Stroke Prevention

Authored by , Reviewed by Dr Colin Tidy | Last edited | Certified by The Information Standard

This article is for Medical Professionals

Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Stroke article more useful, or one of our other health articles.

Prevention of stroke may be classified as:

  • Primary prevention, if there is no previous history of stroke or transient ischaemic attack (TIA).
  • Secondary prevention, if there has been such an event.

See also the separate Prevention of Cardiovascular Disease and Cardiovascular Risk Assessment articles. For tertiary prevention, see also the separate Cerebrovascular Event Rehabilitation article.

  • Well-documented and modifiable risk factors for stroke include hypertension, exposure to cigarette smoke, diabetes, atrial fibrillation (AF), dyslipidaemia, carotid artery stenosis, sickle cell disease, postmenopausal hormone therapy, poor diet, physical inactivity, and obesity - especially truncal obesity[1].
  • Less well-documented or potentially modifiable risk factors include the metabolic syndrome, alcohol misuse, drug misuse, oral contraceptive use, obstructive sleep apnoea, migraine headaches, hyperhomocysteinaemia, elevated lipoprotein(a), elevated lipoprotein-associated phospholipase, and hypercoagulability[1].
  • After a stroke or TIA, there is a high risk of stroke and of other serious vascular events. Medical treatments with clear evidence of benefit include[2]:
    • Lowering blood pressure after all types of stroke or TIA.
    • Lowering blood cholesterol with a statin after ischaemic stroke or TIA.
    • Antiplatelet treatment after ischaemic stroke or TIA.

The GMS Contract Quality and Outcomes Framework 2019-20[4]includes 10 points for providing statins to people aged 30-74 diagnosed with hypertension (excluding those with pre-existing coronary heart disease (CHD), diabetes, stroke and/or TIA), who have had a CVD risk assessment 'using an assessment tool agreed with their NHS Commissioning Board'.

  • Use an appropriate cardiovascular risk assessment tool (eg, Joint British Societies' (JBS2) risk calculator) to assess cardiovascular disease (CVD) risk[5]:
    • CVD risk should be calculated as 10-year risk of fatal and non-fatal stroke, including TIA, + 10-year risk of CHD.
    • CHD risk includes the risks of death from CHD, and non-fatal CHD, including silent myocardial infarction (MI), angina and coronary insufficiency (acute coronary syndrome).
  • The QRISK®3 calculator has been developed specifically for the UK population[6].
  • While QRISK®3 includes weighting for ethnicity, the ETHRISK® calculator may be more appropriate in British black and minority ethnic groups[7].

Lifestyle factors[3]

  • Dietary advice:
    • Advise eating at least five portions of fruit and vegetables per day.
    • Advise eating at least two portions of fish per week, including a portion of oily fish.
    • Advise people to eat a diet in which the total fat intake is 30% or less of total energy intake, saturated fats are 7% or less of total energy intake, dietary cholesterol is less than 300 mg/day, and saturated fats are replaced by mono-unsaturated and polyunsaturated fats.
    • Advise pregnant women to limit their intake of oily fish to two portions a week.
    • Advise people to reduce their intake of sugar and food products containing them, and to choose wholegrain varieties of starchy foods.
    • Do not routinely recommend omega-3 fatty acid supplements or plant sterols and stanols for primary prevention.
  • Physical activity:
    • Advise people to take 30 minutes of at least moderate-intensity exercise a day at least five days a week.
    • Encourage people who cannot manage this to exercise at their maximum safe capacity.
    • Recommend exercise that can be incorporated into everyday life, such as brisk walking, using stairs and cycling.
    • Tell people that they can exercise in bouts of 10 minutes or more throughout the day.
    • Take into account the person's needs, preferences and circumstances.
    • Agree goals and provide written information about the benefits of activity and local opportunities to be active.
  • Weight management:
    • Offer people who are overweight or obese advice and support to work towards achieving and maintaining a healthy weight.
  • Alcohol consumption[8]:
    • Advise men and women to limit alcohol intake to no more than 14 units a week.
    • Advise everyone to avoid binge drinking.
  • Smoking cessation:
    • Advise all people who smoke, to stop.
    • If people want to stop:
      • Offer support and advice.
      • In addition, provide medication to help with smoking cessation when indicated.

Drug treatment

Before starting statin therapy, offer people the opportunity to change their lifestyle and reassess their risk[3].

See also the separate Atrial Fibrillation article for more information about the prevention of strokes in people with AF. AF is responsible for 25% of all strokes[9].

Hypertension

  • Screen for hypertension and treat appropriately according to National Institute for Health and Care Excellence (NICE) guidelines[10].

Antithrombotic treatment

  • Following acute MI: anticoagulation is appropriate in those who are at increased risk of thromboembolism, including those with a large anterior MI, left ventricular aneurysm or thrombus, paroxysmal tachyarrhythmias, chronic heart failure or a history of thromboembolic events[5].
  • Anticoagulation is indicated for other cardiovascular risk factors for thromboembolism - eg, prosthetic valves, rheumatic heart disease and AF. Anticoagulation instead of antiplatelet treatment should be used for patients who have AF and no contra-indications to anticoagulation[1].

Aspirin

  • Aspirin produces a 12% proportional reduction in serious vascular events, mainly due to a 20% reduction in non-fatal MI. There was no net effect on stroke and vascular mortality[11].
  • If low-dose aspirin is used in primary prevention, the balance of risk and benefits should be discussed with the patient.
  • The risk of gastrointestinal bleeding probably outweighs the small benefit in stroke prevention unless the risk of stroke is particularly high.

Lipid-lowering drugs[3]

  • Consider the possibility of familial hypercholesterolaemia (FH) and investigate as appropriate if total cholesterol is over 7.5 mmol/L and there is a family history of premature CHD.
  • NICE recommends statin therapy as part of the management strategy for the primary prevention of CVD for adults who have a 20% or greater 10-year risk of developing CVD .
  • Total, HDL and non-HDL cholesterol should be measured in all people started on high-intensity statins, including 20 mg atorvastatin, three months after treatment commencement. Aim for a greater than 40% reduction in non-HDL cholesterol. If not achieved:
    • Discuss adherence and timing of dose.
    • Optimise diet and lifestyle measures.
    • Consider increasing dose if started on less than atorvastatin 80 mg and the person is judged to be at higher risk because of comorbidities, risk score or using clinical judgement.

Atrial fibrillation (AF)[12]

See also separate Atrial Fibrillation article for more information about the prevention of strokes in people with AF. AF is responsible for 25% of all strokes[9].

  • All patients with AF should be assessed for their risk of stroke and the need for thromboprophylaxis balanced with the patient's risk of bleeding.
  • NICE recommends using the CHA2DS2-VASc assessment tool for stroke risk and the HAS-BLED tool for bleeding risk prior to and during anticoagulation.
  • Risk factors for stroke included in CHA2DS2-VASc include prior ischaemic stroke, transient ischaemic attacks or thromboembolic events, heart failure, left ventricular systolic dysfunction, vascular disease, diabetes, hypertension, females and patients over 65 years.
  • Patients with a very low risk of stroke (CHA2DS2-VASc score of 0 for men or 1 for women) do not require any antithrombotic therapy for stroke prevention.
  • Oral anticoagulation should be offered to patients with confirmed diagnosis of atrial fibrillation in whom sinus rhythm has not been successfully restored within 48 hours of onset, patients who have had or are at high risk of recurrence of AF (eg, structural heart disease, prolonged history of AF longer than 12 months), a history of failed attempts at cardioversion, and patients with a greater risk of stroke than risk of bleeding.
  • Oral anticoagulation is with a vitamin K antagonist (eg, warfarin or, in non-valvular AF, with apixaban, dabigatran etexilate, rivaroxaban or edoxaban.
  • Anticoagulants are also indicated during cardioversion procedures.
  • Aspirin is less effective than oral anticoagulation and the modest benefit is offset by the risk of bleeding. Therefore, aspirin should not be offered as monotherapy for stroke prevention in AF.
  • If anticoagulant treatment is contra-indicated or not tolerated, left atrial appendage occlusion can be considered.
  • People with a suspected TIA should be offered aspirin 300 mg a day, to be started immediately.
  • All people who have a suspected TIA should be referred immediately for specialist assessment and seen within 24 hours.
  • All patients should be given appropriate advice on lifestyle factors as described for primary prevention, including smoking cessation, physical activity, diet, weight control and avoiding excess alcohol.
  • All patients should receive regular review and treatment of risk factors for vascular disease for the rest of their lives after a stroke with inclusion on a stroke register and a minimum of annual follow-up.
  • Blood pressure: see the separate Hypertension Treatment article.
  • Antithrombotic treatment:
    • People with acute stroke should be started on 300 mg aspirin daily for two weeks once intracerebral haemorrhage has been excluded. At this time a definitive longer antithrombotic treatment plan should be implemented.
    • An alternative antiplatelet should be offered to anyone who is allergic to or genuinely intolerant of aspirin
    • If there is a history of persistent or paroxysmal AF in a non-haemorrhagic stroke, consider anticoagulation first-line:
      • Anticoagulation should be started in every patient with persistent or paroxysmal AF (valvular or non-valvular) unless contra-indicated, following an initial two-week course of aspirin 300 mg daily.
      • Anticoagulation is indicated for other cardiovascular risk factors for thromboembolism - eg, prosthetic valves[1]. Anticoagulation should be stopped for one week following diagnosis of cerebral infarction in people with prosthetic valves if there is a significant risk of haemorrhagic transformation. During this week, 300 mg aspirin should be substituted.
      • Anticoagulants should not be started until brain imaging has excluded haemorrhage and usually not until 14 days have passed from the onset of an ischaemic stroke.
    • Patients with TIA or ischaemic stroke (not due to AF) should be on clopidogrel (only use modified-release dipyridamole in combination with aspirin if clopidogrel is not tolerated)[14, 15]. Clopidogrel is also the preferred treatment option in patients with peripheral arterial disease or multivascular disease[16].
    • Dual therapy with aspirin and clopidogrel may be initiated in secondary care for the first three months following ischaemic stroke or TIA due to severe symptomatic intracranial stenosis or for another condition such as acute coronary syndrome[15].
  • Anti-lipid agents:
    • Treatment with a statin should be given to all patients with ischaemic stroke or TIA unless contra-indicated[3].
    • Following an ischaemic stroke or TIA with evidence of atherosclerosis, people with a target LDL cholesterol of less than 1.8 mmol/L (70 mg/dL) have a 22% lower risk of subsequent cardiovascular events than those with a target LDL of 2.3 mmol/L (90 mg/dL)[17].

Carotid endarterectomy for people with carotid artery stenosis

Carotid endarterectomy has been the standard in atherosclerotic stroke prevention but carotid artery stenting has emerged as a less invasive alternative for revascularisation[18]. See also the separate Carotid Artery Stenosis article.

  • Carotid endarterectomy:
    • All people who have a TIA should have consideration given at their specialist assessment of their suitability for carotid endarterectomy. If they are considered as a possible candidate, they should have urgent carotid imaging[13].
    • People with stable neurological symptoms from acute non-disabling stroke or TIA who have symptomatic carotid stenosis of 50-99% according to the North American Symptomatic Carotid Endarterectomy Trial (NASCET) criteria, or 70-99% according to the European Carotid Surgery Trialists' (ECST) Collaborative Group criteria, should:
      • Be assessed and referred urgently for carotid endarterectomy to a service following current national standards.
      • Receive best medical treatment (control of blood pressure, antiplatelet agents, cholesterol lowering through diet and drugs, lifestyle advice)[13].
    • People with stable neurological symptoms from acute non-disabling stroke or TIA who have symptomatic carotid stenosis of less than 50% according to the NASCET criteria, or less than 70% according to the ECST criteria, should:
      • Not undergo surgery.
      • Receive best medical treatment (control of blood pressure, antiplatelet agents, cholesterol lowering through diet and drugs, lifestyle advice)[13].
    • Carotid endarterectomy is of some benefit for patients with 50-69% symptomatic stenosis and is very beneficial for 70-99% stenosis without near-occlusion[19].
    • Carotid endarterectomy for asymptomatic carotid stenosis reduces the risk of any stroke by approximately 30% over three years. However, the absolute risk reduction is small and there is a 3% perioperative stroke or death rate[20].
  • Carotid angioplasty and stenting:
    • Stenting with the use of an embolic protection device is a less invasive revascularisation strategy than endarterectomy in carotid artery disease. For patients with severe carotid artery stenosis and co-existing conditions, carotid stenting with the use of an embolic protection device appears to be as safe and as effective as carotid endarterectomy[21].
    • Endovascular treatment and carotid endarterectomy appear to have similar early risks of death or stroke and similar long-term benefits in the treatment of carotid artery stenosis[20].
    • The efficacy of carotid artery stenting compared with endarterectomy has not yet been fully established[22]. It is not recommended within the 2019 NICE guidance on management of stroke and TIA[13].
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Further reading and references

  1. Meschia JF, Bushnell C, Boden-Albala B, et al; Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2014 Dec45(12):3754-832. doi: 10.1161/STR.0000000000000046. Epub 2014 Oct 28.

  2. Sudlow C; Preventing further vascular events after a stroke or transient ischaemic attack: an update on medical management. Pract Neurol. 2008 Jun8(3):141-57.

  3. Lipid modification - cardiovascular risk assessment and the modification of blood lipids for the prevention of primary and secondary cardiovascular disease; NICE Clinical Guideline, July 2014 (updated September 2016)

  4. 2019/20 General Medical Services (GMS) contract Quality and Outcomes Framework (QOF); NHS England/BMA, April 2019

  5. Report of the Joint British Societies for the Prevention of Cardiovascular Disease; JBS3, 2014

  6. QRISK®3-2018 risk calculator

  7. ETHRISK®. A modified Framingham CHD and CVD risk calculator for British black and minority ethnic groups

  8. Alcohol Guidelines Review – Report from the Guidelines development group to the UK Chief Medical Officers; Department of Health, January 2016

  9. Ahmad Y, Lip GY; Stroke Prevention in Atrial Fibrillation: Where are We Now? Clin Med Insights Cardiol. 20126:65-78. Epub 2012 Feb 23.

  10. Hypertension: management of hypertension in adults in primary care; NICE Clinical Guideline (August 2011)

  11. Baigent C, Blackwell L, Collins R, et al; Aspirin in the primary and secondary prevention of vascular disease: collaborative meta-analysis of individual participant data from randomised trials. Lancet. 2009 May 30373(9678):1849-60.

  12. British National Formulary (BNF); NICE Evidence Services (UK access only)

  13. Stroke and transient ischaemic attack in over 16s: diagnosis and initial management; NICE Guidance (May 2019)

  14. Stroke Guidelines; Royal College of Physicians (2016)

  15. Stroke and TIA; NICE CKS, March 2017 (UK access only)

  16. Clopidogrel and modified-release dipyridamole for the prevention of occlusive vascular events; NICE Technology Appraisal Guidance, December 2010

  17. A Comparison of Two LDL Cholesterol Targets after Ischemic Stroke; NEJM, 2019

  18. Skerritt MR, Block RC, Pearson TA, et al; Carotid endarterectomy and carotid artery stenting utilization trends over time. BMC Neurol. 2012 Mar 2912(1):17.

  19. Rerkasem K, Rothwell PM; Carotid endarterectomy for symptomatic carotid stenosis. Cochrane Database Syst Rev. 2011 Apr 13(4):CD001081.

  20. Chambers BR, Donnan GA; Carotid endarterectomy for asymptomatic carotid stenosis. Cochrane Database Syst Rev. 2005 Oct 19(4):CD001923.

  21. Hopkins LN, Myla S, Grube E, et al; Carotid artery revascularization in high surgical risk patients with the NexStent Catheter and the Filterwire EX/EZ: 1-year results in the CABERNET trial. Cardiovasc Interv. 2008 Jun 171(7):950-60.

  22. Ederle J, Dobson J, Featherstone RL, et al; Carotid artery stenting compared with endarterectomy in patients with symptomatic carotid stenosis (International Carotid Stenting Study): an interim analysis of a randomised controlled trial. Lancet. 2010 Mar 20375(9719):985-97. Epub 2010 Feb 25.

I suffered an epileptic criss again last week. Can anybody help me understand why it happened? And how to avoid any other criss? Thank you all. Faycal in Paris.

faycal23939
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