Anemia I Flashcards

(42 cards)

1
Q

anemia

A

decrease in circulating RBC mass

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2
Q

volume of packed RBC

A

Hematocrit

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3
Q

usual ratio of Hgb to Hct

A

Hgb:Hct = 1:3

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4
Q

RBC life span

A

120

  • old RBCs are removed by the spleen
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5
Q

reticulocyte count

A

indication of bone marrows production of RBC

  • normal 1-2%
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6
Q

polychromasia

A

reticulocytosis

  • except to see lots of blue on peripheral smear
    • “lots of blue means lots of new”
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7
Q

nomenclature for RBC size

A
  • normocytic: normal size RBC
  • microcytic: small than normal
  • macrocytic: larger than normal
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8
Q

Mean corpuscular volume. List MCV values for Micro, Normo, and Macro

A
  • calculated value to determine average volume of RBC
  • Microcytic: < 80 fL
  • Normocytic: 80-100 fL
  • Macrocytic: > 100 fL
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9
Q

mean corpuscular hemoglobin concentration

A

a measure of the concentration of hemoglobin in a given volume of packed red blood cells

  • normochromic vs hypochromic
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10
Q

anisocytosis

A

variation in size of RBC

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11
Q

red cell distribution width

A

measurement of variation in the size of RBC

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12
Q

symptoms often occur when Hgb drops below

A

7 g/dL

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13
Q

What conditions falls under microcytic, hypochromic

A
  • iron deficiency
  • thalassemia
  • sideroblastic
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14
Q

What conditions falls under normocytic, normochromic

A
  • Hypothyroidism
  • liver disease
  • chronic disease
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15
Q

What conditions falls under macrocytic (megaloblastic)

A
  • folate defiency
  • vitamin B12 deficiency
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16
Q

Presentation

  • MCV low <80
  • Low Fe
  • High TIBC
  • low ferritin
A
  • iron deficiency: determine cause
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17
Q

Presentation

  • MCV low <80
  • Low Fe
  • Normal or low TIBC
  • normal or high ferritin
A
  • anemia of chronic disease
    • infection
    • inflammation
    • malignancy
18
Q

Presentation

  • MCV low <80
  • normal to high Fe
  • any TIBC
  • normal to high ferritin
A
  • sideroblastic anemia

OR

  • alpha or beta thalassemia
19
Q

Which test is most sensitive for iron defiency

A

decrased ferritin: depletion of iron stores occurs first

20
Q

TIBC. High or low in iron deficiency anemia

A

total iron binding capacity

  • measures transferrin (what serum iron binds to in the body)
  • transferrin will increrase to maximize the low iron available
21
Q

IS RDW increased or decreased in iron deficiency anemia

A

increased: variation in RBC size

22
Q

Clinical presentation

  • glossitis, cheilitis, koilonychia
  • pica
  • dysphagia
  • restless leg syndrome
A

iron deficiency anemia

23
Q

treatment of iron deficiency anemia

A
  • **treat underlying cause
  • replace iron stores
    • oral ferrous sulfate 325 mg BID-TID until anemia corrected + 3-6 months
    • blood transfusions (select patients)
24
Q

what is considered a low ferritin level

25
Alpha thalassemia is a deletion of
one or more of the four **alpha globin chains**
26
normal Hb genetic makeup
aa/aa + B/B
27
list number of deletions of a-globin chains and manifestation in alpha thalassemia
* 1 deletion: silent carrier (-a/aa + B/B) * 2 deletions: alpha-thalassemia trait * mild microcytic anemia * 3 deletions: hemolytic anemia * 4 deletions: hydrops fetalis * not compatible with life
28
beta thalassemia
reduced or absent beta-globulin chains
29
list number of deletions of b-globin chains and manifestation in beta thalassemia
* dysfunction of one B-globin chain -\> thalassemia minor * asymptomatic * microcytic, hypochromic anemia * severe dysfunction of both B globin chains -\> thalassemia major (cooley anemia) * patients die before age 30
30
poikilocytosis
abnormal shaped RBC
31
RDW is normal or elevated in thalassemia
normal
32
diagnosis of thalassemia
Hgb electrophoresis
33
peripheral smear of thalassemia
* target cells * teardrop red cells * poikilocytosis
34
treatment of thalassemia
* folic acid supplementation * regular transfusion schedule (severe cases) * hematopoietic cell transplantation (severe Beta-T) * Avoid iron supplementation\*\*
35
presentation * MCV normal to decreased * Serum FE normal to decreased * TIBC: normal to decreased * Ferritin: normal to increased
anemia of chronic disease/inflammation
36
What is Myelodysplastic syndromes
* acquired disorder to hematopoietic stem cells * ineffective blood cell production
37
Myelodysplastic syndromes can progress to what conditions
* marrow failure * leukemia
38
What is Sideroblastic anemia
* hereditary or acquired RBC disorder * abnormal RBC iron metabolism -\> diminished heme synthesis * bone marrow produces ringed sideroblasts
39
what are sideroblasts
* normally found in bone marrow of healthy people * nucleated RBC precursors (erythroblasts) * contains iron-containing granules in cytoplasm * \*\*abnormal form: ringed
40
sideroblastic anemia is most often a subtype of what condition
myelodysplastic syndrome
41
Presentation * MCV varied * moderate anemia (Hct 20-30%) * normal or elevated ferritin * marked anisocytosis and poikilocytosis * systemic iron overload
sideroblastic anemia
42
what are some other causes of sideroblastic anemia
* chronic alcoholism * lead poisoning * medications * chronic infection or inflammation