Should patients on high doses of levophed (norepinephrine) be fed?

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Last updated: July 20, 2025View editorial policy

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Feeding Patients on High-Dose Norepinephrine

Patients on high doses of norepinephrine (≥0.3 μg/kg/min) should not receive full enteral nutrition until they are hemodynamically stabilized and weaned from high-dose vasopressors.

Rationale for Delaying Full Feeding During Vasopressor Support

Enteral nutrition (EN) during high-dose vasopressor therapy presents significant risks due to:

  1. Compromised Splanchnic Circulation: High-dose vasopressors cause significant vasoconstriction in the splanchnic circulation, potentially leading to:

    • Intestinal ischemia
    • Impaired nutrient absorption
    • Increased risk of feeding intolerance
  2. Evidence-Based Concerns: Recent guidelines specifically caution against early high-dose feeding in patients on high-dose vasopressors:

    • The Personalized Nutrition in Critical Care guidelines (2023) recommend avoiding higher doses of protein in "well-nourished mechanically ventilated patients admitted to ICU in shock on high doses of vasopressors (doses of norepi. ≥0.2 μg/kg/min)" 1
    • The Nutrirea-3 trial showed increased ICU length of stay by one day in patients on high-dose vasopressors (admission norepinephrine: 0.5 μg/kg/min) who received full nutrition compared to those on low-dose nutrition 1

Recommended Feeding Approach for Patients on High-Dose Norepinephrine

Phase 1: During High-Dose Vasopressor Support (≥0.3 μg/kg/min)

  • Provide hypocaloric nutrition (not exceeding 70% of energy expenditure)
  • Limit protein to ≤0.8 g/kg/day until patient is stabilized and weaning off vasopressors 1
  • Consider low-dose enteral nutrition (10-15 kcal/kg/day) if the patient has an intact and functioning GI tract

Phase 2: During Vasopressor Weaning (Norepinephrine <0.3 μg/kg/min)

  • Gradually increase nutrition as vasopressor requirements decrease
  • Monitor for feeding intolerance (high gastric residuals, abdominal distension)
  • Consider prokinetic agents (metoclopramide) if feeding intolerance occurs 1

Phase 3: After Vasopressor Discontinuation

  • Progress to full nutritional support (25-30 kcal/kg/day) 1
  • Increase protein to >1.2 g/kg/day 1

Monitoring Parameters During Feeding

  1. Signs of Feeding Intolerance:

    • Increased gastric residual volumes (>500 ml/6h) 1
    • Abdominal distension
    • Worsening hemodynamic parameters after feeding initiation
  2. Metabolic Parameters:

    • Lactate levels (rising levels may indicate intestinal ischemia)
    • Blood glucose (maintain appropriate glycemic control)

Special Considerations

  • Alternative Feeding Routes: Post-pyloric feeding may be considered in patients with high gastric residuals but should still follow the hypocaloric approach during high-dose vasopressor therapy
  • Parenteral Nutrition: Consider supplemental parenteral nutrition only if enteral route is contraindicated and after patient is hemodynamically stabilized 1

Common Pitfalls to Avoid

  1. Aggressive Early Feeding: The ESPEN guidelines caution that "early high-dose feeding should be avoided until patient is stabilized early in ICU stay" 1

  2. Ignoring Signs of Intestinal Ischemia: Abdominal distension, increasing lactate, or worsening hemodynamics after feeding initiation should prompt immediate feeding cessation

  3. One-Size-Fits-All Approach: While general guidelines recommend caution with feeding during high-dose vasopressor therapy, individual assessment of hemodynamic stability and resuscitation status remains important

The evidence clearly supports a cautious approach to feeding patients on high-dose norepinephrine, with gradual advancement of nutrition as hemodynamic stability improves and vasopressor requirements decrease.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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