Depletion Anemia Flashcards
what are the two main types of depletion anemia
abnormal loss of RBCs
abnormal destruction of RBC’s
abnormal loss of RBCs
hemorrhage
abnormal destruction of RBC’s
hemaglobinopathies/ hemolytic anemia
classification of hemolytic anemia
intracorpuscular defects
extracorpuscular defects
results in free hemoglobin in circulation and starts a potential cascade of events
hemolysis
hemolysis:
____ will damage tissues esp. renal
free Hb
hemolysis:
the protein ____ binds with Hb for elimation
haptoglobin
hemolysis:
once haptoglobin is saturated it binds with the protein albumin to form ______ (indicating there has been considerable hemolysis)
methemalbumin
hemolysis:
continue free ___ is serum will result in hemoglobinuria
Hb
extrinsic agents:
anemias due to iso or auto antibodies are hemolytic such as…
IMHA - immune mediated hemolytic anemia
MAHA - microangiopathic hemolytic anemia
fetal Rh incompatibility
intrinsic defects (-opathies):
in normal adults…
Hb is:
Hb A is:
Hb: 98%+
Hb A: <2%
intrinsic defects (-opathies): newborns have >50% \_\_\_\_ but it is normally replaced by 6 months of age
Hb F
intrinsic defects (-opathies): \_\_\_ is compromised by Hb A1 (95-98%) and Hb A2 (1-2%), a minor component
Hb A
Hb structural abnormalities:
mostly african americans; trait about 8%, dz about 1%
sickle cell dz
Hb structural abnormalities:
Hb S levels at >80% is the dz
sickle cell dz
Hb structural abnormalities:
Hb S at 20-40% with Hb A at 60-80% in the trait
sickle cell dz
Hb structural abnormalities:
sickle cell prep screens for ____ but not in small quantities, therefore useful only after 6 months of age
Hb S
Hb structural abnormalities:
____ electrophoresis is definitive in sickle cell dz
Hb
Hb structural abnormalities:
causes no anemia except under unique situations
sickle trait
Hb synthesis abnormalities:
___ thalassemia Hb, but a complex genetic abnormality of globin chain synthesis
NO
Hb structural abnormalities:
in ____, Hb A1 is 20% or less, Hb A2 is 3%, and Hb F is >65%
thalassemia
Hb structural abnormalities:
in the _____, the Hb A1 makes up more than 50% of Hb A1, Hb A2 is 4-6%, and Hb F is up to 3%
thalassemia TRAIT
Hb structural abnormalities:
presents as a severe anemia with microcytosis, target cells, marked hypochromia, and family history of mediterranean origin
thalassemia major DZ
Hb structural abnormalities:
differs from IDA in the
1. RDW is normal
2. anemia is unlikely; as a matter of fact, the RBC may be greater than 5x10^6 even though the Hb may be as low as 9gr/dl
thalassemia minor TRAIT