5. Anticoagulant and Inherited Bleeding Flashcards

(35 cards)

1
Q

Contraindications of anticoagulant and inherited bleeding disorders (3)

A

Aspirin
NSAIDs
Antithrombotic medication (anticoagulants, antiplatelets)

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2
Q

Indications for oral anticoagulation (4)

A

AF
DVT
Heart valve disease/ mechanical heart valves
Thrombophilia

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3
Q

Types of oral anticoagulants (4)

A

Coumarins
Indanediones
Direct thrombin inhibitors
Factor Xa inhibitor

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4
Q

Types of wafarin drug interactions (2)

A

Potentiating drugs

Inhibiting drugs

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5
Q

Examples of warfarin potentiating drugs (4)

A

Amiodarone
Antibiotics
Alcohol (with liver disease)
NSAIDs

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6
Q

Examples of warfarin inhibiting drugs (4)

A

Carbamazepine, barbiturates
Cholesystramine
Griseofulvin
Alcohol (without liver disease)

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7
Q

Dangers of warfarin (overdose)

A

Haemorrhage

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8
Q

How do anti platelet drugs affect clotting (2)

A

Inhibiting platelet aggregation

Inhibiting thrombus formation in arterial circulation

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9
Q

Examples of anti platelet medications (8)

A
Low dose aspirin
Clopidogrel
Dipyridamole
Prasugrel and aspirin
Abciximab
Eptifibate and aspirin
Ticagrelor
Tirofaban
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10
Q

Definition of inherited bleeding disorder

A

Acquired defects which affect blood coagulation

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11
Q

What may inherited bleeding disorders affect (3)

A

Coagulation cascade
Platelet number
Platelet function
Combo

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12
Q

Types of rare bleeding disorders (2)

A

Inherited defects of other factors in coagulation pathway (not FVIII, IX, XI)
Inherited defect of platelet number/function

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13
Q

Types of haemophilia (3)

A

Haemophilia A
Haemophilia B
Haemophilia C

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14
Q

Genetics of haemophilia (2)

A

Sex-linked recessive inheritance

Males affected, females carriers

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15
Q

Definition of Haemophilia A

A

FVIII deficiency

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16
Q

Definition of Haemophilia B

A

FIX deficiency

17
Q

Treatment of severe/moderate Haemophilia A

A

Use of recombinant factor VIII

18
Q

Treatment of mild/carriers of Haemophilia A (2)

A

DDAVP

Very mid - oral tanexamic acid

19
Q

Treatment of Haemophilia B (2)

A

No response to DDAVP

Prophylactic cover requires recombinant FIX

20
Q

Definition of von Willebrand disease

A

Deficiency of von Willebrand factor

21
Q

Genetics of von Willebrand disease (2)

A

Autosomal dominant

Both sexes equally affected

22
Q

Types of von Willebrand disease (3)

A
Type 1 (dominant, mild)
Type 2 (dominant, mild)
Type 3 (recessive, severe)
23
Q

Treatment of von WIllebrand disease (2)

A

Majority respond to DDAVP

Very mild cases - oral tranexamic acid

24
Q

LA issues with inherited bleeding disorders (2)

A

IDB, lingual infiltration, post. sup. nerve block

Buccal infiltration, intra-ligamentary, intra-papillary safe

25
Definition of thrombophilia
Acquired condition superimposed on a genetic condition
26
Increased risk of what with thrombophilia
Clot development
27
Types of inherited bleeding syndromes (4)
Protein C deficiency Protein S deficiency Factor V leiden Antithrombin III deficiency
28
How can acquired syndromes be obtained (7)
``` Antiphospholipid syndrome (lupus anticoagulants) Oral contraceptives Surgery Trauma Cancer Pregnancy Immobilisation ```
29
Types of platelet abnormalities (3)
Thrombocytopenia Thrombocythaemia Qualitative disorders (normal platelet number but abnormal function)
30
Definition of thrombocytopenia
Reduced platelet numbers
31
Definition of thrombocythaemia
Increased platelet numbers
32
Types of thrombocytopenia (3)
Idiopathic Drug-related Secondary to lymphoproliferative disorder
33
Types of inherited qualitative disorders (3)
Bernard Soulier syndrome Hermansky Pudlak Glanzmann's thromboasthenia
34
Types of acquired qualitative disorders (4)
Cirrhosis Drugs Alcohol Cardiopulmonary bypass
35
Definition of Haemophilia C
Deficiency of FXI