Hypothyroidism Flashcards

1
Q

Newborn visit checklist

A

Prenatal history
Birth history
Feeding history
Development

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2
Q

Weight gain in newborn period

A

can lose up to 10% of birth weight and then expected to regain by 2 weeks

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3
Q

Breastfeeding

A

ideal nutrition for kids (HIV, herpes lesion, drugs only reasons not to)

  • 8-12 feedings every 24 hrs
  • getting enough? –> weight gain, UO, trend in feeding history
  • Vit D supplement (400 units)
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4
Q

Definition of lethargy

A

level of consciousness characterized by poor or absent eye movements
*DIFFICULT TO ASSESS IN NEWBORN

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5
Q

DDx for lethargy in infant

A

infection (sepsis)
intracranial patholgy
metabolism error
chromosomal anomaly

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6
Q

Abnormal movements in infants

A

seizures aren’t like regular ones -> weird jerky movements, fluttering eyelids or smacking lips
- myoclonic jerks - normal for infants when falling asleep

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7
Q

Risks of out-of-hospital birhts

A

neonatal tetanus
Omphalitis - infection of umbilical stump
Hemorrhagic disease - no Vit K

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8
Q

Congenital hypothyroidism

A

feeding problems, decreased activity, constipation, prolonged jaundice, umbilical hernia

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9
Q

Shaken baby syndrome

A

young single parents, home stressors, low education level

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10
Q

Down syndrome

A

hyptonia –> poor feeding

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11
Q

Sepsis

A

fever, infection, poor feeding, vomiting, decreased activity

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12
Q

Congenital adrenal hyperplasia

A

decreased feeding and activity

  • salt-wasting –> decreased activity, dehydration –> shock
  • most common is 21-OH –> no production of cortisol or aldosterone –> hyponatremia and hyperkalemia
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13
Q

inborn error in metabolism

A

typically in first 1-2 days of life due to protein load in milk
- somnolence, lethargy, poor feeding –> vomiting

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14
Q

Measuring fontanels

A

Mean = 2.1 cm

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15
Q

Significance of abnormal fontanels

A

Large - skeletal disorders, chromosomal, hypothyroidism, malnutrition
Small - microcephaly, craniosynostosis, hyperthyroidism
Sunken - dehydration
Bulging - meningitis, hydrocephalus, subdural hematoma, lead poisoning

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16
Q

Epicanthal fold

A

folds of skin between medial eye and nose

17
Q

Palpebral fissures

A

eye slits on lateral sides of eyes

18
Q

Hypoglycemia

A

decreased temp, irritability, tremors, jittery

- can be essentially asymptomatic

19
Q

Labwork for infant with hypotonia

A

Sodium, potassium –> congenital adrenal hyperplasia
Ammonia –> encephalopathy, inborn errors
TSH, T4 –> congenital hypothyroidism (T4 low, TSH high)
Glucose –> check all with hypotonia

20
Q

Etiology of congenital hypothyroidism

A

1:4000 births
aplasia, hypoplasia, ectopic gland
maternal autoimmune thyroiditis
iodine deficiency

21
Q

Primary vs Secondary Hypothyroidism

A

Primary - >95% of all cases (hypothalamic-pituitary axis function is elevated)
Secondary - 5% (abnormality at just hypothalamus or just pituitary) –> low TSH and low T4 respectively

22
Q

Presentation of congenital hypothyroidism

A
feeding problems
decreased activity
constipation
prolonged jaundice
skin mottling
umbilical hernia
23
Q

Newborn screeing of CH

A

performed in all 50 states

*early detection can completely reverse the disease and has great prognosis if caught and treated early

24
Q

Diagnosis and treatment of CH

A

low TSH and T4 is CH until proven otherwise in infant

  • give levothyroxine (maintain level around 1)
  • CLOSE FOLLOW UP
25
Q

PKU

A

if not caught and treated -> developmental delay, microcephaly, cognitive impairment, seizures, musty odor, albinism

26
Q

Benefits/Risks of screening tests

A

Benefits- detect serious fatal diseases and treat them appropriately
Risks - false negatives, anxiety, treatment not effective