ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: TH-OR025

Treatment (Rx) and Outcomes of Profound Hyponatremia

Session Information

Category: Fluid, Electrolytes, and Acid-Base Disorders

  • 1102 Fluid, Electrolyte, and Acid-Base Disorders: Clinical

Authors

  • Sterns, Richard H., Rochester Regional Health, Rochester, New York, United States
  • Silver, Stephen M., Rochester Regional Health, Rochester, New York, United States
  • Salhab Altamimi, Tamer, Rochester Regional Health, Rochester, New York, United States

Group or Team Name

  • PRONATREOUS Investigators.
Background

A thirty-year controversy on how severe, symptomatic hyponatremia should be treated gave way to consensus guidelines published in 2013 and 2014 recommending correction limits of 8 to 10 mmol/L/day to avoid osmotic demyelination syndrome (ODS) in high-risk patients. Recently, guidelines have been challenged by studies suggesting that ODS is “exceedingly rare” and unrelated to rate of correction (NEJM Evid, 2023;2:EVIDe2300014). A multi-center study to update data supporting current guidelines is in progress. Preliminary data from one of the study sites are presented here.

Methods

We reviewed medical records of all 23 patients admitted to four hospitals between 2015 and 2023 with serum sodium (SNa) ≤105 mmol/L and compared Rx and outcomes to a 1987 study of patients with SNa ≤105 mmol/L from the same region (Ann Int Med 1987;107:656).

Results

In the current study, 3 of 7 patients whose largest 24 hour increase in SNa (dSNa) was ≥12 mmol/L developed ODS -- 1 with MRI-documented central pontine myelinolysis (CPM) and 2 with CPM and extrapontine myelinolysis (EPM). Two of the patients with ODS developed severe neurological complications and one had only mild dysarthria. Median dSNa for all 23 patients was 10 mmol/L (IQR = 5); 12 were given DDAVP & D5W to re-lower SNa because of dSNa ≥8 mmol/L. In 11 of 11 patients Rx'd. with proactive DDAVP and 3% NaCl ("DDAVP clamp"), dSNa was ≤10 mmol/L; in 9 of 11, dSNa was ≤ 8 mmol/L. In the 1987 study, the hourly rate of correction to reach a SNa ≥ 120 mmol/L was nearly twice as fast as in the current study.

Conclusion

Preliminary data suggest that ODS is not exceedingly rare in patients with SNa ≤105 mmol/L who are corrected by ≥12 mmol/L/24h. ODS may be less common now than it was in the 1980s because of changes in practice patterns. Additional data from other study sites will be needed to validate these conclusions.

Digital Object Identifier (DOI)