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Reducing Contamination of Enteral Formulations

Introduction

VI. Reducing Contamination of Enteral Formulations

A. Complications related to contamination

1. Some degree of microbial contamination of formulations is almost inevitable during feedings. Contamination of enteral feedings may cause GI colonization, septicemia, nosocomial pneumonia, and diarrhea.69–75 Sources of contamination include formulation ingredients, mixing equipment, delivery systems, handling during assembly of the administration system, unsanitary formula prepa- ration areas and patient care units, health care providers, family members, and patients. Dangerous concentrations of organisms result from heavy initial contamination or inappropriately long hang times of the formulation or administration set.69Because infants are more susceptible to infection, guidelines for prepa- ration, storage, and administration of infant feedings are more conservative than those for children and adults.70

2. Hazard Analysis Critical Control Point (HACCP) is a systematic approach to minimizing the potential for contamination. It is important to identify critical points where contamination of enteral formulations may occur to reduce the possibilities for microbial contamination and/or food-borne disease. HACCP also aids in pro- viding safe and accurate nutrition products as mandated by the Joint Commission on Accreditation of Healthcare Organizations.

3. Reducing contamination during preparation.

a) When possible, formulations should be mixed, reconstituted, and diluted in a centralized location (eg, enteral formulary room or pharmacy). Mixing equipment must be cleaned meticulously.

b) In most instances, formulations can be reconstituted and diluted with tap water. However, in areas where the water supply is of questionable quality or in severely immunocompromised patients, it may be prudent to use distilled or sterile water.

c) Infant feedings require additional formulation preparation safeguards. Whenever possible, sterile ready-to-feed formu- lations or concentrated liquid formulations should be used.

Formulation powders should be weighed (not measured) and should be used only when no liquid forms are available.70For- mulations should always be prepared with sterile water.70 4. Formulations should be stored according to manufacturers’ rec-

ommendations.

a) Expired or damaged formula containers should be discarded.70 b) Unopened ready-to-feed formulations should be stored in a cool, dark place. They should not be stored in direct sunlight or near direct heat such as a radiator. Once opened, formula- tions may be stored in a refrigerator for up to 48 hours.71 c) Reconstituted or diluted formulations be stored in a refriger-

ator for a maximum of 24 hours.71

d) Additional guidelines for infant formulation storage include the following:

(1) Prepared infant formulations should be chilled to 40°F within 1 hour of preparation.70

(2) Opened ready-to-feed containers and prepared infant for- mulations should be stored in a refrigerator and used within 24 hours.70

(3) Human milk may be stored frozen in a home-style freezer for 3 months. It may be stored in a deep freeze (−20°C or

−4°F) for 12 months.70

(4) Fresh human milk may be stored in a refrigerator for 48 hours. Thawed or fortified human milk should be stored and used within 24 hours.70

5. Reducing contamination during administration a) Formulation hang time

(1) Canned, ready-to-use formulations generally can be hung for 8 to 12 hours at room temperature, but manufacturers’

guidelines should be followed. In general, it is best to fill the reservoir using clean technique as infrequently as hang time restrictions allow.

(2) Reconstituted powdered formulations generally can be hung for 4 to 6 hours at room temperature.

(3) Prefilled administration sets (bag/container) can generally be hung for 2 to 48 hours, or according to the manufac- turers’ recommendations.74

b) Administration set hang time

(1) Refillable sets (bag/container and tubing) can be used in a short-term care setting for about 24 hours.74

(2) It has been suggested that refillable administration sets (bags/containers and tubing) may be used for up to 72 hours in long-term care facilities; no differences in adverse effects (eg, fever, pneumonia, diarrhea, vomiting) were noted between delivery sets used for 24 versus 72 hours. How- ever, no bacterial counts were performed. Thus, use of refill- able delivery sets for longer than 24 hours in settings other than long-term care facilities requires further investigation.75 c) Infant feeding delivery guidelines

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74 A.S.P.E.N. Nutrition Support Practice Manual 2nd Ed. © 2005 A.S.P.E.N. www.nutritioncare.org.

(1) Hang times for human milk and infant formulas should not exceed 4 hours.70

(2) Syringe tubing should be changed every 4 hours in infants receiving continuous infusion feedings.70

(Enteral Formulations chapter from the 1st edition was contributed by Kelley Olree, Joseph Vitello, Jacqueline Sullivan, and Carol Kohn- Keeth)

R E F E R E N C E S

1. Storm HM, Lin P. Forms of carbohydrate in enteral nutrition formulas.

Support Line.1996;18:7–9.

2. Abrams SA, Griffin IJ, Davila PM. Calcium and zinc absorption from lactose-containing and lactose-free infant formulas. Am J Clin Nutr.

2002;76:442–446.

3. Bell SJ, Mascioli EA, Bistrian BR. Alternative lipid sources for enteral and parenteral nutrition: long- and medium-chain triglycerides, structured triglycerides, and fish oils. J Am Diet Assoc.1991;91:74–78.

4. Innis S. Perinatal biochemistry and physiology of long-chain polyunsatu- rated fatty acids. J Pediatr.2003;143:81–88.

5. Uauy R, Hoffman DR, Mena P, Llanos A, Birch EE. Term infant studies of DHA and ARA supplementation on neurodevelopment: results of random- ized controlled trials. J Pediatr.2003;143(suppl 4):S17–25.

6. Auestad N, Scott DT, Janowsky JS, et al. Visual, cognitive, and language assessments at 39 months: a follow-up study of children fed formulas con- taining long-chain polyunsaturated fatty acids to 1 year of age. Pediatrics.

2003;112(3 Pt 1):e177–183.

7. Mehta NR, Hamosh M, Bitman J, Wood DL. Adherence of medium-chain fatty acids to feeding tubes of premature infants fed formula fortified with medium-chain triglyceride. J Pediatr Gastroenterol Nutr.1991;13:267–269.

8. Coster J, McCarty R, Hall J. Role of specific amino acids in nutritional sup- port. ANZ J Surg.2003;73:846–849.

9. Platell C, Kung S-E, McCauley R, Hall JC. Branched chain amino acids.

J Gastroenterol Hepatol.2000;15:706–717.

10. Lacey JM, Wilmore DW. Is glutamine a conditionally essential amino acid? Nutr Rev.1990;48:297–309.

11. Neu J, DeMarco V, Li N. Glutamine: clinical applications and mechanisms of action. Curr Opin Clin Nutr Metab Care.2002;5:69–75.

12. Spapen H, Diltoer M, Van Malderen C, Opdenacker G, Suys E, Huyghens L. Soluble fiber reduces the incidence of diarrhea in septic patients receiv- ing total enteral nutrition: a prospective, double-blind, randomized, and controlled trial. Clin Nutr.2001;20:301–305.

13. Spiegel JE, Rose R, Karabell P, et al. Safety and benefits of fructooligosac- charides as food ingredients. Food Technol.1994;48:85–89.

14. Evans MA, Shronts EP. Intestinal fuels: glutamine, short-chain fatty acids, and dietary fiber.J Am Diet Assoc.1992;92:1239–1246.

15. Daly JM, Lieberman MD, Goldfine J, et al. Enteral nutrition with supple- mental arginine, RNA, and omega-3 fatty acids in patients after operation:

immunologic, metabolic, and clinical outcome. Surgery.1992;112:56–67.

16. Daly JM, Lieberman MD, Goldfine J, et al. Immune and metabolic effects of arginine in the surgical patient. Ann Surg.1988;208:512–522.

17. Gianotti L, Braga M, Nespoli L, et al. A randomized controlled trial of preoperative oral supplementation with a specialized diet in patients with gastrointestinal cancer. Gastroenterology.2002;122:1763–1770.

18. McCowen KC, Bistrian B. Immunonutrition: problematic or problem solv- ing? Am J Clin Nutr.2003;3:764–770.

19. Sax HC. Effect of immune enhancing formulas (IEF) in general surgery patients. J Parenter Enteral Nutr.2001;25:S19–S23.

20. Fearon KCH, von Meyenfeldt MF, Moses AGW, et al. Effect of a protein and energy dense m-3 fatty acid enriched oral supplement on loss of weight and lean tissue in cancer cachexia. Gut.2003;53:1479–1486.

21. Kudsk KA, Minard G, Croce MA, et al. A randomized trial of isonitroge- nous enteral diets after severe trauma: an immune-enhancing diet reduces septic complications. Ann Surg.1996;224:531–543.

22. Bower RH, Cerra FB, Bershadksy B, et al. Early enteral administration of a formula (Impact) supplemented with arginine, nucleotides and fish oil in

intensive care unit patients: results of a multicenter, prospective, random- ized, clinical trial. Crit Care Med.1995;23:436–449.

23. Heys SD, Walker LG, Smith I, Eremin O. Enteral nutritional supple- mentation with key nutrients in patients with critical illness and cancer:

a meta-analysis of randomized controlled clinical trials. Ann Surg.

1999;229:467–477.

24. Beale RJ, Bryg DJ, Bihari DJ. Immunonutrition in the critically ill: a sys- tematic review of clinical outcome. Crit Care Med.1999;27:2799–2805.

25. Kudsk KA, Moore F, Martindale RT, et al. Consensus recommendations from the U.S. Summit on Immune-Enhancing Enteral Therapy. J Parenter Enteral Nutr.2001;25(suppl):S61–62.

26. Sacks GS, Kudsk KA. Maintaining mucosal immunity during parenteral feeding with surrogates to enteral nutrition. Nutr Clin Pract.2003;18:

483–488.

27. Bower RH, Muggia-Sullam M, Vallgren S, et al. Branched chain amino acid-enriched solutions in the septic patient. A randomized, prospective trial. Ann Surg.1986;203:13–20.

28. van den Berghe G, Wouters P, Weekers F, et al. Intensive insulin therapy in critically patients. N Engl J Med.2001;345:1359–1367.

29. Franz MJ. 2002 diabetes nutrition recommendations: grading the evidence.

Diabetes Educ.2002;28:756–759, 762–764, 766.

30. American Diabetes Association. Nutrition principles and recommenda- tions in diabetes. Diabetes Care.2004;27(suppl):S36–46.

31. Munoz SJ. Nutritional therapies in liver disease. Semin Liver Dis.1991;11:

278–291.

32. Silk DBA, O’Keefe SJD, Wick C. Nutritional support in liver disease. Gut.

1991;31(suppl):S29–33.

33. Sleisenger MH, Kim YS. Protein digestion and absorption. N Engl J Med.

1979;300:659–663.

34. Mowatt-Larson CA, Brown RO, Wojtysiak SL, et al. Comparison of tol- erance and nutritional outcome between a peptide and a standard enteral formula in critically ill, hypoalbuminemic patients. J Parenter Enteral Nutr.1992;16:20–24.

35. Heimburger DC, Geels WJ, Thiesse KT, Bartolucci AA. Randomized trial of tolerance and efficacy of a small-peptide enteral feeding formula versus a whole-protein formula. Nutrition.1995;11:360–364.

36. Deitch EA, Xu D, Qi L, et al. Elemental diet-induced immune suppression is caused by both bacterial and dietary factors. J Parenter Enteral Nutr.

1993;7:332–336.

37. Serizawa H, Miura S, Tashiro H, et al. Alteration of mucosal immunity after long-term ingestion of an elemental diet in rats. J Parenter Enteral Nutr.1994;18:141–147.

38. Windsor ACJ, Kanwar S, Li AGK, et al. Compared with parenteral nutrition, enteral feeding attenuates the acute phase response and improves disease severity in acute pancreatitis. Gut.1998;42:431–435.

39. Kalfarentzos F, Kehagias J, Mead N, et al. Enteral nutrition is superior to parenteral nutrition in severe acute pancreatitis: results of a randomized prospective trial. Br J Surg.1997;84:1665–1672.

40. Olah A, Pardavi G, Belagyi T, et al. Early nasojejunal feeding in acute pancreatitis is associated with a lower complication rate. Nutrition.

2002;18:259–262.

41. Al-Saady N, Blackmore C, Bennet ED. High fat, low carbohydrate enteral feeding reduces PaCO2and the period of ventilation in ventilated patients.

Intensive Care Med.1989;15:290–295.

42. Frankfurt JD, Fischer CE, Stansburg DW, et al. Effects of high- and low- carbohydrate meals on maximum exercise performance in chronic airflow obstruction. Chest.1991;100:792–795.

43. Talpers SS, Romberger DJ, Bunce SB, et al. Nutritionally associated increased carbon dioxide production. Excess of total calories vs high proportion of carbohydrate calories.Chest.1992;102:551–555.

44. Gadek J, DeMichele S, Karlstad M, et al. Effect of enteral with eico- sapentanoic acid, γ-linolenic acid, and antioxidants in patients with acute respiratory distress syndrome. Crit Care Med.1999;27:1409–1420.

45. Saffle JR, Wiebke G, Jennings K, et al. Randomized trial of immune- enhancing enteral nutrition in burn patients. J Trauma.1997;42:793–802.

46. Shepherd AA. Nutrition for optimum wound healing. Nurs Stand.2003;

18:55–58.

S E C T I O N I Fundamentals of Nutrition Support Practice and Management

© 2005 A.S.P.E.N. www.nutritioncare.org. A.S.P.E.N. Nutrition Support Practice Manual 2nd Ed. 75

47. Gottschlich MM, Jenkins M, Warden GD, et al. Differential effects of three enteral dietary regimens on selected outcome variables in burn patients.

J Parenter Enteral Nutr.1990;14:225–236.

48. A.S.P.E.N. Board of Directors and the Clinical Guidelines Task Force.

Guidelines for the use of parenteral and enteral nutrition in adult and pediatric patients. J Parenter Enteral Nutr.2002;26:188SA–190SA.

49. Kaufman SS, Scrivner DJ, Murray ND, Vanderhoof JA, Hart MH, Antonson DL. Influence of portagen and pregestimil on essential fatty acid status in infantile liver disease. Pediatrics.1992;89(1):151–154.

50. Pickering LK, Granoff DM, Erickson JR, et al. Modulation of the immune system by human milk and infant formula containing nucleotides. Pediatrics.

1998;101:242–249.

51. American Academy of Pediatrics. Committee on Nutrition. Iron fortification of infant formulas. Pediatrics.1999;104:119–123.

52. Zeiger RS, Sampson HA, Bock SA, et al. Soy allergy in infants and children with IgE-associated cow’s milk allergy. J Pediatr.1999;134:614–622.

53. American Academy of Pediatrics. Committee on Nutrition. Soy protein- based formulas: recommendations for use in infant feeding. Pediatrics.

1998;101:148–153.

54. Vanderhoof JA, Murray ND, Paule CL, Ostrom KM. Use of soy fiber in acute diarrhea in infants and toddlers. Clin Pediatr (Phila).1997;36:

135–139.

55. Burks AW, Vanderhoof JA, Mehra S, Ostrom KM, Baggs G. Randomized clinical trial of soy formula with and without added fiber in antibiotic- induced diarrhea. J Pediatr.2001;139:578–582.

56. Brown KH, Perez F, Peerson JM, et al. Effect of dietary fiber (soy poly- saccharide) on the severity, duration, and nutritional outcome of acute, watery diarrhea in children. Pediatrics.1993;92:241–247.

57. American Academy of Pediatrics. Committee on Nutrition. Hypoaller- genic infant formulas. Pediatrics.2000;106:346–349.

58. Jakobsson I, Lothe L, Ley D, Borschel MW. Effectiveness of casein hydrolysate feedings in infants with colic. Acta Paediatr.2000;89:18–21.

59. Nelson SP, Chen EH, Syniar GM, Christoffel KK. Prevalence of symptoms of gastroesophageal reflux during infancy. A pediatric practice-based survey.

Pediatric Practice Research Group. Arch Pediatr Adolesc Med.1997;6:

569–572.

60. Rudolph CD, Mazur LJ, Liptak GS, et al. Guidelines for evaluation and treatment of gastroesophageal reflux in infants and children: recommen- dations of the North American Society for Pediatric Gastroenterology and Nutrition. J Pediatr Gastroenterol Nutr.2001;32(suppl 2):S1–31.

61. Vanderhoof JA, Moran JR, Harris CL, Merkel KL, Orenstein SR. Effi- cacy of a pre-thickened infant formula: a multicenter, double-blind, ran-

domized, placebo-controlled parallel group trial in 104 infants with symptomatic gastroesophageal reflux. Clin Pediatr (Phila).2003;42:

483– 495.

62. Wenzl TG, Schneider S, Scheele F, Silny J, Heimann G, Skopnik H.

Effects of thickened feeding on gastroesophageal reflux in infants: a placebo-controlled crossover study using intraluminal impedance. Pedi- atrics.2003;111:e355–359.

63. Kuschel C, Harding J. Multicomponent fortified human milk for promoting growth in preterm infants. Cochrane Database Syst Rev.2004;1:CD000343.

64. Morley R, Lucas A. Randomized diet in the neonatal period and growth performance until 7.5–8 y of age in preterm children. Am J Clin Nutr.

2000;71:822–888.

65. Lucas A, Fewtrell MS, Morley R, et al. Randomized trial of nutrient- enriched formula versus standard formula for postdischarge preterm infants. Pediatrics.2001;108:703–711.

66. Carver JD, Wu PY, Hall RT, et al. Growth of preterm infants fed nutrient- enriched or term formula after hospital discharge. Pediatrics.2001;107:

683–689.

67. Koo WW, Poh D, Leong M, Tam YK, Succop P, Checkland EG. Osmotic load from glucose polymers. J Parenter Enteral Nutr.1991;15:144 –147.

68. Fomon SJ, Ziegler EE. Renal solute load and potential renal solute load in infancy. J Pediatr.1999;134:11–14.

69. Anderton A. Reducing bacterial contamination in enteral tube feeds.

Nutrition.1999;15:55–57.

70. Pediatric Nutrition Practice Group of the American Dietetic Association.

Infant Feedings: Guidelines for Preparation of Formula and Breast Milk in Health Care Facilities.Chicago, IL: American Dietetic Association;

2003.

71. Campbell SM. Preventing Microbial Contamination of Enteral Formulas and Delivery Systems.Columbus, OH: Ross Products Division of Abbott Laboratories; 1995.

72. Kohn CL. The relationship between enteral formula contamination and length of enteral delivery set usage. J Parenter Enteral Nutr.1991;15:

567–571.

73. Thurn J, Crossley K, Gerdts A, et al. Enteral hyperalimentation as a source of nosocomial infection. J Hosp Infect.1990;15:203–217.

74. Donius MA. Contamination of a prefilled ready-to-use enteral feeding sys- tem compared with a refillable bag. J Parenter Enteral Nutr.1993;17:

461– 464.

75. Graham S, Chicone J, Gerard B, et al. Frequency of changing enteral ali- mentation bags and tubing, and adverse clinical outcomes in patients in a long term care facility. Can J Infect Control.1993;8:41– 43.

76 A.S.P.E.N. Nutrition Support Practice Manual 2nd Ed. © 2005 A.S.P.E.N. www.nutritioncare.org.

Linda Lord, NP, RN, MS, CNSN;

Michelle Harrington, MS, RD, CSP, CNSD, LDN

5

Enteral Nutrition

Implementation and Management

Introduction

When the gastrointestinal (GI) tract is functional, enteral feeding is the preferred route for nutrition support. This type of feeding provides many physiologic, metabolic, safety, and cost benefits over parenteral feedings.1Tube feedings can range from providing adjunctive support to providing complete nutrition therapy. Enteral feedings can be admin- istered and scheduled in a variety of ways. Practitioners who are famil- iar with these options can recommend regimens that accommodate each patient’s needs and lifestyle. Selection of the optimal enteral regimen depends on a number of factors, such as the patient’s nutritional and clinical status, GI function, age, and level of activity. Practitioners need to be aware of these factors so that enteral feedings can be administered successfully and safely. A well-tolerated enteral regimen that meets the patient’s needs can reduce the length of time that support is necessary and improve the disease treatment outcome; it can also assist in the growth and development of the pediatric patient.2

I. Benefits, Indications, and Contraindications for Enteral Feedings II. Implementation of Enteral Feedings

III. Monitoring and Management of Enteral Feedings IV. Complications and Management of Enteral Feedings

V. Transitioning from Enteral Nutrition Support References

I. Benefits, Indications, and Contraindications for