44 - Anemia Case Study Flashcards

1
Q

What is the chief complain of our anemia case study?

A
  • 22 year old white female, Amy W., presents to your office for pre-op surgical consult prior to elective hammertoe repair of the 2nd toe, bilateral, under local anesthesia
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2
Q

What is the patient’s history?

A
  • Family history of hammertoes
  • Patient wears high-heels regularly in her job as a fashion model and finds it more difficult due to hammertoes
  • Relates that most members of her family have long 2nd toes
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3
Q

Describe the other patient history

A
- MH: unremarkable
= SH: no alcohol, 4 cans of diet Coke®/day, no illicit drugs, vegetarian, works out daily in health club
- FH: unremarkable
- Drugs: None
- Allergies: None
- ROS: occasional fatigue
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4
Q

What did the pre-op CBC indicate?

A
  • Low hemoglobin -anemia
  • Low MCV -microcytic anemia

Hb –> if there is low hemoglobin, you have anemia, this is the clinical definition (NOT RBCs, Hb***)

MCV –> mean corpuscular volume, tells you the size of the RBCs – if size is lower than normal, it is MICROCYTIC anemia , if size is higher than normal, it is MACROCYTIC anemia

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5
Q

What is the next step?

A

Call the patient to ask questions

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6
Q

What questions will you ask?

A

Is there any family history of anemia or blood disorders?
- Nephew receives regular blood transfusions for clotting problem

Do you have normal menstruation?
- “Heavy” bleeding

Do you take vitamins?
- Yes, with an iron supplement as suggested by OB-GYN

Have you been diagnosed with an iron deficiency anemia?
- “Yes, by my OB-GYN who is also my PCP”

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7
Q

What will you want to call and ask the OBGYN?

A

Past blood work

Nurse relates that last 4 CBC’s taken at time of annual PAP smear and pelvic exam showed similar values. No other hematological studies performed.

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8
Q

You decide to do a peripheral blood smear. What would you see?

A

Smear shows microcytes with…

  • Anisocytosis (different sizes)
  • Poikilocytosis (different shapes)
  • Hypochromia (excess pallor in center of RBC)
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9
Q

What is your differential diagnosis?

A

Microcytic Anemia** –> you will now look at ISAT for the major differential of what is going on **

ISAT

I - Iron deficiency anemia
S - Sideroblastosis
A - Anemia of chronic disease
T - Thalassemia

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10
Q

What tests will you order?

A

Serum ferritin-42 ug/ml (10-300)

With a normal ferritin, diagnosis of iron deficiency is unlikely

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11
Q

What do you order next?

A

Hemoglobin electrophoresis-increased hemoglobin A2

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12
Q

What is the diagnosis?

A

Beta thalassemia trait

This is more common in Mediterranean populations - could have asked about background - she is Italian

Like you will find out, Sickle cell anemia and thalassemia are blood disorders that have evolved to protect people from malaria***

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13
Q

What is beta thalassemia trait?

A
  • Genetic disease characterized by globin chain imbalance
  • Mutations partially or completely inactivate production of a globin chain leading to imbalance in ratio of α- and β-globin chains
  • Alpha has decreased alpha chains
  • Βeta has decreased beta chains
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14
Q

What does it mean if you have the “trait”?

A

Trait: Hb production reduced in RBC, leading to microcytic anemia, but does NOT affect RBC production and survival

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15
Q

What does it mean if you have the “major”?

A

Major: profound imbalance in chain production with affects on RBC production or survival

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16
Q

What should you know about the beta trait?

A
  • Autosomal recessive disorder
  • Child has 25% chance of acquiring disorder if both parents have the trait
  • Patients are asymptomatic
  • Increased alpha chains need something to bind to, so they usually combine with δ chains to form HbA2 (α2δ2) which increases in concentration above normal 4-7%
  • No surgical precautions necessary
  • No treatment
17
Q

What you NEED to know is the mnemonic for the different types of anemia

A

“I sat in a ham damn”

18
Q

Microcytic anemia

A

I-iron deficiency
S-sideroblastic anemia
A-anemia of chronic disorder
T-thalassemia

19
Q

Normocytic anemia

A

I-infiltrative bone marrrow disorder
N-nutritional anemia

A-anemia of chronic disorder

H-hemolytic anemia
A-anemia of renal insufficiency
M-myelodysplastic anemia

20
Q

Macrocytic anemia

A

D-drugs [metformin (glucophage®)]

A-alcohol

M-malabsorption syndromes

N-nutritional anemias

21
Q

What is the most common anemia you will see clinically?

A

MOST COMMON ANEMIA (that you will see clinically based on your patient population) – normocytic anemia due to chronic disorder

Chronic diseases cause normocytic anemia

22
Q

Can you still take your patient to surgery?

A

Yes

But you do need to recommend genetic counseling to the patient