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Is my child too short

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Recurrent URI's including AOM x 3 (eventually leading to diagnosis of mild, ... FH: 4 y/o brother had Kawasaki's, now doing well. Uncle with asthma. ... – PowerPoint PPT presentation

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Title: Is my child too short


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Is my child too short?
  • Theresa A. Allison, M.D., M.Mus.
  • UCSF/CHN Family Practice Residency Program
  • Patient Care Conference

3
The CaseT.T.
  • ID/CC Vietnamese boy with devoted parents (born
    in June, 2003) first seen in my clinic at 14
    months of age for routine well-child care
  • PMH
  • Pulmonic stenosis, followed at UCSF
  • Recurrent URIs including AOM x 3 (eventually
    leading to diagnosis of mild, intermittent
    asthma)
  • S/P term NSVD to a 38 y/o G3P1?2 with mild
    neonatal hyperbilirubinemia, and a negative r/o
    sepsis
  • Micrognathia, 5th digit campylodactyly
    brachydactyly evaluated by Genetics at birth

4
The Case T.T.
  • FH 4 y/o brother had Kawasakis, now doing
    well. Uncle with asthma.
  • SH lives with parents, both Vietnamese, and one
    sibling. Supportive home environment
  • ROS poor eating during multiple URIs, including
    3 episodes AOM, and 2 episodes of gastroenteritis
  • Clinical concern Falling off his growth curve

5
Is the child too small?
  • Standardized Growth Charts
  • Individual curves
  • Failure to Thrive (FTT) and Idiopathic Short
    Stature (ISS)

6
Growth Chart from Birth to 15 months
7
Growth Chart from Birth to 15 months
8
Growth Chart from Birth to 15 months
9
Growth Chart from Birth to 15 months
10
Failure to Thrive Syndrome
  • Less than 3rd or 5th percentile by weight or
    length2,3,6,7
  • Growth curve that has crossed two standard
    deviations in a short time2,3,6,7
  • A fall to less than 75 of median weight-for
    height in children less than 2 y/o7
  • Caveats no underlying medical disorder and
    lasting at least 12 months7

11
Failure to Thrive
  • Differential Diagnosis
  • Environment
  • Nutrition
  • Disease
  • Hormonal Deficiencies
  • Genetic Disorders

12
1. Environment
  • Neglect inadequate intake equals inadequate
    resources for growth
  • Growing evidence that growth hormone, like the
    rest of the HPA, is affected by stress levels
  • Psychological dwarfism obscene extreme of
    neglect, marked by short stature, bizarre
    behavior and limited speech
  • (Remember, this child has devoted parents! The
    above is for learning, and is not this patients
    problem)

13
2. Nutrition
  • (Excluding neglect)
  • Affected greatly by acute illnesses, like URIs
    and gastroenteritis
  • Inadequate food choices and intake Toddlers are
    notoriously picky but, over time, they tend to
    get what they need

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3. Disease
  • Nelson Textbook of Pediatrics (Table 36-1) Major
    Organic Causes of Failure to Thrive
  • System Cause
  • Gastrointestinal Gastroesophageal reflux, celiac
    disease, pyloric stenosis, cleft palate/cleft
    lip, lactose intolerance, Hirschsprung's disease,
    milk protein intolerance, hepatitis,
    cirrhosis, pancreatic insufficiency, biliary
    disease, inflammatory bowel disease,
    malabsorption, food alkalines
  • Renal Urinary tract infection, renal tubular
    acidosis, diabetes insipidus, chronic renal
    insufficiency
  • Cardiopulmonary Cardiac diseases leading to
    congestive heart failure, asthma,
    bronchopulmonary dysplasia, cystic fibrosis,
    anatomic abnormalities of the upper airway,
    obstructive sleep apnea (snoring)
  • Endocrine Hypothyroidism, diabetes mellitus,
    adrenal insufficiency or excess, parathyroid
    disorders, pituitary disorders, growth hormone
    deficiency

15
3. Disease
  • Nelson Textbook of Pediatrics (Table 36-1) Major
    Organic Causes of Failure to Thrive
  • (continued)
  • System Cause
  • Neurologic Mental retardation, cerebral
    hemorrhages, degenerative disorders
  • Infectious Parasitic or bacterial infections of
    the gastrointestinal tract, tuberculosis,
    human immunodeficiency virus disease
  • Metabolic Inborn errors of metabolism
  • Congenital Chromosomal abnormalities, congenital
    syndromes (fetal alcohol syndrome), perinatal
    infections
  • Miscellaneous Lead poisoning, malignancy,
    collagen vascular disease, recurrently infected
    adenoids and tonsils

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First Interlude
  • Birth and routine well-child care
  • At delivery, the patient was found to have a
    harsh III/VI systolic murmur and he had
    evaluation by the Cardiology and Genetics
    services (ruled out for genetic issues)
  • At his outpatient visits (up to 1 year), T.T.s
    growth was on a reasonable curve, so no workup
    was initiated
  • Lead and anemia screening, per routine for WIC
    Hgb/HCT 11.6/31.8 MCV 69.7
  • Empiric initiation of iron was discussed with
    T.T.s mother, as there was no FH of thalassemia

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3. Disease as a nutrition issue
  • Anemia ? the oxygen-carrying component Includes
    sickle cell anemias, thalassemias and iron
    deficiency anemia
  • Celiac and other GI Disease ? inadequate
    absorptive ability secondary to gut lining issues
  • Chronic Kidney Disease ? protein deficiency due
    to protein loss

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3. Disease as a nutrition issue
  • Chronic Lung Disease (cystic fibrosis and
    asthma) ? hypoxia and breathing requirements
    interfere with the mechanics of eating
  • Congenital Heart Disease (cyanotic lesions and
    left-to-right shunts) ? oxygenation requirements
    interfere with both the mechanics of eating and
    the metabolic requirements of digestion
  • Illness and injury ? Decreased ability to take in
    nutrients and increased metabolic requirements

19
Second Interlude
  • T.T. has pulmonic stenosis, initially moderate,
    improving with growth to a mild case. At this
    point, he does not require balloon valvuloplasty
    per his mother
  • Parent agrees to bring in contact information for
    Pediatric Cardiologist at UCSF to discuss
    patients case (last consult note from 11/2003)

20
Pulmonic Stenosis
  • Differs from other cardiac lesions with respect
    to growth
  • One study suggests that mild PS has a near normal
    distribution of growth, and
  • Severe PS actually is marked by small but
    significant increase in growth for unclear
    reasons5

21
4. Hormonal deficiencies
  • Isolated Growth Hormone Deficiency the hot
    topic, as the availability of manufactured GH
    opens up the option of cosmetic endocrinology
  • Hypothyroidism Acquired hypothyroidism can
    present as early as the first 2 years of life
    with deceleration of growth as the first
    manifestation6
  • Any derangement of the HPA axis via alterations
    in metabolic state and feedback mechanisms that
    involve growth hormone

22
5. Genetic Disorders
  • When to suspect the zebras?
  • Dysmorphic features
  • Developmental delay
  • Cosanguinity
  • Family History

23
5. Genetic Disorders
  • Turners syndrome
  • Downs syndrome
  • Achondroplasia and other Skeletal dysplasias
  • Zebras Many rare genetic disorders, only some of
    which have associations with other disabilities

24
Constitutional Short Stature (ISS)
  • In the rush to give everything a diagnosis, we
    even have a name for normal, idiopathic short
    stature
  • As long as the child is staying on a curve, we
    are reassured
  • Once a child falls off of the curve or loses
    weight, we need to think about the appropriate
    workups

25
Third Interlude
  • At his most recent visit, TTs mother says But
    he is bigger than the 16 month old Vietnamese
    girl he usually plays with. What does that
    mean?
  • Is the child the right size for that child, or is
    he developing as normally as he should?
  • At what point do we need to embark on a workup?

26
Vietnamese Growth Chart
27
The Workup for FTT
  • Labs CBC, LFTs, Renal panel, urinalysis.
    Consider TSH, ESR, Insulin Growth Factor-BP3
    (IGF-BP3), Insulin Growth Factor 1 (IGF-1),
    specific antibody testing for celiac disease,
    karyotyping. In this case consider a hemoglobin
    electophoresis
  • Do not do a growth hormone stimulation test1
  • Bone age plain film left hand to evaluate
    ossification, consider a skeletal survey
  • Referral to the appropriate specialty as indicated

28
Treatment Options at SFGH
  • UCSF Pediatric Gastroenterology Because so much
    of growth failure is due to nutritional issues,
    our pediatrics GI service has a formed strong
    collaborative program with Nutrition in order to
    maximize nutritional status
  • UCSF Pediatric Endocrinology If indicated, may
    require evaluation for growth hormone replacement
  • UCSF Genetics UCSF has leading experts in both
    dysmorphology and genetic testing

29
Workup and Treatment for T.T.
  • TREAT WHAT YOU KNOW
  • Re anemia, T.T.s mother had opted to increase
    organ meats in his diet and had not started
    FeSO4. Contracted with mother to initiate FeSO4
    while awaiting results. Screen for thalassemia
    because a positive result ? d/c FeSO4
  • Re Asthma 6M clinic had referred patient to
    Asthma clinic for further evaluation and testing.
    He received one home visit but did not f/u in
    clinic. Appointment now scheduled for March
  • Flu vaccine, childhood immunizations up to date

30
Workup and Treatment for T.T.
  • At his last visit, the 19 month old pt ate a
    good-sized peanut butter sandwich during the
    history, and per mothers report feeding is no
    longer an issue
  • Given ABSENCE OF WEIGHT GAIN, check bone age and
    labs to rule out anything ominous or treatable
  • Lots of reassurance, as this child may well be
    just the right size for himself and recovering
    from an illness-malnutrition cycle
  • Weight check in one month

31
Is my child too small?
  • Research on the psychological effects of short
    stature
  • Controversy over use of growth hormone for ISS
  • Childs sense of his/her own size appears to be
    more important than actual size in terms of
    self-image
  • Data on psychological effects of short stature is
    for the most part of poor quality design8. There
    is no solid evidence that short stature is
    inherently, psychologically damaging.

32
References
  • Badaru, A. and D.M. Wilson. Alternatives to
    Growth Hormone Stimulation Testing in Children.
    Trends in Endocrinology and Metabolism. 15(6)
    252-258. 2004.
  • Behrman, R.E. et al. Nelson Textbook of
    Pediatrics, 17th ed. PhiladelphiaSaunders. 2004
  • Blair, P.S., et al. Family, Socioeconomic and
    Prenatal Factors Associated with Failure to
    Thrive in the Avon Longitudinal Study of Parents
    and Children (ALSPAC). International Journal of
    Epidemiology. 33(4) 839847. 2004.
  • Erling, A. Why Do Some Children of Short Stature
    Develop Psychologically Well While Others Have
    Problems? European Journal of Endocrinology.
    151S35-S39. 2004.

33
References, continued
  • Ferber, B. et al. Accelerated Weight Gain with
    Pulmonic Stenosis. Pediatric Cardiology.
    18(1)8-10. 1997.
  • Gunn, V.L. and C. Nechyba, eds. The Harriet Lane
    Handbook A Manual for Pediatric House Officers.
    Philadelphia Mosby. 2002.
  • Perrin, E.C. et al, investigators. Criteria for
    Determining Disability in Infants and Children
    Failure to Thrive. Evidence Report/Technology
    Assessment. Number 72. Rockville, MD Agency for
    Healthcare Research and Quality. 2003.
    www.ahrq.gov.
  • Voss, L.D. and D.E.Sandberg. The Psychological
    Burden of Short Stature Evidence Against.
    European Journal of Endocrinology. 151S29-S33.
    2004.

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