Chapter 8 Nutrition in Critically ill Patients
6 How many calories should critically ill patients receive?
Energy expenditure varies with age, sex, body mass, and type and severity of illness. During critical illness, total energy expenditure (TEE) can be measured with indirect calorimetry. However, in clinical practice, resting energy expenditure (REE) is usually estimated by using a variety of available equations and is then multiplied by a stress factor of 1.0 to 2.0 to estimate TEE (and therefore caloric requirements). Roughly 25 kcal/kg ideal body weight is often the standard practice, and other equations, such as Harris-Benedict, Ireton-Jones, and Weir, are commonly used (Table 8-1). Unfortunately, predictive equations tend to be inaccurate. The optimal amount of calories to provide critically ill patients is unclear given the paucity of existing data, but studies do suggest that providing an amount of calories closer to goal calories is associated with improved clinical outcomes.
Table 8-1 Examples of Predictive Equations for Ree in Critical Illness
Harris-Benedict | Men: [66.5 + (13.8 × AdjBW) + (5 × Ht) − (6.8 × Age)] × 1.3 Women: [655 + (9.6 × AdjBW) + (1.8 × Ht) − 4.7 × Age)] × 1.3 |
Owen | Men: 879 + (10.2 × ActBW) Women: 795 + (7.2 × ActBW) |
Mifflin | Men: 5 + (10 × ActBW) + (6.25 × Ht) − (5 × Age) Women: 161 + (10 × ActBW) + (6.25 × Ht) − (5 × Age) |
Ireton-Jones equation for obesity | Men: 606 + (9 × ActBW) − (12 × Age) + 400 (if ventilated) + 1400 Women: ActBW − (12 × Age) + 400 (if ventilated) + 1444 |
Ireton-Jones for patients with mechanical ventilation | Men = 2206 − (10 × Age) + (5 × ActBW) + 292 (if trauma) + 851 (if burn) Women = 1925 − (10 × Age) + (5 × ActBW) + 292 (if trauma) + 851 (if burn) |
25 kcal/kg | BMI < 25: ActBW × 25 BMI ≥ 25: IBW × 25 |
ActBW, Actual body weight = weight on admission (kilograms); AdjBW, adjusted body weight = ideal body weight + 0.4 (actual body weight − ideal body weight); BMI, body mass index; Ht, height (centimeters); IBW, ideal body weight = 50 + 2.3 per inch > 60 inches (men), 45.5 + 2.3 per inch > 60 inches (women).
16 What are some complications of enteral feeding, and how can they be minimized?
EN is not without risks, and complications can be categorized as GI, mechanical, or metabolic.
GI complications include diarrhea, nausea, vomiting, constipation, aspiration, and ischemic bowel. Decreased gastric motility occurs in a majority of critically ill patients, and therefore nausea and vomiting with resultant aspiration are not uncommon. These can be minimized with semirecumbent positioning, placement of a small-bowel feeding tube, and continuous rather than bolus enteral feeding (discussed earlier). Ileus also commonly occurs in a critical care setting, often as a result of opioid administration, and can be treated with small doses of oral naloxone that do not affect the analgesia of opioids. Diarrhea is common in the ICU and may be due to antibiotics or other medications. If diarrhea develops in a patient receiving EN, infectious causes (i.e., Clostridium difficile) should first be ruled out. If those tests are negative, stool-bulking agents such as banana flakes can be administered. Alternative strategies to decrease diarrhea include increasing soluble fiber intake or changing to another enteral formula.
Mechanical complications include obstruction of the feeding tube with medications; erosion of the feeding tube into nasal or gastric mucosa with risk of bleeding, infection, or perforation; accidental insertion of the feeding tube into the pulmonary tree with risk of injury; displacement of the tube with risk of aspiration; and sinusitis. To minimize these complications, tubes should be soft and well lubricated for insertion, and tube position should always be verified radiographically before use (auscultation over the stomach alone is not adequate).
Metabolic complications include hyperglycemia, electrolyte derangements, and overfeeding. Monitoring of blood glucose and electrolytes can detect these and lead to appropriate changes in feedings. If overfeeding is a concern, a metabolic cart (indirect calorimetry) can be performed to measure TEE.
17 When should PN be used in critically ill patients?
After 7 days of hospitalization in critically ill patients who are not malnourished but in whom enteral feeding has not been feasible or who have only received a fraction of goal calories
On admission in critically ill patients who are malnourished and in whom enteral feeding is not feasible
During the perioperative period in a patient undergoing major GI surgery who is either malnourished or when the period of time during which EN is not feasible is expected to be longer than 5 to 7 days
Given these recommendations, very few patients in a medical ICU should need PN.
18 What are some complications of PN?
Mechanical complications in patients receiving PN include those related to the catheter used for delivery of PN, such as pneumothorax and venous thromboembolism.
Metabolic complications from PN include hyperglycemia and electrolyte abnormalities. Hyperglycemia can be treated with an appropriate insulin protocol for hyperglycemia associated with critical illness.
Infectious complications from parenteral feeding include central line–associated bloodstream infection and sepsis.
Hepatobiliary complications. PN can occasionally cause elevated hepatic transaminase, alkaline phosphatase, and bilirubin levels, as well as steatosis (i.e., fatty liver), and acalculous cholecystitis may result.
19 Which pharmaconutrients or specialized formulas should critically ill patients receive?
Glutamine. Although data are limited, supplemental enteral glutamine (when using a feeding formula that is not already supplemented with glutamine) decreases hospital length of stay, ICU length of stay, and mortality in burn and mixed ICU patients and therefore should be added to enteral regimens when feasible. This effect is likely explained by glutamine’s role in maintaining the integrity of the GI lumen. It can be administered as a powder mixed with water and infused through the feeding tube, and the dose should be 0.3 to 0.5 g/kg per day.
Parenteral glutamine potentially has an even larger benefit than enteral glutamine and has been shown to reduce mortality and infections in patients receiving PN. Outside of North America, the dipeptide formulation of intravenous glutamine is available and should be used. In North America, however, intravenous glutamine is available only in a formulation that has limited solubility and requires excess fluid administration.
Antioxidants: A prior meta-analysis found that antioxidants and minerals reduced mortality in critically ill patients. On the basis of these results, critically ill patients (particularly those with burns or trauma and receiving mechanical ventilation) should receive antioxidant vitamins (vitamins E and C) and minerals (selenium, zinc, and copper). Very few data are currently available on individual nutrients.
Arginine: Enteral feeding formulas containing arginine should be used in patients undergoing major elective surgery and in those with trauma, burns, and head and neck cancer. On the basis of results from prior studies, however, patients with sepsis should not receive arginine because it has been suggested that it may increase mortality.
Omega-3 fatty acids: The use of feeding formulas containing omega-3 fatty acids (fish oil) in patients with acute lung injury and sepsis is currently quite controversial. Three prior trials comparing an enteral formula containing omega-3 fatty acids, borage oil (γ-linolenic acid [GLA]), and antioxidants with placebo found benefit. However, two additional recent randomized trials (one used a liquid fish oil supplement and another used a twice-daily supplement containing fish oil, GLA, and antioxidants) found no benefit.
22 How might propofol influence the nutritional support provided to critically ill patients?
Key Points Nutrition in Critically Ill Patients
1. EN should be used in the vast majority of ICU patients rather than PN.
2. EN should be started within 24 to 48 hours of ICU admission.
3. After patients with shock are resuscitated and hemodynamically stable, they can safely receive EN even if they are receiving stable lower doses of vasopressors.
4. In patients intolerant of EN, measures such as semirecumbent positioning and motility agents should be attempted before starting PN.
5. Patients with acute pancreatitis, even if it is severe, should receive EN, which can be delivered either gastrically or jejunally.
1 Canadian critical care nutrition clinical practice guidelines: topics. Accessed August 1 http://criticalcarenutrition.com/docs/cpg/1.0envspn_07_FINAL.pdf, 2011.
2 Canadian critical care nutrition clinical practice guidelines: topics. http://criticalcarenutrition.com/docs/cpg/2.0early_FINAL.pdf, 2011. Accessed August 1
3 Cerra F.B., Benitez M.R., Blackburn G.L., et al. Applied nutrition in ICU patients. A consensus statement of the American College of Chest Physicians. Chest. 1997;111:769–778.
4 Drakulovic M.B., Torres A., Bauer T.T., et al. Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomised trial. Lancet. 1999;354:1851–1858.
5 Gadek J.E., DeMichele S.J., Karlstad M.D., et al. Effect of enteral feeding with eicosapentaenoic acid, gamma-linolenic acid, and antioxidants in patients with acute respiratory distress syndrome. Crit Care Med. 1999;27:1409–1420.
6 Heyland D.K., Dhaliwal R., Suchner U., et al. Antioxidant nutrients: a systematic review of trace elements and vitamins in the critically ill patient. Intensive Care Med. 2005;31:327–337.
7 Heyland D.K., Drover J.W., Dhaliwal R., et al. Optimizing the benefits and minimizing the risks of enteral nutrition in the critically ill: role of small bowel feeding. JPEN J Parenter Enteral Nutr. 2002;26(6 Suppl):S51–S55.
8 Ibrahim E.H., Mehringer L., Prentice D., et al. Early versus late enteral feeding of mechanically ventilated patients: results of a clinical trial. JPEN J Parenter Enteral Nutr. 2002;26:174–181.
9 Khalid I., Doshi P., DiGiovine B. Early enteral nutrition and outcomes of critically ill patients treated with vasopressors and mechanical ventilation. Am J Crit Care. 2010;19:261–268.
10 McClave S.A., Chang W.K., Dhaliwal R., et al. Nutrition support in acute pancreatitis: a systematic review of the literature. JPEN J Parenter Enteral Nutr. 2006;30:143–156.
11 McClave S.A., Martindale R.G., Vanek V.W., et al. Guidelines for the Provision and Assessment of Nutrition Support Therapy in the Adult Critically Ill Patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.). JPEN J Parenter Enteral Nutr. 2009;33:277–316.
12 Meissner W., Dohrn B., Reinhart K. Enteral naloxone reduces gastric tube reflux and frequency of pneumonia in critical care patients during opioid analgesia. Crit Care Med. 2003;31:776–780.
13 Pontes-Arruda A., Aragão A.M., Albuquerque J.D. Effects of enteral feeding with eicosapentaenoic acid, gamma-linolenic acid, and antioxidants in mechanically ventilated patients with severe sepsis and septic shock. Crit Care Med. 2006;34:2325–2333.
14 Rice T.W., Wheeler A.P., Thompson B.T., et al. for the NHLBI ARDS Clinical Trials Network: Enteral omega-3 fatty acid, gamma-linolenic acid, and antioxidant supplementation in acute lung injury. JAMA. 2011;306:1574–1581.
15 Singer P., Theilla M., Fisher H., et al. Benefit of an enteral diet enriched with eicosapentaenoic acid and gamma-linolenic acid in ventilated patients with acute lung injury. Crit Care Med. 2006;34:1033–1038. Erratum in: Crit Care Med 34:1861, 2006
16 Stapleton R.D., Martin T.R., Weiss N.S., et al. A phase II randomized placebo-controlled trial of omega-3 fatty acids for the treatment of acute lung injury. Crit Care Med. 2011;39:1655–1662.
17 Suchner U., Heyland D.K., Peter K. Immune-modulatory actions of arginine in the critically ill. Br J Nutr. 2002;87(1 Suppl):S121–S132.
18 van Nieuwenhoven C.A., Vandenbroucke-Grauls C., van Tiel F.H., et al. Feasibility and effects of the semirecumbent position to prevent ventilator-associated pneumonia: a randomized study. Crit Care Med. 2006;34:396–402.