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Seminar on:
Failure to thrive
GROUP – 5
BDU, CMHS
C-1
01/01/ 2008 E.C
05/01/2008 E.C 1
Contents
Definition
Overview of Normal growth patterns
Epidemiology
Classification of FTT
Risk factors
Etiologies
Approach a child with FTT
Clinical manifestations
Assessment of FTT
Work UP
Severe Acute Malnutrition
05/01/2008 E.C 2
Definition
05/01/2008 E.C 3
Definition
Failure to thrive (FTT) is a descriptive term
applied when a young child’s physical growth
is less than that of his or her peers
failure to attain the potentials expected for a
child of that specific age and sex
Sign of unexplained Wt lose or poor Wt gain
linear growth and head circumference also
may be affected
05/01/2008 E.C 4
Cont’d...
common terms to describe FTT;
Failure to gain weight
Failure to grow
Growth deficiency
Growth faltering
Undernutrition
05/01/2008 E.C 5
Cont’d...
Greatest Growth velocity of A Child
occurs at ;
First 2 years of life &
Earliest teens
It is at these times that the children most
probably fail to thrive.
05/01/2008 E.C 6
Cont’d...
The term FTT is not a disease
The best definition for FTT is the one that refers
to it as inadequate physical growth diagnosed
by observation of growth over time using a
standard growth chart
05/01/2008 E.C 7
The most common definition is weight less than
the 3rd or 5th 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)
(MEDscape)
05/01/2008 E.C 8
Overview of Normal Growth patterns
Introduction
Normal growth is the progression of
changes in height, weight, and head
circumference that are compatible with
established standards for a given population
The progression of growth is
interpreted within the context of the
genetic potential for a particular child.
05/01/2008 E.C 9
Term infants: Lose 5-10% of birth Wt, regain by
10-14 days
Infant Wt gain pattern:
1kg/mo for the first 3 months
0.5kg/mo from age 3-6 months
0.33kg/mo from age 6-9 months
0.25kg/mo from age 9-12 months
Double the birth Wt by 4-6 mo
Triple the birth Wt by 1yr of age
05/01/2008 E.C 10
Cont....d
Normal growth is a reflection of overall health
and nutritional status.
Understanding the normal patterns of growth
enables
Early detection of pathologic deviations (eg, poor
weight gain due to a metabolic disorder, short
stature due to inflammatory bowel disease) and
Prevent the unnecessary evaluation of children
with acceptable normal variations in growth
05/01/2008 E.C 11
Growth velocity
The change in growth over time,
A more sensitive index of growth than is a
single measurement.
Current growth points should be compared to
previous growth points, if possible, to determine
the interval growth velocity
05/01/2008 E.C 12
Height velocity
Average normal length or height velocities are
as follows
0 to 6 months –--- (2.5 cm) per month
7 to 12 months – (1.25 cm) per month
12 to 24 months – (10 cm) per year
24 to 36 months – (8 cm) per year
36 to 48 months – (7 cm) per year
4 to 10 years ------- (5 to 6 cm) per year
05/01/2008 E.C 13
Head Growth
05/01/2008 E.C 14
Head circumference:
Average at birth is 35cm
47cm by 1yr of age, rate then slows
Average of 55cm by 6 yrs of age
 Brain weight doubles by four to 6 months of age and
triples by one year of age
 The majority of head growth is complete by 4 years of
age
Cont’d...
 Corrections for gestational age should be made for
premature infant
– for weight through 24 months of age,
– for stature through 40 months of age, and
– for head circumference through 18 months of age
 Special growth charts exist for some genetic disorders,
such as Down syndrome
05/01/2008 E.C 15
Exception to the definition
Children with genetically short stature, SGA
infants, and preterm infants
preterm infants: plot using corrected age
until 2yrs of age if birth Wt > 1000gm
until 3yrs of age if birth Wt < 1000gm
Catch-up growth for premature infants:
18mo for HC
24mo for Wt
40mo for Ht
05/01/2008 E.C 16
Epidemiology
05/01/2008 E.C 17
EPIDEMIOLOGY
True incidence of FTT is not known
In developed nations
5–10% of young children
3–5% of children admitted into teaching hospitals
Prevalence higher in developing countries , why?
Poverty
malnutrition
HIV infection
05/01/2008 E.C 18
Cont’d...
Under-feeding is the single commonest cause
of FTT
95% of cases of FTT inadequate food
peak incidence of FTT the age of 9–24 mo
No significant gender difference
Majority of children ≤18 months old
Uncommon after the age of 5 years
05/01/2008 E.C 19
Risk Factors
05/01/2008 E.C 20
Medical risk factors for FTT include;
prematurity
Intrauterine growth restriction(IUGR)
Developmental delay
Congenital anomalies (e.g., cleft lip and/or palate),
Intrauterine exposures (e.g., alcohol, anticonvulsants,
infection, lead poisoning, anemia) and
Any medical condition that results in inadequate
intake, increased metabolic rate, maldigestion, or
malabsorption
05/01/2008 E.C 21
Psychosocial risk factors for FTT include:
Poverty
Certain health and nutrition beliefs (e.g., fear of obesity
or cardiovascular disease, prolonged exclusive breastfeeding),
Social isolation
Life stresses
Poor parenting skills
Disordered feeding techniques
Drug or substance abuse
Other psychopathology
violence, and abuse
05/01/2008 E.C 22
Classification
05/01/2008 E.C 23
Classification
Traditionally, classified as
1.Organic FTT
2○ to underlining medical illnesses
Account for less than 20% of cases
2.Nonorganic FTT (NOFT)
Psychosocial FTT
No known medical condition that causes poor
growth
Inadequate food or undernutrition
Accounts for over 70% of cases
05/01/2008 E.C 24
3 . Mixed FTT
Organic and non organic causes coexist.
Those with organic disorders may also suffer
from environmental deprivation
Likewise, those with severe undernutrition
From non-organic FTT can develop organic
medical problems
05/01/2008 E.C 25
Cont’d...
Based on pathophysiology, FTT may be classified
into those due to:
1. inadequate caloric intake
2. inadequate absorption
3. increased caloric requirement, and
4. defective utilization of calories
This classification leads to a logical organization of many
conditions that cause or contribute to FTT; which is the
preferred classification,
05/01/2008 E.C 26
Etiologies of FTT
05/01/2008 E.C 27
Etiologies
Etiologies of FTT by pathophysiology
1. Inadequate caloric intake
Inappropriate feeding technique
Inappropriate nutrient intake :
excess fruit juice consumption
inappropriate preparation of formula
inadequate quantity of food,
inappropriate food for age,
neglect
Inappropriate parental knowledge
05/01/2008 E.C 28
Disturbed caregiver/child relationship
Economic deprivation
Insufficient lactation in mother
Mechanical problems (cleft palate, nasal
obstruction, adenoidal hypertrophy, dental
lesions)
Sucking or swallowing dysfunction (CNS,
neuromuscular)
05/01/2008 E.C 29
2. Inadequate Absorption or Increased Losses
Malabsorption
lactose intolerance
cystic fibrosis
cardiac disease
malrotation
inflammatory bowel disease(IBD)
milk allergy
parasites
celiac disease
05/01/2008 E.C 30
Biliary atresia
Cirrhosis
Vomiting
Infectious gastroenteritis
Increased intracranial pressure
Intestinal tract obstruction (pyloric stenosis,
hernia, malrotation, intussusception)
Infectious diarrhoea
Necrotizing enterocolitis or short bowel
syndrome
05/01/2008 E.C 31
3. Increased Caloric Requirement
Hyperthyroidism
Malignancy
Chronic inflammatory bowel disease
Chronic systemic disease (juvenile idiopathic
arthritis)
systemic infection
Urinary tract infection
Tuberculosis
Toxoplasmosis
05/01/2008 E.C 32
Chronic metabolic problems
Hypercalcemia
Storage diseases
Inborn errors of metabolism
galactosemia
diabetes mellitus
adrenal insufficiency
Chronic respiratory insufficiency
bronchopulmonary dysplasia
cystic fibrosis
Congenital or acquired heart disease
05/01/2008 E.C 33
CARDIAC
Cyanotic heart
lesions
Congestive heart
failure
Vascular rings
PULMONARY/RESPIRATORY
Severe asthma
Cystic fibrosis
Cronchiectasis
Chronic respiratory failure
Bronchopulmonary dysplasia
Adenoid/ tonsillar hypertrophy
Obstructive sleep apnea
05/01/2008 E.C 34
Organic Causes Of FTT
GASTROINTESTINAL
Pyloric stenosis
Gastroesophageal reflux
Malrotation
Malabsorption syndromes
Celiac disease
Food allergy
Milk intolerance: lactose,
protein
Pancreatic insufficiency
syndromes (cystic fibrosis)
Chronic cholestasis
Inflammatory bowel
disease
Chronic congenital
diarrhea states
Short bowel syndrome
05/01/2008 E.C 35
…
NEUROLOGIC
Cerebral palsy
Hypothalamic and other CNS tumors
Neuromuscular disorders
Neurodegenerative disorders
RENAL
Urinary tract infection
Renal tubular acidosis
Renal failure
05/01/2008 E.C 36
…
ENDOCRINE
Diabetes mellitus
Diabetes insipidus
Hypothyroidism/hyperthyroidism
Growth hormone deficiency
Adrenal insufficiency
05/01/2008 E.C 37
GENETIC/METABOLIC/CONGENITAL
Sickle cell disease
Inborn errors of metabolism (organic acidosis,
hyper- ammonemia, storage disease)
Fetal alcohol syndrome
Skeletal dysplasia
Chromosomal disorders
Multiple congenital anomaly syndromes (VATER,
CHARGE)
05/01/2008 E.C 38
MISCELLANEOUS
Collagen-vascular
disease
Malignancy
Primary
immunodeficiency
Transplantation
INFECTIONS
Perinatal infection
(TORCH)
Occult/chronic
infections
Parasitic infestation
Tuberculosis
HIV
05/01/2008 E.C 39
Non-organic FTT (Psychosocial/Behavioral)
Commonest Cause
Inadequate diet because of poverty/food
insufficiency
Errors in food preparation
Child/parent interaction problem
Poor parenting skill (lack of knowledge of
sufficient diet/feeding techniques)
Food refusal
Parental mental health/cognitive problems
05/01/2008 E.C 40
….
Child abuse/neglect
Family dysfunction: marital stress, mental
illness, substance abuse, …
Infant co-morbidities
Unintentional
Emotional deprivation
05/01/2008 E.C 41
05/01/2008 E.C 42
05/01/2008 E.C 43
APPROACH TO A CHILD WITH
FAILURE TO THRIVE
1. History Taking
Prenatal History
Smocking
Alcohol consuming
Use of medication
Any illness during pregnancy
History
Postnatal History
Neonatal asphyxia/Apgar scores
Prematurity
Small for gestational age
Birth weight and length
Congenital malformations or infections
Maternal bonding at birth
Length of hospitalization
Feeding difficulties during neonatal period
History
Feeding history
Details breast and formula feeding
Typical feeding schedule, plus food preparation
(formula prep, portion size)
Methods of feeding, length of time spent feeding,
and diet supplementation/medication
Description of type of solid foods taken
(quantitative composition and frequency of meals
and snacks)
Prospective 3-day food diary
History
A direct observation- issues of sucking ability,
choking, regurgitation, vomiting, and diarrhea,
mother’s affect and attitude.
Change in formula, change from breast milk to
formula, and changes in the primary individuals
responsible for feeding the child
Parents’ attitude about feeding (restrictions of
food based on finances, religion
History
History
History
Family History
stature and growth patterns
Medical problems
Genetic diseases
Developmental delays
History
Age and occupation of parents
Who feeds the child?
Life stressors (loss of job, divorce, death in
family)
Availability of social and economic support
Perception of growth failure as a problem
History of violence or abuse of care-giver
Psychosocial History
Family composition
Any major events in the child’s life
Family stressors
Chronic Illness,
Martial stress
Single parenthood
Depression
Domestic violence
Substance abuse,
Employment / financial obligations
History
Growth and eating pattern of other siblings
Young parental age
Affluent circumstances or parents engaged in career
development
Child rearing beliefs
History
Poverty,
Certain health and nutrition beliefs (eg, fear of
obesity or cardiovascular disease, prolonged
exclusive breastfeeding),
Social isolation, life stresses,
Poor parenting skills,
Disordered feeding techniques,
Substance abuse or other psychopathology,
violence, and abuse
2. Physical Examination
The four main goals of physical examination
include
1. Identification of dysmorphic features
suggestive of a genetic disorder that affects
growth
2. Detection of an underlying disease that may
impair growth
3. Assessment for signs of possible child abuse
4. Assessment of the severity and possible effects
of malnutrition
Physical examination
General appearance
Cachexia, temporal wasting, sparse hair or
alopecia  malnutrition
Dysmorphic features
Small palpebral fissures
Midface hypoplasia
Flat philtrum
Thin vermilion border of fetal alchohol syndrome)
Physical examination
Vital signs
Temperature  hypothermia
PR  tachycardia
RR  tachypenic
BP  hypotension
Anthropometry derangements
Physical examination
HEENT
Microcephaly
Delayed closure of fontanelle
Cataracts
Papilledema
Oropharyngeal lesions (eg, caries, tongue
enlargement, mandibular hypoplasia, tonsillar
hypertrophy, defects in soft or hard palate)
Delayed tooth eruption
Thyroid enlargement Thyroid disease
Physical examination
Chest
Wheezing
Crackles
Prolonged expiratory phase
Hyperexpansion
Abdomen
Abdominal distension
hyperactive bowel sounds
Hepatosplenomegaly
Physical examination
Genitourinary
Genitourinary abnormality
Rectal fistulae
Musculoskeletal
Bony deformities
Craniotabes
Beading of the ribs
Scoliosis
Bowing of the legs or distal radius and ulna
Enlargement of the wrist
Edema
Physical examination
Skin and Mucous Membranes
Pallor
Clubbing
Scaling skin
Spoon-shaped nails
Iron deficiency
Cheilosis
Vitamin deficiency
Chronic diaper rash
Physical examination
Neurologic
Abnormal deep tendon reflexes
Hypotonia
Weakness
Spasticity
Neuropathy
Red Flag Signs and Symptoms Suggesting
Medical Causes of Failure to Thrive
• Cardiac findings suggesting congenital heart disease
or heart failure (e.g., murmur, edema, jugular venous
distention)
• Developmental delay
• Dysmorphic features
• Failure to gain weight despite adequate caloric intake
• Organomegaly or lymphadenopathy
• Recurrent or severe respiratory, mucocutaneous, or urinary
• Infection
• Recurrent vomiting, diarrhea, or dehydration
05/01/2008 E.C 64
Clinical Features
Most common clinical presentation is poor
growth
Accompanied by physical signs;
Alopecia
Reduced subcutaneous fat or muscles
Dermatitis
Syndromes of marasmus or kwashiorkor
Failure to meet expected age norms for ht and
wt
Recurrent infections
Depending on the severity infants with FTT
may exhibit
Thin extremities
Narrow face
Prominent ribs and wasted buttocks
Cont’d…
Neglect of hygiene
Diaper rash
Unwashed skin
Uncut and dirty finger nails or
unwashed clothing
Delays in social and speech development
Expressionless face and hypotonic
05/01/2008 E.C 69
Assessment of FTT
Anthropometric criteria:
1. A child younger than 2 years of age whose weight is
less than the 3rd or 5th percentile for age on > 1
occasion
2. A child younger than 2 years of age with weight is
less than 80% of the ideal weight for age
3. A child younger than 2 years whose weight for age
percentile crosses two major percentiles lines on a
standard weight curves below a previously
established growth rate
,,,,
05/01/2008 E.C 71
05/01/2008 E.C 72
Growth Charts
• Standard growth charts are commonly used to
define how the growth of a child compares to
normal.
• Growth charts are constructed using a group of
normal children living:
–In a given area at a given time.
05/01/2008 E.C 73
Recommended growth charts
WHO growth charts :
For both boys and girls
• Weight-for-age
• Length-for-age
• Head circumference-for-age, and
• Weight-for-length
CDC/NCHS growth charts :
For both boys and girls
• Weight-for-age
• Length-for-age
• Head circumference-for-age, and
• Weight-for-length
05/01/2008 E.C 74
05/01/2008 E.C 75
Work Up
05/01/2008 E.C 76
LABORATORY EVALUATION
Laboratory evaluation for organic disease should be
guided by the signs and symptoms found in the initial
evaluation.
A careful history and physical examination in the child
with failure to thrive (FTT) may suggest clues to an
organic disease
Laboratory studies that are not suggested on the basis
of the initial history and examination rarely are helpful.
One study revealed that only 1.4 % of the laboratory
studies performed in evaluating children with FTT were
useful diagnostically
05/01/2008 E.C 77
Simple routine tests includes:
Random Blood Sugar(RBS)
complete blood count(CBC)
Urinalysis(U/A)
electrolyte levels
stool exam
PIHCT
TB
05/01/2008 E.C 78
Severe Acute Malnutrition
05/01/2008 E.C 79
Child with visible severe wastingChild with edematous malnutrition
 Severe acute malnutrition is defined by a very low weight for height
(below -3z scores of the median WHO growth standards), by
visible severe wasting, or by the presence of nutritional oedema
one of the most common causes of morbidity and mortality
among children under the age of 5 years WW
– Dx is made based on:
1. In infants < 6 months
 WFH < 70%(Severe wasting) of NCHS median, OR
 Bilateral pitting oedema of nutritional origin, OR
 Visible Severe Wasting if it is difficult to determine W/L
2. children 6 months up to 5 years
 WFH < 70%(Severe wasting) of NCHS median, OR
 Bilateral pitting oedema of nutritional origin, OR
 MUAC <11cm (for infants above 6months or >65cm length)
05/01/2008 E.C 80
Investigation:
RBS-------Hypoglcemia
CBC--------Hct, Hb
U/A-------- UTI
Serum electrolytes---
↑Na+, ↓K+
stool exam---
parasites
chest X-ray-
Blood culture
sepsis
HIV test
05/01/2008 E.C 81
Pneumonia ,TB
05/01/2008 E.C 82

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Failure To Thrive

  • 1. Seminar on: Failure to thrive GROUP – 5 BDU, CMHS C-1 01/01/ 2008 E.C 05/01/2008 E.C 1
  • 2. Contents Definition Overview of Normal growth patterns Epidemiology Classification of FTT Risk factors Etiologies Approach a child with FTT Clinical manifestations Assessment of FTT Work UP Severe Acute Malnutrition 05/01/2008 E.C 2
  • 4. Definition Failure to thrive (FTT) is a descriptive term applied when a young child’s physical growth is less than that of his or her peers failure to attain the potentials expected for a child of that specific age and sex Sign of unexplained Wt lose or poor Wt gain linear growth and head circumference also may be affected 05/01/2008 E.C 4
  • 5. Cont’d... common terms to describe FTT; Failure to gain weight Failure to grow Growth deficiency Growth faltering Undernutrition 05/01/2008 E.C 5
  • 6. Cont’d... Greatest Growth velocity of A Child occurs at ; First 2 years of life & Earliest teens It is at these times that the children most probably fail to thrive. 05/01/2008 E.C 6
  • 7. Cont’d... The term FTT is not a disease The best definition for FTT is the one that refers to it as inadequate physical growth diagnosed by observation of growth over time using a standard growth chart 05/01/2008 E.C 7
  • 8. The most common definition is weight less than the 3rd or 5th 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) (MEDscape) 05/01/2008 E.C 8
  • 9. Overview of Normal Growth patterns Introduction Normal growth is the progression of changes in height, weight, and head circumference that are compatible with established standards for a given population The progression of growth is interpreted within the context of the genetic potential for a particular child. 05/01/2008 E.C 9
  • 10. Term infants: Lose 5-10% of birth Wt, regain by 10-14 days Infant Wt gain pattern: 1kg/mo for the first 3 months 0.5kg/mo from age 3-6 months 0.33kg/mo from age 6-9 months 0.25kg/mo from age 9-12 months Double the birth Wt by 4-6 mo Triple the birth Wt by 1yr of age 05/01/2008 E.C 10
  • 11. Cont....d Normal growth is a reflection of overall health and nutritional status. Understanding the normal patterns of growth enables Early detection of pathologic deviations (eg, poor weight gain due to a metabolic disorder, short stature due to inflammatory bowel disease) and Prevent the unnecessary evaluation of children with acceptable normal variations in growth 05/01/2008 E.C 11
  • 12. Growth velocity The change in growth over time, A more sensitive index of growth than is a single measurement. Current growth points should be compared to previous growth points, if possible, to determine the interval growth velocity 05/01/2008 E.C 12
  • 13. Height velocity Average normal length or height velocities are as follows 0 to 6 months –--- (2.5 cm) per month 7 to 12 months – (1.25 cm) per month 12 to 24 months – (10 cm) per year 24 to 36 months – (8 cm) per year 36 to 48 months – (7 cm) per year 4 to 10 years ------- (5 to 6 cm) per year 05/01/2008 E.C 13
  • 14. Head Growth 05/01/2008 E.C 14 Head circumference: Average at birth is 35cm 47cm by 1yr of age, rate then slows Average of 55cm by 6 yrs of age  Brain weight doubles by four to 6 months of age and triples by one year of age  The majority of head growth is complete by 4 years of age
  • 15. Cont’d...  Corrections for gestational age should be made for premature infant – for weight through 24 months of age, – for stature through 40 months of age, and – for head circumference through 18 months of age  Special growth charts exist for some genetic disorders, such as Down syndrome 05/01/2008 E.C 15
  • 16. Exception to the definition Children with genetically short stature, SGA infants, and preterm infants preterm infants: plot using corrected age until 2yrs of age if birth Wt > 1000gm until 3yrs of age if birth Wt < 1000gm Catch-up growth for premature infants: 18mo for HC 24mo for Wt 40mo for Ht 05/01/2008 E.C 16
  • 18. EPIDEMIOLOGY True incidence of FTT is not known In developed nations 5–10% of young children 3–5% of children admitted into teaching hospitals Prevalence higher in developing countries , why? Poverty malnutrition HIV infection 05/01/2008 E.C 18
  • 19. Cont’d... Under-feeding is the single commonest cause of FTT 95% of cases of FTT inadequate food peak incidence of FTT the age of 9–24 mo No significant gender difference Majority of children ≤18 months old Uncommon after the age of 5 years 05/01/2008 E.C 19
  • 21. Medical risk factors for FTT include; prematurity Intrauterine growth restriction(IUGR) Developmental delay Congenital anomalies (e.g., cleft lip and/or palate), Intrauterine exposures (e.g., alcohol, anticonvulsants, infection, lead poisoning, anemia) and Any medical condition that results in inadequate intake, increased metabolic rate, maldigestion, or malabsorption 05/01/2008 E.C 21
  • 22. Psychosocial risk factors for FTT include: Poverty Certain health and nutrition beliefs (e.g., fear of obesity or cardiovascular disease, prolonged exclusive breastfeeding), Social isolation Life stresses Poor parenting skills Disordered feeding techniques Drug or substance abuse Other psychopathology violence, and abuse 05/01/2008 E.C 22
  • 24. Classification Traditionally, classified as 1.Organic FTT 2○ to underlining medical illnesses Account for less than 20% of cases 2.Nonorganic FTT (NOFT) Psychosocial FTT No known medical condition that causes poor growth Inadequate food or undernutrition Accounts for over 70% of cases 05/01/2008 E.C 24
  • 25. 3 . Mixed FTT Organic and non organic causes coexist. Those with organic disorders may also suffer from environmental deprivation Likewise, those with severe undernutrition From non-organic FTT can develop organic medical problems 05/01/2008 E.C 25
  • 26. Cont’d... Based on pathophysiology, FTT may be classified into those due to: 1. inadequate caloric intake 2. inadequate absorption 3. increased caloric requirement, and 4. defective utilization of calories This classification leads to a logical organization of many conditions that cause or contribute to FTT; which is the preferred classification, 05/01/2008 E.C 26
  • 28. Etiologies Etiologies of FTT by pathophysiology 1. Inadequate caloric intake Inappropriate feeding technique Inappropriate nutrient intake : excess fruit juice consumption inappropriate preparation of formula inadequate quantity of food, inappropriate food for age, neglect Inappropriate parental knowledge 05/01/2008 E.C 28
  • 29. Disturbed caregiver/child relationship Economic deprivation Insufficient lactation in mother Mechanical problems (cleft palate, nasal obstruction, adenoidal hypertrophy, dental lesions) Sucking or swallowing dysfunction (CNS, neuromuscular) 05/01/2008 E.C 29
  • 30. 2. Inadequate Absorption or Increased Losses Malabsorption lactose intolerance cystic fibrosis cardiac disease malrotation inflammatory bowel disease(IBD) milk allergy parasites celiac disease 05/01/2008 E.C 30
  • 31. Biliary atresia Cirrhosis Vomiting Infectious gastroenteritis Increased intracranial pressure Intestinal tract obstruction (pyloric stenosis, hernia, malrotation, intussusception) Infectious diarrhoea Necrotizing enterocolitis or short bowel syndrome 05/01/2008 E.C 31
  • 32. 3. Increased Caloric Requirement Hyperthyroidism Malignancy Chronic inflammatory bowel disease Chronic systemic disease (juvenile idiopathic arthritis) systemic infection Urinary tract infection Tuberculosis Toxoplasmosis 05/01/2008 E.C 32
  • 33. Chronic metabolic problems Hypercalcemia Storage diseases Inborn errors of metabolism galactosemia diabetes mellitus adrenal insufficiency Chronic respiratory insufficiency bronchopulmonary dysplasia cystic fibrosis Congenital or acquired heart disease 05/01/2008 E.C 33
  • 34. CARDIAC Cyanotic heart lesions Congestive heart failure Vascular rings PULMONARY/RESPIRATORY Severe asthma Cystic fibrosis Cronchiectasis Chronic respiratory failure Bronchopulmonary dysplasia Adenoid/ tonsillar hypertrophy Obstructive sleep apnea 05/01/2008 E.C 34 Organic Causes Of FTT
  • 35. GASTROINTESTINAL Pyloric stenosis Gastroesophageal reflux Malrotation Malabsorption syndromes Celiac disease Food allergy Milk intolerance: lactose, protein Pancreatic insufficiency syndromes (cystic fibrosis) Chronic cholestasis Inflammatory bowel disease Chronic congenital diarrhea states Short bowel syndrome 05/01/2008 E.C 35
  • 36. … NEUROLOGIC Cerebral palsy Hypothalamic and other CNS tumors Neuromuscular disorders Neurodegenerative disorders RENAL Urinary tract infection Renal tubular acidosis Renal failure 05/01/2008 E.C 36
  • 37. … ENDOCRINE Diabetes mellitus Diabetes insipidus Hypothyroidism/hyperthyroidism Growth hormone deficiency Adrenal insufficiency 05/01/2008 E.C 37
  • 38. GENETIC/METABOLIC/CONGENITAL Sickle cell disease Inborn errors of metabolism (organic acidosis, hyper- ammonemia, storage disease) Fetal alcohol syndrome Skeletal dysplasia Chromosomal disorders Multiple congenital anomaly syndromes (VATER, CHARGE) 05/01/2008 E.C 38
  • 40. Non-organic FTT (Psychosocial/Behavioral) Commonest Cause Inadequate diet because of poverty/food insufficiency Errors in food preparation Child/parent interaction problem Poor parenting skill (lack of knowledge of sufficient diet/feeding techniques) Food refusal Parental mental health/cognitive problems 05/01/2008 E.C 40
  • 41. …. Child abuse/neglect Family dysfunction: marital stress, mental illness, substance abuse, … Infant co-morbidities Unintentional Emotional deprivation 05/01/2008 E.C 41
  • 44. APPROACH TO A CHILD WITH FAILURE TO THRIVE
  • 45. 1. History Taking Prenatal History Smocking Alcohol consuming Use of medication Any illness during pregnancy
  • 46. History Postnatal History Neonatal asphyxia/Apgar scores Prematurity Small for gestational age Birth weight and length Congenital malformations or infections Maternal bonding at birth Length of hospitalization Feeding difficulties during neonatal period
  • 47. History Feeding history Details breast and formula feeding Typical feeding schedule, plus food preparation (formula prep, portion size) Methods of feeding, length of time spent feeding, and diet supplementation/medication Description of type of solid foods taken (quantitative composition and frequency of meals and snacks) Prospective 3-day food diary
  • 48. History A direct observation- issues of sucking ability, choking, regurgitation, vomiting, and diarrhea, mother’s affect and attitude. Change in formula, change from breast milk to formula, and changes in the primary individuals responsible for feeding the child Parents’ attitude about feeding (restrictions of food based on finances, religion
  • 51. History Family History stature and growth patterns Medical problems Genetic diseases Developmental delays
  • 52. History Age and occupation of parents Who feeds the child? Life stressors (loss of job, divorce, death in family) Availability of social and economic support Perception of growth failure as a problem History of violence or abuse of care-giver
  • 53. Psychosocial History Family composition Any major events in the child’s life Family stressors Chronic Illness, Martial stress Single parenthood Depression Domestic violence Substance abuse, Employment / financial obligations
  • 54. History Growth and eating pattern of other siblings Young parental age Affluent circumstances or parents engaged in career development Child rearing beliefs
  • 55. History Poverty, Certain health and nutrition beliefs (eg, fear of obesity or cardiovascular disease, prolonged exclusive breastfeeding), Social isolation, life stresses, Poor parenting skills, Disordered feeding techniques, Substance abuse or other psychopathology, violence, and abuse
  • 56. 2. Physical Examination The four main goals of physical examination include 1. Identification of dysmorphic features suggestive of a genetic disorder that affects growth 2. Detection of an underlying disease that may impair growth 3. Assessment for signs of possible child abuse 4. Assessment of the severity and possible effects of malnutrition
  • 57. Physical examination General appearance Cachexia, temporal wasting, sparse hair or alopecia  malnutrition Dysmorphic features Small palpebral fissures Midface hypoplasia Flat philtrum Thin vermilion border of fetal alchohol syndrome)
  • 58. Physical examination Vital signs Temperature  hypothermia PR  tachycardia RR  tachypenic BP  hypotension Anthropometry derangements
  • 59. Physical examination HEENT Microcephaly Delayed closure of fontanelle Cataracts Papilledema Oropharyngeal lesions (eg, caries, tongue enlargement, mandibular hypoplasia, tonsillar hypertrophy, defects in soft or hard palate) Delayed tooth eruption Thyroid enlargement Thyroid disease
  • 60. Physical examination Chest Wheezing Crackles Prolonged expiratory phase Hyperexpansion Abdomen Abdominal distension hyperactive bowel sounds Hepatosplenomegaly
  • 61. Physical examination Genitourinary Genitourinary abnormality Rectal fistulae Musculoskeletal Bony deformities Craniotabes Beading of the ribs Scoliosis Bowing of the legs or distal radius and ulna Enlargement of the wrist Edema
  • 62. Physical examination Skin and Mucous Membranes Pallor Clubbing Scaling skin Spoon-shaped nails Iron deficiency Cheilosis Vitamin deficiency Chronic diaper rash
  • 63. Physical examination Neurologic Abnormal deep tendon reflexes Hypotonia Weakness Spasticity Neuropathy
  • 64. Red Flag Signs and Symptoms Suggesting Medical Causes of Failure to Thrive • Cardiac findings suggesting congenital heart disease or heart failure (e.g., murmur, edema, jugular venous distention) • Developmental delay • Dysmorphic features • Failure to gain weight despite adequate caloric intake • Organomegaly or lymphadenopathy • Recurrent or severe respiratory, mucocutaneous, or urinary • Infection • Recurrent vomiting, diarrhea, or dehydration 05/01/2008 E.C 64
  • 66. Most common clinical presentation is poor growth Accompanied by physical signs; Alopecia Reduced subcutaneous fat or muscles Dermatitis Syndromes of marasmus or kwashiorkor
  • 67. Failure to meet expected age norms for ht and wt Recurrent infections Depending on the severity infants with FTT may exhibit Thin extremities Narrow face Prominent ribs and wasted buttocks
  • 68. Cont’d… Neglect of hygiene Diaper rash Unwashed skin Uncut and dirty finger nails or unwashed clothing Delays in social and speech development Expressionless face and hypotonic
  • 70. Anthropometric criteria: 1. A child younger than 2 years of age whose weight is less than the 3rd or 5th percentile for age on > 1 occasion 2. A child younger than 2 years of age with weight is less than 80% of the ideal weight for age 3. A child younger than 2 years whose weight for age percentile crosses two major percentiles lines on a standard weight curves below a previously established growth rate
  • 73. Growth Charts • Standard growth charts are commonly used to define how the growth of a child compares to normal. • Growth charts are constructed using a group of normal children living: –In a given area at a given time. 05/01/2008 E.C 73
  • 74. Recommended growth charts WHO growth charts : For both boys and girls • Weight-for-age • Length-for-age • Head circumference-for-age, and • Weight-for-length CDC/NCHS growth charts : For both boys and girls • Weight-for-age • Length-for-age • Head circumference-for-age, and • Weight-for-length 05/01/2008 E.C 74
  • 77. LABORATORY EVALUATION Laboratory evaluation for organic disease should be guided by the signs and symptoms found in the initial evaluation. A careful history and physical examination in the child with failure to thrive (FTT) may suggest clues to an organic disease Laboratory studies that are not suggested on the basis of the initial history and examination rarely are helpful. One study revealed that only 1.4 % of the laboratory studies performed in evaluating children with FTT were useful diagnostically 05/01/2008 E.C 77
  • 78. Simple routine tests includes: Random Blood Sugar(RBS) complete blood count(CBC) Urinalysis(U/A) electrolyte levels stool exam PIHCT TB 05/01/2008 E.C 78
  • 79. Severe Acute Malnutrition 05/01/2008 E.C 79 Child with visible severe wastingChild with edematous malnutrition  Severe acute malnutrition is defined by a very low weight for height (below -3z scores of the median WHO growth standards), by visible severe wasting, or by the presence of nutritional oedema one of the most common causes of morbidity and mortality among children under the age of 5 years WW
  • 80. – Dx is made based on: 1. In infants < 6 months  WFH < 70%(Severe wasting) of NCHS median, OR  Bilateral pitting oedema of nutritional origin, OR  Visible Severe Wasting if it is difficult to determine W/L 2. children 6 months up to 5 years  WFH < 70%(Severe wasting) of NCHS median, OR  Bilateral pitting oedema of nutritional origin, OR  MUAC <11cm (for infants above 6months or >65cm length) 05/01/2008 E.C 80
  • 81. Investigation: RBS-------Hypoglcemia CBC--------Hct, Hb U/A-------- UTI Serum electrolytes--- ↑Na+, ↓K+ stool exam--- parasites chest X-ray- Blood culture sepsis HIV test 05/01/2008 E.C 81 Pneumonia ,TB