eMedicine Specialties > Pediatrics: General Medicine > Nutrition

Failure to Thrive: Treatment & Medication

Author: Mohammad F El-Baba, MD, Assistant Professor of Pediatrics, Division of Pediatric Gastroenterology, Wayne State University School of Medicine; Division Chief of Pediatric Gastroenterology, Children's Hospital of Michigan
Coauthor(s): Reda W Bassali, MBChB, Associate Professor, Departments of General Pediatrics and Adolescent Medicine, Medical College of Georgia; John Benjamin, MD, Chief, General Section of Pediatrics and Adolescent Medicine, Vice Chair for Clinical Activities, Professor, Department of General Pediatrics, Medical College of Georgia; Ruby Mehta, MD, Fellow, Division of Pediatric Gastroenterology, Children's Hospital of Michigan
Contributor Information and Disclosures

Updated: May 4, 2009

Treatment

Medical Care

Most children with failure to thrive (FTT) can be treated as outpatients; home visits and close clinical follow-ups often help determine the underlying reason for the failure to thrive. However, hospitalization sometimes is necessary for diagnostic and therapeutic reasons. Diagnostic benefits of admission may include observation of feeding, parental-child interaction, and dietary habits, as well as the ability to perform specific tests and consult subspecialists.

Therapeutic benefits may result from hospitalization. Acute needs, such as dehydration, infection, anemia, or electrolyte imbalance, can be addressed and managed within the hospital. For instance, intravenous fluids, systemic antibiotic therapy, transfusion, and, possibly, parenteral nutrition often are in-hospital procedures. Of course, if an organic etiology is found for the failure to thrive in a particular child, specific therapy can be initiated during the hospitalization.

Another benefit of hospitalization may be the observation of parent-child interaction. In addition to observation of the feeding techniques of the parents, other interactions can be observed more easily in the hospital. For instance, the degrees to which parents bond, speak, and even interact with their children all can be observed during the hospital stay. If children gain weight easily during a hospitalization, the cause of the failure to thrive is most likely nonorganic.

Consultations

When treating children with failure to thrive, an interdisciplinary team approach combining pediatric, nutritional, mental health, and social work expertise often is helpful. An interdisciplinary approach ensures that programs such as women, infants, and children (WIC); food stamps; and Medicaid can be accessed. Using an interdisciplinary approach is also helpful if appropriate home-based intervention needs to be arranged.

Other advantages of using an interdisciplinary team include the fact that the family's psychosocial situation can be addressed and intervention can be provided. For example, an older child with a chronic illness and failure to thrive may benefit from referral to a psychologist. If neglect is suspected, child protective services can become involved as a result of this multidisciplinary approach.

Subspecialists should be involved for the treatment of organic illness when identified.

Diet

The long-term goal for every child with failure to thrive is to provide adequate energy intake for growth. Therefore, even if no etiology is found for a child with failure to thrive, aggressive dietary management is the cornerstone of therapy. Proper feeding can be achieved through infant formulas that are adjusted to meet the child's specific nutrient needs. For instance, some children are given formulas that have as much as 30 kcal/oz, whereas other children may receive regular 20 kcal/oz formulas supplemented with high-calorie food fortifiers, which can be lipids, protein, or carbohydrates (CHO).
 
Infants may be given concentrated formulas, assuming renal function is normal. If this option is chosen, renal function must be normal because the osmolar load of the resultant formula is high. In cases in which this is a problem because of renal insufficiency, increasing the fat content of the formula may be useful as a way of delivering additional calories.

Supplements for older children may include adding cheese, sour cream, butter, margarine, or peanut butter to meals. Also, high-energy (approximately 1 kcal/mL) shakes, which are available in different flavors, provide a good supplement (eg, Pedia Sure, Kindercal, Boost). Multivitamin and mineral supplements, including iron and zinc, usually are recommended to all undernourished children. Tube feeding rarely is indicated except for severe malnutrition and debilitation. In children with organic failure to thrive, continuous nighttime tube feeding also may be used to increase their energy intake.

Whether the child with failure to thrive is an inpatient or an outpatient, increasing energy intake is necessary. In younger children, energy intake is increased by increasing the amount of formula or caloric concentration of formula, using 24 or 27 kcal/oz, or adding calorie fortifiers. In toddlers, supplemental high-energy formulas as much as 30 kcal/oz are used. Sometimes these can be administered through tube feedings.

Table 2. Examples of High-Calorie Fortifiers

Open table in new window

Table
ProductCaloriesSource
Medium-chain triglyceride (MCT) oil7.7 kcal/mLFractionated coconut oil
Microlipid4.5 kcal/mLSafflower oil
Corn oil8.4 kcal/mLCorn
ProMod (protein powder)28 kcal/scoop (4.2 kcal/g)
5 g/scoop
Whey protein with lecithin
Polycose (powder or liquid)Powder - 23 kcal/tbsp
Liquid - 30 kcal/tbsp
Powder - Hydrolyzed cornstarch
Liquid - Glucose polymers derived from hydrolyzed cornstarch
Rice cereal (powder)15 kcal/tbspRice flour
Nonfat dry milk powder15 kcal/T (1.5 g protein)Cow's milk
Powder infant formula40 kcal/tbspCow's milk
Liquid concentrated infant formula40 kcal/ozCow's milk
ProductCaloriesSource
Medium-chain triglyceride (MCT) oil7.7 kcal/mLFractionated coconut oil
Microlipid4.5 kcal/mLSafflower oil
Corn oil8.4 kcal/mLCorn
ProMod (protein powder)28 kcal/scoop (4.2 kcal/g)
5 g/scoop
Whey protein with lecithin
Polycose (powder or liquid)Powder - 23 kcal/tbsp
Liquid - 30 kcal/tbsp
Powder - Hydrolyzed cornstarch
Liquid - Glucose polymers derived from hydrolyzed cornstarch
Rice cereal (powder)15 kcal/tbspRice flour
Nonfat dry milk powder15 kcal/T (1.5 g protein)Cow's milk
Powder infant formula40 kcal/tbspCow's milk
Liquid concentrated infant formula40 kcal/ozCow's milk
Table 3. Examples of High-Calorie Nutritional Products

Open table in new window

Table
Product, 30 kcal/ozCHO, g/100 mLProtein, g/100 mLFat, g/100 mLOsmolalityNutrient Sources
Nutren Junior
(Clintec)
12.834.2350CHO - Maltodextrin, sucrose
Protein - Casein, whey
Fat - Soy, MCT, and canola oils
(Vanilla, also available with fiber)
Kindercal
(Mead Johnson)
13.53.44.4310CHO - Maltodextrin, sucrose
Protein - Caseinates, milk protein concentrate
Fat - Canola, MCT, and high-oleic sunflower oils
Contains soy fiber 6.3 g/L
(Vanilla)
PediaSure
(Ross)
1135310CHO - Corn syrup solids, sucrose
Protein - Caseinate, whey protein concentrate
Fat - High-oleic safflower, soy, and MCT oils
(Vanilla, also available with fiber)
Boost
(Mead Johnson)
17.44.31.7590-620CHO - Sucrose, corn syrup solids
Protein - Milk protein concentrate
Fat - Canola, sunflower, corn oils
(Chocolate, chocolate mocha, strawberry, vanilla)
Product, 30 kcal/ozCHO, g/100 mLProtein, g/100 mLFat, g/100 mLOsmolalityNutrient Sources
Nutren Junior
(Clintec)
12.834.2350CHO - Maltodextrin, sucrose
Protein - Casein, whey
Fat - Soy, MCT, and canola oils
(Vanilla, also available with fiber)
Kindercal
(Mead Johnson)
13.53.44.4310CHO - Maltodextrin, sucrose
Protein - Caseinates, milk protein concentrate
Fat - Canola, MCT, and high-oleic sunflower oils
Contains soy fiber 6.3 g/L
(Vanilla)
PediaSure
(Ross)
1135310CHO - Corn syrup solids, sucrose
Protein - Caseinate, whey protein concentrate
Fat - High-oleic safflower, soy, and MCT oils
(Vanilla, also available with fiber)
Boost
(Mead Johnson)
17.44.31.7590-620CHO - Sucrose, corn syrup solids
Protein - Milk protein concentrate
Fat - Canola, sunflower, corn oils
(Chocolate, chocolate mocha, strawberry, vanilla)

More on Failure to Thrive

Overview: Failure to Thrive
Differential Diagnoses & Workup: Failure to Thrive
Treatment & Medication: Failure to Thrive
Follow-up: Failure to Thrive
Multimedia: Failure to Thrive
References
Further Reading

References

  1. Hoare KJ. A baby presenting with failure to thrive in primary care: a case report. Cases J. Feb 11 2009;2(1):137. [Medline].

  2. [Best Evidence] Picaud JC, Decullier E, Plan O, et al. Growth and bone mineralization in preterm infants fed preterm formula or standard term formula after discharge. J Pediatr. Nov 2008;153(5):616-21, 621.e1-2. [Medline].

  3. Buysse K, Reardon W, Mehta L, et al. The 12q14 microdeletion syndrome: Additional patients and further evidence that HMGA2 is an important genetic determinant for human height. Eur J Med Genet. Mar 17 2009;[Medline].

  4. Leung DH, Chung CT. Cases in pediatric gastroenterology from The Children's Hospital of Philadelphia: a 2-year-old boy with diarrhea, failure to thrive, and hepatomegaly. Medscape J Med. 2009;11(1):13. [Medline].

  5. Levy Y, Levy A, Zangen T, et al. Diagnostic clues for identification of nonorganic vs organic causes of food refusal and poor feeding. J Pediatr Gastroenterol Nutr. Mar 2009;48(3):355-62. [Medline].

  6. Munoz-Hoyos A, Molina-Carballo A, Uberos J, et al. Serum melatonin concentration in the child with non-organic failure to thrive: comparison with other types of stress. J Biol Regul Homeost Agents. Jan-Mar 2009;23(1):15-22. [Medline].

  7. Skuse DH. Non-organic failure to thrive: a reappraisal. Arch Dis Child. Feb 1985;60(2):173-8. [Medline].

  8. Black MM, Dubowitz H, Hutcheson J, et al. A randomized clinical trial of home intervention for children with failure to thrive. Pediatr. 1995;95(6):807-814. [Medline].

  9. Raynor P, Rudolf MC, Cooper K. A randomised controlled trial of specialist health visitor intervention for failure to thrive. Arch Dis Child. Jun 1999;80(6):500-6. [Medline].

  10. Adedoyin O, Gottlieb B, Frank R, et al. Evaluation of failure to thrive: diagnostic yield of testing for renal tubular acidosis. Pediatrics. Dec 2003;112(6 Pt 1):e463. [Medline].

  11. Babson SG, Benda GI. Growth graphs for the clinical assessment of infants of varying gestational age. J Pediatr. 1976;89:815. [Medline].

  12. Berwick DM. Nonorganic failure-to-thrive. Pediatr Rev. 1990;1(9):265-270.

  13. Cronk C, Crocker AC, Pueschel SM. Growth charts for children with down syndrome: 1 month to 18 years of age. Pediatr. 1988;81(1):102-110. [Medline].

  14. Drewett RF, Corbett SS, Wright CM. Cognitive and educational attainments at school age of children who failed to thrive in infancy: a population-based study. J Child Psychol Psychiatry. 1999;40(4):551-561. [Medline].

  15. Drotar D, Sturm L. Prediction of intellectual development in young children with early histories of nonorganic failure-to-thrive. J Pediatr Psychol. Jun 1988;13(2):281-96. [Medline].

  16. Elmer E, Gregg GS, Ellison P. Late results of the "failure to thrive" syndrome. Clin Pediatr (Phila). Oct 1969;8(10):584-9. [Medline].

  17. Frank DA, Zeisel SH. Failure to thrive. Pediatr Clin North Am. Dec 1988;35(6):1187-206. [Medline].

  18. Genero A, Moretti C, Fait P. [Non-organic failure to thrive: retrospective study in hospitalized children]. Pediatr Med Chir. Sep-Oct 1996;18(5):501-6. [Medline].

  19. Hamill PV, Drizd TA, Johnson CL, et al. Physical growth: National Center for Health Statistics percentiles. Am J Clin Nutr. Mar 1979;32(3):607-29. [Medline].

  20. Holmes LB. Fetal environmental toxins. Pediatr Rev. Oct 1992;13(10):364-9. [Medline].

  21. Homer C, Ludwig S. Categorization of etiology of failure to thrive. Am J Dis Child. Sep 1981;135(9):848-51. [Medline].

  22. Horton WA, Rotter JI, Rimoin DL. Standard growth curves for achondroplasia. J Pediatr. Sep 1978;93(3):435-8. [Medline].

  23. Lyon AJ, Preece MA, Grant DB. Growth curve for girls with Turner syndrome. Arch Dis Child. Oct 1985;60(10):932-5. [Medline].

  24. Mackner LM, Starr RH Jr, Black MM. The cumulative effect of neglect and failure to thrive on cognitive functioning. Child Abuse Negl. 1997;21(7):691-700. [Medline].

  25. Maggioni A, Lifshitz F. Nutritional management of failure to thrive. Pediatr Clin North Am. Aug 1995;42(4):791-810. [Medline].

  26. O'Callaghan MJ, Harvey JM, Tudehope DI, Gray PH. Aetiology and classification of small for gestational age infants. J Paediatr Child Health. Jun 1997;33(3):213-8. [Medline].

  27. Oates RK. Similarities and differences between nonorganic failure to thrive and deprivation dwarfism. Child Abuse Negl. 1984;8(4):439-45. [Medline].

  28. Olsen EM, Petersen J, Skovgaard AM, Weile B, Jorgensen T, Wright CM. Failure to thrive: the prevalence and concurrence of anthropometric criteria in a general infant population. Arch Dis Child. Feb 2007;92(2):109-14.

  29. Porter B, Skuse D. When does slow weight gain become 'failure to thrive'?. Arch Dis Child. Jul 1991;66(7):905-6. [Medline].

  30. Reif S, Beler B, Villa Y. Long-term follow-up and outcome of infants with non-organic failure to thrive. Isr J Med Sci. Aug 1995;31(8):483-9. [Medline].

  31. Sills RH. Failure to thrive. The role of clinical and laboratory evaluation. Am J Dis Child. Oct 1978;132(10):967-9. [Medline].

  32. Tanner JM, Davies PS. Clinical longitudinal standards for height and height velocity for North American children. J Pediatr. Sep 1985;107(3):317-29. [Medline].

  33. Treem WR. Emerging concepts in celiac disease. Curr Opin Pediatr. Oct 2004;16(5):552-9. [Medline].

  34. Walravens PA, Hambidge KM, Koepfer DM. Zinc supplementation in infants with a nutritional pattern of failure to thrive: a double-blind, controlled study. Pediatrics. Apr 1989;83(4):532-8. [Medline].

  35. Wright JA, Ashenburg CA, Whitaker RC. Comparison of methods to categorize undernutrition in children. J Pediatr. Jun 1994;124(6):944-6. [Medline].

  36. Zenel JA Jr. Failure to thrive: a general pediatrician's perspective. Pediatr Rev. Nov 1997;18(11):371-8. [Medline].

Keywords

failure to thrive, FTT, growth failure, failure of growth, malnutrition, delayed growth, growth charts, infant growth, normal growth, growth in infants, normal weight in infants, normal height in infants, head circumference in infants, Down syndrome, Turner syndrome, malnutrition, diarrhea, cerebral palsy, seizure, hepatomegaly, marasmus, maternal eating disorders, anorexia, bulimia, psychosocial deprivation, neglect, emotional deprivation syndrome, prematurity, placental insufficiency, alcohol ingestion, hypertension, preeclampsia, heart disease, diabetes mellitus, short stature, Prader-Willi syndrome, craniofacial abnormalities, congestive heart failure, chronic lung disease, bronchopulmonary dysplasia, gastroesophageal reflux, esophagitis, cystic fibrosis, CF, hyperthyroidism, milk protein allergy, Celiac disease, protein-losing enteropathies, Shwachman-Diamond syndrome, renal failure, renal tubular acidosis, hypothyroidism, systemic lupus erythematosus, treatment, diagnosis

Contributor Information and Disclosures

Author

Mohammad F El-Baba, MD, Assistant Professor of Pediatrics, Division of Pediatric Gastroenterology, Wayne State University School of Medicine; Division Chief of Pediatric Gastroenterology, Children's Hospital of Michigan
Mohammad F El-Baba, MD is a member of the following medical societies: American Gastroenterological Association and North American Society for Pediatric Gastroenterology and Nutrition
Disclosure: Nothing to disclose.

Coauthor(s)

Reda W Bassali, MBChB, Associate Professor, Departments of General Pediatrics and Adolescent Medicine, Medical College of Georgia
Reda W Bassali, MBChB is a member of the following medical societies: Ambulatory Pediatric Association and American Academy of Pediatrics
Disclosure: Nothing to disclose.

John Benjamin, MD, Chief, General Section of Pediatrics and Adolescent Medicine, Vice Chair for Clinical Activities, Professor, Department of General Pediatrics, Medical College of Georgia
John Benjamin, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.

Ruby Mehta, MD, Fellow, Division of Pediatric Gastroenterology, Children's Hospital of Michigan
Disclosure: Nothing to disclose.

Medical Editor

Maria Rebello Mascarenhas, MBBS, Associate Professor of Pediatrics, University of Pennsylvania School of Medicine; Section Chief, Division of Gastroenterology and Nutrition, Director, Nutrition Support Service, Children's Hospital of Philadelphia
Maria Rebello Mascarenhas, MBBS is a member of the following medical societies: American Gastroenterological Association, American Society for Parenteral and Enteral Nutrition, and North American Society for Pediatric Gastroenterology and Nutrition
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Jatinder Bhatia, MBBS, Professor of Pediatrics, Chief, Section of Neonatology, Department of Pediatrics, Medical College of Georgia
Jatinder Bhatia, MBBS is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American Dietetic Association, American Federation for Clinical Research, American Pediatric Society, American Society for Clinical Nutrition, American Society for Parenteral and Enteral Nutrition, New York Academy of Sciences, Society for Pediatric Research, and Southern Society for Pediatric Research
Disclosure: Mead Johnson Consulting fee Consulting; Mead Johnson Honoraria Speaking and teaching; Dey LP Consulting fee Consulting; Dey LP Honoraria Speaking and teaching; Ovation Honoraria Speaking and teaching

CME Editor

Merrily P M Poth, MD, Professor, Department of Pediatrics and Neuroscience, Uniformed Services University of the Health Sciences
Merrily P M Poth, MD is a member of the following medical societies: American Academy of Pediatrics, Endocrine Society, and Lawson-Wilkins Pediatric Endocrine Society
Disclosure: Nothing to disclose.

Chief Editor

Jatinder Bhatia, MBBS, Professor of Pediatrics, Chief, Section of Neonatology, Department of Pediatrics, Medical College of Georgia
Jatinder Bhatia, MBBS is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American Dietetic Association, American Federation for Clinical Research, American Pediatric Society, American Society for Clinical Nutrition, American Society for Parenteral and Enteral Nutrition, New York Academy of Sciences, Society for Pediatric Research, and Southern Society for Pediatric Research
Disclosure: Mead Johnson Consulting fee Consulting; Mead Johnson Honoraria Speaking and teaching; Dey LP Consulting fee Consulting; Dey LP Honoraria Speaking and teaching; Ovation Honoraria Speaking and teaching

 
 
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