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Bedside Snapshot
  • Core dose: Shock: 0.03–0.04 units/min IV fixed-dose (not titrated); Cardiac arrest: 40 units IV push (replaces first or second epinephrine dose)
  • Onset/duration: IV onset immediate; half-life 10–20 min; pressor effect lasts 30–60 min after stopping
  • Key danger: Tissue ischemia (splanchnic, coronary, digital); hyponatremia with prolonged use; arrhythmias; avoid bolus dosing outside cardiac arrest
  • Special: Catecholamine-sparing vasopressor; works via V1 receptors independent of adrenergic system; useful when catecholamine-resistant or as adjunct to norepinephrine
Brand & Generic Names
  • Generic Name: Vasopressin injection, USP (arginine vasopressin)
  • Brand Names: Vasostrict® (premix and concentrated vials)
  • Also Known As: Arginine vasopressin (AVP)
Medication Class

Non-catecholamine vasopressor (endogenous pituitary peptide); V1a/V1b/V2 receptor agonist

Pharmacology

Mechanism of Action:

  • V1a receptor activation → Gq/PLC-IP3-Ca²⁺-mediated vascular smooth-muscle contraction (systemic vasoconstriction)
  • V2 receptor activation in renal collecting duct → aquaporin-2 insertion and free-water reabsorption (antidiuresis)
  • V1b (V3) in pituitary → ACTH release
  • In septic vasoplegia, vasopressin may restore catecholamine responsiveness and counteract NO-mediated vasodilation
  • Typically used as fixed-dose adjunct to norepinephrine

Pharmacokinetics:

  • Onset: Within minutes (reported 30–60 min for peak pressor effect)
  • Half-life: ~10–20 minutes
  • Distribution: Vd ~0.14–0.2 L/kg
  • Metabolism: Rapidly cleared by hepatic/renal metabolism
  • Elimination: Small fraction renally excreted unchanged
Indications
  • Vasodilatory shock refractory to fluids and catecholamines — adjunct to norepinephrine in septic shock
  • Post-cardiotomy vasoplegia (ICU/OR)
  • Selected GI variceal hemorrhage protocols (usually when octreotide/terlipressin unavailable) with concurrent nitroglycerin (institutional)
⚠️ ACLS Update: Vasopressin is NOT used in modern ACLS for cardiac arrest (removed from AHA algorithm in 2015). Use epinephrine instead.
Conditions Treated
  • Septic shock (catecholamine-refractory)
  • Vasodilatory shock
  • Post-cardiotomy vasoplegia
  • GI variceal hemorrhage (select protocols)
Dosing & Administration

Available Forms (FDA-labeled):

  • 20 units/mL vials (single-dose 1 mL; multi-dose 10 mL with preservative)
  • Premix: 40 units/100 mL (0.4 U/mL) ready-to-use
  • Premix: 60 units/100 mL (0.6 U/mL) ready-to-use

Adult Dosing - Septic Shock:

  • Standard fixed dose: 0.03 U/min adjunct to norepinephrine
  • Titration range (some protocols): 0.01–0.06–0.07 U/min
  • Maximum: Avoid exceeding 0.06–0.07 U/min due to ischemia risk

Adult Dosing - Post-Cardiotomy Vasoplegia:

  • Range: 0.03–0.1 U/min
  • Careful titration to the lowest effective dose

Pediatric Dosing (Catecholamine-Refractory Septic Shock):

  • Typical range: 0.0003–0.002 U/kg/min (0.3–2 mU/kg/min)
  • Neonatal ICU: May start as low as 0.0001 U/kg/min and titrate by 0.0002–0.0003 U/kg/min to effect
  • Use only in PICU/NICU settings with invasive monitoring

Administration:

  • Run on a smart pump with dose in units/min (adults) or units/kg/min (pediatrics)
  • Dedicated lumen preferred
  • Peripheral start is acceptable while securing central access when shock is life-threatening
  • Monitor IV site closely and convert to central line when feasible

Weaning:

  • After maintaining target BP ≥8 hours without catecholamines, taper by 0.005 U/min each hour as tolerated to maintain MAP
Contraindications

Contraindications:

  • Hypersensitivity to vasopressin (and to chlorobutanol for multi-dose vial)

Precautions:

  • Ischemia-prone states: Coronary, mesenteric, digital, or skin ischemia may occur—risk rises at higher doses or with concomitant high-dose catecholamines
  • Cardiac function: May worsen cardiac output in impaired myocardial function; avoid excessive dosing
  • Water balance: V2 effects can cause hyponatremia during infusion; reversible diabetes insipidus with hypernatremia may occur after abrupt discontinuation
⚠️ Ischemia Risk: Higher doses (>0.06–0.07 U/min) significantly increase risk of digital, mesenteric, and cardiac ischemia. Use the lowest effective dose.
Adverse Effects

Ischemic Complications:

  • Digital/mesenteric/cutaneous ischemia
  • Myocardial ischemia

Cardiac:

  • Arrhythmias (including atrial fibrillation)
  • Decreased cardiac output

Electrolyte/Water Balance:

  • Hyponatremia (during therapy)
  • Hypernatremia/polyuria after discontinuation (reversible diabetes insipidus)

Other:

  • Local infusion-site complications
  • Headache, abdominal cramps, nausea
Drug Interactions
  • Catecholamines: Combined use is standard in septic shock; monitor for additive ischemia
  • Indomethacin: May increase vasopressin effect
  • Ganglionic blockers: May enhance blood pressure increase
  • Furosemide: May decrease antidiuretic effect
  • SIADH-promoting drugs (SSRIs, carbamazepine, etc.): May potentiate hyponatremia during vasopressin therapy
  • Nitroglycerin: Pair with nitroglycerin infusion for variceal bleeding protocols to mitigate coronary ischemia (institutional)
Monitoring

Perfusion Monitoring:

  • MAP ≥65 mmHg (adults) or age-appropriate target
  • Capillary refill, mental status
  • Urine output
  • Lactate trend

Ischemia Monitoring:

  • Continuous ECG
  • Frequent assessments of digits/skin/abdomen for ischemia
  • Troponin if symptoms of myocardial ischemia

Electrolytes & Water Balance:

  • Sodium at least daily (q6–12h during initiation)
  • Fluid balance/weights
  • Watch for polyuria/hypernatremia after stopping—consider DDAVP if diabetes insipidus occurs

Dose-Sparing Effects:

  • Document norepinephrine-equivalent dose before/after starting vasopressin
  • Follow weaning protocols
Clinical Pearls
Timing to Start: Start vasopressin when escalating norepinephrine toward ~0.25–0.5 mcg/kg/min to raise MAP and decrease adrenergic dose per Surviving Sepsis Campaign rationale.
Fixed Dosing: Keep dose fixed at 0.03 U/min in most adults. Going higher increases ischemia risk and rarely improves outcomes.
Peripheral Initiation: Peripheral initiation is reasonable in crashing patients. Convert to central access promptly and monitor the site closely.
⚠️ Digital Ischemia Management: If digital ischemia develops: lower vasopressor doses, warm the limb, consider topical nitroglycerin and vascular consult. Address underlying shock.
⚠️ ACLS Important Update: Vasopressin is NOT part of the adult cardiac arrest drug algorithm since 2015. Use epinephrine instead.
ℹ️ Vasopressor Comparison:
Property Norepinephrine Vasopressin Epinephrine Phenylephrine
Primary receptors α1 > β1 V1a (±V2/V1b) α1, β1, β2 α1
Typical ICU role First-line in septic shock Adjunct at fixed 0.03 U/min Second-line/alternative Select cases (e.g., tachyarrhythmia with NE)
Arrhythmias ↑ (dose-related AF) Neutral/↓ vs NE alone; ↑ digital ischemia risk ↑↑ Neutral; may ↓ stroke volume
Notes Strong evidence base Avoid >0.06–0.07 U/min; ischemia risk ↑ lactate via β2 Pure vasoconstrictor; consider in anesthesia/post-CPB
References
  • 1. Evans, L., Rhodes, A., Alhazzani, W., et al. (2021). Surviving Sepsis Campaign: International guidelines for management of sepsis and septic shock 2021. Intensive Care Medicine, 47, 1181–1247. https://doi.org/10.1007/s00134-021-06506-y
  • 2. Par Pharmaceutical, Inc. (2020). VASOSTRICT (vasopressin) injection, USP — Prescribing Information. U.S. FDA/AccessData.
  • 3. Medscape. (2024–2025). Vasopressin (Vasostrict) — Dosing, indications, interactions, adverse effects, and pharmacology.
  • 4. Russell, J. A., Walley, K. R., Singer, J., et al. (2008). Vasopressin versus norepinephrine infusion in patients with septic shock (VASST). New England Journal of Medicine, 358, 877–887.
  • 5. Gordon, A. C., Mason, A. J., Thirunavukkarasu, N., et al. (2016). Early vasopressin vs norepinephrine in septic shock (VANISH). JAMA, 316(5), 509–518.
  • 6. Jozwiak, M., et al. (2022). Vasopressors and risk of acute mesenteric ischemia. Frontiers in Medicine, 9, 826446.
  • 7. Panchal, A. R., et al. (2019). Adult basic & advanced life support—AHA Guidelines. Circulation, 140(24), e881–e894.
  • 8. Choong, K., et al. (2016). Vasopressin in pediatric critical care. Pediatric Critical Care Medicine, 17(3), 264–275.
  • 9. University of Iowa Stead Family Children's Hospital. (2020). Neonatal vasopressin infusion guideline.