Nutritional Considerations in Failure to Thrive 

  • Author: Simon S Rabinowitz, MD, PhD; Chief Editor: Jatinder Bhatia, MBBS   more...
 
Updated: May 4, 2010
 

Background

Failure to thrive (FTT) is both a descriptive term for various entities and a diagnosis. It is defined as a significant interruption in the expected rate of growth during early childhood. Because sequential measurements of growth are vital aspects of preventive pediatrics, failure to thrive is a concern for all pediatric heath care providers. All standard pediatric textbooks have sections on this topic,[1] and numerous review articles have been written.[2, 3, 4, 5, 6] However, despite significant attention, a meta-analysis of studies on industrialized children with this condition failed to demonstrate any significant adverse outcomes in this cohort.[7] Still, failure to thrive can be a prelude to significant morbidity and mortality in the developing world, in impoverished children, and in children with various chronic illnesses.

Although specific anthropometric criteria to define failure to thrive vary, all describe children with inadequate or worsening growth over time. The most common definition is weight less than the third to fifth percentile for age on more than one occasion or weight measurements that fall 2 major percentile lines using the standard growth charts of the National Center for Health Statistics (NCHS).

Some authors have included height measurements as part of the definition; however, height measurements more precisely describe short stature. If weight parameters are significantly compromised, height can also be secondarily affected in individuals with failure to thrive. A European study examined a large cohort of children using various terms associated with pediatric growth compromise and documented a wide variance in the prevalence of this condition.[8] Although serial measurements of head circumference are important in the evaluation of infants and toddlers, isolated failure of the head to grow should not suggest the typical failure to thrive differential.

In the developed world, the published literature indicates that although the differential diagnosis of failure to thrive is comprehensive, most children with this problem are diagnosed with predominantly psychosocial or nonorganic problems. However, because speech and feeding evaluations have become more commonplace and are more sophisticated, psychosocial compromise is now recognized as more likely to yield failure to thrive in those with subtle swallowing dysfunction or other organic conditions.[9] As this fundamental paradigm is reconsidered,[10, 11] the practicing child care provider must make every effort to identify simultaneous pathophysiology, regardless of how deprived the child with failure to thrive may appear.

Conversely, the contributions of dysfunctional familial dynamics, oppositional behavior, and depression to the failure to thrive noted in chronic illnesses must also be appreciated. Some authors have substituted a nonorganic failure to thrive paradigm for the organic failure to thrive paradigm, with individual children lying closer to one extreme or the other.[12]

Normal growth and growth charts of term and premature infants, as well as the etiology, evaluation, management, and outcome of failure to thrive are discussed in this article. For information on energy malnutrition, see the eMedicine article Marasmus.

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Pathophysiology

Although failure to thrive has historically been considered to be organic or nonorganic, a new view attempts to identify all contributing factors, often finding contributors from both categories in a single child. Nonorganic failure to thrive is almost always the result of inadequate energy intake. In addition to that problem, organic failure to thrive may also be the result of compromised use of ingested calories (usually vomiting or malabsorption and/or excessive losses [ie, protein-losing enteropathy]) and excessive metabolic demands. Prior to analyzing these entities, normal growth is reviewed.

Normal growth in term infants

The average birth weight for a term infant is 3.3 kg. Weight drops as much as 10% in the first few days of life, secondary to loss of excess fluid. By 10-14 days of life, birth weight should be regained. Breastfed infants who are fed smaller volumes of colostrum for the first few days regain birth weight a little later than bottle-fed infants.

On average, infants gain 1 kg/mo for the first 3 months, 0.5 kg/mo from age 3-6 months, 0.33 kg/mo from age 6-9 months, and 0.25 kg/mo from age 9-12 months. Term infants double their birth weight by age 4-6 months and triple their weight by age 12 months. An alternative schema to use is that term infants gain almost 30 g (1 oz) per day for 3 months and then almost 15 g (0.5 oz) per day for the next 6 months. From age 9 months until the child is a toddler, the average weight gain is roughly 0.25 kg/mo (or 0.5 lb/mo). Afterwards, the weight gain is about 2 kg/y through early school age.

Caloric intake to assure adequate intake in a normal infant is 100-110 kcal/kg/d for the first half year and 100 kcal/kg/d for the second half of the first year. Beyond 10 kg, 50 kcal/kg/d is required until 20 kg. Beyond 20 kg, 20 kcal/kg/d are necessary.

Term infants grow 25 cm in length during the first year, 12.5 cm in the second year, and then slow down to approximately 5-6 cm between age 4 years and the onset of puberty, at which time, growth can increase up to 12 cm per year.

The average head circumference is 35 cm at birth and rapidly increases to 47 cm by age 1 year. The rate of growth then slows, reaching an average of 55 cm by age 6 years.

Also, the upper-to-lower body segment ratio changes with growth. Normally, the ratio at birth is 1.7, the ratio at age 3 years is 1.3, and the ratio by age 7 years becomes 1. The lower body segment is measured from the symphysis pubis to the floor.

Normal growth in premature infants

When plotting growth charts for premature babies, a "corrected age" should be used. This corrected age can be calculated by subtracting the number of weeks of prematurity from the postnatal age. Special growth charts based on gestational age rather than chronological age have been developed for infants, beginning at 26 weeks' gestational age. However, because these charts represent a compilation of a relatively small number of infants, they may not be completely reliable. Whichever technique is used for premature babies (eg, adjustment of age, using specific premature growth charts), consistency of methodology is essential. Once a method for plotting growth is chosen, that technique should be followed each time plotting occurs. Prior to 40 weeks' gestation, some infants may require as much as 120 kcal/kg/d to ensure adequate weight gain.

Catch-up growth is attained at approximately age 18 months for head circumference, age 24 months for weight, and age 40 months for height. Subsequently, normal growth charts can be used. In some premature babies with very low birth-weight, catch-up growth does not occur until early school age.

Growth charts

Growth charts were developed by the NCHS based on data collected through the Third National Health and Nutrition Examination Survey III. They have been used since 1977 and are available for males and females aged 0-36 months and aged 2-18 years. The growth charts for boys and girls aged 0-36 months include weight and height for age and head circumference; growth charts for both age groups include weight for stature.

These charts have been revised and are available from the Centers for Disease Control and Prevention (2000 CDC Growth Charts: United States).[13] The new charts are applicable to infants, children, and adolescents from birth to age 20 years and have 7 percentile curves (5th, 10th, 25th, 50th, 75th, 90th, 95th). Charts are available for use in subspecialty patients (eg, endocrine, gastroenterology), with additional third and 97th percentile curves. Body mass index (BMI) charts, which are available for individuals aged 2-20 years, have replaced the weight-for-stature charts. BMI is calculated by dividing weight in kilograms by height in meters squared.

Accurate measurements are essential to the interpretation of growth charts. Scales need to be regularly calibrated; length should be carefully measured, and head circumference should be measured using standardized techniques.

Alternate growth charts are available for children who are breast fed and for children with Down syndrome,[14]Turner syndrome,[15] achondroplasia,[16] meningomyelocele, low birth weight, and very low birth weight. No matter which growth chart is used, the most valuable information is obtained by careful measuring and plotting on the same chart over time. Infants and children should remain within 1-2 percentile curves over time.

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Epidemiology

Frequency

United States

In reports from 1980-1989, failure to thrive accounted for 1-5% of tertiary hospital admissions for infants younger than 1 year. As many as 10% of children in primary care settings show signs of failure to thrive. The incidence is highest in children with prematurity and with other medical conditions. The proportion of nonorganic failure to thrive among all infants with failure to thrive is much higher in the United States and other industrialized countries than in the developing nation.

International

In underdeveloped countries, malnutrition manifesting as failure to thrive is more common.

Mortality/Morbidity

Ultimate physical growth and cognitive development may be decreased in children with long standing failure to thrive, especially with an early onset. However, efforts to analyze the published data have not yielded unequivocal confirmation in children in the developing world.[7] Earlier publications have described more cognitive deficits in nonorganic than organic failure to thrive.[17]

In developing countries, malnutrition is a significant cause of mortality, whether directly or secondary to complications (eg, infection). Among children with certain illnesses, failure to thrive is an independent risk factor for premature mortality, such as with HIV infection[18] and epidermolysis bullosa.[19]

Race

Failure to thrive can occur in all socioeconomic strata, although it is more frequent in families living in poverty. Studies indicate increased incidence in children receiving Medicaid, children living in rural areas, and children who are homeless.

Sex

Nonorganic failure to thrive is reported more commonly in females than in males.

Age

The term is mainly reserved for growth compromise in young children.

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Contributor Information and Disclosures
Author

Simon S Rabinowitz, MD, PhD  Professor of Clinical Pediatrics, New York Medical College; Chairman, Chief and Medical Administrator, Department of Pediatrics, Chief, Pediatric Gastroenterology and Nutrition, Richmond University Medical Center

Simon S Rabinowitz, MD, PhD is a member of the following medical societies: American Academy of Pediatrics, American Association for the Advancement of Science, American College of Gastroenterology, American Gastroenterological Association, American Medical Association, New York Academy of Sciences, North American Society for Pediatric Gastroenterology and Nutrition, Phi Beta Kappa, and Sigma Xi

Disclosure: Nothing to disclose.

Coauthor(s)

Madhavi Katturupalli, MD  Resident Physician, Department of Pediatrics, New York Medical College, Richmond University Medical Center

Madhavi Katturupalli, MD is a member of the following medical societies: American Academy of Pediatrics

Disclosure: Nothing to disclose.

Genie Rogers, MA, CCC-SLP, BRS-S  Speech-Language Pathologist, Infant and Child Learning Center, Neonatal Intensive Care Unit, Downstate University Hospital; Clinical Supervisor, Speech Therapy Services, Step by Step Infant Development Program

Genie Rogers, MA, CCC-SLP, BRS-S is a member of the following medical societies: American Speech-Language-Hearing Association

Disclosure: Nothing to disclose.

Specialty Editor Board

Maria Rebello Mascarenhas, MBBS  Associate Professor of Pediatrics, University of Pennsylvania School of Medicine; Section Chief Nutrition, 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.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Pharmacy Editor, eMedicine

Disclosure: Nothing to disclose.

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 Pediatric Society, American Society for Clinical Nutrition, American Society for Parenteral and Enteral Nutrition, Society for Pediatric Research, and Southern Society for Pediatric Research

Disclosure: Nothing to disclose.

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 Pediatric Society, American Society for Clinical Nutrition, American Society for Parenteral and Enteral Nutrition, Society for Pediatric Research, and Southern Society for Pediatric Research

Disclosure: Nothing to disclose.

References
  1. Bauchner H. Failure to Thrive. In: Nelson Textbook of Pediatrics. 18th Ed. Philadelphia, PA: WB Saunders; 2007:37;184-7.

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

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

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

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

  6. 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].

  7. Rudolf MC, Logan S. What is the long term outcome for children who fail to thrive? A systematic review. Arch Dis Child. Sep 2005;90(9):925-31. [Medline].

  8. Olsen EM, Petersen J, Skovgaard AM, et al. Failure to thrive: the prevalence and concurrence of anthropometric criteria in a general infant population. Arch Dis Child. Feb 2007;92(2):109-14. [Medline].

  9. Reilly SM, Skuse DH, Wolke D, Stevenson J. Oral-motor dysfunction in children who fail to thrive: organic or non-organic?. Dev Med Child Neurol. Feb 1999;41(2):115-22. [Medline].

  10. Olsen EM, Skovgaard AM. [Psychosomatic failure-to-thrive in infants and toddlers]. Ugeskr Laeger. Nov 25 2002;164(48):5631-5. [Medline].

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

  12. Manikam R, Perman JA. Pediatric feeding disorders. J Clin Gastroenterol. Jan 2000;30(1):34-46. [Medline].

  13. [Guideline] Centers for Disease Control and Prevention. CDC Growth Charts. August 4, 2009;[Full Text].

  14. [Guideline] Cronk C, Crocker AC, Pueschel SM, et al. Growth charts for children with Down syndrome: 1 month to 18 years of age. Pediatrics. Jan 1988;81(1):102-10. [Medline].

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

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

  17. 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. May 1999;40(4):551-61. [Medline].

  18. Prazuck T, Tall F, Nacro B, et al. HIV infection and severe malnutrition: a clinical and epidemiological study in Burkina Faso. AIDS. Jan 1993;7(1):103-8. [Medline].

  19. Lechner-Gruskay D, Honig PJ, Pereira G, McKinney S. Nutritional and metabolic profile of children with epidermolysis bullosa. Pediatr Dermatol. Feb 1988;5(1):22-7. [Medline].

  20. Berwick DM, Levy JC, Kleinerman R. Failure to thrive: diagnostic yield of hospitalisation. Arch Dis Child. May 1982;57(5):347-51. [Medline].

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

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

  23. Daniel M, Kleis L, Cemeroglu AP. Etiology of failure to thrive in infants and toddlers referred to a pediatric endocrinology outpatient clinic. Clin Pediatr (Phila). Oct 2008;47(8):762-5. [Medline].

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

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

  26. Schwarz SM, Corredor J, Fisher-Medina J, Cohen J, Rabinowitz S. Diagnosis and treatment of feeding disorders in children with developmental disabilities. Pediatrics. Sep 2001;108(3):671-6. [Medline].

  27. Tannenbaum GS, Ramsay M, Martel C, Samia M, Zygmuntowicz C, Porporino M. Elevated circulating acylated and total ghrelin concentrations along with reduced appetite scores in infants with failure to thrive. Pediatr Res. May 2009;65(5):569-73. [Medline].

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

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

  30. Black MM, Dubowitz H, Krishnakumar A, Starr RH Jr. Early intervention and recovery among children with failure to thrive: follow-up at age 8. Pediatrics. Jul 2007;120(1):59-69. [Medline].

  31. Black MM, Dubowitz H, Hutcheson J, Berenson-Howard J, Starr RH Jr. A randomized clinical trial of home intervention for children with failure to thrive. Pediatrics. Jun 1995;95(6):807-14. [Medline].

  32. Reif S, Beler B, Villa Y, Spirer Z. 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].

  33. Corbett SS, Drewett RF. To what extent is failure to thrive in infancy associated with poorer cognitive development? A review and meta-analysis. J Child Psychol Psychiatry. Mar 2004;45(3):641-54. [Medline].

  34. Emond AM, Blair PS, Emmett PM, Drewett RF. Weight faltering in infancy and IQ levels at 8 years in the Avon Longitudinal Study of Parents and Children. Pediatrics. Oct 2007;120(4):e1051-8. [Medline].

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

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Failure of growth in weight, length, and head circumference starting at birth, suggesting an organic etiology that occurred in utero.
Growth failure in length and weight with a normal head circumference in an infant with growth hormone deficiency.
Acquired hypothyroidism.
Constitutional delay of growth.
Failure to thrive secondary to caloric deprivation.
Table 1. Summary of Organic Causes of Failure to Thrive
Prenatal causes
  • Prematurity with complications
  • Maternal malnutrition
  • Toxic exposure in utero
  • Alcohol, smoking, medications, infections
  • IUGR
  • Chromosomal abnormalities
Postnatal causesInadequate intake



  • Lack of appetite (chronic illness)
  • Inability to suck or swallow
  • Vomiting
  • Therapy used to treat primary illness (eg, chemotherapy)
  • Developmental delay
  • GI pain or dysmotility
Poor absorption and/or use of nutrients



  • Malabsorption
  • Anatomical GI problems
  • Pancreatic and cholestatic conditions
  • Inborn errors of metabolism
  • Chronic GI infections
Increased metabolic demand



  • HIV infection
  • Malignancy
  • Cardiopulmonary diseases and inflammatory conditions
  • Renal failure
  • Hyperthyroidism
Table 2. Examples of High-Calorie Fortifiers
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
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)



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