What is the appropriate dosing range for norepinephrine (norepinephrine) intravenous (IV) infusion?

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Last updated: July 22, 2025View editorial policy

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Appropriate Dosing Range for Norepinephrine IV Infusion

The appropriate dosing range for norepinephrine intravenous infusion is 0.1-1.0 mcg/kg/min, titrated to desired clinical effect, with doses up to 5 mcg/kg/min sometimes necessary in severe shock. 1

Initial Dosing and Titration

Norepinephrine is primarily used for shock states after adequate volume resuscitation. The dosing should follow this algorithm:

  1. Starting dose: Begin at 0.1 mcg/kg/min
  2. Titration: Gradually increase dose based on hemodynamic response
  3. Target: Achieve mean arterial pressure (MAP) ≥65 mmHg
  4. Typical range: 0.1-1.0 mcg/kg/min
  5. Maximum dose: Up to 5 mcg/kg/min may be required in severe, refractory shock

Preparation and Administration

Norepinephrine should be administered through a central venous catheter whenever possible to minimize risk of extravasation. However, recent evidence suggests peripheral administration may be safe with proper protocols 2.

Standard preparation methods:

  • Add 4 mg (4 mL) of norepinephrine to 250 mL D5W or NS to yield 16 mcg/mL
  • Alternative concentration: 1 mg in 100 mL saline (10 mcg/mL)

Clinical Scenarios and Dosing Considerations

Cardiogenic/Distributive Shock

  • Pediatric dosing: 0.1-1.0 mcg/kg/min 1
  • Adult dosing: Same range, with careful titration to effect

Septic Shock

  • Early administration (within 1-2 hours) at low doses improves shock control rate by 6 hours 3
  • Target MAP of 75 mmHg may optimize renal perfusion, filtration and oxygenation compared to lower targets 4

Refractory Hypotension

  • For hypotension unresponsive to initial doses, consider:
    • Increasing norepinephrine up to 5 mcg/kg/min
    • Adding a second vasopressor agent
    • Addressing underlying cause

Monitoring and Safety Considerations

Required Monitoring

  • Continuous blood pressure monitoring
  • Heart rate and rhythm
  • Urine output
  • Peripheral perfusion
  • Serum lactate (when available)

Potential Complications

  • Extravasation can result in severe tissue injury
    • If extravasation occurs, consider phentolamine (0.1-0.2 mg/kg up to 10 mg diluted in 10 mL NS) injected intradermally at the site 1
  • Tachyarrhythmias/ectopic beats
  • Peripheral, renal, and splanchnic vasoconstriction at higher doses (>20 mcg/kg/min) 1

Special Populations

Obesity

Weight-based dosing in obese patients may lead to higher cumulative norepinephrine requirements and prolonged vasopressor duration compared to non-weight-based approaches, without improving time to target MAP 5. Consider ideal body weight for dosing calculations in significantly obese patients.

Pediatric Patients

  • Dosing range remains 0.1-1.0 mcg/kg/min, titrated to effect
  • Maximum doses up to 5 mcg/kg/min may be necessary in severe shock 1

Clinical Pearls and Pitfalls

  • Critical pitfall: Administering norepinephrine before adequate volume resuscitation may worsen tissue perfusion
  • Important consideration: Norepinephrine effects are dose-dependent; higher doses (>1 mcg/kg/min) predominantly stimulate α-adrenergic receptors causing vasoconstriction
  • Safety measure: Always use an infusion pump for administration
  • Weaning strategy: Once the patient is stable, gradually reduce the dose by 0.05-0.1 mcg/kg/min while monitoring hemodynamic response

Norepinephrine remains the first-line vasopressor for most shock states, and proper dosing is essential for optimizing outcomes while minimizing adverse effects.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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