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WELL CHILD CARE

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WELL CHILD CARE The Newborn Exam and General Pediatric Screening. By Dr Chi Jokonya General Rules Get a good FHx for congenital problems Perinatal hx ie substance ... – PowerPoint PPT presentation

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Title: WELL CHILD CARE


1
WELL CHILD CARE
  • The Newborn Exam and General Pediatric Screening.
  • By Dr Chi Jokonya

2
General Rules
  • Get a good FHx for congenital problems
  • Perinatal hx ie substance abuse
  • Examine each part of the baby
  • Develop a routine or system

3
Developmental Dysplasia of the Hip (DDH, formerly
CHD)
  • 1 in 100 unstable hip, only 1 in 1000 true
    dislocation.
  • Types a) Typical normal child b) Teratological
    syndrome or abnormal bone
  • FHx (20), firstborn, female (FM 91), breech
    (40)
  • Associations congenital muscular torticollis
    metatarsus adductus

4
DDH contd.
  • Audible click means nothing.
  • Dx highest yield at 1 month newborn screeing
    maybe ineffective and perhaps harmful.
  • Dynamic uss screen breech babies at 4wks
  • X-rays AP and frog
  • Other CT, MRI, arthrography

5
Treatment DDH
  • Double/triple diaper for 2-3wks probably
    ineffective in true DDH
  • Pavlik harness, Frejka splint, van Rosen splint
    95 successful in dysplastic hips, 80 in DDH
  • Surgery at 6-12mths cast and traction
  • 3 recurrence

6
Fingers and Toes
  • Extra digit 2 in 1000 births, 30 FHx, usually
    5th toe or finger tie off EMLA or lidocaine
    anesthesia
  • Syndactyly x-ray to be certain bones present.
    Think of syndrome (toes Smith-Lemli-Opitz)
  • Polydactyly may need x-ray to preclude presence
    of bone in digit

7
Funny Looking Kids
  • FAS
  • Downs/Edwards/Pataus trisomy syndromes
  • Cornelia de Lange

8
Umbilical Problems
  • Single umbilical artery 0.55 deliveries, 27
    associated malformations.
  • Umbilical hernia 35 African American babies, 4
    white babies, increased in LBW. Association
    trisomy 18, 21 and hypothyroidism. Usually close
    spontaneously if not surgery at 3 to 5yrs

9
Umbilical Problems contd
  • Gastrochisis
  • Omphalocoele
  • Omphalitis
  • Umbilical granuloma rx with AgNO3

10
Birth Injuries
  • Cephalohematoma
  • Brachial nerve injury -90 Erbs palsy
    C5,C6,C7-1 Klumpkes palsy C8,T1
  • Facial nerve palsy 0.5, forceps/syndrome
  • Clavicular fracture may occur in utero

11
Nose Disorders
  • Hemangioma
  • Choanal atresia
  • Cleft lip/palate/nose
  • Tilted, flattened or deviated-oligohydramnios
    renal agenesis, Potters syndrome-think syndrome

12
Eyes
  • NB Check red reflex!! - retinoblastoma
  • Cataracts numerous causes. 50 missed at birth
  • Glaucoma 50 primary infantile glaucoma,
    remainder familial so get FHx

13
Ears
  • Low set many syndromes
  • Abnormal pinna-large flabby urogenital
    malformations-flat pressed against head Potters
    syndrome-pits Beckwith Weidemann (BWS)-tags
    (BWS)

14
Screening in Pediatrics
15
When Should PE Be Done
  • Birth 1mo, 6mo, 1yr
  • 1, 2, 5, 10 and 14yrs
  • Both of above for screening purposes and neither
    conforms with recommendations of various primary
    care specialty groups.

16
The Physical Exam
  • A composite of screens, most effective when
    purpose is health maintenance.
  • Yield of new abnormalities LOW
  • Hx defines most abnormal findings
  • NB need to be using BMI to identify obesity,
    chart and review growth curves.

17
Genetic and Metabolic Screens
  • Newborn PKU, tyrosinemia, galactosemia,
    hypothyroidsim, SCD.
  • Potential future screens-CAH in boys, some
    states already doing-biotinidase deficiency (1
    in 70 000) 9 states decided yes cheap and easy
    to treat-cholesterol in late childhood and
    adolescence? Insufficient evidence

18
Tuberculin Testing
  • PPD preferred (most standardized)
  • Low risk screen at 12-15mths, before school and
    at 14-16yrs
  • High risk screen annually
  • 15mm always ve, 10-14mm ve in high risk gps,
    5-9mm doubtful unless immunosuppressed.

19
Anemia
  • Screen at 6 and 18mths
  • Hct more reliable than Hb
  • If positive MCV will distinguish IDA from
    thalassemia trait (smaller rbcs in TT)

20
Lead Poisoning
  • Screen all children at 1yr?
  • All abnormal levels interview, educate, give
    questionnaire
  • Levels 10-14mcg/dl repeat in 1yr 15-20mcg/dl
    repeat in 3mths 20-30mcg/dl consider EDTA
    gt30mcg/dl requires intervention
  • www.ahrg.gov/clinic/uspstf/uspslead.htm

21
Scoliosis
  • Late childhood/early adolescent mild types rarely
    progress and almost never cause significant
    disability.
  • Evidence show screening not cost effective and
    harm exceeds benefits.
  • Routine screening NOT recommended
  • www.ahrg.gov/clinic/uspstf/uspsaisc.htm

22
Urinalysis
  • Screening NOT recommended-proteinuria FP
    common fever, exercise-orthostatic proteinuria
    transient and harmless-bacteria non treatment
    of asymptomatic bacteruria does NOT increase freq
    of pyelo or cause renal insufficiency. Rx may
    INCREASE freq of pyelo
  • Screening NOT recommended but high index of
    suspicion in febrile illness

23
Auditory Screening
  • 1 in 2000 severely hearing impaired
  • Healthy Newborns, screening safe insufficient
    evidence to recommend routine screening
  • Older children gross assessment at all CV.
  • Test in kindergarten grades 1,3,5,7
  • Pure tone audimetry at 4yrs refer if fails to
    hear 2 frequencies at 25db (NB r/o OM)

24
Visual Screening
  • During each health maintenance visit, lt5yrs look
    for strabismus, ambylopia and as soon as possible
    visual acuity (USPSTF 2004)
  • Use fixation pattern in lt3yrs. Cover one eye,
    encourage fixation. Child will not like having
    good eye covered.
  • School checks generally suffice in older children

25
Developmental Screening
  • Must be in contesxt of HP, vision and hearing
    screens.
  • Know normal developmental stages.
  • Major focus first year of life then preschool
    years.
  • Newer instruments such as ASQ (The Ages and
    Stages Questionnaires) are easier to use and more
    accurate than the DDST (Denver Developmental
    Screening Test)Journal of FP May 2006 Vol55
    No.5 415-421

26
Sickle Cell Conditions
  • Screen at birth HB electrophoresis
  • Imperative to start penicillin prophylaxis once
    diagnosis is made CT until 10yrs
  • 2-16yrs transcranial doppler screening inc BF
    gt/1 major blood vessel inc reisk of stroke, 2
    ve screens institute chronic transfusion therapy
    to keep HbS lt30

27
Gyn Screening
  • Annual pap once sexually active
  • Routine chlamydia screen all sexually active
    adolescent females.
  • Testicular cancer USPSTF recommends against
    routine screening, however, encourage regular
    self examination and examine at every visit.

28
Short List Birth to 10yrs
  • Ht, wt, BMI
  • BP
  • Vision (3-4yrs)
  • Hemoglobinopathy at birth
  • PKU, T4 and or TSH at birth

29
Short List 11 to 24yrs
  • Ht, wt and BMI
  • BP
  • Pap test
  • Chlamydia screen (females gt20yrs)
  • Rubella serology or vaccination
  • Assess for substance abuse

30
Case Scenarios
  • Cases
  • Questions
  • DiscussionChildren are not little adultsKnow
    age specific milestonesMonitor growth charts/BMI
    !
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