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31 Cards in this Set

  • Front
  • Back
what are the 3 categories of anemia
blood loss, inability for survival, decreased rbc production
how much rapid blood loss can healthy individuals tolerate
1000 ml
when does rapid blood loss lead to shock
2000 ml
hemolysis
decreased rbc survival
what do gi chronic bleeding or menorrhagia typically lead to
iron deficiency
intrinsic hemolysis is usually caused by aquired abnormalities
FALSE.... this is the case for extrinsic

intrinsic is usually inherited
anemia
reduction in red cell mass
3 categories of anemia
rbc loss
decreased rbc survival
decreased rbc production
intravascular hemolysis
destruction of rbc in circulation
extravascular hemolysis
destruction of rbc in reticuloendothelial system; spleen, liver
hereditary spherocytosis
spectrin, structural protien.... rbcs are less deformable .... sequestered and destroyed in spleen
autosomal codominant

hemoglobin SS
sickle cell anemia
hemoglobin S
valine for glutamic acid at 6
what happens to sickle cells
sequestered in spleen/ trapped in microcirculation
sickle cell trait
hemoglobin AS
thalessemias
imbalance in alpha and beta chemoglobin chain..... due to point mutation
g6p deficiency
prone to oxidation .... oxidized hemoglobin denatures..... attaches to rbc membrane.... loses flexibility..... lysed in spleen
hallmark of g6p deficiency
bite cells
genetics of g6p deficiency
x linked inheritance
anti d
binds to fetal rh + in rh - mother after birth and removes it
autoimmune hemolysis
patient makes antibodies for own rbc
hallmark of autoimmune hemolysis
spherocytes
DIC
red cells are lysed as they travel through fibrin clots in microcirculation
hallmark of mechanical trauma to rbc
schistocytes
megaloblastic anemia
low thymidine.... dna synthesis impaired..... delay in mitotic division ... fewer cells grow bigger
hypersegmented neutrophils ...
megaloblastic anemia
pernicious anemia
associated with b12 deficiency and intrinsic factor
2 pathogenic theories of aplastic anemia
aquired stem cell defect

suppression of stem cell by t cell
myelophthisic anemia
bone marrow replaced by tumor
primary polycythemia
neoplastic
secondary polycythemia
erythropoieten production