Depletion Anemia Flashcards

1
Q

what are the two main types of depletion anemia

A

abnormal loss of RBCs

abnormal destruction of RBC’s

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2
Q

abnormal loss of RBCs

A

hemorrhage

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3
Q

abnormal destruction of RBC’s

A

hemaglobinopathies/ hemolytic anemia

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4
Q

classification of hemolytic anemia

A

intracorpuscular defects

extracorpuscular defects

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5
Q

results in free hemoglobin in circulation and starts a potential cascade of events

A

hemolysis

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6
Q

hemolysis:

____ will damage tissues esp. renal

A

free Hb

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7
Q

hemolysis:

the protein ____ binds with Hb for elimation

A

haptoglobin

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8
Q

hemolysis:
once haptoglobin is saturated it binds with the protein albumin to form ______ (indicating there has been considerable hemolysis)

A

methemalbumin

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9
Q

hemolysis:

continue free ___ is serum will result in hemoglobinuria

A

Hb

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10
Q

extrinsic agents:

anemias due to iso or auto antibodies are hemolytic such as…

A

IMHA - immune mediated hemolytic anemia
MAHA - microangiopathic hemolytic anemia
fetal Rh incompatibility

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11
Q

intrinsic defects (-opathies):
in normal adults…
Hb is:
Hb A is:

A

Hb: 98%+

Hb A: <2%

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12
Q
intrinsic defects (-opathies):
newborns have >50% \_\_\_\_ but it is normally replaced by 6 months of age
A

Hb F

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13
Q
intrinsic defects (-opathies):
\_\_\_ is compromised by Hb A1 (95-98%) and Hb A2 (1-2%), a minor component
A

Hb A

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14
Q

Hb structural abnormalities:

mostly african americans; trait about 8%, dz about 1%

A

sickle cell dz

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15
Q

Hb structural abnormalities:

Hb S levels at >80% is the dz

A

sickle cell dz

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16
Q

Hb structural abnormalities:

Hb S at 20-40% with Hb A at 60-80% in the trait

A

sickle cell dz

17
Q

Hb structural abnormalities:

sickle cell prep screens for ____ but not in small quantities, therefore useful only after 6 months of age

18
Q

Hb structural abnormalities:

____ electrophoresis is definitive in sickle cell dz

19
Q

Hb structural abnormalities:

causes no anemia except under unique situations

A

sickle trait

20
Q

Hb synthesis abnormalities:

___ thalassemia Hb, but a complex genetic abnormality of globin chain synthesis

21
Q

Hb structural abnormalities:

in ____, Hb A1 is 20% or less, Hb A2 is 3%, and Hb F is >65%

A

thalassemia

22
Q

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%

A

thalassemia TRAIT

23
Q

Hb structural abnormalities:
presents as a severe anemia with microcytosis, target cells, marked hypochromia, and family history of mediterranean origin

A

thalassemia major DZ

24
Q

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

A

thalassemia minor TRAIT

25
in thalassemia ____ TIBC is low with normal ferritin
minor
26
in ____ TIBC is high and ferritin is low
iron deficiency anemia (IDA)
27
sex linked to X chromosome; affects men more than females | brought on by ASA, phenacetin, sulfas, nitrofurntoin
G-6-PD deficiency | RBC enzyme def
28
what increases in RBC membrane abnormalities
MCHC
29
lack of protein spectrin which forms an important part of the cytoskeleton of the cell diagnosed early, hemolysis, jaundice, splenomegaly
hereditary spherocytosis and hereditary eliptocytosis | RBC membrane abnormalities
30
slow and chronic bleeds usually result in
factor deficiencies
31
examples of factor deficiencies
males: peptic dz females: menstrual disorders
32
index of mature RBC production (bone marrow activity)
reticulocyte (tic) count
33
increases mean increased RBC's lost due to depletion (hemorrhage or hemolysis) or treatment of anemia with iron, B12, or folate
reticulocyte (tic) count
34
normocytic-normocytic: acute bleeds or hemolytic dz
depletion
35
normo-normo: chronic dz
produciton deficit
36
microcytic and hypochromic
factor deficiency | IDA
37
normocytic-normochromic/ hypochromic
factor deficiency | early IDA
38
macrocytic-normochromic/ hypochromic
factor deficiency | B12 or foliate