demyelination (ODS) have been identified, including SNa ≤ 105 mEq/L at presentation, overcorrection itself, malnutrition, hypokalemia, and liver disease [15,16,17,18,19,20,21,22]

  • Prophylactic and therapeutic interventions for overcorrection included the use of 5% dextrose in water (D5W) in 18 (32.1%) patients, free water intake in 2 (3.6%) patients, and DDAVP in 11 (19.6%) patients

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Summary

Introduction

Even with abundant evidence for osmotic demyelination in patients with hyponatremia, the risk factors for overcorrection have not been fully investigated. The purpose of this study is to clarify the risks for overcorrection during the treatment of chronic profound hyponatremia. The problem of overcorrection makes the treatment of hyponatremia difficult because it can provoke osmotic demyelination (ODS), which is a dreaded neurologic complication associated with high mortality [9]. There is a paucity of literature on the risk factors for overcorrection [14], especially in “Chronic” profound hyponatremia, which carries a greater risk of neurologic complications from overcorrection, even though several risk factors for ODS have been identified, including SNa ≤ 105 mEq/L at presentation, overcorrection itself, malnutrition, hypokalemia, and liver disease [15,16,17,18,19,20,21,22]. We hypothesized that the identification of risk factors for overcorrection can improve the safety and efficacy of the treatment of chronic hyponatremia

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