• Medientyp: E-Artikel
  • Titel: Sodium Polystyrene Sulfonate Treatment for Lithium Toxicity: Effects on Serum Potassium Concentrations
  • Beteiligte: Linakis, James G.; Hull, Keith M.; Lacouture, Peter G.; Lockhart, Gregory R.; Lewander, William J.; Maher, Timothy J.
  • Erschienen: Wiley, 1996
  • Erschienen in: Academic Emergency Medicine
  • Sprache: Englisch
  • DOI: 10.1111/j.1553-2712.1996.tb03446.x
  • ISSN: 1069-6563; 1553-2712
  • Schlagwörter: Emergency Medicine ; General Medicine
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>ABSTRACT</jats:title><jats:p>Objective: To examine the effects of sodium polystyrene sulfonate (SPS) on serum potassium (K) concentrations in mice pretreated with parenteral lithium (Li).</jats:p><jats:p>Methods: A placebo–controlled murine model trial of SPS therapy following IV Li was performed. Sixty male CD–I mice weighing 18–22 g were administered either IV LiCl (125 mg/kg) or a control solution (normal saline). Half of the mice in each of these groups were then given orogastric water 20, 40, 90, 150, and 210 minutes after LiCl or normal saline; the other half received SPS (5 g/kg/dose) at equivalent times. Subgroups of each of these four groups were sacrificed at one, two, and six hours after pretreatment and the serum was analyzed for K concentration. Serum K concentrations for the various groups were compared with analysis of variance and Newman–Keuls tests for the comparison of multiple means.</jats:p><jats:p>Results: A statistically significant reduction of serum K concentrations occurred in the animals that received SPS treatment following either IV saline or LiCl solutions. The degree of K reduction that resulted from the combination of LiCl and SPS treatment (35% reduction at six hours, compared with the placebo–treated controls) was larger than that which resulted from eimer IV Li with oral water (15% reduction) or IV saline with oral SPS (20% reduction).</jats:p><jats:p>Conclusions: These findings suggest that development of hypokalemia may represent a potential limitation in the use of SPS in the treatment for Li toxicity.</jats:p>
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