Bleeding Disorders Flashcards

(52 cards)

1
Q

why are your blood vessels less efficient as you age?

A

lose collagen more easily

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2
Q

causes of vessel wall problems that affect platelet plug formation?

A
steroids
ageing
vasculitis eg HSP (antibodies stick to vessel wall)
vitamin C deficiency
inherited eg marfans
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3
Q

why can aspirin cause failure of platelet plug formation?

A

it is an antiplatelet so causes a reduced number

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4
Q

VW disease is more commonly presented in women/men

A

women

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5
Q

main clinical sign of thrombocytopenia

A

petechial rash in the lower limbs

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6
Q

thromocytopenia is more commonly hereditary/acquired

A

acquired

autoimmune is most common

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7
Q

causes of platelet destruction in thrombocytopenia

A

coagulopathy eg DIC
ITP
hypersplenism

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8
Q

what is ITP?

A

making antibodies against your own platelets

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9
Q

1st line Tx ITP

A

prednisolone

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10
Q

platelets last for _ days

A

7

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11
Q

why do you get hypersplenism in portal HT

A

blood backs up from the liver and diverts to the spleen

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12
Q

is acquired or hereditary VWF disease more common?

A

hereditary

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13
Q

inheritance for hereditary VWF disease?

A

AD

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14
Q

commonest cause of primary haemostatic failure

A

thrombocytopenia

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15
Q

multiple clotting factor deficiencies are generally acquired/hereditary

A

acquired

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16
Q

4 clotting factors need vitamin K activated to form, what are they?

A

2
7
9
10

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17
Q

what step do the vitamin K dependent CFs need and why?

A

carboxylation

makes them negative

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18
Q

causes of multiple factor deficiencies?

A

warfarin therapy
liver failure
coagulopathy eg DIC

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19
Q

why does warfarin therapy cause CF deficiency?

A

reduces vit K levels which is required for some CF formation

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20
Q

what does vitamin K need to be absorbed?

A

bile salts

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21
Q

where is vit K absorbed?

A

jejeunum

ileum

22
Q

why can obstructive jaundice cause Vit K deficiency

A

gallstones block bile duct = reduced bile salt release = vit k deficiency

23
Q

causes of reduced vit k?

A
poor diet
malabsorption
obstructive jaundice
vit k antagonists eg warfarin
haemorrhagic disease of newborn
24
Q

define DIC

A

excessive activation of the haemostatic system (primary, secondary, fibrinolysis)

25
pathophysiology of DIC
TF expressed -> clotting -> more damage -> more clotting -> thrombus -> overuse of clotting factors = massive bleeding
26
screening test for extrinsic pathway (TF)?
PT | play tennis - outside
27
screening test for intrinsic pathway (8 etc)?
APTT | play table tennis - inside
28
if PT and PTT are low, where is the problem?
problem with 5, 10 or | multiple clotting factor deficiency
29
how are fibrin degradation products measured?
D dimers
30
high D dimers means..
using up clotting fibres to cause fibrinolysis eg in DIC
31
causes of DIC
sepsis eg meningitis/gram -ve obstetric emergencies malignancy hypovolaemic shock
32
what obstetric emergencies cause DIC and why?
placental abruption infarction from PET triggers TF release, inducing DIC
33
Tx DIC
get a senior treat cause eg antibiotics/delivery of placenta REPLACE- platelets/plasma/fibrinogen transfusions
34
FFP can be used to replace what?
blood clotting factors | CFs are present in plasma
35
cryoprecipitate is good for replacing what?
fibrinogen (to make fibrin)
36
inheritance of haemophilia
X linked so only affects boys
37
where does bleeding most commonly present in haemophiliacs?
1. ankle joint 2. knee joint 3. elbow joint
38
haemophilia A/B is more common
A
39
clinical features of haemophilia
haemarthrosis recurrent soft tissue bleeds bleeding after surgery/dental extractions
40
complications of haemophilia?
iron inflames the synovium from haemarthrosis and causes neovascularisation of new vessels which are prone to bleeding
41
haemophilia is a disruption of primary haemostasis T or F
F, secondary haemostasis as cant make factor 8/9 to form fibrin
42
what screening test will be abnormal in haemophilia?
APTT
43
medical term for a normal bruise
purpura
44
people with thrombocytopenia get a __ rash
petechial
45
thrombocytopenia means...
low platelets
46
what initiates the extrinsic pathway
tissue thromboplastin
47
what initiates the intrinsic pathway
contact activators
48
how is warfarin screened and why?
PT as factor 7 is most sensitive
49
how is heparin screened and why?
aPTT
50
VWF is carried around on...
factor 8
51
what age does VWF disease present?
adulthood
52
ideal INR?
2-3