Haemolysis Flashcards

(46 cards)

1
Q

What is Bleeding time?

A

Measure of the time from the appearance of the first drop of blood until the cessation of bleeding.

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2
Q

What tests can you use for coagulation time and how do you carry them out?

A

Clotting time on a watch glass, Clotting time in plastic syringe, Clotting time in activated clotting time tube

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3
Q

What is coagulation in an ACT test tube?

A

Si02 with fresh blood to check the coagulation without the contact factor (Hagemann factor) at 37c.

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4
Q

How long does each test take to coagulate?

A

3 minutes is normal

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5
Q

What are the causes of thrombocytopenia?

A

Decrecreased production of thrombocytes in the bone marrow, increased utilization of thrombocytes, (DIC), increased destruction of thrombocytes automimmune thrombocytopenia (AITP), increased sequestration of thrombocytes

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6
Q

Which factors are dependent on vitamin K?

A

Proconvertin (Factor 7), Christmas (Factor 9), Stuart Prower (Factor 10), and Prothrombin (Factor 2)

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7
Q

What is prothrombin time?

A

Gives information about the function of the extrinsic pathway because the coagulation cascade is triggered by adding tissue factor.

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8
Q

How long is a normal PT?

A

10-15 seconds

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9
Q

What is APTT?

A

Activated partial thromboplastin time – gives information on the function of the intrinsic pathway through the provision of surface activation

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10
Q

How long is a normal APTT?

A

How long is a normal APTT?

20-30 seconds

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11
Q

What is the general platelet count?

A

200-800 x 10 to the 9

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12
Q

What is DIC?

A

Disseminated intravascular coagulopathy. Secondary problem where microthrombus formation and fibrinolysis are present at many different places in the body simultaneously because of severe tissue damage or necrosis

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13
Q

Something about Von Willebrands disease, basically wanted to know which clotting factor was messed up.

A

Factor VIII is deficient

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14
Q

What are the major groups of haemostasis disorders?

A

Vasculopathy, Thrombocytopathy, Coagulopathy

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15
Q

What tests were used to investigate coagulopathies?

A

Bleeding time, (buccal mucosal bleeding time test,) clotting time, clotting time on different
surfaces, clot retraction time.

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16
Q

What tests investigate platelet count (can’t remember the exact phrasing of her question there but its
pretty much what she wanted.)

A

blood smear test, automatic cell counters, Burker chamber count

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17
Q

What is the clot retraction test?

A

The measure of the decrease in clot size with a contractile protein called thrombostenin. Slower or
no contraction happening is a sign of thrombocytopathy

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18
Q

In dicumarol posioning what is increased?

A

The PT and APTT is increased

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19
Q

what was increased in Haemophilia type A

20
Q

How can you count platelets in a sample

A

Burker chamber (haemocytometer), blood smear, automatic cell counters.

21
Q

Which hemostatic disorder lead to more sever clinical signs, thrombocytpathys or coagulopathys?

A

Thrombocytopathy as there is no connection between thrombocyte-thrombus

22
Q

Shortest coagulation factor life time?

A

(7) 3 minutes with the CT in ACT

23
Q

Which factor is involved in measuring thrombin time

24
Q

Time until the first fibrin strain

25
What does silicon dioxide influence in ACT
The contact factor Hagemann factor
26
How does dicoumarol anticoagulant work
It is the competitive antagonist of vitamin k which is responsible for the gamma carboxylation of proconvertin(Factor 7) Christmas factor (Factor 9), Stuart Prower (Factor 10) and he Prothrombin (Factor 2). It removes Ca2+ from these factors so they cannot activate
27
Clot retraction test
Measure of the effectiveness of thrombostenin for reducing the clot via the release of serum.
28
Platelet count normal number
200-800 x 10 to the 9 | Platelet count formula for smear (20*10^9/l)
29
Which anticoagulant used for platelet count examination
EDTA, K2, Na2-
30
Dicumarol toxicosis effect on PT an APTT
Increases quickly on PT then gradually on APTT
31
Ratio of anticoagulant (citrate:blood)
1:9
32
Thrombocytopenia, name 3 causes
Decreased production of thrombocytes in the bone marrow, increased utilization of thrombocytes DIC (disseminated intravascular coagulopathy), increased loss of thrombocytes: subacute/chronic bleeding
33
How does sodium citrate inhibit coagulation
Citrate prevents coagulation by binding calcium ions
34
DIC
Disseminated intravascular coagulopathy (DIC) microthrombus formation and fibrinolysis are present at many different locations in the body due to necrosis or severe tissue damage.
35
BMBT time
3-5 minutes
36
How is BMBT performed
0.5 cm incision on the skin of the inner part of the external ear or the buccal mucosal surface. Wipe away excess blood under the incision until the cessation of bleeding
37
What level of platelets are considered a clinical bleeding disorder
Above 50x10 to the 9/Liter
38
Function of platelets
They bind thrombocytes along with fibrin to form clots in damaged blood vessels
39
What do factors need for their synthesis
Calcium ion
40
Which factor is 13 and what is its function
Von Willebrand Factor is responsible for plately adhesion and aggregation and anti haemophylic factor.
41
What factor are in extrinsic pathway
3, 7, 5, 10, 2, 13
42
Which factors can bind to Calcium
Proconvertin (Factor 7), Christmas (Factor 9), stuart prower (Factor 10), Prothrombin (Factor 2)
43
What molecule can activate factor 12 (hagemann)
Free collagen fibres, kininogen, and kallikrein
44
What is the glue that sticks the thrombocytes to each other
Polymerized fibrin network
45
What factor initiates the intrinsic pathway
Hagemann factor Factor 12
46
What factor is calcium
Factor 4