More questions Flashcards

1
Q

What natural anticoagulant is required for heparin to work?

A

antithrombin

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2
Q

Why do we need to bridge coumadin?

A

coumadin will decrease protein C and S so it will cause an acute hypercoagulable state

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3
Q

What is the formula to calculate ANC?

A

ANC = [ (% neutrophils + % band) x WBC]/ 100

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4
Q

Elevated LDH, indirect bilirubin, and haptoglobin, combined with anemia is consistent with what?

A

hemolytic anemia

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5
Q

Thalassemia is a _________ problem, while sickle cell is a _________ problem

A
  • thalassemia = quantitative

- sickle cell = qualitative

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6
Q

What is the treatment for hereditary spherocytosis?

A

remove spleen

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7
Q

What is the treatment for warm hemolytic anemia (IgG+)?

A

steroids immunesuppression

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8
Q

What is the diagnostic test for G6PD deficiency?

A

G6PD enzyme level

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9
Q

If a patient is receiving a transfusion and develops hives ONLY what do you do?

A

antihistamines and keep going

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10
Q

What is the difference in terms of pathophysiology between ITP and TTP?

A
  • ITP = auto-antibody against platelets

- TTP = deficiency in Adams TS13 which cleaves vWF

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11
Q

What is the treatment for TTP?

A

plasma exchange to give back Adams TS13

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12
Q

How do you diagnose TTP?

A

check Adams TS13 level

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13
Q

HUS is typically d/t to what?

A

E. coli infection

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14
Q

How can you use labs to differentiate between HUS and TTP?

A

TTP will have low Adams TS13 but normal in HUS

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15
Q

What is HELLP associated with?

A

pre-eclampsia in pregnancy

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16
Q

How is HELLP treated?

A

deliver the baby

17
Q

What are the 5 MAHAs discussed in class?

A
  • ITP
  • TTP
  • HUS
  • HELLP
  • DIC
18
Q

How can you differentiate DIC from the rest of the MAHAs?

A
  • look at coags they will be prolonged!
19
Q

What are the 2 main consequences of renal disease?

A
  • EPO deficiency causing anemia

- qualitative platelet defect

20
Q

What is the treatment for hereditary hemochromatosis?

A

phlebotomy

21
Q

How do you a qualitative platelet abnormality secondary to uremia?

A
  • DDAVP to increase factor 8 and vWF
22
Q

There is no risk of spontaneous bleeding until platelet count is how low?

A

<10-20,000

23
Q

Before initiating workup of new onset thrombocytopenia you must rule out _________________ .

A

pseudothrombocytopenia

24
Q

How is immune thrombocytopenia diagnosed?

A

diagnoses of exclusion

BUT on PBS can see large platelets

25
What is the treatment for immune thrombocytopenia?
corticosteroids
26
What is the treatment for DIC?
fix underlying cause
27
What is the clinical pentad consistent with TTP?
- fever - anemia - thrombocytopenia - renal failure - neurologic dysfunction
28
How is TTP treated?
plasmapheresis with plasma exchange
29
How is HUS diagnosed and treated?
- diagnosed = stool culture for EHEC | - treated = supportive, NO ANTIBIOTICS