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Infant Nutrition: Conditions

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Down's syndrome may be 108 kcal/kg. Correction for Gestational Age ... Di George Syndrome. Down Syndrome. Trisomy 21. Sucking problems due to hypotonicity ... – PowerPoint PPT presentation

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Title: Infant Nutrition: Conditions


1
Infant Nutrition Conditions Interventions
  • Chap 9 Brown

2
See Cloud Feeding Problems DVD
  • Follow Cloud Power point
  • Answer Cloud questions Midterm on Website

3
Infants At Risk
  • Most infants are born healthy and then grow and
    develop in a usual manner
  • Some have special needs
  • Infant mortality decreased 39 between 1980 and
    1995 in US. Health Care is now better at saving
    ill children than preventing chronic conditions
  • Advances in Neonatal intensive care
  • Preterm infants who died in the past are now
    being saved

4
Preterm Infants
  • Much more likely to have nutrition needs
  • Questions to ask in all cases
  • How is the baby growing?
  • Is the diet providing all of the necessary
    nutrients?
  • How is the infant being fed?

5
Energy and Nutrient Needs of Infants with Health
Conditions
  • Best determined by indirect calorimetry
  • Generally 120 cal/kg
  • Modifications to this based on condition
  • Eg. Downs syndrome may be 108 kcal/kg

6
Correction for Gestational Age
  • 40 weeks from last menstrual cycle is a term
    delivery
  • If born at 30 weeks, 10 weeks or approx. 2.5
    months early
  • 2.5 months subtracted from infants current
    chronological age and plotted on Infant Health
    and Development Program (IHDP) Growth Premature
    Growth Charts
  • http//www.cdc.gov/growthcharts/
  • http//www.who.int/childgrowth/en/

7
Severe Preterm Birth
  • Preterm 11.6 of all births
  • LBW 7.6 of all births, almost 300,000 in 1998.
    Most observed and go home in a week.
  • VLBW(under 1500 grams) 1.4 of all births, over
    55,000 in 1998.
  • Near 1500 grams, Usually 28-32 weeks gestation
    Nearly 90 survival immediate intensive care
    long term nutritional care
  • ELBW(Extremely Low) less than 1000g 23-28 weeks
    Often lifelong consequences.

8
How Sick Babies are Fed
  • VLBW and ELBW babies are at high risk for GI
    tract problems
  • Necrotizing enterocolitis damage to a section of
    the GI tract resulting in bleeding
  • Parenteral Nutrition required

9
Feeding Methods
  • If GI tract works, use it
  • Oral gastric feeding
  • Transpyloric feeding
  • Gastrostomy feeding
  • Jenunostomy feeding

10
What to Feed Preterm Infants?
  • Breast Milk Recommended, by the mother if
    possible with active feeding
  • If not possible, use banked breast milk
  • May require supplementation
  • If Breast milk not possible, pre-term formula is
    recommended.

11
Problems Feeding Preterm
  • Fatigue
  • Low tolerance to volume
  • Disorganized feeding

12
Case Study 9.1
  • Premature Birth in an At-risk Family

13
Infants With Genetic Disorders
  • Maple Syrup Urine Disease
  • Rare genetic condition of protein metabolism in
    which breakdown by-products build up in blood and
    urine, causing coma and death if untreated.
    Branched chain aas (leucine, isoleucine and
    valine) accumulate and their keto acid
    derivatives become toxic
  • http//www.msud-support.org

14
Maple Syrup Urine Disease
  • Diet needed within days of birth or brain damage
    or death will occur
  • Referred to Genetic Centers for additional
    screening and treatment.
  • Screening is done in some states at birth. Not
    Washington.
  • Washington Screens for PKU and congenital
    hypothyroidism but not the 30 other screenable
    disorders.

15
MSUD Symptoms
  • Infant with poor appetite
  • Irritable
  • Characteristic odor in urine burnt sugar
  • Within days of birth lost sucking reflex
  • Listless, high-pitched cry, rigid and limp
    episodes
  • With no treatment seizures, come and death

16
MSUD Inheritance
  • Recessive disorder
  • Parents are carriers of MSUD gene so dont show
    the disease
  • Each pass the gene on to their offspring

17
MSUD Treatment
  • Carefully controlled diet with synthetic formula
    with no leucine, isoleucine, valine
  • These aas are added to diet in carefully
    controlled amounts of food to provide for
    necessary growth and development

18
Genetic Problems
  • Galactosemia Inability to convert galactose to
    glucose. Galactose part of lactose Avoid
    lactose No breastfeeding Not screened for in
    Washington
  • DiGeorge Syndrome
  • Chromosome 22 has a small deletion resulting in
    wide range of speech, heart, and learning
    difficulties

19
DiGeorge Syndrome(22q11.2)
  • Genetic Problem with part of Chromosome 22
    missing. Symptoms may include
  • Heart defects in 74 of patients
  • Cleft palate or palate anomalies in 69 of
    patients
  • Results in 30 of patients having feeding
    problems
  • May require naso-gastric or gastrostomy

20
DiGeorge Syndrome
  • Hypocalcemia is common
  • Impaired immune function with poor thymus
    function and T cell production
  • Dx with facial features(hooded eyelids, long
    face) and then FISH (Fluorescence in situ
    hybridization) a chromosome test which shows a
    missing portion of the 22nd chromosome.

21
DiGeorge Syndrome
  • Nutritonal Tx Variable
  • Cleft palate may require tube feeding until
    repaired
  • Heart defects may affect energy level and tires
    infant significantly during feeding.

22
Case Study 9.2
  • Di George Syndrome

23
Down Syndrome
  • Trisomy 21
  • Sucking problems due to hypotonicity
  • Other contributing factors
  • Cardiac Problems
  • Fatigue
  • Delayed dentition
  • Show Cloud Module II G

24
Prader-Willi Syndrome
  • http//www.pwsausa.org/
  • Disorder of 15th chromosome 2 mother 15s and no
    father 15
  • Dx FISH (Fluorescence in situ hybridization, a
    chromosome test)
  • Hypotonia in neonate and infant
  • Feeding problems
  • Excessive wt gain between 1 and 6 years

25
Prader-Willi Syndrome
  • Distinctive facial features narrow face, almond
    shaped eyes, small-appearing mouth with thin
    upper lip, down-turned corners of mouth
  • Hypogonadism
  • Global developmental delay before age 6
  • Food foraging/obsession with food maybe due to
    hypothalmic dysfunction Urge to eat is
    physiological and overwhelming
  • High calorie intake coupled with low energy
    expenditure results in wt gain

26
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27
Prader-Willi Syndrome
  • Treatment
  • Early feeding problems failure to thrive may
    require tube feedings
  • Later food obsession lock kitchen cupboards
    increase activity
  • Behavior management with positive rewards
  • Meds psychotropic meds serotonin uptake
    inhibitors such as fluoretine and sertoline are
    used to treat obsession-compulsive eating
    behavior.
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