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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.
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.