Professional Documents
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Anthropometry
Anthropometry
Dr/GihanFouad
MDpediatrics,IBCLC,TQM,
fellowship board Hospital Management
Head of infection control unit ,Quality
unit
Nutritional requirements and growth
department
National Nutrition Institute
Nutritional Assessment
Anthropometric Biochemical
Clinical Dietary
§ Growth is an important index of a child’s nutritional
status and should be monitored on a regular basis.
Accurate measurements of growth parameters plotted on
an appropriate growth curve is one of the simplest but
most powerful tools in our care of infants.
§ Anthropometry refers to comparative measurements of
the human body.
- The primary measures used as indices of growth and
development include stature (length or height), weight,
and head circumference (for young children).
- The secondary measures used to estimate body
composition include triceps skinfold thickness,
subscapular skinfold thickness, and mid-upper arm
circumference
I am a person not a dot
§ Factors that alter Energy needs
§ Body composition
§ Body size
§ Gender
§ Growth
§ Genetics
§ Ethnicity
§ Environment
§ Adaptation and accommodation
§ Activity/work
§ Illness/Medical conditions
Variability of Normal Infant growth
Growth channels
§ Some times after 6 or 9 months will have fallen to a lower one,
sometimes crossing more than two percentile lines. He or she
then stays on that particular growth percentile. This is perfectly
normal because early growth may represent intrauterine
growth factors. These can persist in early infancy, but the child
then finds his genetically determined channel of growth and
remains there
Growth spurt of infancy
§ . Many infants born at or below the tenth percentile for length
may not reach their genetically appropriate growth channel until
1 year of age.
§ pattern of
growth
• Triceps skinfold less than
5thpercentile.
§ Children in their early teenage look very thin, because the
corresponding weight and muscle mass gain of
adolescence is delayed by several months.
§ Anemia is also seen in early infancy growth spurt and with
catch up growth in premature low birth weight babies. Here
also it is due to rapid growth and is described as “bleeding
within circulation” -
Growth spurt of adolescence(Tanner staging of the adolescent)
§ In May 2000 the U.S. CDC released growth charts, which
are based on 5 nationally representative surveys
conducted between 1963 and 1994.
Walking alone
Standing alone
Motor milestone
Hands-&-knees crawling
3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21
Age in months
Primary Measures
Head Circumference
Head Circumference
§
Stunting VS Wasting
§ Tables of
adjustment have been developed based on the
research of Himes, Roche
Calculation of Mid-Parental Height
--- Person A
-----Person B
Weight Measurements
‘Ideal” Body Weight
1 to 6 years [ Age(yr) x 2 ] + 8
§ Frisancho RA. New norms of upper limb fat and muscle
areas for assessment of nutritional status. Am J Clin
Nutr, 1981; 34:2540-2545.
All neonates typically loss some weight after birth. Preterm's have more ECF
than term and thus tend to lose more weight(15%).term infant regained wt by
2nd or 3rd ws ,but small and sick neonate take longer time.
How to Distinguish ????????????????
§ Natural" slow gainer § slow-weight-gain
§ A baby that is a "natural" slow-gainer § does not gain at least one-half an
still gains weight steadily, albeit ounce (15 g) a day by the fourth or
slowly: fifth day after birth.
§ maintains a particular growth curve. § does not regain birth weight by two
to three weeks after birth.
§ increases in length and head
circumference increase according to § does not gain at least one pound
typical rates of growth.
(454 g) a month for the first four
§ wakes on his/her own and is alert months (from lowest weight after
and cues to breastfeed about eight to birth versus birth weight).
12 times in 24 hours.
§ exhibits a dramatic drop in rate of
§ produces wet and dirty diaper counts growth (weight, length, or head
similar to a faster-growing baby. circumference) from her/his
previous curve
Down syndrome
Williams syndrome (WS, also Williams-Beuren syndrome), now recognized
to be caused by a microdeletion of chromosome 7, is a multisystem disorder first identified as
a distinct clinical entity in 1961.1 It is present at birth and affects boys and girls equally
Williams syndrome
HeadCircumferance
Prader-willi syndrome