Untitled Deck Flashcards

1
Q

What are the main antifibrinolytic agents used in coagulation support?

A

Tranexamic acid.

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2
Q

How is warfarin reversal achieved?

A

With vitamin K or Octaplex (factors II, VII, IX, X).

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3
Q

What is used in patients with inhibitors during bleeding?

A

Factor VIIa or increased doses of factor VIII to overpower antibodies. FEIBA or Octaplex can also be used.

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4
Q

What is disseminated intravascular coagulation (DIC)?

A

An acquired thrombophilia where widespread clotting and bleeding occur.

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5
Q

Why do many elderly patients not switch from warfarin to DOACs?

A

Warfarin is cheaper but requires complex management, whereas DOACs are simpler but more expensive.

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6
Q

What is haemarthrosis?

A

Bleeding into joints, often seen in untreated haemophiliacs, leading to joint fixation.

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7
Q

How much factor level is required to maintain hemostasis?

A

At least 25% of factor levels, but up to 100% is targeted before surgery to reduce transfusion needs.

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8
Q

What is desmopressin (DDAVP) and how does it work?

A

Desmopressin increases von Willebrand factor (vWF) and factor VIII levels by 2-6 times. It is cheap, safe, and widely available.

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9
Q

What is the half-life of desmopressin (DDAVP) and its implication in surgery?

A

12 hours. If surgery is delayed beyond 24 hours, factor levels return to baseline.

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10
Q

What is the role of tranexamic acid in coagulation?

A

It is an antifibrinolytic that prevents clot breakdown by inhibiting the conversion of plasminogen to plasmin.

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11
Q

How are patients with von Willebrand disease (vWD) treated?

A

Type 1: Desmopressin or tranexamic acid mouthwash.

Type 2: Treated with vWF concentrates like Willate.

Type 3: Requires vWF concentrates; DDAVP is ineffective.

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12
Q

What is the preferred method for managing warfarin reversal in severe cases (INR > 20)?

A

Octaplex is preferred over plasma to avoid adding fuel to the fire.

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13
Q

What factors are included in Octaplex?

A

Factors II, VII, IX, X, as well as proteins C and S.

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14
Q

Why is Hepatitis B considered particularly resilient?

A

It is highly durable and survives in various conditions.

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15
Q

What led to significant HIV and Hepatitis C transmission in haemophiliacs in the past?

A

Contaminated plasma-derived products before the advent of viral inactivation methods.

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16
Q

How are plasma-derived products inactivated to ensure safety?

A

Through methods such as solvent detergent treatment, dry heat, and pasteurization.

17
Q

What is the Ristocetin cofactor assay used for?

A

To test if vWF is effectively binding platelets.

18
Q

How is cryoprecipitate discovered and what does it contain?

A

Discovered accidentally; it contains fibrinogen, vWF, and factor VIII.

19
Q

What are the advantages of recombinant factors over plasma-derived products?

A

Recombinant factors are safer, with no risk of viral transmission, although human-derived products are cheaper.

20
Q

What is the role of FEIBA in haemophilia management?

A

It is used to bypass inhibitors by providing activated clotting factors.

21
Q

How is tranexamic acid used in dental procedures for coagulation disorders?

A

It can be applied as a mouthwash every 6 hours or incorporated into tissue packs to control bleeding.

22
Q

What makes vWF a ‘sticky’ protein?

A

It binds platelets and factor VIII, playing a key role in clot formation.

23
Q

Why are human-derived products still used in some countries?

A

They are cheaper, although they are now viral-inactivated to ensure safety.

24
Q

What cells are used to produce recombinant factor VIII?

A

Chinese hamster ovary cells, as they allow proper glycosylation required for function.

25
Q

What is the treatment of choice for haemophiliacs with intracranial hemorrhage?

A

Rapid infusion of factor concentrates to restore adequate clotting factor levels.

26
Q

What is the role of monoclonal antibody columns in coagulation product preparation?

A

They are used to purify specific clotting factors, such as factor VIII, enhancing product safety and efficacy.

27
Q

Why is factor VIII often administered with von Willebrand factor (vWF)?

A

vWF stabilizes factor VIII in circulation, enhancing its half-life and efficacy in preventing bleeds.

28
Q

What is the effect of prosthetic joints on haemophilia treatment?

A

Prosthetic joints can improve mobility for haemophiliacs with chronic joint damage caused by repeated bleeds.

29
Q

What is the primary cause of haemarthrosis in children with haemophilia?

A

Repeated bleeding into joints due to low clotting factor levels.

30
Q

What happens if surgery for a haemophiliac is delayed beyond 24 hours?

A

Factor levels, increased by treatments like DDAVP, return to baseline, necessitating repeated dosing.

31
Q

How is haemophilia treatment different for ‘low responders’ with inhibitors?

A

Increased doses of factor VIII can be used to overpower antibodies, or alternative agents like FEIBA are employed.

32
Q

What is the primary advantage of recombinant products over plasma-derived products?

A

They eliminate the risk of viral contamination.

33
Q

What is the impact of delayed recognition of moderate haemophilia?

A

Patients may only be diagnosed during events like dental extractions, leading to unanticipated bleeding complications.

34
Q

Why is octaplex used in Ireland for coagulation support?

A

It is a cost-effective option that provides multiple clotting factors along with proteins C and S.

35
Q

How do antifibrinolytics support haemostasis?

A

By preventing the breakdown of clots, thus stabilizing formed thrombi in bleeding patients.