• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/43

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

43 Cards in this Set

  • Front
  • Back
three broad categories for failure to thrive
inadequate intake
increaed metabolic demand
increaed output
MCC failure to thrive
inadequate intake (usually from psychosocial issues)
failure to thrive labs
CBC, BMP, albumin, total protein, sweat chloride, UA/culture, stool O&P
when to change car seat from rear to front facing
1 year and 20 lbs
work-up in suspected child abuse
skeletal survey (bucket handle or corner fracture, spiral fracture in femur or humerus, posterior ribs, skull)
ophthalmologic exam
CT scan
CBC, coags, lft's
define SIDS
unexplained death <1 yr old despite thorough investigation
spina bifida patient's often have what allergy?
latex
is physiologic jaundice direct or indirect hyperbilirubinemia?
indirect

also will not occur within first 24 hours of life
differentiate gastroschisis from omphalocele
omphalocele has intestines, sometimes liver and other organs, protruding through umbilicus and contained within a sac, often with other anomalies

gastroschisis is protrusion without a surrounding sac through an abdominal wall defect
in hirschprung's disease, is the aganglionic segment narrow or dilated?
narrow with dilation of proximal normal colon
four most common sites for neonatal sepsis
bacteremia
UTI
meningitis
pneumonia
treatment of neonatal sepsis
ampicillin (for listeria)
and claforan or gentamicin
fever in first month of life?
in months 2-3 and non-sick?
full work-up
CBC, UA, CXR
if normal -->
urine culture, blood culture, +/- LP, may give one dose ceftriaxone and reevaluate in 24 hours
initial treatment of bites
augmentin PO x 10 days
cellultiis
cephalexin PO x 10 days
initial treatment of neonatal conjunctivitis
PO erythromycin for chlamydia
x 14 days
IV ceftriaxone for gC x 7 days
initial treatment of suppurative conjunctivitis
polymyxin b/TMP
initial treatment of salmonella
cefotaxime only if <6 mo, toxic or immunocompromised
initial treatment of mastoiditis
augmentin
initial treatment of meningitis <1 mo old
amp and cefotaxime x 21 days
initial treatment of meningitis 1-3 mo
amp and cefotaxime
initial treatment of meningitis for kids >3 mo
cefotaxime and vanc
initial treatment of orbital cellulitis
cefotaxime and clindamycin
initial treatment of
osteomyelitis?
if <5 yrs old?
if foot puncture?
if sickle cell?
oxacillin or clinda
add cefotaxime (Hib)
add ceftazidime (pseudomonas)
add cefotaxime (salmonella)
initial treatment of AOM?
high dose amoxicillin
initial treatment of GAS pharyngitis?
PO- pen VK
IV benzathine pcn
initial treatment of vp shunt infection
vanc and cefotaxime
cause and treatment of respiratory distress syndrome
surfactant deficiency

maternal antenatal steroids and surfactant
cause and treatment of transient tachypnea of newborn
retained fetal lung fluid

mild to moderate O2 req
initial treatment of congenital CMV
ganciclovir
initial treatment of congenital toxo (3!)
pyrimethamine
sulfadiazine
and
spiramycin
characterized by blueberry muffin rash, cataracts, hearing loss, PDA, encaphalitis
congenital rubella
initial treatment of congenital herpes
acyclovir
Kawasaki's symptoms
(CRASH and Burn)
conjunctivitis (bilateral, nonpurulent)
rash (truncal)
adenopathy (one cervical node >1 cm)
strawberry tongue
hand feet swelling
fever > 5 days
lab abnormalities with Kawasaki's
increaed ESR/CRP
thrombocytosis
tx of kawasaki's
IVIg x1
high dose aspirin QID until fever resolves and then low dose qd for 2 months
follow with echo (at dx, at 2 months, at 1 year)
most common immunodeficiency
IgA
B-cell deficiency in Boys
Bruton's agammaglobulinemia (recurrent URIs and encapsulated organism bacteremia)
how to tell (broadly) congenital B-cell deficiency from T-cell?
B-cell presents after 6 months

T-cell has wider range of infections (viral, fungal, intracellular bacterial) and presents 1-3 months
patient with eczema, thrombocytopenia, decreased IgM, increased IgE and IgA
Wiskott-Aldrich
common mucous membrane infections and poor wound healing suggestive of
phagocytic disease
(chronic granulomatous disease or chediak-Higashi syndrome)
complement deficiency leads to what infection?
neisseria
prophylactic treatment for hereditary angioneurotic edema
this is C1 esterase deficiency

tx is danazol (it increases C1 inhibitor protein synthesis in liver)