Treatment Options for Hyponatremia
The treatment of hyponatremia should be based on symptom severity, volume status, and underlying cause, with careful attention to correction rates to prevent osmotic demyelination syndrome. 1
Initial Assessment and Classification
- Hyponatremia evaluation should include serum and urine osmolarity, urine electrolytes, uric acid, and assessment of extracellular fluid volume status to determine the underlying cause 2, 1
- Categorize patients according to volume status: hypovolemic, euvolemic, or hypervolemic hyponatremia 1, 3
- A serum sodium value less than 131 mmol/L should prompt a comprehensive workup 2
Treatment Based on Symptom Severity
Severe Symptomatic Hyponatremia (seizures, coma, altered mental status)
- Administer 3% hypertonic saline with an initial goal to correct 6 mmol/L over 6 hours or until severe symptoms resolve 2, 1, 4
- Total correction should not exceed 8 mmol/L in 24 hours to prevent osmotic demyelination syndrome 2, 1, 4
- After initial 6 mmol/L correction, limit to only 2 mmol/L in the following 18 hours 4
- Consider ICU admission for close monitoring during treatment 1
- Discontinue 3% saline when severe symptoms resolve and transition to protocols for mild symptoms or asymptomatic hyponatremia 4
Mild to Moderate Symptomatic Hyponatremia
- For chronic hyponatremia, avoid rapid correction exceeding 1 mmol/L/hour 2, 1
- Patients with advanced liver disease, alcoholism, malnutrition, or prior encephalopathy require more cautious correction (4-6 mmol/L per day) 1
Treatment Based on Volume Status
Hypovolemic Hyponatremia
- Discontinue diuretics and administer isotonic saline (0.9% NaCl) for volume repletion 1, 5
- Address the underlying cause (e.g., gastrointestinal losses, renal losses) 1, 6
Euvolemic Hyponatremia (SIADH)
- Fluid restriction to 1L/day is the cornerstone of treatment for mild/asymptomatic cases 1, 7
- Consider pharmacological options for resistant cases:
- Tolvaptan (vasopressin receptor antagonist) for clinically significant hyponatremia resistant to fluid restriction, starting at 15 mg once daily 1, 8
- Tolvaptan showed significant improvement in serum sodium levels compared to placebo in clinical trials 8
- Other options include demeclocycline, lithium, or urea 1, 3
Hypervolemic Hyponatremia (heart failure, cirrhosis)
- Implement fluid restriction to 1000-1500 mL/day for moderate hyponatremia (120-125 mmol/L) 1, 5
- For severe hyponatremia (<120 mmol/L), consider more severe fluid restriction plus albumin infusion 1
- Avoid hypertonic saline unless life-threatening symptoms are present, as it may worsen edema and ascites 1
Special Considerations
Cerebral Salt Wasting (CSW)
- Treatment focuses on volume and sodium replacement, not fluid restriction 2, 1
- For severe symptoms, administer 3% hypertonic saline and fludrocortisone 2, 1
- Subarachnoid hemorrhage patients receive treatment even for sodium levels of 131-135 mmol/L 2, 4
Patients with Liver Disease
- Require more cautious correction (4-6 mmol/L per day) due to higher risk of osmotic demyelination syndrome 1
- Consider albumin infusion alongside fluid restriction in cirrhotic patients 1
Monitoring During Treatment
- For severe symptoms: monitor serum sodium every 2 hours during initial correction 1
- After resolution of severe symptoms, monitor every 4 hours 4
- Calculate sodium deficit using formula: Desired increase in Na (mEq/L) × (0.5 × ideal body weight in kg) 1
Common Pitfalls to Avoid
- Overly rapid correction of chronic hyponatremia leading to osmotic demyelination syndrome 2, 1, 3
- Using fluid restriction in cerebral salt wasting, which can worsen outcomes 2, 1
- Failing to recognize and treat the underlying cause 1, 6
- Using hypertonic saline in hypervolemic hyponatremia without life-threatening symptoms 1
- Inadequate monitoring during active correction 1
Pharmacological Considerations
- Tolvaptan may cause gastrointestinal bleeding in patients with cirrhosis (10% vs 2% with placebo) 8
- Common adverse effects of tolvaptan include thirst (14%), dry mouth (13%), and polyuria (11%) 8
- Hypernatremia occurred in 1.7% of patients receiving tolvaptan vs. 0.8% receiving placebo 8
- Avoid concomitant use of tolvaptan with strong CYP3A inhibitors 8