• 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

1/25

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;

25 Cards in this Set

  • Front
  • Back
Most common inherited bleeding disorder is?
Von willebrands
Most common acquired bleeding disorder is?
vit k deficiency
What are the key features of von willebrand disease
lack of factor 8-R

aPTT prolonged, bleeding time prolonged
what are the key features of hemophilia a?
lack of factor 8

aPTT prolonged
normal bleeding time
what are the features of hemophilia b?
lack of factor 9

aPTT prolonged
normal bleeding time
vit k defiency key features?
PT prolonged
fat malabsorption
antibiotics (dminished gut flora)
coumadin therapy
What are key feature of idiopathic thrombocytic purpura
immune mediated
childrean: acute, after viral infect
adults: often chronic
What are key features of TTP?
young women
microthrombi
fragmented RBCs (helmet cells)
bleeding time depends on?
platelet function
PT time depends on?
extrinsic pathway plus common
aPTT depends on?
intrinsic pathway plus common
TT (bleeding) depends on
common pathway
key features of spherocytosis?
autosomal dominant
defective spectrin
splenomegaly
g6pd defiency key features
hemolysis during oxidative stress

so..viral infections, fava beans, sulfa drugs, nitrofurantoin, quinine

heinz bodies present
sickle cell key features?
vaso-occlusive crisis, sequestration crisis (swollen spleen)
autosplenectomy
aplastic crisis

worsened by HYPOXIA, DEHYDRATION, ACIDOSIS
key features of alpha thalassemias
HBH beta 4

common in SE ASIA
hypochromic cells, TARGET CELLS

Hb Bart (gamma 4) hydrops fetalis
key features of beta thalassemias
HbA2 (alpha 2 beta 2) and HbF (alpha 2 and gamma 2)

common in Meditteraen and US,
hypochromic and target cells
whats the difference between immune mediated anemias with warm antibodies and cold antibodies
cold antibodies are on peripheral anemias, caused by IgM(minnesota) mycoplasma pneumo, mononucleosis, and lymphoma

warm IgG caused by drugs, malignancies, SLE
direct coombs test detects what?
cell bound antibodies, mix rbcs with anti-IgG
indirect coombs test measures
free antibodies

mix pts plasma with normal RBCs
key features of megaloblastic anemia
HYPOchromic, macrocytic

hypersegmented neutrophils

if neuro symptoms, then b12 def, if none then consider folate
key features of iron defiency anemia
HYPOchromic, MICROcytic RBCs

chronic blood loss, if elderly consider malignancy, esp right sided colon cancer and FOB positive
key features of aplastic anemia aka BM failure
viral infections
toxins
drugs- alkylating agents, chloramphenicol
plummer vinson sydrome triad?
IDA
atrophic glossitis (esophagitis)
esophageal webs (dysphagia)
key features of fanconi anemia
autosomal recessive
hypoplastic thumbs
absent radii
aplastic anemia