Blood Flashcards

(44 cards)

1
Q

What is serum?

A

Plasma minus clotting factors

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2
Q

What is plasma?

A

Serum plus clotting factors

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3
Q

Where are all blood cells derived from?

A

Multipotential haemopoietic cell (myeloid or lymphoid)

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4
Q

Which is the universal accepter of blood?

A

AB

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5
Q

Which is the universal donor of blood?

A

O

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6
Q

Rhesus blood group is dependent on?

A

D antigen being present

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7
Q

What % of blood is plasma?

A

55%

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8
Q

Albumin in the range of what?

A

35-50g/l protein

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9
Q

Immunoglobulins amount?

A

15g/l

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10
Q

Fibrinogen amount?

A

3-5g/l

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11
Q

What does iron deficiency anaemia lead to?

A

Macrocytic, pale and small RBC low Haemoglobin

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12
Q

B12 or folate deficiency may lead to what anaemia?

A

Macrocytic or megoblastic

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13
Q

Rh + is common or rare?

A

Common

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14
Q

Rh- is common or rare?

A

rare

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15
Q

haemolytic anaemia could be caused by?

A

Acquired or inherited, is due to destruction of the cells. sickle cell and thallasaemia.

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16
Q

Factor ten does what?

A

Prothrombin to thrombin and then thrombin converts fibrinogen to fibrin

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17
Q

Factor 13 is important in doing what?

A

consolidation of the clot?

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18
Q

Platelets are made by what?

A

megakaryocytes

19
Q

What does injury expose which causes platelet expression?

A

Sub endothelial collagen

20
Q

Platelets bind to what? via GPVI and GP1 and VWF

21
Q

What do platelets release after binding?

A

Thromboxane, and ADP causes further activation through binding P2Y and TP receptors

22
Q

What is major bleeding defined as?

A

more than half a litre

23
Q

what is DIC

A

Disseminated intravascular coagulation is due to sepsis, small clots forming in the microvasculature, clotting factors and platelets used up.

24
Q

Spontaneous bleeding can be caused by

A

factor deficiencey, vit K, or thrombocytopenia.

25
Vitamin K modifies what on platelet membranes
modifies glutamic acid to gamma carboxyglutamic aicd and binds phospholipids via ca2+
26
haemophillia A is a deficiency in what?
Factor 8 (cofactor)
27
haemophillia B is a deficiency in what?
Factor 9 (conversion)
28
most common bleeding disorder is?
Von willebrand
29
Thrombocytopenia
lack of platelets
30
von willebrand factor is produced
Weibel - palade bodies
31
What does VWF do?
Stabilise factor 8 platelet aggregation and platelet adhesion
32
What is virchows triad?
Hypercoaguability, stasis, endothelial injury
33
What can factor 5 leiden lead to?
Risk of DVT resistance to protein C
34
What is protein C?
Inactivates factors 5 and 8 (thrombolitic)
35
Protein s is the cofactor for what?
Protein C
36
Thrombin inhibitors include
melgatran and dabigatran
37
what does heparin do?
helps anti thrombin to inhibit thrombin and factor X
38
A haemoglobin level of less than what in men is indicative of anaemia?
13.5g/l
39
A haemoglobin level of less than what in women is indicative of anaemia?
11g/l
40
Most common cause of anaemia is?
iron deficiency
41
Inherited condition causing hameolytic anaemia affects what part of the cytoskeleton?
alpha and beta spectrin (spherocytosis)
42
Alpha thallasaemia is caused by large what of the chains?
deletion
43
Beta thallasaemia is caused by what of beta chains?
point mutations
44
Sickle cell anaemia is caused by what mutation?
Glu-val