Treatment of acute hyponatremia: ensuring the excretion of a predictable amount of electrolyte-free water
- PMID: 10890640
- DOI: 10.1097/00003246-200006000-00037
Treatment of acute hyponatremia: ensuring the excretion of a predictable amount of electrolyte-free water
Abstract
Background: Hypertonic saline is the recommended therapy to shrink swollen brain cells in patients with acute hyponatremia accompanied by seizures.
Objectives: In the absence of hypertonic saline, hypertonic mannitol will shrink the cell volume. Because mannitol is excreted rapidly, our aim was to ensure that it would be excreted with electrolyte-free water (EFW) and to evaluate the renal mechanisms responsible for EFW excretion.
Design: A randomized, prospective, placebo-controlled study in rats was carried out in a research laboratory.
Subjects: Adult male Wistar rats.
Interventions: The control group of rats (n = 6) was administered hypotonic saline, a loop diuretic, vasopressin, and glucose by the intraperitoneal route; in the experimental group (n = 6), glucose was replaced with mannitol. Plasma electrolytes were measured at 0 and 210 mins, and balances for water, sodium, and potassium were obtained from 0 to 90 mins and from 90 to 210 mins.
Measurements and main results: Virtually 100% of the administered mannitol was excreted within 210 mins, and half was excreted in the first 90 mins. The urine contained EFW only in the mannitol group because of a larger volume in the first 90 mins (EFW, 3.7 mL) and to a lower excretion of NaCl in the next 120 mins (EFW, 3.5 mL).
Conclusions: The combined use of mannitol and a loop diuretic caused the excretion of a predictable volume of EFW because the urine was iso-osmotic to plasma and contained all the administered mannitol. The calculated decrease in intracellular fluid volume was equivalent when mannitol was retained or excreted.
Comment in
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Mannitol: a therapeutic alternative in the treatment of acute hyponatremia?Crit Care Med. 2000 Jun;28(6):2152-3. doi: 10.1097/00003246-200006000-00092. Crit Care Med. 2000. PMID: 10890690 No abstract available.
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