bleeding disorders Flashcards

1
Q

causes of DIC

A

sepsis, obstetric emergencies, malignancies, hypovolaemic shock

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
1
Q

what are DICs

A

conditions that inappropriately activate the clotting cascade

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what causes the bruising and purpura and generalised bleeding in DIC

A

clotting factor consumption

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

blood film in DIC

A

fragmented red blood cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

bloods in DIC

A

PT, APTT are very prolonged and fibrinogen is markedly reduced
high levels of D-dimer
severe thrombocytopenia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

haemophilia has what inheritance

A

X linked recessive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what haemophilia is more common

A

A

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Haemophilia bleeding mostly occurs into

A

joints

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

is there an abnormality of primary haemostats in haemophilia

A

No

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

bloods for haemophilia

A

isolated prolonged. APTT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

complication of clotting factor infusions

A

your body becomes resistant

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what drug can be used for minor bleeds in haemophilia

A

desmopressin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

VWF gene is on chromosome

A

12

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

reduced VWF in VW disease leads to what factor deficiency

A

8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

immune thrombocytoopenic purpura is when there is a decreased number of circulating

A

platelets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

immune thrombocytopenia purpura is caused by what hypersensitivity reaction

A

2

16
Q

how does immune thrombocytopenia purpura tend to present

A

In a child under 10 and often there is a history of a recent viral illness

17
Q

there is an isolated thrombocytopenia in what

A

immune thrombocytopenia purple

18
Q

mx for ITP

A

usually non but can give prednisolone, IV immunoglobulins

19
Q

Thrombotic thrombocytopenic purpura due to a deificnecy of

A

metalloproteinase ADAMTS13

20
Q

classic pentad in:- Fever
- Microangiopathic haemolytic anaemia (MAHA)
- Thrombocytopaenic purpura
- CNS involvement: headache, confusion, seizures
- AKI

A

TTP

21
Q

blood film can show what in TTP

A

schistocytes

22
Q

difference between TTP and DIC

A

coagulation screen will be normal in TTP, whereas it will be prolonged in DIC with low plasma fibrinogen

23
Q

what assay is diagnostic in TTP

A

low ADAMST13

24
Q

what does fresh frozen plasma do

A

replace coagulation factors

25
Q

what does cryoprecipitate replace

A

fibrinogen

26
Q

in what system are platelets not activated

A

venous system

27
Q

what is first line for DVT

A

apixaban or rivaroxaban

28
Q

options for secondary prevention of DVT

A

warfarin, DOAC, LMWH

29
Q

aetiology for what:- Factor V Leiden
- Prothrombin 20210 mutation
- Antithrombin deficiency
- Protein C deficiency
- Protein S deficiency

A

hereditary thrombophilias

30
Q

some examples of when you might suspect herediatary thrombophilias

A

venous thromboses in under 45
recurrent venous thromboses

31
Q

are thromboses arterial or venous in anti phospholipid syndrome

A

both

32
Q

lived reticualris is what ? it can be seen in antiphospholipid syndrome

A

purplish, net like discolouration of the skin

33
Q

at least one positive blood test on 2 occasions at least 12 weeks apart to diagnose anti phospholipid syndrome. the three are

A
  1. anticardiolipin antibodies
  2. anti-β2-GPI antibodies
  3. positive lupus anticoagulant assay