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Actions for Practice Teams Management of primary hypertension in adults October 2012 www.pctsla.org Actions for Practice Teams Why are we covering this? • • Hypertension is a major preventable cause of morbidity and mortality Lowering blood pressure (BP) in patients with hypertension decreases the risk of1,2: o o o o • 2 stroke coronary events heart failure renal impairment Hypertension may be underdiagnosed in the West Midlands o QOF-reported prevalence of hypertension in the West Midlands in 2010/11 was 14.6%. Public health (Eastern Region Public Health Observatory ) estimated prevalence was 32.6%.3 • Improved identification, diagnosis and treatment of hypertension could improve outcomes, reduce hospital admissions and costs to the NHS. Actions for Practice Teams What are we covering? The following slides provide information on primary hypertension in adults including: • Background • Definitions and classification of hypertension • Risk factors for hypertension and clinical events • Measurement of blood pressure • Hypertension diagnosis • Assessment of cardiovascular (CV) risk and target organ damage • Lifestyle advice • Blood pressure targets • Drug treatment • Patient education and counselling • Review of patients with hypertension We are not covering hypertension in pregnancy or children, secondary hypertension, accelerated hypertension or acute hypertension in emergency care settings 3 Actions for Practice Teams Background • • • • • 4 Hypertension is defined as a persistently raised BP (above a designated threshold). Estimated hypertension prevalence in West Midlands (2011)33.2% of men and 31.0% of women aged over 16 years.3 Hypertension is a major risk factor for stroke, myocardial infarction, heart failure, chronic kidney disease (CKD), cognitive decline and premature death.4 Hypertension is usually symptomless- screening and accurate diagnosis are therefore vital Diastolic pressure is more commonly elevated in younger people (age < 50 years). With aging, elevated systolic BP is a greater problem.4 Actions for Practice Teams Definitions and classification of hypertension4 Stage 1 Hypertension Stage 2 Hypertension Clinic BP ≥ 140/90 mmHg AND Daytime average ABPM or HBPM ≥ 135/85 mmHg Severe Hypertension Clinic BP ≥ 160/100 mmHg AND Daytime average ABPM or HBPM ≥ 150/95 mmHg Clinic systolic BP ≥ 180 mmHg OR Clinic diastolic BP ≥ 110 mmHg Isolated systolic Hypertension Systolic BP ≥ 160 mmHg, diastolic BP < 90 mmHg ABPM = ambulatory BP measurement HBPM = home BP measurement 5 Actions for Practice Teams Who is most at risk of hypertension? Predisposing risk factors for hypertension include5: • • • • • • • • • Increasing age Family history of CV disease African or Caribbean origin High intake of salt Sedentary lifestyle Co-existing disorders such as diabetes, obesity and hyperlipidaemia Smoking High intake of alcohol Stress 6 Actions for Practice Teams Risk factors for clinical events • 7 The risk of clinical events in hypertensive patients depends on o BP level o Calculated CV risk (estimated from factors such as age, gender, smoking history etc.) o Presence of target organ damage o Presence of established CV disease o Concomitant disease associated with CV risk (e.g. diabetes or CKD) • The risk associated with raised BP is continuous. o Each 20/10 mmHg rise in BP doubles risk of CV disease across the entire BP range starting from 115/75 mmHg.6 o Each 2 mmHg rise in systolic BP is associated with increased risk of mortality (7% from ischaemic heart disease, 10% from stroke).4 Actions for Practice Teams Measurement of BP 8 Method Brief Description of equipment Clinic BP measurement An automated device or the auscultatory (listening) method may be used. The auscultatory method involves use of a sphygmomanometer (mercury or alternative) and stethoscope by a trained healthcare professional. Automated machines detect oscillation in the arterial wall as blood flows though. Algorithms are used to calculate BP. Easier to use but less accurate than auscultatory method, particularly if pulse irregularity. Home BP measurement Fully automated, electronic, oscillometric devices are most commonly used. Upper arm devices are recommended (wrist and finger devices discouraged). BP values tend to be lower than clinic readings and treatment threshold and targets should be adjusted accordingly. Ambulatory BP measurement The patient wears a BP cuff attached to an automatic device that inflates the cuff at regular intervals (e.g. every 20 to 30 minutes during the day). Readings are recorded by the device and average day or night BP is determined from the data by a computer. BP readings are 10/5 mmHg lower than clinic BP readings. Ambulatory BP monitoring monitors use an oscillometric technique and are not suitable for patients with pulse irregularity. Actions for Practice Teams Clinic BP measurement • • • • 9 Detailed information on clinic BP measurement, including an educational video is available on the British Hypertension Society (BHS) website (http://www.bhsoc.org/resources/bhsdvd/). A list of validated BP-measuring devices can be obtained from the BHS Website (http://www.bhsoc.org/bp-monitors/bpmonitors/) . Devices for measuring BP should be properly validated, maintained and regularly recalibrated according to manufacturer’s instructions Healthcare professionals taking BP measurements need adequate training and periodic review of their performance Actions for Practice Teams Home BP measurement • • 10 A video of home BP measurement and list of suitable devices are available on the Blood Pressure UK Website http://www.bpassoc.org.uk/BloodPressureandyou/Thebasics/H omemonitoring Advise patients to: o Choose an upper arm pressure monitor with appropriate cuff size (finger and wrist monitors are less accurate). o Always use the same arm. Take three measurements twice a day in the morning before BP treatment and 12 hours later. o Avoid taking measurements when bladder is full, after exercise or within 30 minutes of taking caffeine or smoking o Record measurements with date and time, particularly in relation to when BP tablets are taken. Actions for Practice Teams Ambulatory BP monitoring (1) • Detailed information on ambulatory BP monitoring is now available on the BHS website. This includes a: o o o o • • • 11 Standard operating procedure for ambulatory BP monitoring Clinic checklist for fitting an ambulatory BP monitor A patient information leaflet Patient diary Ambulatory BP monitoring devices should be validated and properly maintained. A list of suitable devices is available from the BHS Website. Ambulatory BP monitoring machines are sold with software packages. Some provide basic data (e.g. average day and night-time values and a visual plot), others provide more detail. Clinicians responsible for delivering an ambulatory BP monitoring service should be fully trained. Actions for Practice Teams Ambulatory BP monitoring (2) • • • • 12 Patients must be capable of coping with and caring for the recorder. Consider whether they will be able to cope with the cuff inflating every half hour. Relax patient in a quiet room. The ambulatory BP monitoring process should be explained to the patient. Consider asking patients to make diary records of events that are known to affect BP. Sleep times should be recorded. Instruct patient on how to remove and inactivate monitor after 24 hours. Actions for Practice Teams NICE CG127: Hypertension • diagnosis4 13 NICE recommend that if the clinic BP ≥ 140/90 mmHg, 24-hour ambulatory BP monitoring should be offered to confirm the diagnosis of hypertension. o Take at least two measurements/hour during the day and use the average. Use average of at least 14 measurements. • Home BP measurement may be used to confirm diagnosis if ambulatory BP monitoring is unsuitable: o Two consecutive measurements should be taken at least one minute apart with the person seated. Use average values (discard first day’s measurements) o Record BP twice daily in the morning and evening for ≥ 4 days (ideally 7 days) • If hypertension is not diagnosed, measure BP in clinic at least every 5 years (more frequently if close to 140/90 mmHg). o If there is evidence of target organ damage, investigate causes Actions for Practice Teams • • • • • Why ambulatory BP monitoring for hypertension diagnosis? 14 Studies suggest that ambulatory BP monitoring is more accurate than clinic BP measurement for diagnosis of hypertension.7 “White coat effect” can lead to artificially high clinic BP readings Up to 25% of people with high clinic BP readings subsequently have normal BP on ambulatory BP monitoring4 Ambulatory monitoring is a better predictor of heart disease and stroke associated with hypertension than single clinic measurements.8-10 Use of ambulatory BP monitoring for patients with high clinic BP measurements may reduce misdiagnosis and ultimately reduce costs.11 Actions for Practice Teams • Assessment of CV risk and target organ damage (1) 15 The 10-year risk of CV disease in hypertensive patients should be estimated using a validated risk assessment tool. This should be used to discuss prognosis and healthcare options.4 • Follow local advice regarding which tool should be used. • Examples of validated risk assessment tools are: o QRISK®2 Cardiovascular Risk Score (http://qrisk.org) o Joint British Societies risk prediction chart (see BNF or http://www.bhsoc.org/latest-guidelines/cvd-risk-chart-andcalculators/ ) o Framingham risk equation (http://hp2010.nhlbihin.net/atpiii/calculator.asp ) Actions for Practice Teams Assessment of CV risk and target organ damage (2) 16 The following tests are recommended by NICE to help assess CV risk, identify diabetes, hypertensive damage to heart and kidney, and secondary causes of hypertension (e.g. renal disease): o 12-lead electrocardiogram o Test urine for presence of protein o Take blood to measure plasma glucose, electrolytes, creatinine, estimated glomerular filtration rate, serum total cholesterol and HDL cholesterol o Examine fundi for hypertensive retinopathy • If initial clinical examination suggests possibility of secondary hypertension, NICE recommends patient is referred for specialist review. Actions for Practice Teams Specialist referral • • 17 If initial clinical examination suggests possibility of secondary hypertension, NICE recommend patient is referred for specialist review.4 Refer the same day if o accelerated hypertension (BP > 180/110 mmHg with signs of papilloedema and/or retinal haemorrhage) o suspected phaechromocytoma Actions for Practice Teams Key lifestyle advice and associated BP reductions Modification 18 Approximate mean BP reduction Weight reduction (if overweight) Cochrane systematic review (2011): mean reduction in systolic and diastolic BP of 4.5 mmHg and 3.2 mm Hg respectively12 Exercise e.g. 30 to 60 mins, 3 to 5 times each week NICE meta-analysis (2011): mean reduction in systolic BP (3.1 mmHg) and diastolic BP (1.8 mmHg)4 Alcohol consumption Men: max 21 unit/week Women: max 14 unit/week Meta-analysis of 15 RCTs (2001): mean reduction in systolic BP of 3.3 mmHg, diastolic BP 2 mmHg13 Dietary sodium reduction (< 6 g of salt) NICE meta-analysis (2011): mean systolic BP reduction of 3.4 mmHg, diastolic BP reduction of 2.2 mmHg4 Caffeine consumption Consumption of five or more cups a day associated with small increase in BP14 Smoking cessation Smoking is associated with poor CV and pulmonary outcomes Evidence does not support use of calcium, magnesium or potassium supplementation.4 Relaxation therapies are not provided by the NHS. Patient information on lifestyle changes is available from the Blood Pressure Association Website http://www.bpassoc.org.uk/BloodPressureandyou/Yourlifestyle Actions for Practice Teams Initiation of drug treatment4 (1) 19 For stage 1 hypertension: • If aged less than 80 years, offer antihypertensive drugs to people if they also have one or more of the following: o o o o o • • • target organ damage established CV disease renal disease diabetes a 10-year CV risk ≥ 20% If aged 40 to 80 years with none of the above conditions, advise on lifestyle changes (see slide 18) If aged ≤ 40 years with none of the above conditions, seek specialist advice regarding evaluation for secondary causes If aged > 80 years and newly diagnosed with stage 1 hypertension, decision to treat should be based on the presence of other co-morbidities Actions for Practice Teams Initiation of drug • • • treatment4 (2) All patients with stage 2 hypertension should receive treatment, regardless of age. For patients with isolated systolic hypertension, treat as for patients with both a raised systolic and diastolic BP. For patients with severe hypertension, consider starting antihypertensive treatment immediately 20 Actions for Practice Teams Blood pressure targets • • • • • 21 Monitor blood pressure at least annually (more frequently if titrating drug treatment) using clinic blood pressure measurements (note: QOF requires practices to record blood pressure at least every nine months). In patients with “white coat effect”, consider ambulatory BP monitoring or home BP measurement as adjunct. Non-diabetic patients aged less than 80 years4: o target clinic BP < 140/90 mmHg o target ambulatory BP or home BP < 135/95 mmHg Non-diabetic patients aged over 80 years4 o target clinic BP < 150/90 mmHg o target ambulatory BP or home BP < 145/85 mmHg Patients with diabetes15 o target clinic BP < 140/80 mmHg (< 130/80 mmHg if kidney, eye or cerebrovascular disease) Actions for Practice Teams Antihypertensive drug treatment • The choice of a specific drug or a drug combination should take into account the following: o o o o o o o o NICE/local guidelines CV risk profile of the patient Comorbidities Severity of hypertension Interactions with drugs used for concomitant conditions Age Ethnicity Previous patient experience of the drug (favourable or unfavourable) o Cost 22 Actions for Practice Teams Antihypertensive therapy: 23 adverse effects/contraindications/monitoring Contraindications/ Adverse effects Monitoring Drug class Angiotensin converting enzyme inhibitors (ACEi) (e.g. ramipril, lisinopril) Angiotensin-II receptor antagonists (ARBs) (e.g. losartan, candesartan, valsartan) Dihydropyridine calcium channel blockers (CCBs) (e.g. felodipine, amlodipine) Rate-limiting CCBs (e.g. diltiazem, verapamil) Thiazide-like diuretics (e.g. chlortalidone, indapamide) Thiazide diuretics (e.g. bendroflumethiazide, hydrochlorthiazide) precautions Generally well tolerated but may cause dry cough (about 15%), loss of taste, rarely angioedema, first dose hypotension, hyperkalaemia, renal impairment Contraindicated in pregnancy, not recommended if breastfeeding. Caution in renal impairment or peripheral vascular disease. Monitor renal function and serum electrolytes particularly in elderly and in renal impairment. Well tolerated but may cause dizziness and syncope, hyperkalaemia, impairment of renal function Contraindicated in pregnancy, not recommended if breastfeeding. Caution in renal impairment and in peripheral vascular disease. Monitor renal function and serum electrolytes, particularly in elderly and in renal impairment. Dihydropyridinesheadache and facial flushing, tachycardia and palpitation, ankle swelling Rate-limiting CCBsbradycardia, atrioventricular conduction delay. Verapamil may cause constipation. Avoid diltiazem and verapamil in heart failure. Max dose for simvastatin in combination with amlodipine, verapamil or diltiazem is 20 mg. Do not combine a beta- blocker with verapamil, caution with diltiazem. Prescribe SR nifedipine and diltiazem (except 60 mg) by brand. Hypokalaemia, may cause or exacerbate diabetes or gout, hypercalcaemia, erectile dysfunction Avoid in gout, not recommended during pregnancy. Caution in combination with beta-blocker. Monitor renal function and serum electrolytes, particularly potassium levels. Actions for Practice Teams Antihypertensive therapy: 24 contraindications/cautions/monitoring Drug class Beta-blockers (e.g. atenolol, bisoprolol, metoprolol) Alpha blockers (e.g.doxazosin, terazosin) For resistant hypertension Adverse effects Contraindications/ precautions Bronchospasm in susceptible individuals, bradycardia, lethargy, depression, sleep disturbances, coldness of the extremities, risk of new onset diabetes, masking of hypoglycaemia in insulindependent diabetes Contraindicated in asthma, COPD with significant reversibility and heart block. Caution advised in unstable heart failure, peripheral vascular disease, diabetes, with concomitant thiazide or thiazide-like diuretics. Do not combine a beta- blocker with verapamil, caution with diltiazem. Dizziness, drowsiness, postural hypotension, headache, flushing, nasal congestion, fluid retention, weakness Vary by drug Monitoring Actions for Practice Teams NICE: Antihypertensive treatmentnon-diabetes4 Based on CG127 Hypertension slide set, published August 2011 by NICE to be used in conjunction with guidance CG127 Aged under 55 years 25 Aged over 55 years or black person (African, Caribbean origin) of any age CCB Step 1 ACEi and ARBs contraindicated Step 2 in pregnancy Step 3 ACEi or low-cost ARB (if CCB not suitable, consider thiazidelike diuretic) ACEi (or low-cost ARB) + CCB (or thiazide-like diuretic if CCB not suitable) (ARB is preferred to ACEi for black people of African or Caribbean origin) ACEi (or low-cost ARB) + CCB + thiazide-like diuretic Resistant Hypertension Step 4 ACEi (or low-cost ARB) + CCB + thiazide-like diuretic + consider further diuretic or alpha- or beta-blocker Consider seeking expert advice Where possible, use drugs that are taken once a day and prescribe non-proprietary drugs. Titrate to optimum or maximum tolerated dose at each step of treatment. Unless it is necessary to lower blood pressure urgently, an interval of at least 4 weeks should be allowed to determine response. Blood pressure targets: • If kidney, eye or cerebrovascular damage, set a target < 130/80 mmHg • Others, set a target < 140/80 mmHg 26 Based on NICE clinical guideline 87 Type 2 Diabetes published in May 2009 Monitor BP 1-2 monthly until consistently below target BP above target Maintain lifestyle measures Actions for Practice Teams NICE: Antihypertensive drug treatmenttype 2 diabetes15 Offer ACEi (titrate dose); for people of African-Caribbean descent, offer ACEi plus diuretic or CCB BP above target Add CCB or diuretic If there is a possibility of the person becoming pregnant, start with a CCB. If continuing intolerance to ACEi (other than renal deterioration or hyperkalaemia), change to an ARB BP above target Add other drug (diuretic or CCB – see above) BP above target Add alpha-blocker, beta-blocker or potassium-sparing diuretic Use a potassium-sparing diuretic with caution if already taking ACEi or ARB Actions for Practice Teams Annual cost comparison of selected antihypertensive drugs 27 £207.66 irbesartan Aprovel® (75mg to 300mg) £126.32 £205.57 eprosartan Teveten® (300mg to 800mg) £95.29 £147.56 felodipine (5mg to 20mg) £54.88 £129.58 perindopril arginine Coversyl Arginine® (2.5mg to 10mg) £53.90 £96.73 valsartan capsules (80mg to 320mg) £37.28 £61.40 candesartan (8mg to 32mg) £36.50 £50.06 lisinopril (2.5mg to 80mg) £9.65 £41.37 indapamide M/R (1.5mg) losartan (25mg to 100mg) £25.42 £20.21 perindopril erbumine (4mg to 8mg) £25.29 £23.33 £21.38 chlortalidone Hygroton® (50mg) ramipril capsules (1.25mg to 10mg) £15.12 £11.08 indapamide (2.5mg) £13.56 £11.08 £10.17 amlodipine (5mg to 10mg) Maximum £9.26 bendroflumethiazide (2.5mg) £0 Minimum £50 £100 £150 £200 £250 Actions for Practice Teams Other measures to reduce CV risk • Review use of drugs that may potentially exacerbate hypertension (prescribed or OTC) including: o o o o o • 28 Non-steroidal anti-inflammatory drugs (NSAIDs) Soluble analgesics (high sodium content) Combined hormonal contraceptives Steroids Sympathomimetics (in some cold medicines) Additional therapy to lower CV risk should be considered for patients with target organ damage, established CV disease, diabetes, CKD or estimated 10 year CVD risk ≥ 20% o Aspirin for patients with established CV disease (unless contraindicated) o Aspirin is not licensed for primary prevention of vascular events and is of unproven benefit (with or without diabetes).16-20 Consider benefits and risks for each individual. o Statins should be used in line with NICE guidance on lipid lowering drugs (CG67). 21 Actions for Practice Teams Patient education and counselling (1) • • • Repeated in-depth patient education and counselling improves adherence to treatment and reduces CV risk factors. Support adherence to antihypertensive drugs as this is often suboptimal. Poor adherence has been associated with complications including CV death. o Recent systematic review suggests that adherence may be particularly poor in those prescribed diuretics and beta-blockers22 Interventions to support adherence may include23: o o o o o • 29 suggesting that patients record their medicine-taking encouraging patients to monitor their condition simplifying the dosing regimen using alternative packaging for the medicine using a multi-compartment medicines system. Explain that although high BP is usually symptomless, it increases the chance of strokes, heart attacks, heart failure, or kidney failure. Actions for Practice Teams Patient education and counselling (2) • 30 Provide information on benefits and side effects of drugs. o Advise patients on what to do if they develop an adverse reaction to their medication o Explain that hypertensive medication usually needs to be taken for life. • Advise patients that although medication may be stopped if blood pressure becomes well controlled, particularly after lifestyle changes, it should be regularly checked thereafter o Blood pressure may rise again a year or more after treatment withdrawal • • Discuss appropriate lifestyle changes (see slide 18) Patient information on blood pressure and antihypertensive drugs is available from Blood Pressure UK (http://www.bpassoc.org.uk ) and the British Heart Foundation (http://www.bhf.org.uk ) Actions for Practice Teams Follow-up and monitoring • • • • • 31 NICE recommend that patients with hypertension are reviewed annually Check blood pressure, renal function and test for proteinuria Reinforce lifestyle advice and check adherence to antihypertensive drugs Is a change to antihypertensive drug treatment indicated? Consider: o Is blood pressure adequately controlled? o Adverse effects? If the person is not taking a statin, assess CV risk and consider whether this treatment would be appropriate. For patients requiring secondary prevention, review need for antiplatelets. Actions for Practice Teams References 1) 2) 3) 4) 5) 6) 7) 8) 9) 10) 11) 12) 13) 14) 15) 16) 17) 18) 19) 20) 21) 22) 23) 24) 32 Law MR, Morris JK, Wald NJ. Use of blood pressure lowering drugs in the prevention of cardiovascular disease: meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ 2009;338:b1665. Lv J, Neal B, Ehteshami P et al. Effects of intensive blood pressure lowering on cardiovascular and renal outcomes: a systematic review and meta-analysis. PLoS Med 2012;9:e1001293. East of England Public Health Observatory. Modelled estimate of prevalence of hypertension in England. 2011 http://www.apho.org.uk/resource/item.aspx?RID=111119 Hypertension: Clinical management of primary hypertension in adults. National Institute for Health and Clinical Excellence. CG127 2011. http://publications.nice.org.uk/hypertension-cg127 <accessed 7/2012> Maryon-Davis A, Press V. Hypertension: the public health burden. Faculty of Public Health and National Heart Forum. 2005. http://www.fph.org.uk/uploads/Section%20Ahypertension.pdf <accessed 9/2012> Chobanian AV, Bakris GL, Black HR et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA 2003;289:2560-72. Hodgkinson J, Mant J, Martin U et al. Relative effectiveness of clinic and home blood pressure monitoring compared with ambulatory blood pressure monitoring in diagnosis of hypertension: systematic review. BMJ 2011;342:d3621. Ohkubo T, Hozawa A, Nagai K et al. Prediction of stroke by ambulatory blood pressure monitoring versus screening blood pressure measurements in a general population: the Ohasama study. J Hypertens 2000;18:847-54. Staessen JA, Thijs L, Fagard R et al. Predicting cardiovascular risk using conventional vs ambulatory blood pressure in older patients with systolic hypertension. Systolic Hypertension in Europe Trial Investigators. JAMA 1999;282:539-46. Imai Y, Ohkubo T, Sakuma M et al. Predictive power of screening blood pressure, ambulatory blood pressure and blood pressure measured at home for overall and cardiovascular mortality: a prospective observation in a cohort from Ohasama, northern Japan. Blood Press Monit 1996;1:251-4. Lovibond K, Jowett S, Barton P et al. Cost-effectiveness of options for the diagnosis of high blood pressure in primary care: a modelling study. Lancet 2011;378:1219-30. Siebenhofer A, Jeitler K, Berghold A et al. Long-term effects of weight-reducing diets in hypertensive patients. Cochrane Database Syst Rev 2011;CD008274. Xin X, He J, Frontini MG et al. Effects of Alcohol Reduction on Blood Pressure. Hypertension 2001;38:1112-7. Jee SH, He J, Whelton PK et al. The effect of chronic coffee drinking on blood pressure: a meta-analysis of controlled clinical trials. Hypertension 1999;33:647-52. Type 2 diabetes: The management of type 2 diabetes. CG87. National Institute for Health and Clinical Excellence. 2009. http://publications.nice.org.uk/type-2-diabetescg87/guidance <accessed 9/2012> 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;373:1849-60. Fowkes FG, Price JF, Stewart MC et al. Aspirin for prevention of cardiovascular events in a general population screened for a low ankle brachial index: a randomized controlled trial. JAMA 2010;303:841-8. De Berardis G, Sacco M, Strippoli GF et al. Aspirin for primary prevention of cardiovascular events in people with diabetes: meta-analysis of randomised controlled trials. BMJ 2009;339:b4531. Lip GYH, Felmeden DC, Dwivedi G. Antiplatelet agents and anticoagulants for hypertension. Cochrane Database of Systematic Reviews 2011, Issue 12. Art. No.: CD003186. DOI: 10.1002/14651858.CD003186.pub3 Aspirin: not licensed for primary prevention of thrombotic vascular disease. Drug Safety Update. Volume 3, Issue 3. Medicines and Healthcare products Regulatory Agency. 2012. http://www.mhra.gov.uk/Safetyinformation/DrugSafetyUpdate/CON087716 <accessed 9/2012> Lipid modification. CG67. National Institute for Health and Clinical Excellence. 2008. http://www.nice.org.uk/nicemedia/live/11982/40689/40689.pdf <accessed 9/2012> Kronish IM, Woodward M, Sergie Z et al. Meta-analysis: impact of drug class on adherence to antihypertensives. Circulation 2011;123:1611-21. Medicines adherence: Involving patients in decisions about prescribed medicines and supporting adherence. CG76. National Institute for Health and Clinical Excellence. 2009. http://publications.nice.org.uk/medicines-adherence-cg76/guidance#supporting-adherence <accessed 7/2012> Hypertension in people who do not have diabetes-management. Clinical Knowledge Summaries. 2010. <accessed 10/2012>