CLIPP 9 Flashcards

1
Q

feedings per day and duration

A

8-12 per day for 10-15min/time

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2
Q

stool and urines / day at d3-5 and d5-7

A

d3-5: 3-4, 3-5

d5-7: 3-6, 4-6

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3
Q

what vitamin do newborns need and in what amount? who is exempt?

A

D - 400 IU daily

-exempt if formula-fed exclusively and having 1L to 1Q per day

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4
Q

seizures vs jitters in infants

A
  • newborns rarely have generalized tonic clonic seizures and instead may have apnea, lip smacking etc, eye fluttering, horizontal deviation
  • jitters are stimulated, go away with passive gentle flexion and are generalized and symmetric
  • clonus up to 10 beats in newborn if no other neuro sx and no asymmetric or up to 3 in 1-2 month old is normal, brief myoclonus is also okay esp when falling asleep
  • clonus = twitching and rhythmic jerks when trying to hold in stretched state vs myoclonus = involuntary jerks
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5
Q

presentation of salt-wasting CAH

A

dehydration, lethargy, vomiting, virilization

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6
Q

one cause / association of hypoglycemia

A

low temperature

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7
Q

common finding in congenital hypothyroidism

A

constipation, may also see umbilical hernia, hypotonia, jaundice

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8
Q

calculating fontanel size, associations with large, small, sunken, bulgy, exemptions

A

h+w / 2
AF: mean is 2.1, @SD is .6 and 3.6
PF: most is below .5
large: skeletal, chromosomal, malnutrition, hypothyroid, high ICP
small: microcephaly, craniosynostosis, hyperthyroidism, normal variant
sunken: dehydrated
bulging: hydrocephalus, meningitis, lead poisoning, subdural hematoma
exempt: if crying or if lying vs sitting - can change it.

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9
Q

important cause of decreased feeding

A

CAH

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10
Q

inborn errors of metabolism - sx and lab

A

appear fine in 1-2 days of life but then can get lethargic, dehydrated–>encephalopathy
-hyperammonemia and elevated urine orotic acid

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11
Q

most common cause worldwide of hypothy

A

iodine deficiency

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12
Q

hypothyroidism transiently due to

A

babies of graves mothers who take anti-thy drugs or passage of thyrotropin receptor blocking Ab via placenta

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13
Q

two populations in whom congenital hypothyroidism is common in

A

native americans, hispanics

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14
Q

primary vs secondary, tertiary hypothyroidism

A
  • primary: HPA is functioning, TSH high

- secondary, tertiary: abnormalities at pituitary or hypothalamus

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15
Q

why do CH patients appear normal at birth?

A

moms thyroid hormone can protect hypothyroid fetus and only several months after birth does the baby start to show signs

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16
Q

one of most common causes of preventable mental retardation

A

CH

17
Q

next steps in dx CH and tx

A

confirmatory measurements of TSH and T4 and started on Levo

18
Q

musty sweaty odor, seizures

A

PKU ( due to phenylacetate)

19
Q

timing of specimen collection

A

asap - initial likely before 24h age (no later than d/c time and no later than 7d of age), another before 2w

20
Q

goal of Levo tx

A

maintain TSH at 1 and t4 in upper half of normal range - normalization of TSH within 1-2 months has good prognosis for neurologic outcomes

21
Q

after starting levo, measure TSH at..

A

2 and 4 weeks post tx and..
every 1-2 months if under 1y old
eery 2-3 months til 3 yo
every 3-12 months til growth is done

22
Q

Levo at 0-6months of age

A

10-15 mcg/kg/day

23
Q

large tongue, puffy skin around eyes, bad muscle tone, outty bellybutton

A

hypothyroidism

24
Q

botulism

A

hypotonia, lethargy, constipation , absent dTRs, weka cry, respi failure