Vasopressin

Vasopressin

Vasopressin, also known as antidiuretic hormone (ADH), is a peptide hormone synthesized in the hypothalamus and stored in the posterior pituitary gland. It plays a critical role in regulating water retention in the kidneys and maintaining vascular tone. As a medication, vasopressin is utilized in various clinical settings, including vasodilatory shock, diabetes insipidus, gastrointestinal bleeding, and cardiac arrest.


Uses

  1. Vasodilatory Shock: Used in septic and vasodilatory shock unresponsive to catecholamines to increase blood pressure through vasoconstriction.
  2. Diabetes Insipidus: Treats central diabetes insipidus by reducing urine output and controlling fluid balance.
  3. Gastrointestinal Bleeding: Manages esophageal variceal bleeding by reducing portal pressure.
  4. Cardiac Arrest: Acts as an alternative to epinephrine in advanced cardiac life support (ACLS) during resuscitation.
  5. Hemodynamic Support: Used in post-cardiotomy shock to improve hemodynamics.


Dosage and Administration

Vasodilatory Shock:

  • IV Infusion: 0.01-0.04 units/min, titrate based on blood pressure response.

Cardiac Arrest (ACLS):

  • IV/IO: 40 units as a single dose, can replace the first or second dose of epinephrine in adult cardiac arrest.

Diabetes Insipidus:

  • IM/Subcutaneous: 5-10 units 2-4 times daily as needed.
  • Intranasal: 10-40 mcg daily, divided into 1-3 doses.

Esophageal Variceal Bleeding:

  • IV: 0.2-0.4 units/min infusion. Adjust to control bleeding.


Dose Adjustment in Different Diseases

  • Hepatic Impairment: Monitor closely; metabolism may be altered.
  • Renal Impairment: Adjust dose or increase monitoring due to reduced excretion.
  • Elderly: Use with caution due to increased risk of hyponatremia and ischemia.
  • Cardiac Disease: Lower doses may be required to reduce the risk of myocardial ischemia.


Drug Combinations in Use

  • Catecholamines (e.g., norepinephrine): Enhances vasopressor effects.
  • Corticosteroids: May improve outcomes in shock management.
  • Diuretics: Increased risk of hyponatremia when combined with vasopressin.
  • Carbamazepine, Chlorpropamide, Clofibrate, Tricyclic Antidepressants: Potentiate the antidiuretic effect.


Presentation or Form

  • Injection: 20 units/mL in 1 mL ampoules or vials.
  • Intranasal Spray: Available for use in diabetes insipidus.


Pharmacokinetics

  • Onset: Immediate with IV use.
  • Duration: 30-60 minutes for IV administration; longer duration with subcutaneous use.
  • Half-life: 10-20 minutes when given intravenously.
  • Metabolism: Primarily in the liver and kidneys.
  • Excretion: Renal and hepatic.

Pharmacodynamics

  • V1 Receptors: Located on vascular smooth muscle, cause vasoconstriction and increase blood pressure.
  • V2 Receptors: Located in the renal collecting ducts, promote water reabsorption and reduce urine output.
  • V3 Receptors: Located in the anterior pituitary, stimulate ACTH release.


Drug Interactions

  • Catecholamines: Enhances vasopressor effects.
  • Corticosteroids: May enhance vasopressor effects.
  • Diuretics: Risk of hyponatremia.
  • Potentiators: Carbamazepine, chlorpropamide, clofibrate, tricyclic antidepressants.
  • Antagonists: Lithium and demeclocycline may reduce vasopressin efficacy.


Comparison with Other Drugs of Same Category

Drug

Mechanism of Action

Indications

Onset (IV)

Half-life (IV)

Key Side Effects

Vasopressin

V1 and V2 receptor agonist

Shock, DI, bleeding

Immediate

10-20 min

Hyponatremia, ischemia

Desmopressin

Selective V2 agonist

DI, bleeding disorders

30 min

1-2 hours

Headache, hyponatremia

Terlipressin

V1 receptor agonist

Variceal bleeding

30 min

4-6 hours

Ischemia, abdominal pain


Precautions and Special Considerations

  • Cardiovascular Disease: Increased risk of myocardial ischemia.
  • Elderly: Higher risk of adverse effects, especially hyponatremia.
  • Seizure Disorders: Use with caution.
  • Pregnancy: Category C; use only if the potential benefit justifies the risk.
  • Extravasation: Monitor for tissue necrosis at infusion sites.


Side Effects

Common:

  • Abdominal cramps
  • Nausea
  • Headache

Serious:

  • Hyponatremia
  • Arrhythmias
  • Ischemia (myocardial, mesenteric, or peripheral)
  • Tissue necrosis at infusion site

Less Common:

  • Water intoxication
  • Allergic reactions
  • Bronchial constriction


Recent Updates and Guidelines

  • 2023 ACC/AHA Guidelines: Vasopressin recommended as an adjunct to norepinephrine in septic shock when MAP remains below target.
  • Evolving ACLS Protocols: Emphasis on epinephrine as first-line, with vasopressin reserved for specific cases.
  • New Formulations: Development of slow-release intranasal formulations for diabetes insipidus management.


Facts to Remember

  • Vasopressin can be life-saving in vasodilatory shock and refractory cardiac arrest.
  • Monitor serum sodium and urine output to avoid hyponatremia.
  • Extravasation requires immediate treatment to prevent tissue necrosis.
  • Use cautiously in patients with coronary artery disease or seizure disorders.
  • Continuous monitoring of hemodynamics is essential during administration.


References

  1. NCBI - Vasopressin: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672256/
  2. Goodman & Gilman's The Pharmacological Basis of Therapeutics, 13th Edition.
  3. Stoelting's Pharmacology and Physiology in Anesthetic Practice, 5th Edition.
  4. UpToDate - Vasopressin in the treatment of vasodilatory shock.
  5. Lexicomp Online - Vasopressin Drug Information.

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