Treatment for Haemostasis, thrmobosis, coagulation, stroke lecture Flashcards

1
Q

What are the 4 classes of drug agents used to treat conditions involving thrmbus?

A

Anticoagulants
Platelet inhibitors (anti-platelet drugs)
Fibrinolytic enzymes
Antifibrinolytics

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2
Q

What is the function of Anticoagulants?

A

These prevent thrombus (clot) formation, commonly known as blood thinners.

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3
Q

What are the different types of Anticoagulatns?

A

Unfractionated Heparin (parenteral)
Low molecular weight heparins (parenteral)
Vit K antagonists (oral) e.g. warfarin
non-vit K antagonists (oral) e.g. Apixaban

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4
Q

Unfractionated Heparins are of what origin?

What is their main function?

A

Medical heparin is of animal origin i.e. bovine lung.

They inhibit thrombin from converting fibrinogen into fibrin

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5
Q

What inhibits their action naturally in the blood?

And what can we give to inhibit their action?

A

Heparinases inhibit heparin naturally in the blood.
Protamine Sulphate is used to reverse the effect of heparin mostly in heparin overdose by binding and inactivating heparin.

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6
Q

What is a major adverse effect of prolonged heparin treatment?

A

Heparin-induced Thrombocytopenia - massive reduction in platelet count.
Happens in two stages -
first 2-3 days, won’t show any symptoms
then 5-7 days, will produce an immune-mediated response. Typically would stop giving the heparins.

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7
Q

How long does it take for Unfractionated Heparin to work?

A

It is quick acting and short acting which is a benefit if there is a contra-indication or an issue as the infusion can be stopped immediately.

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8
Q

Low- molecular weight Heparins: Where are their origins?

A

These were developed from UNfractionated Heparins so can be called Fractionated Heparins.

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9
Q

What is the difference in the Low- molecular weight Heparin mechanism of action compared to Unfractionated Heparin?

A

LMWHs don’t inactivate thrombin, instead they inactivate Xa, which has a central role of linking the extrinsic and intrinsic pathway in the coagulation cascade.

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10
Q

What is an advantage of LMWH compared to Unfractionated Heparin?

A

LMWHs are less likely to induce Thrombocytopenia.

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11
Q

How would LMWHs be administered and why?

A

They are highly ionized so would not be absorbed from the GI, so must be given as an IV or Deep Subcutaneous Injection.

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12
Q

What is the only issue with the administration of LMWHs?

A

If longer treatment was required, then the patinet would have to be taught how to use them at home.

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13
Q

Vitamin K antagonists: how do thesework?

A

They work by inducing a deficiency in Vitamin K, therefore inhibiting factor II, VII, IX and X

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14
Q

Where are Vitamin K antagonists active?

A

In-vivo

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15
Q

How do Vitamin K antagonists cause a reduction in vit K?

A

They prevent Vitamin K reductase from breaking down Vitamin K to its active form.

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16
Q

What is the most commonly used Vitamin K antagonist?

A

Warfarin - the S-isomer is the most potent at inhibiting Vitamin K reduction

17
Q

What is the disadvantages of Vit K antagonist?

A

Slow onset of action due to no action on already carboxylated factors - the already active Vitamin K.
They have an enormous range of drug interactions causing deccreased or increased anticoagulation effects.

18
Q

What is the aim of treatment of any thrombus i.e. DVT, PE etc

A

The aim is to resolve normal circulation to the limbs, prevent damage to valves and prevent PE or DVT. The ail is to break down the clot, and prevent any more clots form forming.

19
Q

What is the Immediate treatment for anticoagulation in an emergancy?

A

Would choose LMWHs over Unfractionated Heparins unless there is increased risk of bleeding or renal impairment, then would choose Unfractionated first due to the more control of being able to withdraw the drug if required and limit the action.

20
Q

What would be the treatment for a PE for a patient who is haemodynamically unstable

A

Offer Unfractionated Heparin, then depending on location of the thrombus, may initiate thrombolytic therapy. May have to intervene surgically to remove the clot especially if in a major vessel in the lung.

21
Q

What would be the treatment for a patient with confirmed DVT or PE within?

A

Vitamin K antagonist e.g. Warfarin that should be used for 3 months (prophylaxis) then asses the risk/benefit of continuing treatment.

22
Q

Platelet Aggregation Inhibitors: how do these work?

A

Prevent platelet aggregation by targeting a variety of mechanisms, mainly inhibiting Glycoprotein IIb/IIIa from coming together which is essential for clot formation.

23
Q

Give example drugs of Platelet Aggregation inhibitors:

A

Aspirin, Clopidogrel, Dihydromole

24
Q

Fibrinolytic enzymes: How do these work?

A

Clot-busting drugs. These PROMOTE plasminogen conversion to plasmin which is an enzyme that dissolves clots by removing fibrin.

25
Q

When would Fibrinolytic enzymes be given?

A

These would be given for DVT, Ischaemic stroke, also licensed for use after an S/T elevated myocardial infarction.

26
Q

Give the name of the drug used for DVT that is a fibrinolytic enzyme:

A

Streptokinase

27
Q

What is the issue with streptokinase?

A

Strepotkinase is antigenic so there will be antibody production against the drug within the first 4 days of use, therefore will not be active if used again within 1 year of first administration. Would have to use another Fibrinolytic enzymes e.g. alteplase.

28
Q

WHat is the first line treatment for the presentation of Stroke ot TIA (you don’t know which one it is until after further investigation)

A

1: Aspirin loading dose 300mg immediately, followed by a specialist assessement and investigation to find out if it is a stroke or TIA.

29
Q

WHat is the treatment for a confirmed case of TIA?

A

Immediate acute treatment with Altepase which is a fibrinolytic enzyme adiministered as an IV bolus 10% followed by an infusion of the remaining 90% over an hour (60 mins)

30
Q

When is treatment most effective for stroke and TIA?

When do the risk of treatment outweigh the benefits?

A

Most effective within 90mins of onset, much poorer outcome after 3.5 hours.
After 4.5 hours, no point due to risks.

31
Q

What is the new treatment that is promoted by the NHS for Clots in large vessles?

A

Thrombecotomy - remove the drug mechacnially to resotre the blood flow

32
Q

What are Antifibrinolytic drugs?

A

These are pro-coagulation = they prevent bleeding and are opposite to fibrinolytic drugs (that promote fibrinolysis) by prefenting fibrinolysis.

33
Q

Give an example drug of Antifibrinolytic drugs?

A

Tranexamic acid - a sythnetic lysine derivative.

34
Q

What is the mechanism of action of Antifibrinolytic drugs?

A

They reversibly block the lysine binding sites on plasminogen, therefore preventing its conversion to Plasmin, preventing the breakdown of clots.

35
Q

WHen are Antifibrinolytic drugs used?

A

To prevent heavy bleeding after surgery or dental operation, thrombolytic overdose, menorrhagia (heavy periods)

36
Q

Summary of treatment: What type of thrombosis is LMWH and UFH used?

A

short-to mid term primarily VENOUS THROMBOSIS

37
Q

Summary of treatment: What type of thrombosis is Warfarin - Vit K antagonist used for?

A

Long term prevention of mainly VENOUS THROMBOSIS

38
Q

Summary of treatment: What type of thrombosis is Anti-platelet drugs used for e.g. aspirin, clopdogrel, dihydromole?

A

Prevent arterial thrombosis, also used for NSTEMI and unstable angina