Drugs Affecting Coagulation Flashcards

1
Q

What is thrombosis?

A

The pathological formation of a haemostatic plug in a blood vessel in the absence of blood loss

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2
Q

What kind of cells are present in a arterial thrombus?

A

Platelets, white blood cells, fibrin

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3
Q

What kind of cells are present in a venous thrombus?

A

Platelets, red blood cells, fibrin

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4
Q

What is the first step in haemostasis?

A

Vasoconstriction - an initial vasoconstriction occurs because of the release of endothelin from the epithelium

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5
Q

What is the second step in haemostasis?

A

Primary haemostasis - the formation of the initial platelet plug - the exposed collagen in the damaged blood vessel causes platelets to adhere, activate and aggregate

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6
Q

What is the third step in haemostasis?

A

Secondary haemostasis - activation of the coagulation cascade to convert fibrinogen to fibrin - initiated by the exposure of tissue factor in the damaged endothelium which activates thrombin which converts fibrinogen to fibrin

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7
Q

What is present in the subendothelial ECM which when exposed causes platelets to adhere to the blood vessel?

A

Von willebrands factor - a factor which binds to platelets via GpIb platelet receptor

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8
Q

What causes platelet activation?

A

Platelet adhesion (binding to vWF via GpIb), thromboxane A2 and ADP

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9
Q

What happens when platelets are activated?

A

They release their granule contents (calcium and ADP and serotonin) and synthesise thromboxane A2 and express the GpIIb-IIIa receptor

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10
Q

What is the role of calcium released by platelets?

A

It is a cofactor in many reactions in the coagulation cascade

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11
Q

What is the role of ADP released by platelets?

A

It activates other platelets

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12
Q

What is the role of serotonin released by platelets?

A

vasoconstriction

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13
Q

What is platelet aggregation?

A

Where fibrinogen binds to GpIIb-IIIa receptors on platelets to form a bridge

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14
Q

How are endothelial cells activated to release tissue factor?

A

By cytokines such as IL-1 and TNF or by bacterial products such as endotoxin

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15
Q

How is coagulation controlled?

A

By enzymes which inhibit the cascade e.g. antithrombin or by lysis via plasmin

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16
Q

What are the three factors which lead to thrombosis (Virchow’s triad)?

A

blood stasis, hyper coagulability, vessel damage

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17
Q

When does blood stasis occur?

A

in atrial fibrillation or deep vein thrombosis

18
Q

When does vessel damage occur?

A

atherosclerosis

19
Q

What is heparin?

A

A drug which enhances the activity of antithrombin III (which inhibits factor Xa and thrombin)

20
Q

What are the pharmacokinetics of heparin?

A

It has a high molecular weight and is not orally available

21
Q

What is low molecular weight heparin?

A

A lower molecular weight version of heparin with less effect on thrombin that has a longer half life - used for patients self administration

22
Q

What test is used to monitor heparin?

A

The APTT test (intinsic pathway)

23
Q

What are the adverse effects of heparin?

A

haemorrhage, platelet deficiency, osteoporosis

24
Q

Which factors are vitamin K dependent?

A

II, VII, IX, X - these factors require gamma carboxylation after synthesis which requires reduced vitamin K as a cofactor

25
Q

What is warfarin?

A

A drug which inhibits the reduction of vitamin K so inhibits gamma carboxylation of factors II, VII, IX and X

26
Q

What are the properties of warfarin?

A

It is only active in vivo, has a delayed onset of action and doesn’t effect already active factors

27
Q

What are the adverse effects of warfarin?

A

haemorrhage

28
Q

What test is used to monitor warfarin?

A

INR (extrinsic pathway)

29
Q

What happens if you administer vitamin K and warfarin?

A

vitamin K will outcompete and overcome the warfarin

30
Q

What are the pharmacokinetics of warfarin?

A

orally active, rapidly absorbed, strongly bound to plasma protein

31
Q

What causes increased warfarin activity?

A

vitamin K deficiency, hepatic disease, hyper metabolic state, drug interactions

32
Q

What drugs interact with warfarin to increase activity ?

A

Drugs which affect platelet aggregation (aspirin), drugs which compete for plasma protein binding (NSAIDs), drugs which compete for the cytochrome p450 pathway (alcohol)

33
Q

What causes decreased warfarin activity?

A

pregnancy, drug interactions

34
Q

What drugs interact with warfarin to decrease activity?

A

drugs which induce liver enzymes - e.g. barbiturates or chronic alcohol use and also vitamin K supplements

35
Q

Why are new anticoagulants needed?

A

To have a lower molecular weight so they can be given orally, to get a more predictable dose-response relationship and to reduce laboratory monitoring

36
Q

What drugs affect platelet activation and adhesion?

A

ADP receptor antagonists (clopidigrel), thromboxane synthesis inhibitors (aspirin), glycoprotein receptor antagonists (abciximab)

37
Q

What is aspirin?

A

An irreversible COX inhibitor - leads to decreased platelet activation and vasoconstriction

38
Q

What drugs are used to cause fibrinolysis?

A

streptokinase and alteplase

39
Q

What does streptokinase do?

A

It activates plasminogen

40
Q

Why can streptokinase only be used once?

A

Because it is antigenic (derived from bacterium)

41
Q

What does alteplase to?

A

Activates fibrin bound plasminogen (clot selective)

42
Q

Can alteplase be given more than once?

A

Yes