Topic 12 Anemia Flashcards

1
Q

Anemia Therapeutics

A

Iron
B12
Folic Acid (B9)
Erythropoietin (Epogen, Procrit)

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2
Q

Why is Iron a treatment of Anemia?

A

Required for the hemoglobin molecule to carry
O₂
Iron deficiency results from inadequate iron stores &/or intake.

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3
Q

Iron is stored in what?

A

Stored in intestinal mucosal cells as ferritin.

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4
Q

Oral Iron supplement adverse effects?

A

Injections HURT!

Oral iron supplements can cause “GI upset”

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5
Q

Iron deficiency anemia classically causes what kind of anemia?

A

hypochromic, microcytic anemia

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6
Q

Folate (B9) deficiencies are caused by what?

A

pregnancy, lactation, intestinal pathology (Crohn’s Disease, etc.) preventing absorption, alcoholism, certain drugs.
Folate is require for DNA synthesis

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7
Q

Folate deficiency anemia classically causes what type of anemia

A

megaloblastic anemia

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8
Q

Most common cause of deficiency is what?

A

poor B₁₂ absorption aka “pernicious anemia”

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9
Q

pernicious anemia

A

poor B₁₂ absorption

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10
Q

B₁₂ deficiency also causes what type of anemia

A

megaloblastic anemia

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11
Q

Therapies for megaloblastic anemia

A

B₁₂ and Folate

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12
Q

Epogen and Procrit (Erythropoietin) are what chemically?

A

Both are synthetic forms of erythropoietin-alfa

•Both have identical protein structure and vary in their glycosylation

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13
Q

Darbepotin (Aranesp)

A

is a longer-acting cousin of Epogen and is “albumin-free”
•Part of a comprehensive blood. conservation/blood management program.
•Require week(s) to “kick in” bone marrow so not appropriate for acute blood loss.
•Usually given with iron

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14
Q

Darbepotin

A

(Aranesp)

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15
Q

Darbepotin (Aranesp) side affects?

A
High potential for abuse!
–Stroke
–Increased tumor risk
–Thromboembolic events
–Severe HTN–Death
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16
Q

Sickle cell drugs?

A

Hydroxyurea (Hydrea, Droxia)

Pentoxifylline (Trental)

17
Q

Hydroxyurea

A

Hydrea, Droxia

Sickle cell drugs

18
Q

Pentoxifylline

A

Trental

Sickle cell drugs

19
Q

Hydroxyurea (Hydrea, Droxia) - how does it work?

A

Fairly effective in preventing painful acute
“crises” associated with sickling claudication.
*Causes sickle cell hemoglobin (HbS) to get diluted by an increased production of fetal hemoglobin (HbF) particularly when used with epo-alfa

20
Q

Claudication

A

Pain caused by too little blood flow

21
Q

Pentoxifylline is what kind of modifier

A

rheologic modifier!

-It increases the “flexibility” of RBC’s so they are less likely to clog capillaries

22
Q

Pentoxyifylline does what?

A

Decreases blood viscosity so interesting future possibilities…TIA, strokes, Raynaud’s, diabetic ulcers, etc