RECOGNIZING A NORMAL NEWBORN Flashcards

1
Q

CATEGORIES OF PRETERM BIRTH

Overall PT :
- Moderately PT:
- Very PT :

A
  • Overall PT : <37 wks gestation
  • Moderately PT: between 32 and 36 weeks
  • Very PT : <32 weeks gesatation
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2
Q
  • method of systematically assessing NB after birth
  • Assessed at 1 and 5 minute of life infants immediately
  • If the 5 min score is <7, additional scores should be
    assigned every 5 min up to 20 min
A

APGAR SCORE

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3
Q
  • between 34-36 6/7 wk
  • 37 0/7 wks - 38 6/7 wks
  • 39 0/7 wks — 40 6/7 wks
  • 41 0/7wks - 41 6/7 wks
  • 42 0/7 wks and beyonce
A

Late preterm: between 34-36 6/7 wk
Early Term: 37 0/7 wks - 38 6/7 wks
Full Term: 39 0/7 wks — 40 6/7 wks
Later Term: 41 0/7wks - 41 6/7 wks
Post Term : 42 0/7 wks and beyonce

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4
Q
  • To obtain a more accurate idea of the GA
  • Most accurate if performed within the 1st 12 hrs of life
  • Infant’s true GA can he estimated with an accuracy of about 2 wks
  • If scored age 18 W/T 2 wks of the GA suggested by the mother’s dates, then accept her dates as correct
A

Ballard Score

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5
Q
  • Scalp pressure from the uterus
  • Circular boggy areca of edema w ith indistinct borders
A

Caput succedaneum

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6
Q

Well-circumscribed fluid-filled mass; does not cross the midline

A

Cephalhematoma

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7
Q
  • Not restricted by the houndaries of the sutures
  • Larger and more diffuse
  • Result in hypovolemuc shock
A

Subgaleal hemorrhage

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8
Q

genetic d/0, congenital intxn, drug exposure

A

Microcephaly

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9
Q

Hyrocephalus, storage dse, achondroplasia, cerebral gigantism, neurocutaneous syndrome, IEM

A

Megalencephaly

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10
Q

premature fusion of sutures

A

Craniosynostosis

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11
Q
  • Large anterior fontanel: achondroplasia, Apert syndrome, hypothyroidism, cleidocranial dysostosis, congenital rubella syndrome, Halierman-Streiff syndrome, hydrocephaly, hyphophosphatasia, IUGR, Kenny syncrome, OI, PT, Trisomies, Vit. D def rickets
  • Small fontanels: microcephaly craniosynostosis, CH of wormian bones
  • Presence of third fontancl suggest T21, but seen in preterm infants
A

Fontales: anterior fontanel

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12
Q
  • Atrophic or alopecic scalp
    Sporadic or alopecic autosomal dominant
  • Asstd with T13, chromosome 4 deletion, or Johanson- Blizzard syndrome
A

Aplasia cutis congenita

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13
Q
  • In utero positioning
  • Asstd with torticollis and vertex positioning
A

Deformational plagiocephaly

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14
Q
  • Symmetric acial palsy
  • Absent/hypoplasia of 7th nerve nucleus
A

Mobius syndrome

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15
Q

Cornea >1cm in dia with photophobia and tearing or clouding

A

Glaucoma

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16
Q
  • White pupillary reflex
  • Cataract, tumor, chornoretinitts ROP
A

Leukocoria

17
Q
  • Abduction of the thighs with external rotation
  • If the femoral head can be felt to slip forward into the acetabulum on pressure from behind, it is dislocated (positive) .
  • Sometimes an audible “chunk” can be heard.
A

Ortolani test

18
Q
  • Pressure from the front
  • lf the femoral head is felt to slip out over the posterior lip of the acetabulum and immediately slips back in place when pressure 1s released, there is dislocation or “unstable”
A

Barlow sign

19
Q

4 mechanisms of heat loss

A
  • Convection of heat energy the cooler surrounding air
  • Conduction of heat to the colder materials touching the infant
  • Heat radiation from the infant to other nearby cooler objects
  • Evaporation from skin and lungs