Professional Documents
Culture Documents
N u t r i t i o n a l Th e r a p y
Following Major Burn Injury
Christina Rollins, RD, CNSCa, Franziska Huettner, MD, PhDb,
Michael W. Neumeister, MD, FRCSCb,*
KEYWORDS
Nutritional therapy Enteral and parenteral nutrition support Burn recovery Wound healing
KEY POINTS
Nutrition assessment and intervention are vital components of the burn recovery process.
Hypermetabolic state and increased caloric needs are dependent on burn severity and may remain
elevated up to 2 years following injury.
Supplemental nutrition therapy and pharmacologic support may expedite recovery.
serious complications, such as hyperglycemia, portive measures like bacitracin and petroleum-
fatty liver, and prolonged ventilator dependency.3 based dressing application are beneficial for
a
Food and Nutrition Services, Memorial Medical Center, 701 North 1st Street, Springfield, IL 62781, USA;
b
Department of Surgery, Institute for Plastic Surgery, Southern Illinois University School of Medicine, Baylis
Medical Building, P.O. Box 19653, 747 North Rutledge Street, 3rd Floor, Springfield, IL 62794-9653, USA
* Corresponding author.
E-mail address: mneumeister@siumed.edu
superficial, whereas deep second-degree burns generalized stress.12 A, PA, and T alone poorly
benefit from excision and grafting. Full-thickness reflect malnutrition or the adequacy of calorie/pro-
burns involve damage to the epidermis and tein intake12,13 and should alone not be used as in-
dermis, including the skin appendages and free dicators of nutritional status or adequacy of
nerve endings and are therefore not painful to the nutrition support therapy.14 Using other laboratory
touch. Full-thickness burns require surgical inter- values such C-reactive protein in addition to serum
vention, such as wound debridement and skin protein values will help assess the inflammatory
grafting, to heal.2 impact on serum protein levels.12,13,15
Major burn injuries can be defined as injuries
with greater than 20% burned total body surface CALORIES
area (TBSA),4 and severe burns can be defined
as greater than 40% TBSA. Early massive capillary Calculating precise energy (calorie) requirements
leaks and fluid shifts can lead to hypovolemic can be challenging for clinicians. An ebb-and-
shock and need for aggressive resuscitation in flow response is often seen in burn injuries, where
these patients.5 Physiologic changes can include an initial reduction of metabolic rate occurs fol-
a 10- to 50-fold increase in catecholamines and lowed by hypermetabolism that can last for weeks.
corticosteroids, which can last up to up to Energy expenditure typically begins to increase
9 months postburn6,7; an increase in energy about 72 hours postburn, peaks in 5 to 7 days,
expenditure and metabolic rate,6 which can still and can remain elevated for up to 2 years.16 Fac-
be at 120% 6 months postburn; an increase in car- tors that may impact energy expenditure postburn
diac work with an increase in myocardial con- include wound closure, surgical procedures, initia-
sumption, which can be increased into the tion of nutrition support, physical therapy, certain
rehabilitation phase.8,9 Other changes can include medications,2 sepsis, and ambient temperature.17
lipolysis, liver dysfunction, severe muscle catabo- Size of the burn is also a key determinant of caloric
lism with net protein loss, insulin resistance, in- need. For burns greater than 10% TBSA, resting
crease in cytokine levels, and decrease in sex metabolic rate will likely be close to or at the
hormones and endogenous growth hormone normal range. However, patients with major burn
release. The increased metabolism and hyperdy- injury are as much as double baseline, with a sub-
namic circulation can lead to fatality if untreated. sequent rate decline.
Severity of the physical response to burns de- The 2 most common methods used to estimate
pends on many factors, including burn size and calorie needs are IC and mathematical calcula-
depth, gender, age, presence of inhalation injury, tions. Both methods have pros and cons that
timeliness of medical treatment, and other comor- must be considered.
bid conditions present.10 Complications following Indirect calorimetry (IC) is a respiratory test that
burn injury vary in severity. Negative outcomes calculates actual resting energy expenditure (REE)
are also associated with inadequate nutritional by measuring the exchange of oxygen and carbon
care. Insufficient intake of calories and protein dioxide by the lungs by using IC to measure calorie
can lead to a loss of lean muscle mass, which needs, factors that may impact energy expendi-
can induce immune dysfunction, impair wound ture measured, resulting in a more reliable estima-
healing, and increase mortality at 10%, 20%, and tion of calorie needs.18 It is important to note that
40% loss, respectively.11 IC only provides a measurement of energy expen-
diture for the time frame testing was completed,
LABORATORY TESTING which is typically at rest. To compensate,
measured REE should be multiplied by 1.2 to
There has been a historic link between low serum 1.3.19 Although IC has long been coined the
hepatic proteins, including serum albumin (A), “gold standard” in estimating energy needs,20
serum prealbumin (PA), and transferrin (T) and the financial cost often prohibits its use. IC adds cost
presence of malnutrition. However, current evi- to both the facility and the patient, including an
dence shows that, in hospitalized patients, serum upfront cost to purchase the machine and employ
levels of these proteins have a more positive corre- trained staff as well as a procedural cost to the
lation with inflammation, stress, and mortality. patient.21
Levels may be falsely increased by dehydration, Mathematical calculations are a lower-cost
blood, and intravenous A infusion, severe renal fail- alternative to IC and more readily available,
ure, corticosteroid and oral contraceptive use, and although multiple studies have indicated that
falsely low with fluid resuscitation, hepatitis and he- mathematical equations are less accurate in esti-
patic failure, dialysis, hyperthyroidism, pregnancy, mating caloric need because burn patients have
hyperglycemia, infection, inflammation, and highly variable energy expenditure. Inaccuracy
Clinician’s Guide to Burn Nutrition Therapy 557
Table 1
Mathematical calculations to estimate energy needs after burns
Abbreviations: A, age in years; AF, activity factor; H, height in centimeters; IF, injury factor; TBSA, total body surface area
burned; W, weight in kilograms.
558 Rollins et al
Fig. 1. Decision tree. GI, gastrointestinal; NPO, nothing by mouth; PO, orally.
560 Rollins et al
should be initiated. Initiating PN before day 8 in in postburn injury, this does increase the risk of
well-nourished individuals has shown little func- refeeding syndrome, a condition characterized by
tional benefit.37 very low levels of potassium, magnesium, and
phosphorus, which may become lethal if left un-
COMPLICATIONS OF ENTERAL NUTRITION treated. In addition, PN formulations with insufficient
AND PARENTERAL NUTRITION lipid content can lead to essential fatty acid defi-
ciency. Aggressive treatment is warranted following
Although both EN and PN have functional benefits standard treatment guidelines following a compre-
postburn injury, each presents with its own risk for hensive medical and nutritional assessment.
complications. EN is often associated with Hepatobiliary complications, also known as
nausea, vomiting, abdominal distention, diarrhea, parenteral nutrition associated liver disease
constipation, and aspiration. Using measures (PNALD), have also been associated with PN,
such as the use of chlorhexidine mouthwash twice including steatosis, cholestasis, and gallbladder
per day in orally intubated patients,14 elevating the sludge/stones. Overfeeding of calories, dextrose
head of the bed to 30 to 45 ,38,39 and the use of infusion greater than 5 to 7 mg/kg/min and lipid
prokinetic agents (metoclopramide or erythro- infusion greater than 1 g/kg/d have been associ-
mycin) may reduce the risk of some gastrointes- ated with the onset of PNALD. Care should be
tinal upset and even aspiration of stomach taken to not only assess but also routinely reas-
contents with subsequent decreased risk of pneu- sess nutritional requirements to support burn re-
monia. However, the routine use of prokinetic covery without exceeding the body’s need to
agents must be cautioned because of the potential metabolize and digest these nutrients.43
side effects, like cardiac toxicity and tachyphylaxis Also, the use of PN is to be done with caution,
for erythromycin use, tardive dyskinesia for the use because it carries an increased risk of infection,44
of Reglan, and potential QT prolongation for both specifically, pneumonia rate,45 compared with
of these agents.40,41 Although both have shown EN therapy alone. PN does carry an increased
an improvement in the GRV, no decrease in length risk of bloodstream infections because central
of stay or mortality was associated with their venous access is required for PN infusion suffi-
use.42 cient to meet estimated nutritional requirements.
Laboratory imbalances are also common with PN infusion can also lead to atrophy of the
both EN and PN, including but not limited to electro- gastrointestinal tract and carries an increased
lytes, acid/base balance, and glucose levels. risk of bacterial translocation. Care should be
Although early aggressive feeding is recommended taken to limit the use of PN to what is medically
Table 2
Micronutrient repletion and laboratory monitoring
Fig. 2. Initial burn admission order guidelines example (to be considered in addition to standard admission orders
and according to individual hospital guidelines). BID, twice a day; IV, intravenously; PEG, percutaneous endo-
scopic gastrostomy; PRN, as needed; TID, 3 times a day.
562 Rollins et al
Fig. 2. (continued)
Clinician’s Guide to Burn Nutrition Therapy 563
Fig. 2. (continued)
necessary, with the introduction of EN as soon as decrease in gram-negative bacteremia and hospi-
possible to avoid further and possibly long-term tal mortality.49,50
complications. To support adequate wound healing postburn,
the following supplementation regimen should
be considered in addition to EN formula infusion:
MICRONUTRIENT SUPPLEMENTATION multivitamin with minerals, vitamin C, zinc, cop-
The increased inflammatory response paired per, vitamin A, and thiamine.51–53 Administration
with burn-induced oxidative stress leads to of very high doses of vitamin C in first 24 hours
depletion of the endogenous antioxidant defense helps to stabilize the cell membrane and can
mechanism.4 For this reason, burn patients reduce the fluid resuscitation needs by 30%.54
have much higher vitamin and trace element re- Table 2 provides dosing information and labora-
quirements when compared with other patient tory monitoring. The supplementation has to
populations. Low plasma levels of micronu- be used with caution in patients with renal and
trients have been associated with exudative los- hepatic failure.
ses, hypoalbuminemia, and induced oxidative
stress.2,20 Zinc and copper in particular have OTHER PHARMACOLOGIC AGENTS
been reported as significantly lower than healthy
controls at postburn days 3, 7, and 14.46 Simi- One potentially beneficial pharmacologic agent
lar findings were also reported by Berger,47 often used postburn is propranolol. In a recent
who correlated copper, selenium, and zinc systematic review, propranolol was associated
supplementation with improved clinical out- with significant decreases in REE and insulin resis-
comes, namely fewer pulmonary infections and tance.55 Treatment recommendations include initi-
improved burn wound healing. ation of propranolol as early as 24 hours postburn.
Commercially available EN and PN products are Following initial resuscitation and achievement
not sufficient to provide adequate amounts of of hemodynamic stability, propranolol is often
micronutrients to meet the increased micronutrient given in combination with oxandrolone.4 A syn-
demand. In addition, because of antagonist mech- thetic analogue to testosterone, oxandrolone im-
anisms and competing forces, additional enteral proves muscle protein synthesis and protein
substitution is not enough,4 and intravenous sup- metabolism leading to increases lean body mass,
plementation is indicated. The exception to this bone mineral content, and muscle strength. In a
statement is glutamine. Enteral glutamine has recent meta-analysis and systematic review,
been shown to have a tropic effect in maintaining oxandrolone was shown to be significantly effec-
gut integrity postburn, and sufficient intake of tive without obvious side effects, including
glutamine can be obtained via enteral formula infu- decreased length of stay, decreased donor site
sion alone.48 Although literature is mixed regarding healing time, reduced weight and nitrogen loss,
the effectiveness of glutamine postburn, glutamine decreased time between surgeries, gain in lean
supplementation has been associated with a body mass,56,57 and decreased mortality.58 With
564 Rollins et al
close monitoring of liver function, oxandrolone is 7. Wilmore DW, Aulick LH. Metabolic changes in burned
safe for both genders. Side effects are rare, and patients. Surg Clin North Am 1978;58(6):1173–87.
the risk of masculinization effect and hirsutism 8. Cuthbertson DP, Angeles Valero Zanuy MA, Leon
are low at 5% and 1%, respectively. Sanz ML. Post-shock metabolic response. 1942.
Intensive insulin therapy to achieve blood sugar Nutr Hosp 2001;16(5):176–82 [discussion: 175–6].
levels of 80 to 110 mg/dL has also been linked to a 9. Baron PW, Barrow RE, Pierre EJ, et al. Prolonged
decreased mortality as well as sepsis rates post- use of propranolol safely decreases cardiac work
burn.46 Tight glycemic control with insulin therapy in burned children. J Burn Care Rehabil 1997;
stimulates muscle protein synthesis and increased 18(3):223–7.
lean body mass. However, current critical care 10. Graves C, Saffle J, Cochran A. Actual burn nutrition
nutrition guidelines recommend more liberal blood care practices: an update. Presented at the Amer-
sugar control at target range of 140 to 180 mg/dL. ican Burn Association conference in Chicago, IL,
Care must be taken to avoid hypoglycemic events April 29 – May 2, 2008.
with tight blood sugar control. 11. Chang DW, DeSanti L, Demling RH. Anticatabolic
and anabolic strategies in critical illness: a review
of current treatment modalities. Shock 1998;10(3):
ADDITIONAL CONSIDERATIONS
155–60.
In addition to pharmacologic agents, maintaining 12. Davis CJ, Sowa D, Keim KS, et al. The use of preal-
an ambient temperature of 28 C to 33 C17 has bumin and C-reactive protein for monitoring nutrition
been shown to reduce energy requirements, support in adult patients receiving enteral nutrition in
decrease protein and muscle catabolism, and an urban medical center. JPEN J Parenter Enteral
improve overall survival. Early excision and Nutr 2012;36(2):197–204.
coverage59 of burned tissue has also been 13. Jensen GL, Hsiao PY, Wheeler D. Adult nutrition
shown to improve survival rate by reducing infec- assessment tutorial. JPEN J Parenter Enteral Nutr
tious complications and overall inflammatory 2012;36(3):267–74.
response. 14. McClave SA, Taylor BE, Martindale RG, et al. Guide-
lines for the provision and assessment of nutrition
support therapy in the adult critically ill patient: Soci-
SUMMARY
ety of Critical Care Medicine (SCCM) and American
Adequate nutritional intake is crucial to the burn Society for Parenteral and Enteral Nutrition
recovery process. Care of the burn patient should (A.S.P.E.N. JPEN J Parenter Enteral Nutr 2016;
be individualized to include adequate calorie, pro- 40(2):159–211.
tein, and fluid intake. Nutrition therapy, vitamin and 15. Ferrie S, Allman-Farinelli M. Commonly used “nutri-
mineral supplementation, and other pharmaco- tion” indicators do not predict outcome in the criti-
logic agents should also be considered to support cally ill: a systemic review. Nutr Clin Pract 2013;
wound healing. For a comprehensive list of 28(4):463–84.
nutrition-related order options, see Fig. 2. 16. A.S.P.E.N. Board of Directors and the Clinical Guide-
lines Task Force. Guidelines for the use of parenteral
and EN in adult and pediatric patients. JPEN J Pa-
REFERENCES
renter Enteral Nutr 2002;26S:88SA–90SA.
1. American Burn Association. Burn Incidence Fact 17. Wilmore DW, Mason AD Jr, Johnson DW, et al. Effect
Sheet. Available at: http://www.ameriburn.org/ of ambient temperature on heat production and
resources_factsheet.php. Accessed July 14, 2016. heat loss in burn patients. J Appl Physiol 1975;
2. Herndon D. Total burn care. Philadelphia: Saunders 38(4):593–7.
Elsevier; 2007. 18. Prelack K, Dylewski M, Sheridan R. Practical guide-
3. Merritt R. The A.S.P.E.N. Nutrition support practice lines for nutritional management of burn injury and
manual. 2nd edition. Silver Springs (MD): recovery. Burns 2007;33:14–24.
A.S.P.E.N; 2005. 19. Academy of Nutrition and Dietetics Nutrition Care
4. Rousseau AF, Losser MR, Ichai C, et al. ESPEN Manual. Burns Nutrition Prescription. 2011. Available
endorsed recommendations: nutritional therapy in at: www.nutritioncaremanual.com. Accessed May 26,
major burns. Clin Nutr 2013;32(4):497–502. 2016.
5. Deitch EA. Intestinal permeability is increased in 20. Turza K, Krenitsky J, Sawyer R. Enteral feedings and
burn patients shortly after injury. Surgery 1990; vasoactive agents: suggested guidelines for clini-
107(4):411–6. cians. Pract Gastroenterol 2009;78:11–22.
6. Jeschke MG, Chinkes DL, Finnerty CC, et al. Patho- 21. Davis K. Nutritional gain versus financial gain: the
physiologic response to severe burn injury. Ann role of metabolic carts in the surgical ICU.
Surg 2008;248(3):387–401. J Trauma 2006;61:1436–40.
Clinician’s Guide to Burn Nutrition Therapy 565
22. Cresci G, Gottschlich M, Mayes T, et al. Trauma, sur- 38. Drakulovic MB, Torres A, Bauer TT, et al. Supine
gery, and burns. The A.S.P.E.N. nutrition support body position as a risk factor for nosocomial pneu-
core curriculum: a case-based approach – the adult monia in mechanically ventilated patients:
patient. Silver Springs (MD): A.S.P.E.N; 2007. p. a randomised trial. Lancet 1999;354(9193):1851–8.
455–72. 39. van Nieuwenhoven CA, Vandenbroucke-Grauls C,
23. Dickerson R, Gervasio JM, Riley ML, et al. Accuracy van Tiel FH, et al. Feasibility and effects of the semi-
of predictive methods to estimate resting energy recumbent position to prevent ventilator-associated
expenditure of thermally-injured patients. J Parenter pneumonia: a randomized study. Crit Care Med
Enteral Nutr 2002;26:17–29. 2006;34(2):396–402.
24. Wolfe RR, Goodenough RD, Wolfe MH. Isotopic ap- 40. Al-Khatib SM, LaPointe NM, Kramer JM, et al. What
proaches to the estimation of protein requirements in clinicians should know about the QT interval. JAMA
burn patients. Adv Shock Res 1983;9:81–98. 2003;289(16):2120–7.
25. Vicic VK, Radman M, Kovacic V. Early initiation of 41. Li EC, Esterly JS, Pohl S, et al. Drug-induced QT-
enteral nutrition improves outcomes in burn disease. interval prolongation: considerations for clinicians.
Asia Pac J Clin Nutr 2013;22(4):543–7. Pharmacotherapy 2010;30(7):684–701.
26. Chiarelli A, Enzi G, Casadei A, et al. Very early nutri- 42. Nguyen NQ, Chapman M, Fraser RJ, et al. Proki-
tion supplementation in burned patients. Am J Clin netic therapy for feed intolerance in critical
Nutr 1990;51(6):1035–9. illness: one drug ortwo? Crit Care Med 2007;
27. Peng YZ, Yuan ZQ, Xiao GX. Effects of early enteral 35(11):2561–7.
feeding on the prevention of enterogenic infection in 43. Gottschlich MM. The APSEN nutrition support core
severely burned patients. Burns 2001;27(2):145–9. curriculum: a case based approach – the adult patient.
28. Chen Z, Wang S, Yu B, et al. A comparison study be- 2007. Available at: https://www.valorebooks.com/
tween early enteral nutrition and parenteral nutrition textbooks/aspen-nutrition-support-core-curriculum-a-
in severe burn patients. Burns 2007;33(6):708–12. case-based-approach-the-adult-patient-1st-edition/
29. Jabbar A, Chang WK, Dryden GW, et al. Gut immu- 9781889622088.
nology and the differential response to feeding and 44. Herndon DN, Barrow RE, Stein M. Increased mortal-
starvation. Nutr Clin Pract 2003;18(6):461–82. ity with intravenous supplemental feeding in
30. Windsor AC, Kanwar S, Li AG, et al. Compared with severely burned patients. J Burn Care Rehabil
parenteral nutrition,enteral feeding attenuates the 1989;10(4):309–13.
acute phase response and improves disease 45. Lam NN, Tien NG, Khoa CM. Early enteral feeding
severity in acute pancreatitis. Gut 1998;42(3):431–5. for burned patients–an effective method which
31. Ammori BJ. Importance of the early increase in in- should be encouraged in developing countries.
testinal permeability in critically ill patients. Eur J Burns 2008;34(2):192–6.
Surg 2002;168(11):660–1. 46. van den Berghe G, Wouters P, Weekers F, et al.
32. Lewis SJ, Andersen HK, Thomas S. Early enteral Intensive insulin therapy in critically ill patients.
nutrition within 24 h of intestinal surgery versus later N Engl J Med 2001;345(19):1359–67.
commencement of feeding: a systematic review 47. Berger M. Trace element supplementation modu-
and meta-analysis. J Gastrointest Surg 2009;13(3): lates pulmonary infection rates after major burns: a
569–75. double-blind, placebo controlled trial. Am J Clin
33. MacLeod JB, Lefton J, Houghton D, et al. Prospec- Nutr 1998;68:365–71.
tive randomized control trial of intermittent versus 48. Garrel D, Patenaude J, Nedelec B, et al. Decreased
continuous gastric feeds for critically ill trauma pa- mortality and infectious morbidity in adult burn pa-
tients. J Trauma 2007;63(1):57–61. tients given enteral glutamine supplements: a pro-
34. Jenkins ME, Gottschlich MM, Warden GD. Enteral spective, controlled, randomized clinical trial. Crit
feeding during operative procedures in thermal in- Care Med 2003;31(10):2444–9.
juries. J Burn Care Rehabil 1994;15(2):199–205. 49. Lin JJ, Chung XJ, Yang CY, et al. A meta-analysis of
35. Caddell KA, Martindale R, McClave SA, et al. Can trials using the intention to treat principle for gluta-
the intestinal dysmotility of critical illness be differen- mine supplementation in critically ill patients with
tiated from postoperative ileus? Curr Gastroenterol burn. Burns 2013;39(4):565–70.
Rep 2011;13(4):358–67. 50. van Zanten AR, Dhaliwal R, Garrel D, et al. Enteral
36. Khalid I, Doshi P, DiGiovine B. Early enteral nutrition glutamine supplementation in critically ill patients:
and outcomes of critically ill patients treated with va- a systematic review and meta-analysis. Crit Care
sopressors and mechanical ventilation. Am J Crit 2015;19:294.
Care 2010;19(3):261–8. 51. Falder S, Silla R, Phillips M, et al. Thiamine supple-
37. Casaer MP, Mesotten D, Hermans G, et al. Early mentation increases serum thiamine and reduces
versus late parenteral nutrition in critically ill adults. pyruvate and lactate levels in burn patients. Burns
N Engl J Med 2011;365(6):506–17. 2010;36(2):261–9.
566 Rollins et al
52. Al-Jawad FH, Sahib AS, Al-Kaisy AA. Role of antiox- 56. Li H, Guo Y, Yang Z, et al. The efficacy and safety of
idants in the treatment of burn lesions. Ann Burns oxandrolone treatment for patients with severe
Fire Disasters 2008;21(4):186–91. burns: a systematic review and meta-analysis.
53. Barbosa E, Faintuch J, Machado Moreira EA, et al. Burns 2016;42(4):717–27.
Supplementation of vitamin E, vitamin C, and zinc at- 57. Wolf SE, Edelman LS, Kemalyan N, et al. Effects of ox-
tenuates oxidative stress in burned children: a ran- androlone on outcome measures in the severely
domized, double-blind, placebo-controlled pilot burned: a multicenter prospective randomized
study. J Burn Care Res 2009;30(5):859–66. double-blind trial. J Burn Care Res 2006;27(2):131–
54. Tanaka H, Matsuda T, Miyagantani Y, et al. Reduc- 9 [discussion: 140–1].
tion of resuscitation fluid volumes in severely burned 58. Pham TN, Klein MB, Gibran NS, et al. Impact of ox-
patients using ascorbic acid administration: a ran- androlone treatment on acute outcomes after severe
domized, prospective study. Arch Surg 2000; burn injury. J Burn Care Res 2008;29(6):902–6.
135(3):326–31. 59. Hart DW, Wolf SE, Chinkes DL, et al. Effects of early
55. Flores O, Stockton K, Roberts JA, et al. The efficacy excision and aggressive enteral feeding on hyper-
and safety of adrenergic blockade after burn injury: metabolism, catabolism, and sepsis after severe
a systematic review and meta-analysis. J Trauma burn. J Trauma 2003;54(4):755–61 [discussion:
Acute Care Surg 2016;80(1):146–55. 761–4].