national-clinical-guidelines-for-stroke-fourth-edition
national-clinical-guidelines-for-stroke-fourth-edition
national-clinical-guidelines-for-stroke-fourth-edition
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Primary care concise guide <strong>for</strong> <strong>stroke</strong> 2012<br />
National <strong>clinical</strong> guideline <strong>for</strong> <strong>stroke</strong><br />
personal preference and compatibility with<br />
safety in the home environment<br />
● be aware of how to obtain further supplies<br />
of medication<br />
● have a regular review of their medication<br />
● have their capacity (eg cognition, manual<br />
dexterity, ability to swallow) to take full<br />
responsibility <strong>for</strong> self-medication assessed<br />
by the multidisciplinary team prior to<br />
discharge as part of their rehabilitation.<br />
Blood pressure (5.4.1)<br />
A All patients with <strong>stroke</strong> or TIA should have<br />
their blood pressure checked. Treatment should<br />
be initiated and/or increased as is necessary or<br />
tolerated to consistently achieve a clinic blood<br />
pressure below 130/80, except <strong>for</strong> patients with<br />
severe bilateral carotid stenosis, <strong>for</strong> whom a<br />
systolic blood pressure target of 130–150 is<br />
appropriate.<br />
Antithrombotic treatment (5.5.1)<br />
A recent NICE technology appraisal recommends<br />
generic clopidogrel as the most cost-effective<br />
antiplatelet therapy <strong>for</strong> secondary prevention<br />
following ischaemic <strong>stroke</strong> (National Institute <strong>for</strong><br />
Health and Clinical Excellence 2010a). Aspirin<br />
plus modified-release dipyridamole is<br />
recommended <strong>for</strong> those unable to take<br />
clopidogrel, although this combination may be<br />
more difficult to tolerate, with a 29%<br />
discontinuation rate compared with 23% <strong>for</strong><br />
clopidogrel in the PRoFESS study.<br />
Clopidogrel is not licensed <strong>for</strong> the management of<br />
TIA and there<strong>for</strong>e NICE recommends aspirin plus<br />
modified-release dipyridamole <strong>for</strong> this indication.<br />
Clinicians have tended to treat TIA and ischaemic<br />
<strong>stroke</strong> as different manifestations of the same<br />
disease and there<strong>for</strong>e it is illogical to have different<br />
treatment strategies <strong>for</strong> the two presentations. In<br />
producing this guideline, the members of the<br />
working party felt that a unified approach to the<br />
treatment of TIA and ischaemic <strong>stroke</strong> would be<br />
appropriate. Whilst clopidogrel does not have a<br />
licence <strong>for</strong> use after TIA, as the more cost-effective<br />
and better tolerated option, it was felt that the<br />
benefits of recommending this drug as first-line<br />
outweighed any disadvantages.<br />
A For patients with ischaemic <strong>stroke</strong> or TIA in<br />
sinus rhythm, clopidogrel should be the<br />
standard antithrombotic treatment:<br />
● Clopidogrel should be used at a dose of 75<br />
mg daily.<br />
● For patients who are unable to tolerate<br />
clopidogrel, offer aspirin 75 mg daily in<br />
combination with modified-release<br />
dipyridamole 200 mg twice daily.<br />
● If both clopidogrel and modified-release<br />
dipyridamole are contraindicated or not<br />
tolerated, offer aspirin 75 mg daily.<br />
● If both clopidogrel and aspirin are<br />
contraindicated or not tolerated, offer<br />
modified-release dipyridamole 200 mg<br />
twice daily.<br />
● The combination of aspirin and clopidogrel<br />
is not recommended <strong>for</strong> long-term<br />
prevention after TIA or <strong>stroke</strong> unless there<br />
is another indication such as acute coronary<br />
syndrome or recent coronary stent<br />
procedure.<br />
B For patients with ischaemic <strong>stroke</strong> or TIA in<br />
paroxysmal, persistent or permanent atrial<br />
fibrillation (valvular or non-valvular)<br />
anticoagulation should be the standard<br />
treatment. Anticoagulation:<br />
● should not be given after <strong>stroke</strong> or TIA until<br />
brain imaging has excluded haemorrhage<br />
● should not be commenced in patients with<br />
uncontrolled hypertension<br />
● of patients with disabling ischaemic <strong>stroke</strong><br />
should be deferred until at least 14 days<br />
have passed from the onset; aspirin 300 mg<br />
daily should be used until this time<br />
● of patients with non-disabling ischaemic<br />
<strong>stroke</strong> should be deferred <strong>for</strong> an interval at<br />
the discretion of the prescriber, but no later<br />
than 14 days from the onset<br />
● should be commenced immediately<br />
following a TIA once brain imaging has<br />
ruled out haemorrhage, using an agent with<br />
a rapid onset such as low molecular weight<br />
heparin or an oral direct thrombin or factor<br />
Xa inhibitor.<br />
162 © Royal College of Physicians 2012