Exam 3 Blood Disorders Flashcards

1
Q

What are the S/S of vWF disorder?

A

Easy bruising
epistaxis
menorrhagia

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2
Q

What would lab values be for someone with vWF deficiency?

A
  • Normal PT & aPTT
  • Bleeding time is prolonged
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3
Q

What is the treatment for vWF deficiency?

A
  • Desmopressin
  • Cryoprecipitate
  • Factor VIII
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4
Q

How does DDAVP work?

A

Stimulates vWF release from endothelial cells

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5
Q

What is the dose for DDAVP?

A

0.3 mcg/kg in 50 mL over 15-20 mins (Do not bolus)

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6
Q

What is the onset & duration of DDAVP?

A
  • Onset in 30mins
  • duration is 6-8hrs
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7
Q

What are side effects of DDAVP?

A
  • HA
  • hypotension
  • tachycardia
  • hyponatremia
  • water intoxication(excessive water retention)
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8
Q

Someone that gets DDAVP needs to be on what?

A

Fluid restriction 4-6hrs before & after DDAVP

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9
Q

1 unit of Cryo raises the ____ level by ___?

A

Fibrinogen by 50 mg/dL

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10
Q

What is a potential risk factor with cryoprecipitate?

A

Increased risk of infection (not submitted to viral attenuation)

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11
Q

What is Factor VIII concentrate made of?

A

Pool of plasma from a large number of donors.

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12
Q

When is Factor VIII given?

A

Preop or intraop

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13
Q

When should DDAVP be given?

A

30-60mins before Sx

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14
Q

Pts with coagulopathies undergoing neuraxial anesthesia are at increased risk for what?

A
  • Hematoma &
  • compression of neurological structures
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15
Q

What are the anesthesia considerations for someone with vWF deficiency?

A
  • Avoid trauma
  • avoid IM sticks
  • avoid arterial lines (if feasible)
  • avoid spinals,
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16
Q

How does heparin work?

A
  • It inhibits thrombin
  • activates antithrombin III
17
Q

What labs are monitored with heparin?

A

PTT &/or ACT

18
Q

What factors are affected by Coumadin?

A

Vitamin K-dependent factors II, VII, IX & X

19
Q

What is the onset for Vitamin K?

A

6-8hrs

20
Q

What can be given to reverse coumadin faster than Vit K?

A
  • Prothrombin complex concentrates
  • Factor VIIa
  • FFP
21
Q

How do UK, streptokinase & tPA act?

A

Convert plasminogen to plasmin, which cleaves fibrin

22
Q

How do TXA, aminocaproic acid & aprotinin work?

A

Inhibit conversion of plasminogen to plasmin

23
Q

What will labs show for someone in DIC?

A
  • Reduced Plt.
  • Prolonged PT, PTT & TT.
  • Elevated fibrin degradation products
24
Q

When is antifibrinolytic therapy given to someone in DIC?

A

It shouldn’t, it can lead to catastrophic thrombotic complications

25
Q

What is Factor V Leiden?

A
  • Genetic mutation that leads to increased fibrin production.
  • Activated protein C cannot stop factor V
26
Q

What does Activated Protein C do?

A

Inactivates factor V when enough fibrin has been made.

27
Q

Who is usually tested for Factor V Leiden?

A

Pregnant women. Especially ones with unexplained late stage abortions

28
Q

What anticoags could someone with Factor V Leiden be put on?

A
  • Warfarin
  • LMWH & unfractionated heparin
29
Q

What is the hallmark sign of HIT?

A

Plt count <100,000

30
Q

HIT results in ____ activation and potential____?

A
  • Platelet activation
  • venous & arterial thrombosis
31
Q

What is heparin replaced with when HIT is identified?

A

Agratroban or bivalirudin

32
Q

What is Fonaparinaux & when is it used?

A
  • A synthetic Factor Xa inhibitor
  • used to treat VTE in HIT