7-Failure To Thrive
7-Failure To Thrive
7-Failure To Thrive
Learning Objectives
■ By the end of this lecture, the student should be able to:
– Define FTT
– Describe the normal growth pattern in full term & pre-term infants
– Plot growth parameters on growth charts
– List the important points in the history (risk factors)
– List the important physical signs on examination.
– Know the classification of FTT
– Know non-organic FTT
– List the causes of organic FTT
– List the differential diagnosis
– List the lab tests.
– List the imaging studies
– Describe the dietary managements
– Describe the monitoring indices.
Introduction
■ Growth is determined by plotting serial measurements of
weight, length or height, and head circumference, using the
WHO growth charts for boys or girls.
■ Failure to thrive (TOT) or Weight faltering is suboptimal
weight gain in infants or young children.
■ If prolonged and severe, it will result in reduction in height or
length (stunting) and reduction in head growth and may be
associated with delayed development.
Introduction
■ Healthy children's weight will fluctuate, but it will usually progress within
one centile space.
■ size at birth is determined not only by genes but also by the intrauterine
environment.
■ Over the first few weeks, infants who are large at birth will often cross
down centiles (catch-down growth), whereas small babies will move up
centiles (catch-up growth) to find their genetic centile growth lines.
■ Infants who become acutely ill will often lose weight, but will regain their
weight centile within 2 to 3 weeks.
Identifying weight faltering
■ Weight faltering describes a sustained drop down two centile
spaces.
■ A single observation of weight is difficult to interpret unless
markedly discrepant from the head circumference or length.
■ All babies should be weighed during the 1st week, and then at
around 8, 12, and 16 weeks, then at 1 year, and whenever
concerns are raised.
■ the further the weight is below the second centile, the more
likely the child is ‘weight faltering’.
Identifying weight faltering
■ Any child whose weight crosses two centile lines or is below the 0.4th
centile or has a body mass index (BMI) less than the second centile
should be evaluated.
■ The infant with growth faltering needs to be differentiated from a normal
but small or thin baby.
■ If the child was born preterm, this should be allowed for when plotting
growth during the first 1–2 years of age, depending on the degree of
prematurity.
■ Some infants with severe intrauterine growth restriction remain small,
though most exhibit catch-up growth.
failure to thrive constitutionally small infant
Causes
■ In most, the cause is inadequate intake of food, but the reason for this is often
multifactorial.
■ the causes have been divided into:
■ ‘organic’ causes: found in 5% to 10%, and there are almost always
symptoms and signs pointing to the underlying disease.
■ ‘nonorganic’ causes: Although weight faltering is often considered to be
a manifestation of poverty (and is certainly true in poorer societies),
studies in the UK have not found an association with low socioeconomic
status or poor educational attainment.
■ Neglect and child abuse must always be considered, it account for 5% of
cases.
Clinical features and investigation
■ In some children with growth faltering, a full blood count and serum
ferritin may be helpful to identify iron-deficiency anaemia. This is usually
secondary to inadequate iron intake and correcting it may improve
appetite.
■ In most instances, no investigations are required.
■ Further information about the child and family from the health visitor,
general practitioner or other professionals involved with the family can be
particularly helpful.
Investigations to be considered in weight faltering in a child with worrying signs or symptoms of
disease
Investigation Interpreting result
Full blood count and differential white cell count Anaemia, neutropenia, lymphopenia (immune deficiency)
Serum creatinine, urea, electrolytes, acid–base Renal failure, renal tubular acidosis, metabolic disorders, William syndrome
protein)
Ferritin Iron-deficiency anaemia
Urine microscopy, culture, and dipsticks Urinary tract infection, renal disease
Stool microscopy, culture, and elastase Intestinal infection, parasites, elastase decreased in pancreatic insufficiency
■ health visitors can assess and support families to improve feeding and
increase calorie intake.
Behavioural
■ Offer meals at regular times with other family members
■ Praise when food is eaten, ignore when not
■ Limit mealtime to 30 minutes
■ Eat at same time as child
■ Avoid mealtime conflict
■ Never force feed
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