Anemia Flashcards

1
Q

Identify function of erythropoietin – what does it do, where is it produced & what stimulates its production

A

What:

Where:

How:

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2
Q

Identify the laboratory test that provides an index of the erythropoietic action of the bone marrow

A
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3
Q

Differentiate between adult and fetal hgb

A

Adult

Fetal

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4
Q

Define anemia and associated values

A
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5
Q

A megaloblastic anemia caused by gastritis with decreased production of intrinsic factor; accompanied by neurologic changes:

A

B-12

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6
Q

A megaloblastic anemia associated with malnutrition, for example, in elderly people or people with alcoholism; not accompanied by neurologic changes:

A

Folic Acid Deficiency

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7
Q

A cause of acute anemia with risk of hypovolemic shock; cells are of normal size and color:

A

Hemorrhagic anemia

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8
Q

Accompanies gastric irritation associated with chronic aspirin use for control of arthritis pain:

A

Iron deficiency

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9
Q

End-stage renal failure, AIDS, or cancer are most likely causes of:

A

Chronic disease anemia

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10
Q

RBCs are injured and destroyed, for example by transfusion reactions, toxins, venoms, malaria, or by mechanical injury with burns or heart valve defects; RBCs are normal size and color:

A

Hemolytic

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11
Q

Signs and symptoms include increased risk of bleeding, infections, and fatigue:

A

Aplastic

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12
Q

Hereditary anemia affecting blacks; hemoglobin HbS causes abnormally shaped RBCs, which lead to hypoxia:

A

Sickle Cell

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13
Q

Hereditary anemia in various racial and ethnic groups; errors occur in synthesis of hemoglobin chains; children with disorder may have severe growth retardation:

A

thalasemmia

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14
Q

An autosomal dominant disorder in which RBCs form tight spheres that are easily destroyed in vessels of the spleen; may be treated by splenectomy:

A

spherocytosis

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15
Q

Macrocytic-normochromic eteology

A

Vitamin B-12

Folic acid

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16
Q

Microcytic-hypochromic eteology

A

Iron deficiency

Decreased heme synthesis

17
Q

Discuss the “common or classic “ clinical manifestations of anemia and the pathogenesis behind them

A
18
Q

Discuss clinical manifestations seen with the hemolytic anemias

A
19
Q

Discuss clinical manifestations seen with the aplastic anemias

A
20
Q

B-12 deficiency:

Etiology

A
21
Q

B-12 deficiency:

pathogenesis

A
22
Q

B-12 deficiency:

Manifestations

A
23
Q

Folic acid deficiency:

eteology

A
24
Q

Folic acid deficiency:

pathogenesis

A
25
Q

Folic acid deficiency:

Manifestations

A
26
Q

Identify the major causes of hemolytic anemias

A
27
Q

Identify the factors that can precipitate sickle cell crisis

A
28
Q

Identify the hemolysis seen in G6PD anemia

A
29
Q

Define polycythemia

A
30
Q

What is relative polycythemia?

Give examples

A
31
Q

What is Primary polycythemia?

Give examples

A
32
Q

What is seconday polycythemia?

Give examples

A
33
Q

Discuss the pathogenesis behind the clinical manifestations seen in primary polycythemia (polycythemia vera)

A