Cerebrovascular (stroke) Flashcards

1
Q

What drug is used for initial treatment of ischaemic stroke

A

Alteplase (rt-PA)

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2
Q

What drugs are used for post-stroke care

A

Anti-platelets, anticoagulants, antihypertensives, statins

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3
Q

E.g. of anti-platelets

A

Aspirin and clopidogrel

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4
Q

What do anti-platelets do

A

Prevent the adherence of platelets to the wall of the injured vessel

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5
Q

When should aspirin be given post-stroke

A

After 48 hours. It should be started as soon as possible but should wait 24 hours after using rt-PA

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6
Q

E.g. of anticoagulants

A

Warfarin, apixaban, dabigatran, rivaroxiban

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7
Q

If the pt has AF oral anticoagulants are…

A

More effective in preventing recurrent stroke than antiplatelet drugs, and they carry a similar risk of bleeding

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8
Q

When can you start anticoagulants post-stroke?

A

Cannot be started until at least a few days (up to 14 days) after ischaemic stroke cos risk of bleeding (including intracranial haemorrhage)

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9
Q

How do antihypertensives help in ischaemic stroke

A

Lowering the BP reduces the risk of recurrent stroke by approximately 25%. Lowering the BP is more important than the type of antihypertensive used.

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10
Q

How do statins help in ischaemic stroke

A

Statins can slightly reduce the risk of any stroke, in people with a history of TIA or ischaemic stroke. Statins also increases the risk slightly of haemorrhagic stroke.

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11
Q

Medication for hemorrhagic stroke:

A

Nimodipine

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12
Q

What does nimodipine do

A

MOA is unclear, may reduce influx of calcium into neurones and vascular smooth muscle cells. Prevents ischaemic damage from cerebral spasm

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13
Q

Drugs that can help with hemorrhagic stroke

A

Analgesia, stool softeners, anti-emetics, anti-epileptic meds

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14
Q

Alteplase stuff

A

It’s a serine protease which binds to fibrin in a clot and the plasminogen that is part of the structure is activated and becomes plasmin. The plasmin further aids in the breakdown of fibrin, and Alteplase only works in its full capacity when there is fibrin present, which minimises systemic effects. After four hours, fibrinogen and plasminogen levels are approximately halved, but increases to about 80% after 24 hours. Contraindicated in patients who have an increased risk of haemorrhaging.

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