Introduction and overview to haemostasis Flashcards

(49 cards)

1
Q

Define haemostasis

A

arrest of bleeding and maintenance of vascular patency

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2
Q

what are the requirements of haemostasis

A

it is ready at any time and immediate to act
acts at local site of injury
protection against unwanted thrombosis

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3
Q

what are components of a normal haemostatic system

A

primary haemostasis - platelet plug
secondary haemostasis - fibrin clot
fibrinolysis
anticoagulant defences

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4
Q

what kind of disorder do you have if your haematostatic system is underactive

A

bleeding disorder

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5
Q

what kind of disorder do you have if your haematostatic system is overactive

A

clotting disorder

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6
Q

what are megakaryocytes

A

large multinucleate cells found in the bone marrow only

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7
Q

how are platelets formed

A

budding off from megakaryocytes

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8
Q

what are platelets

A

small anucleate rings with a lifespan of 7-10days

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9
Q

how long should a patient stop antiplatelets prior to surgery

A

1 week

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10
Q

what is primary haemostasis

A

formation of platelet plug

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11
Q

is a platelet plug strong

A

no, it is weak

suitable for small injuries but not sufficient in greater damage

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12
Q

explain the process of primary haemostasis

A

Endothelial damage exposes collagen
Platelets and VWF bind to collagen
VWF helps platelets adhere to collagen and other platelets
Secretion of other chemicals help platelet aggregation

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13
Q

what are causes of failure of primary haemostasis

A

vascular: collagen deficiency
platelets: reduced number or function
VWF deficiency

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14
Q

what are symptoms and signs of primary haemostatic failure

A
spontaneous bruising 
senile purpura 
purpura on legs 
mucosal bleeding: nose, conjunctiva, mouth, GI tract, menorrhagia 
intracranial haemorrhage
retinal haemorrhage - fundoscopy
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15
Q

what investigation can be done for primary haemostatic failure

A

platelet count

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16
Q

what is the term for high platelets

A

thrombocytosis

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17
Q

what is the term for low platelets

A

thrombocytopaenia

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18
Q

what is secondary haemostasis

A

formation of fibrin clot

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19
Q

is a fibrin clot strong

A

yes, fibrin strengthens the platelet plug

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20
Q

platelets are full of -ve phospholipids and Ca2+, true or false

21
Q

clotting factors are negatively/positively charged

A

negatively charged

22
Q

explain the process of secondary haemostasis

A

Tissue Factor activates factor 7
this complex activates factors 5+10
these then activate prothrombin to form thrombin
thrombin then converts fibrinogen to fibrin
fibrin is the final product
thrombin also acts in a positive feedback to activate factors 8+9
8+9 also activate factors 5+10
whole process is amplified

23
Q

list the main categories for failure of secondary haemostatic failure

A

single deficiency

multiple deficiencies

24
Q

features of single deficiency in secondary haemostatic failure

A

hereditary
rarer
eg haemophilia

25
which clotting factor is deficient in haemophilia A
factor 8
26
which clotting factor is deficient in haemophilia B
factor 9
27
what is a cause of multiple deficiencies in secondary haemostatic failure
disseminated intravascular coagulation DIC
28
list causes of DIC
``` sepsis cancer ABO incompatibility RTA liver disease ```
29
what is the pathophysiology behind DIC
increase in clot formation leading to widespread ischaemia | paradoxically there is also increased bleeding due to depletion of clotting factors
30
what is fibrinolysis and what is its purpose
break down of fibrin clots to maintain vascular patency occurs when fibrin clot has formed and bleeding has stopped
31
what is the process of fibrinolysis
tPA activates plasminogen into plasmin | plasmin breaks fibrin into FDPs
32
what are d dimers
fibrin degradation products
33
generally, failure of secondary haemostasis has characteristic symptoms, true or false
false
34
what are symptoms of single deficiency secondary haemostatic failure
bleeding into joints and muscles
35
what tests can be done to investigate fibrin clot formation as coagulation screen
prothrombin time PTT | activated partial thromboplastin time APTT
36
what does prothrombin time measure
length of time taken for clot formation via extrinsic pathway
37
prothrombin time measure extrinsic/intrinsic pathway
extrinsic
38
which clotting factors can be tested in prothrombin time
TF/3, 7, 5, 10, PT
39
clotting factors 8+9 are tested in prothrombin time, true or false
FALSE
40
what does activated partial thromboplastin time (APTT) measure
length of time taken for clot formation via intrinsic pathway
41
APTT measure extrinsic/intrinsic pathway
intrinsic
42
which clotting factors are tested in APTT
8, 9, 5, 10, PT
43
if there is a deficiency in factor 7, PT/APTT would be prolonged
PT
44
if there is a deficiency in factor 8, PT/APTT would be prolonged
APTT
45
list some naturally occurring anticoagulants
serine protease inhibitors eg anti thrombin | Protein C + S
46
how does anti thrombin work
inhibits thrombin and so switches off haemostasis
47
how do Protein C+S work
bind to factors 5+8 to switch off coagulation
48
what would occur as a result of antithrombin/Protein C/S deficiency
excess clotting because you cant stop anticoagulation
49
define thrombophilia
increased tendency to forming clots eg DVT, PE, VTE