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tolvaptanBlue Cross Blue Shield of Kansas

clinically significant hypervolemic hyponatremia

Initial criteria

  • Requested agent was initiated (or re-initiated) in the hospital AND
  • Prior to initiating therapy, patient has/had clinically significant hypervolemic or euvolemic hyponatremia defined by ONE of the following: (A) serum sodium <125 mEq/L OR (B) serum sodium ≥125 mEq/L and symptomatic hyponatremia that has resisted correction with fluid restriction AND
  • Patient does NOT have underlying liver disease, including cirrhosis AND
  • Medications known to cause hyponatremia have been evaluated and discontinued when appropriate AND
  • Patient will NOT be using the requested agent in combination with another tolvaptan product for the requested indication AND
  • Patient does not have any FDA labeled contraindications to the requested agent AND
  • Patient has not already received 30 days of therapy with the requested agent for the current hospitalization

Approval duration

365 days