Blood Disorders (Exam III) Marcus's Cards Flashcards

1
Q

What are the S/S of vWF disorder?

A
  • Easy bruising
  • epistaxis
  • menorrhagia
  • Patients usually unaware until surgery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What would lab values be for someone with vWF deficiency?

A
  • Normal PT & aPTT
  • Bleeding time is prolonged
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the treatments for vWF deficiency?

A
  • Desmopressin
  • Cryoprecipitate
  • Factor VIII
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How does DDAVP work in regards to treatment of vWF?

A
  • A synthetic analogue of vasopressin
  • Stimulates vWF release from endothelial cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the dose for DDAVP?

A

0.3 mcg/kg-0.8mcg/kg in 50 mL over 15-20 mins (Do not bolus)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the onset & duration of DDAVP?

A
  • Onset: 30mins
  • Duration: 6-8hrs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are side effects of DDAVP?

A
  • HA
  • Stupor
  • hypotension
  • tachycardia
  • hyponatremia
  • water intoxication (excessive water retention)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the most major side effect of DDAVP?

A

Hyponatremia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Someone that gets DDAVP needs to be on what?

A

Fluid restriction 4-6hrs before & after DDAVP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

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

A

Cryoprecipitate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

1 unit of Cryo raises the ____ level by ___?

A

Fibrinogen by 50 mg/dL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is a potential risk factor with cryoprecipitate?

A

Increased risk of infection (not submitted to viral attenuation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is Factor VIII concentrate made of?

A
  • Prepared from pool of plasma from a large number of donors
  • Undergoes viral attenuation, still high risk for infection
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

When is Factor VIII given?

A

Preop or intraop

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

When should DDAVP be given prior to surgery?

A

60mins before Sx

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What blood product poses an increase risk for infection? Why?

A
  • Cryoprecipitate
  • Not sent for viral attenuation
17
Q

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

A
  • Spinal and epidural hematoma
  • Nerve compression
18
Q

What four things to avoid?

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
19
Q

How does heparin work?

A
  • Thrombin inhibition
  • Antithrombin III activation
20
Q

What labs are monitored with heparin?

A

PTT &/or ACT

21
Q

What is the mechanism of action of Coumadin?

A

Inhibition of vitamin K-dependent factors.

22
Q

Which factors are vitamin-K dependent?

A

II, VII, IX & X

23
Q

What is the onset for Vitamin K administration?

24
Q

3

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 —> causing clot lysis

26
Q

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

A

Inhibit conversion of plasminogen to plasmin

27
Q

What is the best way to treat DIC?

A

Treat the underlying cause

28
Q

What will labs show for someone in DIC?

A
  • ↓Platelet count
  • Prolonged PT, PTT & TT.
  • ↑ fibrin degradation products
29
Q

When is antifibrinolytic therapy given to someone in DIC?

A

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

30
Q

Prothrombin disorder

What is factor V Leiden?

A
  • Protein for clotting.
  • When enough fibrin has been made, activated protein C inactivates factor V thus stopping clot growth*.
31
Q

What is Factor V Leiden disease?

A
  • Genetic mutation in factor V
  • Abnormal version of factor V that is resistant to activated protein C —> excessive fibrin and clotting
32
Q

Factor V Leiden is usually silent until?

A
  • Pregnancy
  • First presention of DVT, repeated late-stage abortions/fetal losses occurs
33
Q

What anticoagulant medications could someone with Factor V Leiden be put on?

A
  • Warfarin
  • LMWH & unfractionated heparin
34
Q

What is the hallmark sign of HIT?

A

Plt count <100,000

thrombocytopenia

35
Q

What is HIT?

A
  • An autoimmune-mediated drug reaction
  • HIT activates platelets –> causes clotting –> depletes platelet count
36
Q

Non-heparin anticoagulants used after HIT?

A

Direct-thrombin inhibitors
* Agratroban
* Bivalirudin

Factor Xa Inhibitor
* Fondaparinaux in place of lovenox

37
Q

Diagnosis of HIT should be entertained when?

A
  • For any patient experiencing thrombosis or thrombocytopenia during/after heparin administration