Pharm
Vasopressin Receptor Antagonist
search
Vasopressin Receptor Antagonist
, Vaptan, Conivaptan, Vaprisol, Tolvaptan, Samsca
Indications
Hypervolemic or euvolemic
Hyponatremia
(
Sodium
<125 mEq/L) due to CHF or
SIADH
FDA approved for short-term use only
Limit to hospitalized patients for close
Serum Sodium
monitoring
Contraindications
Severe symptomatic
Hyponatremia
Hypovolemic
Hyponatremia
Anuria
Creatinine Clearance
<30 ml/min/1.73m2 (Conivaptan) or <10 ml/min/1.73m2 (Tolvaptan)
Precautions
Not currently recommended for
Hyponatremia Management
(European Society of Endocrinology)
Risk of rapid
Sodium
over-correction
No mortality benefit
Spasovski (2014) Eur J Endocrinol 170(3): G1-47 [PubMed]
Efficacy
SALT Trial: Tolvaptan increased
Sodium
levels in
SIADH
,
Cirrhosis
, CHF
Schrier (2006) N Engl J Med 355(20): 2099-112 [PubMed]
Dosing
Conivaptan (Vaprisol)
Loading: 20 mg IV (in 100 ml D5W) infused over 30 minutes
In moderate liver disease, use 10 mg IV over 30 minutes
Maintenance: 20 mg IV over 24 hours for 2-4 days (max 40 mg/24 hours)
In moderate liver disease, use 10 mg IV over 24 hours (max 20 mg/24 hours)
Do not use longer than 4 days
Tolvaptan (Samsca)
Start: 15 mg orally daily
Increase to 30 mg daily after 24 hours if needed
Titrate to maximum of 60 mg daily based on goal
Sodium
concentration
Pharmacokinetics
Metabolized by
CYP3A4
(both Conivaptan and Tolvaptan)
Half life
Conivaptan: 5-8 hours
Tolvaptan: 5-12 hours (onset at 2-4 hours, peaks at 4-8 hours)
Excretion
Primarily feces (Conivaptan is 12% renally excreted as metabolites)
Adverse Effects
Conivaptan (Vaprisol) most common adverse effects
Fever
Hypokalemia
IV site inflammation
Orthostatic Hypotension
Tolvaptan (Samsca) most common adverse effects
Nausea
Pollakuria
Polyuria
Thirst
Xerostomia
References
Dahl (2012) Aliment Pharmacol Ther 36(7): 619-26 [PubMed]
Lehrich (2013) Am J Kidney Dis 62(2): 364-76 [PubMed]
Peri (2013) J Clin Endocrinol Metab 98(4): 1321-32 [PubMed]
Type your search phrase here