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 are the treatments for vWF deficiency?

A
  • Desmopressin
  • Cryoprecipitate
  • Factor VIII
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4
Q

How does DDAVP work in regards to treatment of von Willebrand deficiency??

A

Stimulates vWF release from endothelial cells; synthetic analouge of vasopressin

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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: 30 mins
  • Duration: 6-8 hrs
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7
Q

What are side effects of DDAVP?

A
  • HA
  • Stupor
  • Hypotension
  • Tachycardia
  • Hyponatremia
  • Water intoxication (excessive water retention)
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8
Q

What is the most major side effect of DDAVP?

A

Hyponatremia

From dilution

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9
Q

Someone that gets DDAVP needs to be on what?

A

Fluid restriction 4-6hrs before & after DDAVP

Causes thirst which can lead to water intoxication and hyponatremia

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10
Q

At what serum Na+ do you see confusion, restlessness, and widening of QRS?

A

120 mEq/L

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11
Q

What CNS and EKG changes are seen at a serum Na+ of 115 mEq/L?

A
  • CNS: Somnolence and nausea
  • EKG: Elevated ST, widened QRS
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12
Q

What serum Na+ can seizures, coma, and Vtach/Vfib be seen?

A

110 mEq/L

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13
Q

What blood product can be utilized for vWF disease if the patient is unresponsive to DDAVP?
What is its risk?

A
  • Cryoprecipitate
  • Infection risk, not submitted to viral attenuation
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14
Q

1 unit of Cryo raises the ____ level by ___?

A

Fibrinogen by 50 mg/dL

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15
Q

What is Factor VIII concentrate made of?

A
  • Pool of plasma from a large number of donors
  • Contains factor VIII and vWF
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16
Q

When is Factor VIII given?

A

Preop or intraop

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17
Q

When should DDAVP be given prior to surgery?

A

30-60mins before Sx

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18
Q

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

A
  • Hematoma
  • Nerve compression
19
Q

What are the anesthesia considerations for someone with vWF deficiency?

A
  • Avoid trauma (particularly airway)
  • Avoid IM sticks
  • Avoid arterial lines (if feasible)
  • Avoid spinals
20
Q

How does heparin work?

A
  • Thrombin inhibition
  • Antithrombin III activation

ATIII inhibits thromin and factors IX and X

21
Q

What labs are monitored with heparin?

A

PTT and ACT (activated clotting time)

22
Q

What is the mechanism of action of Coumadin?

A

Inhibition of vitamin K-dependent factors (II, VII, IX, X)

23
Q

What is the onset for Vitamin K administration?

24
Q

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

A
  • Prothrombin complex concentrates
  • Factor VIIa
  • FFP
25
Q

What is the mechanism of action for fibrinolytics (UK, streptokinase & tPA)?

A

Convert plasminogen to plasmin, which cleaves fibrin

26
Q

How do tranexamic acid (TXA) and aminocaproic acid work?

A

Inhibit conversion of plasminogen to plasmin

27
Q

Treatment for antiplatelet reversal?

A
  • D/C drugs on time
  • Platelet transfusion
28
Q

Some causes of DIC?

A
  • Trauma
  • Amniotic fluid embolus
  • Malignancy
  • Sepsis
  • Incompatible blood transfusions
29
Q

Patho of DIC?

30
Q

What will labs show for someone in DIC?

A
  • ↓Platelet count
  • Prolonged PT, PTT & TT (thrombin time).
  • ↑ fibrin degradation products
31
Q

What is the best way to treat DIC?
Other treatments?

A
  • Treat the underlying cause
  • Blood component transfusions
32
Q

When is antifibrinolytic therapy given to someone in DIC?

A

Trick question, it shouldn’t. Can lead to catastrophic thrombotic complications

33
Q

What is Factor V Leiden deficiency?

A
  • Genetic mutation of factor V that is resistant to activated protein C
  • Leads to factor V leiden making excess fibrin

Activated Protein C usually inhinits favtor V activity

34
Q

What the symptom for TXA toxicity?

A

Loss of color vision

35
Q

What does Activated Protein C do?

A

Inactivates factor V when enough fibrin has been made.

36
Q

Who is usually tested for Factor V Leiden?

A

Pregnant women. Especially ones with unexplained late stage abortions and DVT

37
Q

What anticoagulant medications could someone with Factor V Leiden be put on?
Why is this good for pregnant woemen?

A
  • Warfarin
  • LMWH & unfractionated heparin
  • Prevents placental thrombosis and leads to better outcomes
38
Q

What is the hallmark sign of HIT?

A

Plt count < 100,000, usually 5-14 days after initial therapy

thrombocytopenia

39
Q

HIT results in ____ activation and potential ____ ?

A

platelet; thrombosis

40
Q

What causes HIT?

A
  • Creation of immune complexes (IgG antibody, platelet factor 4, and heparin)
41
Q

What is heparin replaced with when HIT is diagnosed?

A

Argatroban, lepirudin, bivalirudin (direct-thrombin inhibitors)

42
Q

What is Fondaparinux & when is it used?

A
  • A synthetic Factor Xa inhibitor
  • Used to treat VTE in HIT
43
Q

When do HIT immune complexes clear from the circulation?

A

Typically, within 3 months - should still avoid future heparin exposure