Bleeding disorders Flashcards

1
Q

What history should be taken if a bleeding disorder us suspected?

A

Types of bruising
Severity
Pattern
Congenital vs acquired

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2
Q

What types of bleeding may be reported?

A
Bruising
Epistaxis
Post surgical
Menorrhagia
Post partum haemorrhage
Post trauma
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3
Q

What is the pattern of platelet type bleeding?

A
Mucosal
Epistaxis
Purpura
Menorrhagia
GI
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4
Q

What is the pattern gf coagulation factor bleeding?

A

Articular
Muscle haematoma
CNS

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5
Q

What history should be taken to establish congenital vs acquired?

A

Previous episodes
Age at first event
Previous surgical challenges
Associated history

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6
Q

What is the genetic basis of haemophilia?

A

X linked

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7
Q

What is distinctive about severe haemophilia?

A

Spontaneous bleeding

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8
Q

What are the clinical features of haemophilia?

A
Haemarthrosis- esp in hinge and weight bearing joints
Muscle haematoma
CNS bleeding
Retroperitoneal bleeding
Post surgical bleed
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9
Q

How is haemophilia diagnosed?

A
Clinical
Genetic analysis
Prolonged APTT
Normal prothrombin time
Reduced factor VIII or IX
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10
Q

What is the pharm treatment of haemophilia?

A

Coagulation factor replacement- given as prophylaxis in severe
Demopressin
Tranexemic acid
Analgesia

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11
Q

What is the general management of haemophilia?

A

Splints

Physio

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12
Q

What is the surgical management of haemophilia?

A

Synovectomy

Joint replacement

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13
Q

What are the complications of haemophilia?

A

Synovitis
Chronic haemophilic arthropathy
neuromuscular compression
Other sequelae of bleeding- stroke

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14
Q

What are the complications of demopressin?

A

MI

Hyponatraemia in babies

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15
Q

What is common in those recieving factor VIII?

A

Development of inhibitors

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16
Q

What are the types of von Willebrand disease?

A

Type 1= quantitive deficiency
Type 2= mutation causing poor function
Type 3= complete deficiency

17
Q

What is the genetic basis of von Willebrand disease?

A

Autosomal

18
Q

What is the treatment of von Willebrand?

A

vWF concentrate or demopressin
Tranexemic acid
OCP for women- prevent menorrhagia

19
Q

What are the 2 types of causes of thrombocytopenia?

A

Decreased production

Increased consumption

20
Q

What are the causes of decreased production thrombocytopenia?

A

Marrow failure
Aplasia
Infiltration

21
Q

What are the causes of increased consumption thrombocytopenia?

A

Immune ITP
Non immune DIC
Hypersplenism

22
Q

What are the clinical features of thrombocytopenia?

A

Petechia
Ecchymosis
Mucosal bleeding
Rarely CNS bleeding

23
Q

What is ITP associated with?

A

Infection
Lymphoma
Collagenosis
Drug induced

24
Q

What is the treatment of ITP?

A

Steroids
IV IgG
Splenectomy
Thrombopoietin analogues

25
Q

Why does liver failure cause bleeding?

A

Failure to produce factors I, II, V, VII, VIII, IX, X, XI

26
Q

what are the clinical features of bleeding caused by liver failure?

A

Bleeding from structural lesions

27
Q

how is bleeding due to liver failure diagnosed?

A

Prolonged prothrombin time and APTT

Reduced fibrinogen

28
Q

What are the acquired causes of bleeding disorders?

A
Thrombocytopenia
Liver failure
Renal failure
DIC
Drugs
29
Q

What drugs can cause bleeding disorders?

A

Warfarin
Heparin
Aspirin
Clopidogrel etc

30
Q

What causes haemorrhage disease of the newborn?

A

Vit K deficiency