(MHD) Clin. Eval of Bleeding Patient Flashcards

1
Q

Bleeding into mucosal tissues is associated with what type of bleeding? (immediate or delayed?)

What does it indicate?

A

Immediate bleeding. It indicates an issues with formation of the initial clot

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2
Q

Bleeding into deep tissue is associated with what type of bleeding? (immediate or delayed?)

What does it indicate?

A

Delayed

It is associated with the formation of an initial clot, but missing the factors needed to solidify and reinforce the clot.

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3
Q

Menorrhagia

A

Period in which more than 80ml of blood is loss/cycle

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4
Q

What can we learn/questions can we answer from the CBC? (4)

A
  1. Platelet quantity
  2. Is there involvement of the other cell lines?
  3. What do the platelets look like?
  4. Is there evidence of a systemic disorder?
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5
Q

What can we learn/questions can we answer from the PT/aPTT?

A
  1. Qualitative and quantitative defects in platelets (but won’t differentiate)
  2. Sometimes differentiates the clotting factor which is the culprit
  3. Are there abnormalities in the coagulation system?
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6
Q

What are the differential diagnoses associated with thrombocytopenia? (9)

A
  1. Idiopathic Thrombocytopenic Purpura (ITP)
  2. Gestastional thrombocytopenia
  3. Drug-induced thrombocytopenia
  4. Viral infections (HIV, Rubella, EBV)
  5. Hypersplenism
  6. Narrow infiltration by neoplasia; CLL
  7. Microangiopathic Thrombocytopenia (i.e. HUS-TTP)
  8. DIC
  9. Lupus
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7
Q

Name the inherited platelet dysfunction diseases (2)

A
  1. Glanzmann Thrombasthenia
  2. Bernard-Soulier Syndrome
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8
Q

Name the disorder of platelet activation?

A

vWD

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9
Q

List the acquired causes of abnormalities in clotting factors (5)

A
  1. Vitamin K def
  2. Acquired Inhibitors of clotting factors
  3. Failure of synthetic function of the liver
  4. Drugs-induced
  5. DIC
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10
Q

List the inherited abnormalities in clotting factors (4)

A
  1. Deficiency of factor VIII (Hem A)
  2. Deficiency of IX (Hem. B)
  3. Mutations leading to missense/early stop/ failure to bind
  4. Secondary deficiency of VII
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11
Q

Relationship between circulating vWF and Factor VIII. What issues can come as a result?

A

Circulating vWF carries factor VIII, so if you have low levels of vWF, you will also see low levels of factor VIII, leading to potential issues with the coagulation cascade.

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12
Q

What test tells us if the patient has any vWF?

A

Von Willebrand factor antigen (aka Factor 8 antigen)

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13
Q

What test tells us the vWF that we have works?

A

Vin Willebrand factor Ristocetin cofactor activity test

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14
Q

What test tells us if factor VIII has been affected in a vWF issue?

A

Factor VIII clotting activity test

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15
Q

What test tells us the structure of the vWF?

A

Von Willebrand Multimers (this is a follow up test and not used for initial diagnosis)

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16
Q

Key testing differences between Hem A and vWD

A

Ristocetin activity: Hem A: NL/ vWD: LOW

vWF:Ag: Hem A: NL/ vWD: LOW/NL

17
Q

Function of DDAVP

A

Treatment for vWF deficiency

Therapy which takes storage vWF and moves it to endothelial surface, allowing clots to be produced.

18
Q

Prolonged PT points to what diseases/issues?

A
  1. Liver Disease
  2. DIC (Early Stage)
  3. Warfarin
  4. Factor VII deficiency
19
Q

Prolonged PTT points to what diseases/issues?

A
  1. Heparin
  2. Factors VIII, Ix, XI and XII
  3. Lupus Anticoagulant
20
Q

Prolonged PT and PTT point you towards what diseases/issues?

A
  1. Heparin/Warfarin High-dose
  2. Dilution
  3. Vit K Deficiency
  4. Liver Disease
  5. Paraproteins
21
Q

What are the (2) umbrella reasons for elevated PT or PTT? What test helps us differentiate between the 2?

A
  1. Deficiency of clotting factor
  2. Inhibitor of clotting factor function

Mixing study is used to differentiate between the 2

22
Q

Describe a Mixing Study

A

Used to determine whether there is a deficiency of clotting factors or an inhibitor.

You mix normal plasma with your patient’s plasma. If the problem is deficiency, mixing with normal plasma will lead to clot formation.

23
Q

What is one of the most common inhibitors of coagulative factors

A

Lupus anticoagulant

24
Q

FFP

A

Fresh Frozen Plasma

Given as treatment to low coagulation factors