Hem Onc Review pt2 Flashcards

1
Q

Heparin inhibits activity at what factors?

A

XA and IIA

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2
Q

When doing massive transfusion to treat an aquired bleeding disorder, what must you also give?
Why?

A

FFP

to overcome anticoag fx of sodium citrate

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3
Q

Causes of acute DIC are ____-related

What are they (2)

A

Hyperfibrinolysis
Gram neg sepsis infxn
Malignancies like APL

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4
Q

Subacute/chronic causes of DIC are ____-related

What are they? (4)

A
Prothrombic (increased thrombin)
Mucinous adenocarcinomas
retained dead fetus
venous/pulm thrombosis
connective tissue disorders
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5
Q

All 4 are abnormal, the PT, PTT, Platelet, & Fibrinogen lvls…what is it?

A

DIC

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6
Q

Tx of DIC

A

tx underyling ds, FFP/platelets

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7
Q

In DIC, what do you give for acral cyanosis, digital ischemia, migratory thrombophletbitis, or retained dead fetus?

A

Heparin

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8
Q

what-shape formation of megakaryocytes in bone marrow?

A

Pseudopod

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9
Q

what will prolong bleeding time >9 minutes?

A

Qualitative/quantitative platelets defect/dysfunction

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10
Q

What is ITP?

tx? (3)

A

immune thrombocytopenic purpura
Pathogenic autoantibodies bind platelets, resulting in accelerated platelet clearance

Tx: steroids, if severe: splenectomy
but must also get Pneumococcal, H flu, and meningococcal vaccines 2 weeks prior

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11
Q

Fever, mental status changes, renal insufficiency, microangiopathic hemolytic anemia, and thrombocytopenia is the pentad of sx for

A

Thrombotic microangiopathy

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12
Q

ADAMTS-13 is found in

A

TTP

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13
Q

Common finding in TTP & HUS (2)

The tx?

A

Microangiopathic hemolytic anemia, thrombocytopenia

tx for both: plasma exchange

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14
Q

How to differentiate btwn TTP & HUS

A

TTP: fever, neuro defecit in adults, decreamsed adamts-13
HUS: renal insuff, usu in children, positive stool for e coli 0157-H7

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15
Q

What platelet disorder has stool with e coli 0157-h7?

A

Hemolytic uremic syndrome

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16
Q

What happens withi elevated homocysteine?

tx of homocystenemia

A

endothelial cell dysfunction leading to a prothrombotic surface.

tx: Folic acid

17
Q

What’s the most common protein defect?

A

factor v leiden

18
Q

inactivated protein C leads to increased factor Va in:

A

Factor V leiden

19
Q

increased fibronolysis and increased thrombin formation (related to Vit K dependent clotting factors) is found in

A

Protein C defect

20
Q

What are the vitamin k dependent clotting factors (2)

A

Va, IIIa

21
Q

What happens in antiphospholipid antibody syndrome?

A

antiphospholipid antibodies bind to endothelium and intefere with antocoagulation by messing with Annexin V

22
Q

Annexin V is messed up in what?

A

Antiphospholipid antibody syndrome

23
Q

Protein s leads to what?

A

Protein C and its sx: inc fibrinolysis, inc thrombin formation (with vit-k factors)

24
Q

Aspirin’s MoA

A

inhibits A2 synthesis from arachadonic acid

25
Q

Aspirin blocks COX #?

A

1

26
Q

aspirin and nsaids rule

Why?

A

Take aspirin either 30 min prior or 8 hours post NSAIDS

b/c can obstruct access of aspirin to serine and doing its job

27
Q

Heparin binds to what? to inhibit what?

A

Antithrombin III

Inhibits circulating thrombin and factor XA

28
Q

What test should be used with Heparin?

Should be what its normal lvl?

A

PTT

1.5-2.5 fold

29
Q

HITTS Type 2 is Ig__ mediated.

A

Ig-G

30
Q

Reverse Warfarin OD (2 ways)

A

emergency: FFP

otherwise Vit K

31
Q

MoA of Clopiodrel

A

irrev inhibits binding of ADP to its receptors on platelets.