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National <strong>clinical</strong> guideline <strong>for</strong> <strong>stroke</strong><br />

B People with a suspected TIA, that is, they have no neurological symptoms at the time<br />

of assessment (within 24 hours), should be assessed as soon as possible <strong>for</strong> their risk<br />

of subsequent <strong>stroke</strong> by using a validated scoring system such as ABCD2 .<br />

C Patients with suspected TIA who are at high risk of <strong>stroke</strong> (eg an ABCD2 score of 4 or<br />

above) should receive:<br />

● aspirin or clopidogrel (each as a 300 mg loading dose and 75 mg thereafter) and a<br />

statin, eg simvastatin 40 mg started immediately<br />

● specialist assessment and investigation within 24 hours of onset of symptoms<br />

● measures <strong>for</strong> secondary prevention introduced as soon as the diagnosis is<br />

confirmed including discussion of individual risk factors.<br />

D People with crescendo TIA (two or more TIAs in a week), atrial fibrillation or those<br />

on anticoagulants should be treated as being at high risk of <strong>stroke</strong> (as described in<br />

recommendation 4.2.1C) even though they may have an ABCD2 score of 3 or below.<br />

E Patients with suspected TIA who are at low risk of <strong>stroke</strong> (eg an ABCD2 score of 3 or<br />

below) should receive:<br />

● aspirin or clopidogrel (each as a 300 mg loading dose and 75 mg thereafter) and a<br />

statin, eg simvastatin 40 mg started immediately<br />

● specialist assessment and investigations as soon as possible, but definitely within 1<br />

week of onset of symptoms<br />

● measures <strong>for</strong> secondary prevention introduced as soon as the diagnosis is<br />

confirmed, including discussion of individual risk factors.<br />

F People who have had a TIA but present late (more than 1 week after their last<br />

symptom has resolved) should be treated as though they are at a lower risk of <strong>stroke</strong><br />

(see recommendation 4.2.1E).<br />

G Patients with TIA in atrial fibrillation should be anticoagulated with an agent that has<br />

rapid onset in the TIA clinic once intracranial bleeding has been excluded and if there<br />

are no other contraindications.<br />

4.2.2 Sources<br />

A Consensus; National Institute <strong>for</strong> Health and Clinical Excellence 2010d<br />

B National Institute <strong>for</strong> Health and Clinical Excellence 2008b<br />

C National Institute <strong>for</strong> Health and Clinical Excellence 2008b; Luengo-Fernandez et al<br />

2009; Rothwell et al 2007<br />

D National Institute <strong>for</strong> Health and Clinical Excellence 2008b<br />

E National Institute <strong>for</strong> Health and Clinical Excellence 2008b; Luengo-Fernandez et al<br />

2009; Rothwell et al 2007<br />

F National Institute <strong>for</strong> Health and Clinical Excellence 2008b<br />

G Consensus<br />

4.2.3 Implications<br />

To achieve these recommendations additional training of staff will be required so that<br />

they are able to assess immediate risk in people presenting with a possible TIA, and to<br />

significantly streamline the process of investigation. This may require additional<br />

40 © Royal College of Physicians 2012

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