Microcytic Anemia Flashcards

1
Q

Iron deficiency (hypochromic)- description

A

Iron- essential mineral for functioning Hgb
Most absorbed in duodenum
Absorbed —> transferred —> stored as ferritin in liver, spleen, BM, muscle

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2
Q

Iron deficiency (hypochromic)- cause

A

1 main cause of anemia

Insufficient diet of iron
Poor absorption
Chronic blood loss

W>M- pregnancy/menses

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3
Q

Iron deficiency (hypochromic)- s/s

A

Look for blood loss: GI tract, urinary tract, menses/menorrhagia, blood donations

Tachycardia 
DOE
Fatigue 
Pale skin and mucosa
Brittle nails 
Angular cheilitis- dry corners of mouth 
Pruritus
Pica- crave non foods (ice chips) 
Anxiety
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4
Q

Iron deficiency (hypochromic)- labs and imaging

A

Rectal Exam - is it bleeding??

Ferritin - stored iron

  • <30 + dec H/H -> IDA
  • first lab to become low

Serum Iron

  • can fluctuate daily
  • low or nl

Tranferrin Saturation % - how much serum irion is bound
- low = IDA

Total Iron Binding Capacity (TIBC) - capacity to bind iron

  • inc = IDA -> it can bind, but no iron to bind!
  • Nl = 240-450
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5
Q

Iron deficiency (hypochromic)- treatment

A

Diet - red meat, spinach, beans, lentils

Ferrous Sulfate - 325mg TID

  • start extremely low, and up it slowly - can be poorly tolerated
  • Hct half nl in 3w and full nl in 2m, if not -> wrong dx, blood loss, or pt non-compliant
  • “can” d/c 3-6m after Hct is Nl

Parental - IV
- if fail Ferrous sulfate/diet, GI inhibit absorption, cont blood loss

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6
Q

Thalassememia (hypochromic)- description

A

Hereditary disease of impaired Hgb synthesis- genetic

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7
Q

Thalassememia (hypochromic)- cause

A

Defect in either Hgb is comprised of 2 alpha and 2 beta chains

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8
Q

Thalassememia (hypochromic)- s/s

A
Pallor 
Splenomegaly
Growth failure 
Bone deformities 
Jaundice
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9
Q

Thalassememia (hypochromic)- labs & imaging

A

Retic- nl to inc —> BM trying to compensate
Iron studies- nl

Blood smears- target cells

Hgb electrophoresis- diagnosis

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10
Q

Thalassememia (hypochromic)- treatment

A

Mild:
No spec treatment - monitor
Folate supplements
AVOID - Fe supplement snad Sulfonamides

Major: 
Blood transufions 
Splenectomy - dec risk of bleeding out, but inc risk of infection 
BMT
AVOID- Fe supplements and Sulfonamides
Curre - Allo
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11
Q

Thalassememia (hypochromic)- risks

A

Iron overload —> organ damage
Chelation therapy- poop out iron
Inc infection risk- esp w splenectomy
Bone deformities- BM expansion

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12
Q

Sideroblastic- description

A

Hgb synthesis reduced —> can’t incorporate iron

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13
Q

Sideroblastic- cause

A
Acquired- 
alcoholism
lead/copper/zinc poisoning
dietary B6 or copper deficiency
OCP
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14
Q

Sideroblastic- s/s

A

Consistent w anemia

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15
Q

Sideroblastic- labs & imaging

A

BMB- ringed sideroblasts

Labs show- microcytic anemia w nl Fe studies

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16
Q

Sideroblastic- treatment

A

Rarely needed
Address acquired issues
Transfusion if necessary