3. Blood (2) Flashcards

1
Q

Haemostasis:

A

prevention of blood loss/stopping blood

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2
Q

If a vessel is severed, haemostasis is achieved by:

A
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3
Q
  • Rupture of vessel —-> wall of vessel contracts, sticks
    together
  • Contraction results from: (3)
A
  • nervous reflexes initiated by pain
  • local smooth muscle spasm (main factor)
  • local humoral factors from traumatized tissues and blood platelets (Thromboxane A2)
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4
Q
  • Smaller vessels: platelets mainly responsible for
    vasoconstriction by releasing _______ _____ and
    forming a “plug”
  • Spasm lasts several hours —-> time to form platelet plug and _____ clot.
A

Thromboxane
fibrin

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5
Q

What do they contain? (6)

A
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6
Q

What forms part of the platelet membrane? (3)

A
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7
Q

Dead platelets are removed by macrophages, particularly in the ______.

A

spleen

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8
Q

What is the process of the Formation of the platelet plug?

A
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9
Q

Platelets are also activated by: (4)

A
  • thromboxane A2
  • ADP
  • serotonin
  • thrombin
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10
Q

What are the features of activated platelets? (6)

A
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11
Q

What is on the surface of activated platelets? (2)

A
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12
Q

What are the platelet-limiting factors and anti-platelet
pharmaceuticals?

A
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13
Q

What are the multiple injuries of micro-vessels?

A
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14
Q

What is blood coagulation?

A

Blood coagulation = Secondary Haemostasis

  • Coagulation = transformation of blood from a liquid to a semi-solid, gel state = clot
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15
Q

What is blood coagulation initiated by? (3)

A
  • extravascular cells
  • platelets
  • damaged vessel walls
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16
Q

What is the ultimate effect of blood coagulation?

A

conversion of fibrinogen (soluble plasma
protein) to fibrin (insoluble fibres) = clot

Fibrin clot adheres to the damaged vessel
surface and platelet plug, traps blood cells,
fills the breach and blocks the vessel (~20
minutes).

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17
Q

What are the clotting factors?

A
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18
Q

All clotting factors, except tissue factor, are produced by the _____ and are present in the blood as inactive precursors (______)

A

liver
(zymogens)

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19
Q

When activated, factors IIa (thrombin), VIIa, IXa, Xa, XIa and XIIa are:

A

proteolytic enzymes that activate other clotting
factors, by cutting the proteins

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20
Q

Four factors, II, VII, IX and X, can only be produced if
______ ____ is available in the liver.

A

Vitamin K

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21
Q
  • Factor XIIIa is also an enzyme, but it _____-_____ fibrin.
A

cross-links

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22
Q

What is fibrinogen?

A

Fibrinogen (FI) is not an enzyme or a co-factor. When the
fibrinogen protein is cut by thrombin (FIIa) it becomes
insoluble and forms fibres, called fibrin, which is the clot.

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23
Q

Five clotting factors VIIa, IXa, Xa, XIa and XIIIa
require _____ as a cofactor. (Blocking ____ prevents
coagulation in blood collection tubes.)

A

Ca2+

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24
Q

Two protease clotting factors, IXa and Xa require
platelet _________ for full activity.

A

Phospholipid

25
Q
  • Three protease clotting factors VIIa, Xa and IXa require
    clotting “________” proteins.
A

“co-factor”

26
Q

The cofactor proteins are, respectively, _____ ____ (TF,
FIII —-> TF/FVIIa), FVa (FVa/FXa) and FVIIIa
(FVIIIa/FIXa).

A

tissue factor

27
Q

Clotting proteins are inactive in plasma to avoid ______________ clots and tissue factor is absent.

A

Spontaneous

28
Q

What is the general coagulation sequence?

A
29
Q
  • 3 different coagulation pathways form fibrin, 1 physiological, 2 “biochemical”:
A
30
Q

What is the process of cell-based coagulation? (3)

A
31
Q

Fibrin Formation and Crosslinking: (4)

A
32
Q

Once the clot is formed: (2)

A
33
Q

Platelets secrete growth factors
- Fibroblast cells grow around and into the clot
- ______ tissue forms (1-2 weeks)
- Fibroblasts become _______ cells
- Clot is removed (_______)
Clot Retraction and Fibroblast Invasion

A

Scar
endothelial
fibrinolysis

34
Q

Fibrinolysis and Dissolution of the Clot:

A
35
Q

Vessel injury —> blood oozes out of the vessel. To stop this:

A
36
Q

Biochemical (laboratory) measurement of clotting:
Primary haemostasis:
Secondary hemostasis: (3)

A

—> Bleeding time

Extrinsic pathway —-> Prothrombin Time (PT)
Intrinsic pathway —> Partial Thromboplastin Time (PTT)
also —> Whole blood clotting time

37
Q

Bleeding Time Test Measures Platelet Function:

A
38
Q

Prothrombin Time (PT) test – Extrinsic Pathway, what must be added to the blood?

A
39
Q

Explain the Prothrombin Time (PT) test – Extrinsic Pathway?

A
40
Q
  • Blood is collected into citrate or EDTA tube (to chelate Ca2+). Removal of Ca2+ prevents coagulation in blood collection tube.
  • Blood is _______ to separate the plasma.
  • Plasma is mixed with Ca2+, tissue factor and phospholipid.
  • Time to make a clot is measured —-> usual range = _________
  • Tests function of factors VII, X, V, II & fibrinogen = _____ pathway.
  • ____ is often expressed as INR (international normalized ratio) or prothrombin ratio.
  • INR = (Patient’s PT/Normal PT)
    Normal INR = _____
    Biochemical ________ Pathways
A

centrifuged
12-15s
extrinsic pathway
0.8-1.2
Coagulation

41
Q

What is the Partial Thromboplastin Time (PTT) test
– Intrinsic Pathway?

A

Factor XII is a plasma
protein that activates (cuts)
itself after binding to
negatively-charged surfaces
and molecules, including
* in vitro: glass, silica, kaolin etc.
* in vivo: collagen, platelets, denatured proteins, nucleic acids, microbes

FXIIa activates FXI and also
stimulates inflammation.

42
Q

What is the full intrinsic coagulation pathway?

A
43
Q
  • Blood is collected into _______ or EDTA tube (to chelate Ca2+) and centrifuged.
  • Plasma is mixed with phospholipid,
    Ca2+ and a factor _____ activator
    (kaolin, silica…)
  • Time to form a clot is measured -
    usual range is less than ____ seconds.
  • Tests function of factors XII, XI, IX,
    VIII, X, V, II = intrinsic pathway
  • These factors can also be activated
    by _______
A

citrate
XII
39
inflammation

44
Q

What is a whole blood clotting time test? (4)

A
45
Q

What does the extrinsic and intrinsic pathway start with?

A
46
Q

What are the Mechanisms of Anticoagulation?

A
  1. Clots should not form in healthy/unbroken
    blood vessels.
    * 90% of thrombin is immobilised in the fibrin clot.
  2. Endothelial cells inhibit coagulation by
    * Their smooth endothelial surface and glycocalix layer,
    which repel platelets and clotting factors
    * Stimulating vasodilation (prostacyclin and NO)
    * Stimulating fibrinolysis (secretes tPA)
    * Producing molecules that inhibit clotting factors,
    especially thrombin
    * Producing molecules that break down clotting factors
47
Q

How does Thrombomodulin produce anti-coagulation?

A
48
Q

How does Antithrombin & heparin produce anti-coagulation?

A
49
Q

How does Tissue Factor Pathway
Inhibitor (TFPI) produce anti-coagulation?

A
50
Q

What are the therapeutic anticoagulants? (5)

A
51
Q

Coagulation disorders: (2)

A

Hypercoagulability
Hypocoagulability

52
Q

Hypercoagulability (risk of thrombosis)
* 3 main causes:

A
  1. Haemodynamics
  2. Vessel injury
  3. Excess pro-coagulants vs anticoagulants
53
Q

What are the Haemodynamics of Hypercoagulability? (3)

A
54
Q

What are the vessel injuries associated with Hypercoagulability?

A
55
Q

Hypercoagulability - Excess Pro-coagulants vs
Anticoagulants: (4)

A
56
Q

How does Hypocoagulability (bleeding risk) affect platelet cells?

A
57
Q

How does Hypocoagulability affect the Extrinsic Pathway?

A
58
Q

Vitamin K deficiency has a major disruptive effect on the extrinsic pathway because of its
effect on factor VII, but also disrupts the intrinsic pathway to a lesser extent because it
decreases production of factor IX, in addition to decreasing ___ and ________.

A

FX
thrombin

59
Q

How does Hypocoagulability affect the Intrinsic pathway? (2)

A