E N D
1. Failure to Thrive Joyee G. Vachani, MD
April 21st, 2010
5. Definition <3rd or 5th percentile on growth chart
Change in growth that has crossed two %s
Gomez criteria: compare current wt for age with expected weight for age (at 50th %)
weight <60% of expected = severe FTT
61-75% = moderate FTT
76-90% = mild FTT
6. Growth charts Look at trends over time
Use appropriate growth charts
Premies: corrected age on term growth charts
Trisomy 21
Weight decreases first ? Length
Low wt only: acute undernutrition
Low wt and ht: chronic malnutrion/stunting
Low wt, ht, and HC:
Congenital or genetic abnormalities
Severe malnutrition
7. Normal weight gain - 26 to 31 g/day for those 0 to 3 months
- 17 to 18 g/day for those 3 to 6 months
- 12 to 13 g/day for those 6 to 9 months
- 9 to 13 g/day for those 9 to 12 months
- 7 to 9 g/day for those 1 to 3 years
8. Growth Chart quiz http://emedicine.medscape.com/article/985007-media
9. Your patient You are about to see a patient admitted to FIS for Failure to Thrive… where do you start?
10. History Dietary Hx
Psychosocial Hx
Birth Hx
Family Hx
ROS
Development
Recurrent infections
GI hx
Resp hx
11. History Dietary Hx: quantify caloric intake
Foods and Formula: prep, frequency
Juice and water intake
Behaviors at mealtime
Psychosocial Hx
Pregnancy Hx
Parent mental health and intellectual capacity
Birth Hx
Family Hx
Systemic disease: IBD, asthma, CF
FTT
Short stature
ROS
Development
Recurrent infections
GI hx: vomiting, GER, stool: diarrhea, pattern, frequency, consistency, NBNM
Resp hx: chronic cough, SOB, snoring
12. Physical Exam www.cdc.gov/growthcharts
Dymorphic features
OP: clefts, suck, caries
Chest, Abd, Neuro
Skin: loose skin = muscle wastage
Edema = protein deficiency
Observe interaction between parent and child
13. Back to your patient You have completed your H+P and are formulating an assessment and plan… What are your next steps?
14. Labs Minimal, if any, labs if a proper H+P is done!
Screening tests
CBC, ESR, CMP, UA and Urine Cx
Stool: fat, cx
Sweat test
Other possible tests
Igs, TFTs, Fe/Lead
PPD, HIV
UOA, Karyotype
Bone Age CBC (anemia or malignancy)
ESR
CMP (metabolic disorders, renal disorders, liver disease, electrolyte abnormalities for refeeding)
UA and Urine Cx (UTI, RTA)
CBC (anemia or malignancy)
ESR
CMP (metabolic disorders, renal disorders, liver disease, electrolyte abnormalities for refeeding)
UA and Urine Cx (UTI, RTA)
15. Labs Not much use if a proper H+P is done!
Screening tests
CBC, ESR, CMP, UA and Urine Cx
CBC (anemia or malignancy)
ESR
CMP (metabolic disorders, renal disorders, liver disease, electrolyte abnormalities for refeeding)
UA and Urine Cx (UTI, RTA)
Stool: fat, cx
Sweat test
Other possible tests
Igs, TFTs, Fe/Lead
PPD, HIV
UOA, Karyotype
Bone Age
Familial short stature: bone age = chronological age
Endocrine/Nutritional abnormalities: bone age<chron age
16. DDx: it’s all about the calories Inadequate caloric intake (most common)
Inadequate caloric absorption/utilization
Increased caloric requirements (ie. excess metabolic demand)
Physiologic causes that are not FTT
Prematurity
Familial short stature
Constitutional growth delay
SGA
17. Inadequate Caloric intake Inappropriate volume or type of food
Incorrect formula preparation
Excess juice or water
Poor feeding technique
Oromotor dysfunction or cleft palate
Psychosocial
18. Inadequate caloric absorption/utilization Vomiting
GERD
Obstruction
Increased ICP, meds, illnesses – UTI, metabolic disorders (storage diseases, amino acid disorders)
IBD, CF, Celiac disease, Short gut
MPA, Lactose intolerance, Allergic colitis
Liver disease
Vitamin or mineral deficiencies
19. Increased caloric requirements (? met Demand) Cardiac disease
Chronic lung disease
Endocrine disorders – DM, DI, hyperthyroid, adrenal/pituitary disease
Anemia, Hgb SS, Thalassemia
Genetic/chromosomal abnormalities (Tri 21)
Any chronic disease
20. Treatment Catch up growth
10 days to 1 month 120 kcal/kg/day
1-2 months 115 kcal/kg/day
2-3 months 105 kcal/kg/day
3-6 months 95 kcal/kg/day
6 months to 5 yrs 90 kcal/kg/day
Vitamin and mineral supplementation
Fe and Zinc
Monitor for refeeding
21. When do you admit? Most cases of FTT can be managed outpatient
Admit
Severe FTT/Malnutrition
Moderate dehydration
Infection
Further diagnostic and laboratory evaluation
Lack of catch-up growth
Evaluation of parent-child feeding interaction
22. When do you discharge? Adequate, consistent weight gain demonstrated
Diagnostic tests and consultations complete
Proper follow-up arranged
The caretaker demonstrates understanding of nutrition recommendations and growth expectations
23. Prognosis FTT in 1st year of life (regardless of cause) is particularly ominous
Maximal brain growth occurs in first 6 months of life
1/3 children with psychosocial FTT are developmentally delayed and have social and emotional problems
24. *prematurity, SGA, TORCH, etc.*prematurity, SGA, TORCH, etc.
27. PREP Question #1 You are evaluating a 6 month old child who has a VSD and is scheduled for cardiac surgery. The child’s weight is 6 kg (3rd%), length is 30th%, and HC is 50th%. His mother states she prepares the formula by adding 1 scoop of powder to 2 oz water. She estimates that he drinks 24 oz of formula per day. You estimate the baby’s intake is approx 500 kcal per day of cow milk formula, which is the RDA for his age. According to his mother, he spits up three times per day and passes two soft stools daily. On physical exam, you hear a 3/6 holosystolic murmur and palpate the liver 1 cm below the RCM.
28. PREP Question #1 cont… Of the following, the BEST explanation for the child’s malnutrition is:
A. Caloric requirement exceeding RDA
B. Cow milk protein intolerance
C. Incorrect preparation
D. Pathologic gastro-esophageal reflux
E. Undiagnosed pancreatic insufficiency
29. PREP Question #1 cont… Of the following, the BEST explanation for the child’s malnutrition is:
A. Caloric requirement exceeding RDA
B. Cow milk protein intolerance
C. Incorrect preparation
D. Pathologic gastro-esophageal reflux
E. Undiagnosed pancreatic insufficiency
30. PREP Question #1 ANSWER A. Caloric requirement exceeding RDA
The child in this scenario has a large VSD – a chronic illness which increases his metabolic demand and therefore caloric requirements (RDA).
31. PREP Question #2 During the health supervision visit of a 2-week-old infant, you note that his weight remains below his birthweight. The baby was delivered by a midwife in the parents’ home. There were no complications, and the parents have declined all perinatal testing. His mother says he breastfeeds well, and her milk supply is good compared with that for her previous two children. Recently, though, the infant has been vomiting after feedings. On physical examination, he has total body jaundice, and his liver is enlarged to palpation. He is alert.
32. Prep question #2 cont… Of the following, the test that is MOST likely to aid in diagnosis is:
A. Abdominal ultrasound
B. Serum transaminases measurement
C. Total/direct bilirubin
D. Urine organic acid measurement
E. Urine reducing substance measurement
33. Prep question #2 cont… Of the following, the test that is MOST likely to aid in diagnosis is:
A. Abdominal ultrasound
B. Serum transaminases measurement
C. Total/direct bilirubin
D. Urine organic acid measurement
E. Urine reducing substance measurement
34. Prep question #2 answer E. Urine reducing substance measurement
The child in this scenario has findings suggestive of classic galactosemia: within days of initiation of milk feedings, the infant has vomiting, then develops hepatomegaly, and FTT. Galactosemia results in the inability to oxidize galactose and the accumulation of galactose in organs such as the liver, kidneys, brain, and eyes. Galactose is a urine reducing substance.
35. SUMMARY/Pearls DDx for FTT – think calories!
? Caloric intake (most common)
? Caloric absorption/utilization
? Caloric requirements (? metabolic demand)
A systematic approach to H+P often leads to diagnosis
Detailed feeding hx is especially key
Labs should be minimal and guided by H+P
Children with FTT need solid follow-up to follow weight and developmental progression
36. References 2009 PREP Self-Assessment.
http://emedicine.medscape.com/article/985007-media
Kliegman: Nelson Textbook of Pediatrics, 18th ed. Chapter 37 – Failure to Thrive. 2007.
Olsson, JM. Failure to Thrive. Pediatric Hospital Medicine. 2nd edition. 2008: 97-100.
Stewart, CS. Failure To Thrive. The 5 Minute Pediatric Consult. 5th edition. Ed Schwartz, MW. 2008: 318-319.
37. Thank you! ? “You know you’re a pediatric hospitalist when…
...you've got the art of inpatient FTT down to an amazing, precise science: Give it milk. Watch it grow.”
From the AAP Hospitalist Medicine Listserve
Gregory Plemmons, MD