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Nutrition in the ICU Patient
Notes for MD Anaesthesiology Examination (10 Marks)
1. Introduction and Importance
Malnutrition is common in the critically ill and is independently associated with increased infectious complications, prolonged ICU and hospital stay, impaired wound healing, dysfunctional immune response, and higher mortality. The metabolic response to critical illness involves a catabolic state characterized by:
- Accelerated protein breakdown and muscle wasting
- Insulin resistance and stress hyperglycemia
- Altered fat mobilization
- Increased energy demand with impaired utilization
Nutrition support in the ICU is therefore not merely supportive - it is a therapeutic intervention. Management is guided primarily by the ASPEN/SCCM 2016 & 2021 Guidelines and the ESPEN 2019/2023 Practical Guidelines for Clinical Nutrition in the ICU.
(Harrison's Principles of Internal Medicine, 22e; Mulholland & Greenfield's Surgery, 7e)
2. Nutritional Risk Screening (Step 1 on ICU Admission)
All ICU patients should be assessed for nutritional risk on admission. Two validated screening tools are recommended:
NUTRIC Score (Nutrition Risk in the Critically Ill)
Variables: Age, APACHE II, SOFA, number of comorbidities, days from hospital to ICU admission, ± IL-6
- Score ≥5 (without IL-6) or ≥6 (with IL-6) = high nutritional risk
- Indicates patients most likely to benefit from aggressive nutritional therapy
NRS-2002 (Nutritional Risk Screening 2002)
Assesses nutritional impairment (weight loss, BMI, food intake) + disease severity score
- Score ≥3 = nutritional risk; score ≥5 = high nutritional risk
- ICU patients with APACHE >10 score 3 points for disease severity automatically
(Current Surgical Therapy 14e; Mulholland & Greenfield's Surgery, 7e)
3. Calculating Nutritional Requirements
3a. Energy Requirements
Preferred method: Indirect calorimetry (IC) - measures actual resting energy expenditure (REE) via VO2 and VCO2. This is the gold standard when feasible.
When IC unavailable (most common in routine ICU):
- Use a published predictive equation (Penn State, Mifflin-St Jeor) OR
- Simplistic weight-based equation: 12-25 kcal/kg actual body weight (ABW)/day during the first 7-10 days of ICU stay (ASPEN 2021)
- ESPEN 2023: Target ~20-25 kcal/kg/day in the recovery phase; avoid overfeeding in the acute phase
Target: Achieve 70-100% of REE. Large observational data show optimal survival with caloric intake at ~80% of predicted energy needs (ESPEN 2023).
Avoid overfeeding - especially in the early acute phase (first 48-72 hours). Permissive underfeeding (trophic feeding) of non-protein calories is not inferior to full-goal feeding in some populations (Harrison's Principles, 22e).
3b. Protein Requirements
Protein is the most critical macronutrient in the critically ill:
- Standard range: 1.2-2.0 g/kg ABW/day (ASPEN 2016/2021; Mulholland 7e)
- May be higher in burns or polytrauma patients
- Obese patients (BMI >30): ≥2.0 g/kg ideal body weight (IBW)/day for BMI 30-40; up to 2.5 g/kg IBW/day for BMI ≥40
- Ongoing evaluation of protein adequacy is recommended
- The EFFORT Protein trial (Heyland et al., Lancet 2023) found higher protein dosing did not improve outcomes in all high-risk ICU patients - clinical judgment required
3c. Carbohydrates and Lipids
- Carbohydrates: primary energy substrate; avoid excess (promotes hyperglycemia, fatty liver)
- Lipids (IV): Mixed-oil or 100% soy-oil IV lipids are acceptable in PN patients; fish oil-containing lipids may be used (ASPEN 2021)
- Lipids provide the highest caloric density and are essential for fat-soluble vitamins and cell membrane integrity
4. Route of Nutrition Support
Priority Order (ASPEN/SCCM, ESPEN 2023):
- Oral diet - preferred whenever the patient can eat safely
- Enteral Nutrition (EN) - next preferred; use when GI tract functional
- Parenteral Nutrition (PN) - reserve; use when EN not feasible or insufficient
Why Enteral Nutrition is Preferred:
- Maintains gut mucosal integrity and prevents bacterial translocation
- Preserves gut-associated lymphoid tissue (GALT)
- Maintains secretory IgA production
- Reduces infectious complications (meta-analysis: RR 0.64 for ICU infections vs. PN) - ESPEN 2023
- Avoids complications of PN (hyperglycemia, fatty liver, cholestasis, catheter-related sepsis)
(Harrison's Principles, 22e; Mulholland & Greenfield, 7e)
5. Timing of Nutrition Support
Early Enteral Nutrition (EEN):
- Initiate EN within 24-48 hours of ICU admission in patients unable to maintain volitional intake (ASPEN/SCCM 2016; ESPEN 2023)
- EEN is associated with improved outcomes vs. delayed feeding
- Energy/protein goals should be achieved progressively over 48-72 hours - avoid sudden full target feeding to prevent refeeding syndrome
Parenteral Nutrition Timing:
- Low nutritional risk patients: Delay PN for 7 days if EN is not feasible; initiating PN before day 7-10 when EN is partially feasible does NOT improve outcomes and may be harmful (EPaNIC trial evidence)
- High nutritional risk patients (severely malnourished, GI tract non-functional for >5 days): Start PN as soon as possible after resuscitation
- Supplemental PN: Add PN only if EN fails to meet >60% of energy and protein requirements after 7-10 days of ICU stay
(Mulholland & Greenfield, 7e; ESPEN 2023; ASPEN 2021)
6. Enteral Nutrition: Practical Considerations
Route of Delivery:
- Gastric feeding (nasogastric tube): First-line; most patients tolerate this safely
- Post-pyloric feeding (nasojejunal tube): Use in patients with:
- High aspiration risk
- Gastric feeding intolerance despite prokinetics
- Gastroparesis
Head of Bed Position:
- Elevate head to 30-45° to reduce aspiration risk
Managing Intolerance:
- Prokinetic agents: Metoclopramide (10 mg TDS) or Erythromycin (3-7 mg/kg/day)
- Use if gastric residual volumes (GRV) >500 mL/6 hours
Gastric Residual Volume (GRV) Monitoring:
- Routine GRV monitoring is no longer recommended (ASPEN 2016 bundle statement)
- Do NOT hold EN for GRV <500 mL in the absence of other signs of intolerance
- Avoid inappropriate cessation of EN
Enteral Feeding Protocols:
- Institutionalized volume-based or top-down multi-strategy protocols improve percentage of caloric goal achieved
- Minimize interruptions to EN delivery
Special Situations for EN Caution:
- Vasopressor support / septic shock: EN may be given cautiously after successful resuscitation; start at low rate (20-50% of target) to "open" the gut and advance gradually; bowel ischemia is a rare but serious risk
- Prone positioning: EN can be continued during prone ventilation
- ECMO (VV/VA): Initiate continuous intragastric EN at trophic rate (10-20 mL/h) within 24 hours; increase over 24-36 hours
(ASPEN 2022 EN Indications; ESPEN 2023)
7. Parenteral Nutrition (PN)
Indications:
- GI tract non-functional or inaccessible
- EN not tolerated despite optimization
- High nutritional risk with failure to achieve >60% of targets via EN after 7-10 days
Components of TPN:
- Dextrose (carbohydrate source) - maximum oxidation rate 4-5 mg/kg/min
- Amino acids (protein source) - 1.2-2.0 g/kg/day as standard
- Lipid emulsions - 20-30% of total calories; mixed-oil (soy/MCT/olive/fish) preferred
- Electrolytes: Na, K, Ca, Mg, Phosphate
- Vitamins and trace elements: Essential daily; Vitamin C, B complex, zinc, selenium, copper
Complications of PN:
- Hyperglycemia (most common)
- Fatty liver and cholestasis with long-term use
- Hypertriglyceridemia
- Catheter-related bloodstream infection (CRBSI)
- Metabolic derangements (electrolyte imbalance, refeeding syndrome)
- Gut atrophy and bacterial translocation
Key principle: When PN calories = EN calories, the infectious complication rate becomes similar - overfeeding via PN is the main driver of complications (ESPEN 2023).
8. Immunonutrition and Special Substrates
Glutamine:
- Enteral glutamine in burns (>20% BSA): 0.3-0.5 g/kg/day for 10-15 days (ESPEN 2023, Grade B)
- IV glutamine in PN: NOT recommended routinely in ICU patients (evidence from REDOXS trial showed harm in multi-organ failure)
- Role remains as an essential conditionally indispensable amino acid in gut epithelial repair and immune function
Omega-3 Fatty Acids (EPA/DHA):
- Anti-inflammatory lipid mediators
- May be considered in ARDS patients (weak recommendation); routine use in general ICU not supported
Antioxidants (Selenium, Zinc, Vitamin C, E):
- Critically ill patients have depleted antioxidant reserves
- Adequate replacement doses are recommended; mega-dosing is not supported
Arginine-containing Immune-Modulating Formulas:
- Avoid in sepsis/septic shock (may worsen outcomes via excessive NO production)
- May be considered in elective surgical ICU patients
(ESPEN 2023; Harrison's, 22e)
9. Glycemic Control in the ICU
Hyperglycemia is common due to insulin resistance, stress response, and exogenous glucose. Poor glycemic control worsens outcomes.
Key Evidence:
- Van den Berghe et al. (2001): Intensive insulin therapy (IIT) targeting glucose 80-110 mg/dL reduced surgical ICU mortality by 42% (largely due to high exogenous glucose infusion in controls)
- NICE-SUGAR Trial (2009): Intensive control (81-108 mg/dL) increased 90-day mortality vs. conventional control (144-180 mg/dL); severe hypoglycemia: 6.8% vs. 0.5%
Current Recommendations (Multiple Guidelines, Barash's Clinical Anesthesia 9e):
- Target blood glucose ≤180 mg/dL in all critically ill patients
- Avoid hypoglycemia (<70 mg/dL) - independently associated with mortality
- Use IV insulin infusion protocols for tight-but-not-too-tight control
- Target 140-180 mg/dL is widely accepted (ACP 2011, Surviving Sepsis Campaign)
| Organization | Target Glucose (mg/dL) |
|---|
| SCCM/ASPEN | ≤180 |
| Surviving Sepsis Campaign | <180 |
| ACP | 140-180 |
| Society of Thoracic Surgeons | 150-180 (cardiac surgery ICU) |
(Barash Clinical Anesthesia 9e; Harrison's 22e)
10. Refeeding Syndrome
Definition: Metabolic derangements occurring when nutrition is resumed after prolonged starvation/malnutrition, characterized by:
- Severe hypophosphatemia (hallmark)
- Hypokalemia, hypomagnesemia
- Fluid shifts, cardiac arrhythmias, respiratory failure, seizures, neurological dysfunction
At-risk patients: Prolonged starvation (>5 days), chronic alcoholism, anorexia nervosa, post-surgical ileus, malabsorption syndromes.
Prevention:
- Correct electrolytes (especially phosphate, potassium, magnesium) before initiating feeds
- Start nutrition at low rate (10-20 kcal/kg/day or ~50% target) and advance slowly over 4-7 days
- Monitor electrolytes daily for the first week
- Supplement thiamine (Vitamin B1) before and during refeeding
11. Monitoring Adequacy of Nutrition
| Parameter | Frequency | Goal |
|---|
| Blood glucose | 4-6 hourly | 140-180 mg/dL |
| Serum electrolytes | Daily | Normal ranges |
| Triglycerides (on PN) | 2-3 times/week | <400 mg/dL |
| Serum phosphate | Daily (first week) | Normal |
| Nitrogen balance | Weekly | Aim for zero or positive |
| Indirect calorimetry | When available | Adjust energy targets |
| Weight / fluid status | Daily | Avoid overload |
Visceral proteins (albumin, prealbumin, transferrin) are poor markers of nutritional adequacy in acute illness as they are negative acute-phase reactants. Use NUTRIC/NRS for ongoing risk stratification.
12. Special ICU Populations
| Condition | Nutritional Consideration |
|---|
| Obesity (BMI >30) | Hypocaloric high-protein diet; 65-70% of target energy; ≥2.0 g/kg IBW protein |
| Acute Kidney Injury (non-RRT) | Restrict protein to 0.6-0.8 g/kg/day only if not starting RRT; standard if on CRRT |
| CRRT | Increase protein to 1.5-2.5 g/kg/day to replace amino acid losses in dialysate |
| Burns (>20% BSA) | High energy + protein; add enteral glutamine 0.3-0.5 g/kg/day |
| TBI | Avoid high-dose IV glutamine; early EN within 24-48 h; standard caloric targets |
| Liver failure | Standard or high protein (does NOT worsen encephalopathy at 1.2-1.5 g/kg/day); restrict only in severe refractory hepatic encephalopathy |
| Pancreatitis | Early EN (nasojejunal) within 24-48 h preferred over PN |
Summary: Key Numbers to Remember
| Parameter | Value |
|---|
| Start EN | Within 24-48 hours of ICU admission |
| Energy target | 20-25 kcal/kg/day (adjusted per IC) |
| Protein target | 1.2-2.0 g/kg ABW/day |
| Delay PN (low risk) | Day 7 |
| GRV hold threshold | Do NOT hold for GRV <500 mL/6h |
| Blood glucose target | 140-180 mg/dL (avoid <70) |
| Caloric target associated with best survival | ~80% of predicted REE (ESPEN 2023) |
| EN trophic rate (ECMO) | 10-20 mL/h within 24 h |
| Glutamine in burns | 0.3-0.5 g/kg/day x 10-15 days |
References (for Exam Credit)
- ASPEN/SCCM Guidelines 2016 - McClave SA et al. JPEN 2016;40(2):159-211
- ASPEN Guidelines 2021 - Compher C et al. JPEN 2021 (Compher update)
- ESPEN Practical Guidelines 2023 - Singer P, Blaser AR, Berger MM et al. Clinical Nutrition 2023;42:1671-1689
- ASPEN EN Indications 2022 - Bechtold ML et al. JPEN 2022;46:1470-1496
- NICE-SUGAR Trial - NEJM 2009;360:1283-1297
- EFFORT Protein Trial - Heyland DK et al. Lancet 2023;401(10376):568-576
- Barash Clinical Anesthesia 9e - Chapter 47 (Glycemic Goals in ICU)
- Harrison's Principles of Internal Medicine 22e - Chapter on Critical Illness (Nutrition & Glycemic Control)
- Mulholland & Greenfield's Surgery 7e - Chapter 3 (ICU Nutrition Bundle)
Word of advice for exam writing: In a 10-mark answer, lead with the definition/importance, then systematically cover: screening tools -> energy calculation -> route preference (EN > PN with rationale) -> timing -> practical EN management -> PN indications/complications -> glycemic control -> monitoring. Include the key numbers (24-48 h, 1.2-2.0 g/kg, 140-180 mg/dL) as examiners look for these specifically. Mention ASPEN/SCCM and ESPEN by name to demonstrate awareness of current guidelines.