Hypothyroidism Flashcards
Newborn visit checklist
Prenatal history
Birth history
Feeding history
Development
Weight gain in newborn period
can lose up to 10% of birth weight and then expected to regain by 2 weeks
Breastfeeding
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)
Definition of lethargy
level of consciousness characterized by poor or absent eye movements
*DIFFICULT TO ASSESS IN NEWBORN
DDx for lethargy in infant
infection (sepsis)
intracranial patholgy
metabolism error
chromosomal anomaly
Abnormal movements in infants
seizures aren’t like regular ones -> weird jerky movements, fluttering eyelids or smacking lips
- myoclonic jerks - normal for infants when falling asleep
Risks of out-of-hospital birhts
neonatal tetanus
Omphalitis - infection of umbilical stump
Hemorrhagic disease - no Vit K
Congenital hypothyroidism
feeding problems, decreased activity, constipation, prolonged jaundice, umbilical hernia
Shaken baby syndrome
young single parents, home stressors, low education level
Down syndrome
hyptonia –> poor feeding
Sepsis
fever, infection, poor feeding, vomiting, decreased activity
Congenital adrenal hyperplasia
decreased feeding and activity
- salt-wasting –> decreased activity, dehydration –> shock
- most common is 21-OH –> no production of cortisol or aldosterone –> hyponatremia and hyperkalemia
inborn error in metabolism
typically in first 1-2 days of life due to protein load in milk
- somnolence, lethargy, poor feeding –> vomiting
Measuring fontanels
Mean = 2.1 cm
Significance of abnormal fontanels
Large - skeletal disorders, chromosomal, hypothyroidism, malnutrition
Small - microcephaly, craniosynostosis, hyperthyroidism
Sunken - dehydration
Bulging - meningitis, hydrocephalus, subdural hematoma, lead poisoning
Epicanthal fold
folds of skin between medial eye and nose
Palpebral fissures
eye slits on lateral sides of eyes
Hypoglycemia
decreased temp, irritability, tremors, jittery
- can be essentially asymptomatic
Labwork for infant with hypotonia
Sodium, potassium –> congenital adrenal hyperplasia
Ammonia –> encephalopathy, inborn errors
TSH, T4 –> congenital hypothyroidism (T4 low, TSH high)
Glucose –> check all with hypotonia
Etiology of congenital hypothyroidism
1:4000 births
aplasia, hypoplasia, ectopic gland
maternal autoimmune thyroiditis
iodine deficiency
Primary vs Secondary Hypothyroidism
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
Presentation of congenital hypothyroidism
feeding problems decreased activity constipation prolonged jaundice skin mottling umbilical hernia
Newborn screeing of CH
performed in all 50 states
*early detection can completely reverse the disease and has great prognosis if caught and treated early
Diagnosis and treatment of CH
low TSH and T4 is CH until proven otherwise in infant
- give levothyroxine (maintain level around 1)
- CLOSE FOLLOW UP
PKU
if not caught and treated -> developmental delay, microcephaly, cognitive impairment, seizures, musty odor, albinism
Benefits/Risks of screening tests
Benefits- detect serious fatal diseases and treat them appropriately
Risks - false negatives, anxiety, treatment not effective