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33 Cards in this Set

  • Front
  • Back
what are the 4 common scenarios of picking up anemia?
1. child presents for routine well visit to find low hct; chid 2. child presents with parents complianing of pale, sluggish and picky eater 3. child found to be anemic while being eval for illness, FTT or recurrent infection
what is the definiton of anemia?
decrease in # of RBCs or a decrease in the concentration of hgb
what is the MCV cut off for this class?
80
what are the 3 ways to become anemic?
1. ineffective production 2. increasted destruction 3. blood loss
what are the epidemologic factors rt anemia?
genetic, ethnicity, dietary
what are the MCVs that warrant microcytic anemia in 6 months-2 yrs, 2-5 and 5-12?
<70, <73, <76
what is the equation for MCV in this class?
70 + (2 x age in years)
what are the differentials for microcytic anemia?
IDA, anemia of chronic disease, thalasmia, sideroblastic anemia, lead tox
what are the test that help distinguish lead tox from IDA?
Ferritin and Serum Fe
what is the tx for IDA from cows milk?
decrease milk, 6mg/kg/day for 6 months, test retic in 5-7 days to see if working, or Hgb in 1 month, then if normalizes after 3 months can do 3mg/kg/day
what is the teaching regarding Fe admin?
administer with meals, liquid preps may stain teeth (rinse after), GI symps are constipation, antacids and H2 blockers interfere with absorption, takes 3 months to replenish iron stores
what is the first heme attack of a sickle cell?
dactylitis
what are the test done for a sickler with venous attack?
blood culture, urine c&s, hgb electrophoresis
what is the pattern for sickle cell trait? Sickle C trait?
FAS; FAC
what is the pattern for thalaseemia?
FAA2
what are the lab findings for sicke cell anemia?
increased WBC, decreased hbg, increased retic, increased plts, decreased sed rate, increased serum LDH, increased serum bili
what are sicklers at risk for?
developing sepsis from encapsulated organisms: strep pneumo, and H flu
what is done for febrile sicklers
hospitaized on IV abx
ToF: blood cultures are required for all sicklers with fever
TRUE
ToF: it is necessary to stop breast feeding in physiologic and breast feeding jaundice
FALSE
what is the rule of 2?
for jaundice: bili rises too early (within 24 hours of life), rises too fast (>5/day), too long (>10 days in full term or >2 weeks in preterm infant), bili is too direct (>1.5)
what are the sxs of jaundice?
bili > 5; lethargy, poor feeding, vomiting, poor moro refelx, high pitched cry and constipation
when does physiologic jaundice begin?
usually 3rd day of life and resolves by day 10
what are the causes of non-physiologic jaundice?
hereditary hemolytic anemia (spherocytosis), ABO incomp, G6PD, maternal illness during pregnancy, TORCH, maternal drugs, labor trauma, asphyxia, delayed cord clamp or prematurity
what are the lab findings for physiologic jaundice?
total bili >12 and direct <1.5
what are the etiologies of physiologic jaundice?
1. secondary to polycythemia, birth trauma, decreased survival of RBCs, increased enterohepatic circ 2. decreased hepatic uptake of bili 3. poor conjugation secondary to decreased gluco transferase, decrease excretion of bili
what are the causes of excess bili production?
ABO incompat, red cell mem defects, infections, drugs, hemoglobinopathies, DIC, pyloirc stenosis, dehydration, polycythemia
what are the causes of abnormal bili metabolism>
crigler-najjar syndrome, gilberts disease, dubin-johnson syndrome, rector syndrome, galactosemia, hypothryoidism, and infants with diabetic mothers
when is breast feeding prohibited for breast milk jaundice?
only for diagnostic purposes, bili decreases after 48 hours of cessation
ToF: there is an increase risk of other children having breast milk jaundice after the first does
TRUE
what are the lab tests to workup for jaundice?
Type and coombs (infant and mom); cbc and retic, direct and indirect bili, LFTs, thyroid, TORCH, serum glucose, septic workup
what is the bili cut off to consider phototherapy?
10
at what bili is an exchange transfusion used?
>20