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?

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
Why does liver failure cause bleeding?
Failure to produce factors I, II, V, VII, VIII, IX, X, XI
26
what are the clinical features of bleeding caused by liver failure?
Bleeding from structural lesions
27
how is bleeding due to liver failure diagnosed?
Prolonged prothrombin time and APTT | Reduced fibrinogen
28
What are the acquired causes of bleeding disorders?
``` Thrombocytopenia Liver failure Renal failure DIC Drugs ```
29
What drugs can cause bleeding disorders?
Warfarin Heparin Aspirin Clopidogrel etc
30
What causes haemorrhage disease of the newborn?
Vit K deficiency