BMJ 1999;319:630-635 ( 4 September )

Education and debate

British Hypertension Society guidelines for hypertension management 1999: summary

Lawrence E Ramsay, professor of clinical pharmacology and therapeutics a Bryan Williams, professor of medicine b G Dennis Johnston, professor of clinical pharmacology c Graham A MacGregor, professor of cardiovascular medicine d Lucilla Poston, professor of fetal medicine e John F Potter, professor of medicine for the elderly b Neil R Poulter, director, cardiovascular studies unit f Gavin Russell, consultant renal physician g

a University of Sheffield, Sheffield S10 2TN, b University of Leicester School of Medicine, Leicester Royal Infirmary, Leicester LE2 7LX, c Queen's University of Belfast, Belfast BT7 1NN, d Department of Medicine, St George's Hospital, London SW17 0RE, e Department of Obstetrics and Gynaecology, St Thomas's Hospital, London SE1 7EH, f Imperial College School of Medicine, London W2 1NY, g North Staffordshire Royal Infirmary, Stoke on Trent ST4 7LN

Correspondence to: B Williams bw17{at}leicester.ac.uk

This article summarises the new British Hypertension Society guidelines for management of hypertension, which have been published in full.1 Since the previous guidelines 2 3 much new evidence has emerged on optimal blood pressure targets4; management of hypertension in diabetic patients4-7; treatment of isolated systolic hypertension8; comparison of the antihypertensive efficacy and tolerability of different drug classes9-11; the role of non-pharmacological measures for prevention 12 13 and treatment of hypertension14; and additional benefits associated with the use of aspirin and statins.

Of concern is that national surveys continue to reveal incomplete detection, treatment, and control of hypertension.15 Furthermore, treated hypertensive patients still die prematurely from cardiovascular disease.16 These guidelines aim to present the best currently available evidence on hypertension management and their implementation.


Summary points


Use non-pharmacological measures in all hypertensive and borderline hypertensive people

Initiate antihypertensive drug treatment in people with sustained systolic blood pressure >= 160 mm Hg or sustained diastolic blood pressure >= 100 mm Hg

Decide on treatment in people with sustained systolic blood pressure between 140 and 159 mm Hg or sustained diastolic blood pressure between 90 and 99 mm Hg according to the presence or absence of target organ damage, cardiovascular disease, diabetes, or a 10 year coronary heart disease risk >= 15% according to the Joint British Societies coronary heart disease risk assessment programme or risk chart

Optimal blood pressure treatment targets are systolic blood pressure <140 mm Hg and diastolic blood pressure <85 mm Hg; the minimum acceptable level of control (audit standard) recommended is <150/<90 mm Hg

In the absence of contraindications or compelling indications for other antihypertensive agents, low dose thiazide diuretics or beta  blockers are preferred as first line treatment for the majority of hypertensive people; compelling indications and contraindications for all antihypertensive drug classes are specified

Other drugs that reduce cardiovascular risk must also be considered; these include aspirin and statins


Box 1 : Blood pressure measurement

  • Use the British Hypertension Society's recommendations
  • Use a device with validated accuracy that is properly maintained and calibrated
  • Patient should be seated with the arm at the level of the heart. The bladder size should be adjusted for the arm circumference, the cuff deflated at 2 mm/s and the blood pressure measured to the nearest 2 mm Hg. Diastolic pressure is recorded as disappearance of the sounds (phase V)
  • At least two measurements should be made at each of several visits to determine blood pressure thresholds (see figure).


Box 2 : Indications for ambulatory blood pressure monitoring (ABPM)

  • When clinic blood pressure shows unusual variability
  • Hypertension is resistant to drug treatment (three or more drugs)
  • When symptoms suggest the possibility of hypotension
  • To diagnose "white coat hypertension"



    Blood pressure measurement

All adults should have their blood pressure measured routinely at least every five years until the age of 80 years. Those with high-normal values (135-139/85-89 mm Hg) and those who have had high readings at any time previously should have their blood pressure remeasured annually. The British Hypertension Society's recommendations for measuring blood pressure should be followed (box 1).17 Seated blood pressure recordings are generally sufficient, but standing blood pressure should be measured in elderly or diabetic patients to exclude orthostatic hypotension. Ambulatory blood pressure monitoring may be helpful (box 2).

    Estimating risk of coronary heart disease or cardiovascular disease

Formal estimation of coronary heart disease risk has been proposed as an aid to treatment decisions in hypertension.18 Mindful of the strong relation between blood pressure and stroke risk, the British Hypertension Society acknowledges that targeting cardiovascular disease risk rather than coronary heart disease risk is preferable. However, to be consistent with three existing national guideline recommendations,19-21 we recommend formal estimation of 10 year coronary heart disease risk using the Cardiac Risk Assessor computer program or the coronary heart disease risk chart issued by the Joint British Societies in their recommendations for coronary heart disease prevention.19 This pragmatic recommendation is reasonable because coronary heart disease risk is a good predictor of cardiovascular disease risk, which can be estimated by multiplying the coronary heart disease risk level by 4/3 (for example, 30% coronary heart disease risk=40% cardiovascular disease risk). Moreover, estimates of 10 year stroke risk as well as coronary heart disease risk are provided by the Joint British Societies' Cardiac Risk Assessor computer program. 1 19 The levels of coronary heart disease risk quoted in these guidelines will appropriately precipitate intervention for patients at higher risk of cardiovascular disease.

    Evaluation of hypertensive patients

All hypertensive patients should have a thorough history and physical examination, but need only a limited number of routine investigations (box 3). The purpose of the evaluation is to assess the cause of the hypertension, associated cardiovascular risk factors, evidence of target organ damage, and comorbid diseases, all of which may influence treatment decisions. More complex investigations may require specialist referral (box 4).


Box 3 : Routine investigation of hypertensive people

  • Urine strip test for blood and protein
  • Blood electrolytes and creatinine
  • Blood glucose
  • Serum total:HDL cholesterol ratio
  • 12 lead electrocardiograph


Box 4 : Indications for specialist referral

  • Urgent treatment indicated: malignant hypertension, impending complications
  • To investigate potential underlying causes of hypertension when initial evaluation suggests this possibility
  • To evaluate therapeutic problems or failures
  • Special circumstances: unusually variable blood pressure, possible white coat hypertension, pregnancy



    Non-pharmacological measures

Non-pharmacological advice should be offered to all hypertensive people and those with a strong family history of hypertension. Such measures may obviate the need for drug treatment or reduce the dose or number of drugs required to control blood pressure. 12 14 In patients with mild hypertension but no cardiovascular complications or target organ damage, the response to these measures should be observed during the initial 4-6 month period of evaluation. When drug treatment has to be introduced more quickly, non-pharmacological measures should be instituted in parallel with drug treatment.

Good evidence from trials shows that several lifestyle modifications lower blood pressure: weight reduction to achieve an ideal body weight via reduced fat and total calorie intake12; regular physical exercise designed to improve fitness---this should be predominantly dynamic (brisk walking, for example) rather than isometric (weight training); limiting alcohol consumption to <21 units per week for men and <14 units per week for women; reduced use of salt when preparing food and elimination of excessively salty foods from the diet14; increased consumption of fruit and vegetables.12 Lifestyle modifications that further reduce cardiovascular disease risk are stopping smoking; reducing total intake of saturated fat, replacing it with polyunsaturated or monounsaturated fats; increased intake of oily fish; and regular physical exercise.

Effective implementation of these non-pharmacological measures requires enthusiasm, knowledge, patience, and time spent with patients and their families. It is best undertaken by well trained health professionals---for example, a practice or clinic nurse---and should be backed up by simple clear written information.

    Thresholds for intervention with drug treatment

Systolic blood pressure is at least as important as diastolic blood pressure as a predictor of cardiovascular disease. Systolic and diastolic blood pressure thresholds are thus provided to guide intervention with drug treatment in people with hypertension (figure).



View larger version (42K):
[in this window]
[in a new window]
 
Blood pressure thresholds and drug treatment in hypertension


    Treatment goals or "targets"

The hypertension optimal treatment (HOT) trial was underpowered but provides the best evidence to date on optimal blood pressure targets.4 Optimal blood pressure for reduction of major cardiovascular events (based on an analysis of patients receiving treatment) was reported to be 139/83 mm Hg and reduction of blood pressure below this level caused no harm. However, patients whose blood pressure was below 150/90 mm Hg were not apparently disadvantaged. An intention to treat analysis in hypertensive patients with diabetes showed that lowering blood pressure to below 80 mm Hg rather than below 90 mm Hg was advantageous. Recommendations for target pressures during treatment are shown in table 1. It is emphasised that even with best practice, these targets will not be achieved in all hypertensive people.


                              
View this table:
[in this window]
[in a new window]
 

Table 1. Suggested target blood pressures during antihypertensive treatment. Both systolic and diastolic values should be attained---for example, <140/85 mmHg means less than 140 systolic and less than 85 diastolic



    Choice of antihypertensive drug

For each class of antihypertensive drug there are compelling indications based on sound randomised controlled trial data for use in specific patient groups, and also compelling contraindications. There are also indications and contraindications that are less clear-cut, and which are given different weight by different doctors (possible indications/contraindications). These indications and contraindications for each drug class are summarised in table 2. When none of the special considerations apply, the least expensive drug, with the most supportive trial evidence---a low dose of a thiazide diuretic---should be preferred.


                              
View this table:
[in this window]
[in a new window]
 

Table 2. Compelling and possible indications and contraindications for the major classes of antihypertensive drugs

Since publication of the previous guidelines,3 three long term, double blind studies have compared the major classes of antihypertensive drugs (thiazide, beta  blocker, calcium antagonist, angiotensin converting enzyme inhibitor, and alpha  blocker) and overall showed no consistent or important differences as regards antihypertensive efficacy, side effects, or quality of life.9-11 Differences in average response between drug classes are, however, related to age and ethnic group.10 Few trials have compared different classes of drugs directly as regards reduction in cardiovascular events,22 and none is entirely satisfactory, but they have shown no consistent differences between regimens based on different drug classes. With the exception of the systolic hypertension-Europe and systolic hypertension-China trials and the captopril prevention project study, 8 23 24 most evidence from outcome trials is for treatment based on thiazide or beta  blockers. Indirect comparison between the systolic hypertension in the elderly program,25 based on diuretic treatment, and the systolic hypertension-Europe trial,8 based on a dihydropyridine calcium antagonist, found that the outcome with these regimens was similar.

Controlled trials of dihydropyridine calcium antagonists have not supported earlier concerns about the safety of these drugs, 8 23 although nifedipine in capsule form should no longer be prescribed.

    Dosage and combination therapy

The drug or formulation used should ideally be effective when taken as a single daily dose. An interval of at least four weeks to observe the full response should be allowed, unless it is necessary to lower blood pressure more urgently. The dose of drug (except thiazide diuretics) should be increased according to manufacturers' instructions. If the first drug is well tolerated but the response is small and insufficient, substitution of an alternative drug is appropriate when hypertension is mild and uncomplicated. In more severe or complicated hypertension it is safer to add drugs stepwise until blood pressure control is attained. Treatment can be stepped down later if blood pressure falls substantially below the optimal level.

Most hypertensive people will require combinations of antihypertensive therapy to achieve optimal control. 4 6 Drugs from different classes generally have additive effects on blood pressure when they are prescribed together. Submaximal doses of two drugs result in larger responses of blood pressure and fewer side effects than maximal doses of a single drug. Rational drug combinations combine drugs with different modes of action that are additive---for example, diuretic with beta  blocker, diuretic with angiotensin converting enzyme inhibitor, beta  blocker with calcium antagonist, calcium antagonist with angiotensin converting enzyme inhibitor. Fixed dose combinations may be convenient for patients and are acceptable when monotherapy is ineffective, individual drug components are appropriate, and there are no major cost implications.

    Elderly people with hypertension

Hypertension, including isolated systolic hypertension (>= 160/<90 mm Hg), is found in more than half of all people aged over 60.15 These people have a higher risk of cardiovascular complications, including heart failure and dementia, than do younger people with hypertension, and antihypertensive treatment of diastolic hypertension26 and isolated systolic hypertension reduces this risk. 8 25 Antihypertensive treatment is beneficial until at least age 80, and regular screening of blood pressure should continue until this age. Once treatment is started, it should be continued after the age of 80. When hypertension is first diagnosed in people over 80, there is limited evidence to guide policy but treatment decisions should probably be based on biological rather than chronological age. Low dose thiazides are the accepted first line treatment for elderly people. beta  Blockers are less effective than thiazides as first line treatment; in a meta-analysis they were shown to reduce only stroke events.27 Dihydropyridine calcium antagonists are suitable alternatives for elderly patients when thiazides are ineffective, contraindicated, or not tolerated.8

The full version of the guidelines includes other special groups of patients: those with type I and type II diabetes; those with renal disease; pregnant women; users of oral contraceptives; users of hormone replacement therapy; and ethnic subgroups.1

    Aspirin and hypertension

In the hypertension optimal treatment trial, 75 mg aspirin daily reduced major cardiovascular events in hypertensive patients by 15%, but not fatal events.4 Similar effects were observed in the hypertensive cohort within the thrombosis prevention trial of aspirin.28 In both trials, however, the number of major bleeding episodes due to aspirin was similar to the number of cardiovascular events saved. Hence for primary prevention, aspirin should be considered only for hypertensive people who meet the criteria set out in box 5.    


Box 5 : Other measures to reduce cardiovascular risk

Patients with established cardiovascular disease or at high risk according to the Joint British Societies' Cardiac Risk Assessor computer program or coronary heart disease risk chart should be considered for aspirin and statin therapy as follows:

  • For primary prevention, 75 mg aspirin is recommended for hypertensive patients aged 50 years or older who have satisfactory control of their blood pressure (<150/90 mm Hg) and either target organ damage or diabetes or a 10 year coronary heart disease risk >= 15
  • For primary prevention, statin therapy is indicated up to age 70 when serum total cholesterol is >= 5.0 mmol/l and the 10 year coronary heart disease risk is >= 30
  • For secondary prevention (when there is evidence of cardiovascular disease (angina or myocardial infarction)), statin therapy is indicated up to age 75 when total serum cholesterol is >= 5.0 mmol/l



    Treatment with statins

Several trials have shown that statin treatment reduces coronary events and all cause mortality and is safe, simple, and well tolerated in both secondary and primary prevention.19 Statin treatment also reduces stroke risk substantially in patients who have coronary heart disease.19 In subgroup analyses, benefits were similar in hypertensive patients. Given the persistent high cardiovascular risk in treated hypertensive patients, and the relation of this risk to serum cholesterol,16 these trials have large implications for hypertension management. Statin treatment could now be justified at a 10 year coronary heart disease risk of 6%,29 but this would entail treating over half of all hypertensive patients. The main constraint on statin treatment at present is its cost.

The British Hypertension Society's recommendations for statin therapy are designed to be consistent with three recent sets of UK guidelines.19-21 These are conservative recommendations and represent minimum acceptable levels of treatment. Statin treatment should be prioritised by using the criteria set out in box 5.

    Follow up

The frequency of follow up for treated patients with adequate blood pressure control depends on factors including severity and variability of blood pressure, complexity of the treatment regimen, compliance, and the need for non-pharmacological advice. Three monthly review is sufficient when treatment and blood pressure are stable; the interval should not generally exceed six months. The routine for follow up visits, at which trained nurses have an important role, should be simple: measure blood pressure and weight; inquire about general health and side effects; reinforce non-pharmacological advice; and test urine for proteinuria annually.

    Objectives of the guidelines

  • To promote the primary prevention of hypertension and cardiovascular disease by encouraging changes in the diet and lifestyle of the whole population
  • To increase detection and treatment of undiagnosed hypertension (particularly among those at high risk) by routine screening and increasing awareness of hypertension among the public
  • To increase the proportion of patients on antihypertensive treatment who have optimal blood pressure levels
  • To reduce the cardiovascular risk of treated hypertensive patients by non-pharmacological measures and by appropriate use of aspirin and statin treatment
  • To promote continuation of and compliance with treatment by optimising the choice and use of drugs, minimising side effects, and increasing information and choice for patients.


    Implementation of guidelines

Realisation of these objectives will depend largely on the efforts of doctors and nurses in general practice. Surveys revealing incomplete detection, treatment, and control of hypertension indicate a serious failure to implement the knowledge we have, although there has been some improvement in recent years.15 Ideally, all practices or primary care groups should develop a protocol for hypertension management that covers screening policy; initial evaluation and investigation; estimation of cardiovascular risk; non-pharmacological measures; use of antihypertensive drugs, aspirin, and statins; treatment targets; follow up strategy; and methods for identifying and recalling patients who drop out of follow up. Written information should be available for patients about hypertension and its treatment. The protocol should detail those aspects of management that are in the province of the practice nurse and of the doctor, and the implementation of the practice policy should be audited periodically.

    Acknowledgments

The authors of this manuscript were members of the executive committee of the British Hypertension Society who formed the third working party for the production of these guidelines. LER chaired the working party and produced the first draft after receiving written sections from each member. This draft was reviewed by the membership of the British Hypertension Society and their comments were used by BW to modify subsequent drafts. BW coordinated the final writing and preparation of the manuscript which was reviewed and approved at each draft stage by all members of the working party.

    Footnotes

Competing interests: None declared.

    Appendix

Material for patients

Available from the British Hypertension Society Information Service, Blood Pressure Unit, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE (tel: 0181 725 3412; fax: 0181 725 2959;
www.hyp.ac.uk/bhsinfo/ (for information service); website: www.hyp.ac.uk/bhs/)

Material for doctors

  • Blood Pressure Measurement---Recommendations of the British Hypertension Society. 3rd edition, 1997. (Edited by E O'Brien et al; price £4.95.)
  • BHS/BMJ. Recommendations for Blood Pressure Measurement. CD Rom, price £58.75.

Available from BMJ Publications or the BMJ Bookshop, BMA House, London WC1H 9JR (tel: 0171 383 6244; fax: 0171 383 6455; orders{at}bmjbookshop.com).

  • The Joint British Societies' Cardiac Risk Assessor computer program and copies of the Joint British Societies coronary heart disease risk assessment chart can be downloaded from the British Hypertension Society website (www.hyp.ac.uk/bhs/).
    References

1. Ramsay LE, Williams B, Johnston DG, MacGregor GA, Poston L, Potter JF, et al. Guidelines for management of hypertension: report of the third working party of the British Hypertension Society, 1999. J Hum Hypertens 1999; 13: 569-592[Medline].
2. Swales JD, Ramsay LE, Coope JR, Pocock SJ, Robertson JIS, Sever PS, et al. Treating mild hypertension. BMJ 1989; 298: 694-698.
3. Sever P, Beevers G, Bulpitt C, Lever A, Ramsay L, Reid J, et al. Management guidelines in essential hypertension: report of the second working party of the British Hypertension Society. BMJ 1993; 306: 983-987.
4. Hansson L, Zanchetti A, Carruthers SG, Dahlöf B, Elmfeldt D, Julius S, et al, for the HOT Study Group. Effects of intensive blood-pressure lowering and low-dose aspirin in patients with hypertension: principal results of the hypertension optimal treatment (HOT) randomised trial. Lancet 1998; 351: 1755-1762[Medline].
5. Curb JD, Pressel SL, Cutler JA, Savage PJ, Aplegate WB, Black H, et al, for the Systolic Hypertension in the Elderly Program Co-operative Research Group. Advantage of diuretic-based antihypertensive treatment on cardiovascular disease risk in older diabetic patients with isolated systolic hypertension. JAMA 1996; 276: 1886-1892[Abstract].
6. United Kingdom Prospective Diabetes Study Group. Tight blood pressure control and risk of macrovascular and microvascular complications in type 2 diabetes: UKPDS 38. BMJ 1998; 317: 703-713[Abstract/Free Full Text].
7. Tuomilehto J, Rastenyte D, Birkenhager WH, Thijs L, Antikainen R, Bulpitt CJ, et al. Effects of calcium-channel blockade in older patients with diabetes and systolic hypertension. Syst Eur Investigators. N Engl J Med 1999; 340: 677-684[Abstract/Free Full Text].
8. Staessen JA, Fagard R, Thijs L, Cetis H, Arabidze CG, Birkenhager WH, et al, for the Systolic Hypertension-Europe (Syst-Eur) Trial Investigators. Morbidity and mortality in the placebo-controlled European trial on isolated systolic hypertension in the elderly. Lancet 1997; 360: 757-764.
9. Neaton JD, Grimm RH, Prineas RJ, Stamler J, Grandits GA, Elmer PJ, et al, for the Treatment of Mild Hypertension Study Research Group. Treatment of mild hypertension study. Final results. JAMA 1993; 270: 713-724[Abstract].
10. Materson BJ, Reda DJ, Cushman WC, Massie BM, Freis ED, Kochar MS, et al, for the Department of Veterans Affairs Cooperative Study Group on Antihypertensive Agents. Single-drug therapy for hypertension in men. A comparison of six antihypertensive agents with placebo. N Engl J Med 1993; 328: 914-921[Abstract/Free Full Text].
11. Philipp T, Anlauf M, Distler A, Holzgreve H, Michaelis J, Wellek S, on behalf of the HANE Trial Research Group. Randomised, double blind, multicentre comparison of hydrochlorothiazide, atenolol, nitrendipine, and enalapril in antihypertensive treatment: results of the HANE study. BMJ 1997; 315: 154-159[Abstract/Free Full Text].
12. Appel LJ, Moore TJ, Obarzanek E, Vollmer WM, Svetkey LP, Sacks FM, et al, for the DASH Collaborative Research Group. A clinical trial of the effects of dietary patterns on blood pressure. N Engl J Med 1997; 336: 1117-1124[Abstract/Free Full Text].
13. Trials of Hypertension Prevention Collaborative Research Group. Effects of weight loss and sodium reduction intervention on blood pressure and hypertension incidence in overweight people with high-normal blood pressure: the trials of hypertension prevention, phase II. Arch Intern Med 1997; 157: 657-667[Abstract].
14. Whelton PK, Appel LJ, Espeland MA, Applegate WB, Ettinger WH, Kostis JB, et al, for the TONE Collaborative Research Group. Sodium reduction and weight loss in the treatment of hypertension in older persons. A randomized controlled trial of nonpharmacologic interventions in the elderly (TONE). JAMA 1998; 279: 839-846[Abstract/Free Full Text].
15. Colhoun HM, Dong W, Poulter NR. Blood pressure screening, management and control in England, results from the health survey for England 1994. J Hypertens 1998; 16: 747-753[Medline].
16. Andersson OK, Almgren T, Persson B, Samuelsson O, Hedner T, Wilhelmsen L. Survival in treated hypertension: follow up study after two decades. BMJ 1998; 317: 167-171[Abstract/Free Full Text].
17. O'Brien ET, Petrie JC, Littler WA, De Swiet M, Padfield PD, Dillon MJ, et al. Blood pressure measurement: recommendations of the British Hypertension Society. 3rd ed. London: BMJ Publishing Group , 1997.
18. Alderman MH. Blood pressure management: individualized treatment based on absolute risk and the potential for benefit. Ann Intern Med 1993; 119: 329-335[Abstract/Free Full Text].
19. Joint British recommendations on prevention of coronary heart disease in clinical practice. Heart 1998; 80(suppl 2): S1-29[Free Full Text].
20. Standing Medical Advisory Committee. The use of statins. London: Department of Health , 1997.
21. Scottish Intercollegiate Guideline Network. Lipids and the primary prevention of coronary heart disease. Edinburgh: SIGN , 1999(pc47.cee.h2.ac.uk/sign/; accessed 24 August 1999.)
22. Psaty BM, Smith NL, Siscovick DS, Koepsell TD, Weiss NS, Heckbert SR, et al. Health outcomes associated with antihypertensive therapies used as first-line agents. A systematic review and meta-analysis. JAMA 1997; 277: 739-745[Abstract].
23. Liu L, Wang JG, Gong L, Liu G, Staessen JA. Comparison of active treatment and placebo in older Chinese patients with isolated systolic hypertension. Systolic Hypertension in China (Syst-China) Collaborative Group. J Hypertens 1998; 16: 1823-1829[Medline].
24. Hansson L, Lindholm LH, Niskanen L, Lanke J, Hedner T, Niklason A, et al. Effect of angiotensin-converting enzyme inhibition compared with conventional therapy on cardiovascular morbidity and mortality in hypertension: the captopril prevention project (CAPPP). Lancet 1999; 353: 611-615[Medline].
25. SHEP Cooperative Research Group. Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension. Final results of the systolic hypertension in the elderly program (SHEP). JAMA 1991; 265: 3255-3264[Abstract].
26. Thijs L, Fagard R, Lijnen P, Staessen J, Van Hoof R, Amery A. A meta-analysis of outcome trials in elderly hypertensives. J Hypertens 1992; 10: 1103-1109[Medline].
27. Messerli FH, Grossman E, Goldbourt U. Are ß-blockers efficacious as first-line therapy for hypertension in the elderly? A systematic review. JAMA 1998; 279: 1903-1907[Abstract/Free Full Text].
28. Medical Research Council's General Practice Research Framework. Thrombosis prevention trial: randomised trial of low-intensity oral anticoagulation with warfarin and low-dose aspirin in the primary prevention of ischaemic heart disease in men at increased risk. Lancet 1998; 351: 233-241[Medline].
29. Downs JR, Clearfield M, Weis S, Whitney E, Shapiro DR, Beere PA, et al. Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels. Results of AFCAPS/TexCAPS. JAMA 1998; 279: 1615-1622[Abstract/Free Full Text].

(Accepted 11 August 1999)


© BMJ 1999

Related Articles

Tackling therapeutic inertia: role of treatment data in quality indicators
Bruce Guthrie, Melanie Inkster, and Tom Fahey
BMJ 2007 335: 542-544. [Extract] [Full Text] [PDF]

Aspirin for primary prevention
Lawrence E Ramsay, Philemon S Sanmuganathan, Erica J Wallis, Peter R Jackson, and Abdullah Alkhenizan
BMJ 2000 321: 1472. [Extract] [Full Text]

Management of hypertension
John Wilding, Gareth Williams, Garfield Drummond, Tom Marshall, Andrew Rouse, John Eisenberg, Angela Hey, Tahseen A Chowdhury, Hogne Sandvik, Michael Stewart, N J Sharvill, Bruce M Psaty, Curt D Furberg, Lawrence E Ramsay, Bryan Williams, John F Potter, G Dennis Johnston, Graham A MacGregor, Lucilla Poston, Neil R Poulter, and Gavin Russell
BMJ 2000 320: 576. [Extract] [Full Text] [PDF]

British guidelines on managing hypertension
Bruce M Psaty and Curt D Furberg
BMJ 1999 319: 589-590. [Extract] [Full Text] [PDF]

This article has been cited by other articles:

  • Edwards, C J, Syddall, H, Goswami, R, Goswami, P, Dennison, E M, Arden, N K, Cooper, C, on behalf of the Hertfordshire Cohort Study Group, (2007). The autoantibody rheumatoid factor may be an independent risk factor for ischaemic heart disease in men. Heart 93: 1263-1267 [Abstract] [Full text]  
  • Guthrie, B., Inkster, M., Fahey, T. (2007). Tackling therapeutic inertia: role of treatment data in quality indicators. BMJ 335: 542-544 [Full text]  
  • Verberk, W. J., Kroon, A. A., Kessels, A. G.H., de Leeuw, P. W. (2005). Home Blood Pressure Measurement: A Systematic Review. J Am Coll Cardiol 46: 743-751 [Abstract] [Full text]  
  • Burns, G. E. (2005). Challenges of teaching EBM. CMAJ 172: 1423-1424 [Full text]  
  • Smith, G. D., Lawlor, D. A., Harbord, R., Timpson, N., Rumley, A., Lowe, G. D.O., Day, I. N.M., Ebrahim, S. (2005). Association of C-Reactive Protein With Blood Pressure and Hypertension: Life Course Confounding and Mendelian Randomization Tests of Causality. Arterioscler. Thromb. Vasc. Bio. 25: 1051-1056 [Abstract] [Full text]  
  • Wong, T. Y., Mitchell, P. (2004). Hypertensive Retinopathy. NEJM 351: 2310-2317 [Full text]  
  • Wiggins, B. S., Spinler, S. (2004). Antiplatelet and Antithrombin Therapy for Early Management of Acute Coronary Syndromes. Journal of Pharmacy Practice 17: 347-369 [Abstract]  
  • Feher, M D (2004). Diabetes: preventing coronary heart disease in a high risk group. Heart 90: iv18-iv21 [Abstract] [Full text]  
  • Evans, N (2004). Managing the cost of cardiovascular prevention in primary care. Heart 90: iv26-iv28 [Abstract] [Full text]  
  • McKerracher, A (2004). Treating to hypertension targets. Heart 90: iv33-iv35 [Abstract] [Full text]  
  • Shah, S U, Anjum, S, Littler, W A (2004). Use of diuretics in cardiovascular disease: (2) hypertension. Postgrad. Med. J. 80: 271-276 [Abstract] [Full text]  
  • Hense, H.-W. (2004). Observations, predictions and decisions--assessing cardiovascular risk assessment. Int J Epidemiol 33: 235-239 [Full text]  
  • Howell, S. J., Sear, J. W., Foex, P. (2004). Hypertension, hypertensive heart disease and perioperative cardiac risk{dagger}. Br J Anaesth 92: 570-583 [Abstract] [Full text]  
  • Laurent, S. (2004). Guidelines from the British Hypertension Society. BMJ 328: 593-594 [Full text]  
  • Borzecki, A. M., Wong, A. T., Hickey, E. C., Ash, A. S., Berlowitz, D. R. (2003). Hypertension Control: How Well Are We Doing?. Arch Intern Med 163: 2705-2711 [Abstract] [Full text]  
  • Stanton, A., Jensen, C., Nussberger, J., O'Brien, E. (2003). Blood Pressure Lowering in Essential Hypertension With an Oral Renin Inhibitor, Aliskiren. Hypertension 42: 1137-1143 [Abstract] [Full text]  
  • Oakeshott, P., Kerry, S., Austin, A., Cappuccio, F. (2003). Is there a role for nurse-led blood pressure management in primary care?. Fam Pract 20: 469-473 [Abstract] [Full text]  
  • Jacobson, L., Elwyn, G., Robling, M., Jones, R. T. (2003). Error and safety in primary care: no clear boundaries. Fam Pract 20: 237-241 [Abstract] [Full text]  
  • Hense, H.-W., Schulte, H., Lowel, H., Assmann, G., Keil, U. (2003). Framingham risk function overestimates risk of coronary heart disease in men and women from Germany--results from the MONICA Augsburg and the PROCAM cohorts. Eur Heart J 24: 937-945 [Abstract] [Full text]  
  • Wong, T. Y., Klein, R., Duncan, B. B., Nieto, F. J., Klein, B. E.K., Couper, D. J., Hubbard, L. D., Sharrett, A. R. (2003). Racial Differences in the Prevalence of Hypertensive Retinopathy. Hypertension 41: 1086-1091 [Abstract] [Full text]  
  • Tu, K., Mamdani, M. M., Jacka, R. M., Forde, N. J., Rothwell, D. M., Tu, J. V. (2003). The striking effect of the Heart Outcomes Prevention Evaluation (HOPE) on ramipril prescribing in Ontario. CMAJ 168: 553-557 [Abstract] [Full text]  
  • August, P. (2003). Initial Treatment of Hypertension. NEJM 348: 610-617 [Full text]  
  • Lawlor, D A, Bedford, C, Taylor, M, Ebrahim, S (2003). Geographical variation in cardiovascular disease, risk factors, and their control in older women: British Women's Heart and Health Study. J. Epidemiol. Community Health 57: 134-140 [Abstract] [Full text]  
  • Williams, B. (2003). Drug treatment of hypertension. BMJ 326: 61-62 [Full text]  
  • Fisher, M. (2003). Prevention of macrovascular complications. Eur Heart J Suppl 5: B21-B26 [Abstract]  
  • Cappuccio, F. P, Oakeshott, P., Strazzullo, P., Kerry, S. M (2002). Application of Framingham risk estimates to ethnic minorities in United Kingdom and implications for primary prevention of heart disease in general practice: cross sectional population based study. BMJ 325: 1271-1271 [Abstract] [Full text]  
  • (2002). Prediction of mortality from coronary heart disease among diverse populations: is there a common predictive function?. Heart 88: 222-228 [Abstract] [Full text]  
  • Wallis, E. J, Ramsay, L. E, Jackson, P. R (2002). CARDIOVASCULAR AND CORONARY RISK ESTIMATION IN HYPERTENSION MANAGEMENT. Heart 88: 306-312 [Full text]  
  • Duncan, B B, Wong, T Y, Tyroler, H A, Davis, C E, Fuchs, F D (2002). Hypertensive retinopathy and incident coronary heart disease in high risk men. Br. J. Ophthalmol. 86: 1002-1006 [Abstract] [Full text]  
  • Nanchahal, K., Duncan, J. R, Durrington, P. N, Jackson, R. T (2002). Analysis of predicted coronary heart disease risk in England based on Framingham study risk appraisal models published in 1991 and 2000. BMJ 325: 194-195 [Full text]  
  • Vasan, R.S., Levy, D. (2002). Rates of progression to hypertension among non-hypertensive subjects: implications for blood pressure screening. Eur Heart J 23: 1067-1070 [Full text]  
  • Kothari, V., Stevens, R. J., Adler, A. I., Stratton, I. M., Manley, S. E., Neil, H. A., Holman, R. R. (2002). UKPDS 60: Risk of Stroke in Type 2 Diabetes Estimated by the UK Prospective Diabetes Study Risk Engine. Stroke 33: 1776-1781 [Abstract] [Full text]  
  • Law, M R, Wald, N J (2002). Risk factor thresholds: their existence under scrutiny. BMJ 324: 1570-1576 [Full text]  
  • Horton, R. (2002). Postpublication Criticism and the Shaping of Clinical Knowledge. JAMA 287: 2843-2847 [Abstract] [Full text]  
  • Lauer, M. S. (2002). Aspirin for Primary Prevention of Coronary Events. NEJM 346: 1468-1474 [Full text]  
  • Rabindranath, K S, Anderson, N R, Gama, R, Holland, M R (2002). Comparative evaluation of the new Sheffield table and the modified joint British societies coronary risk prediction chart against a laboratory based risk score calculation. Postgrad. Med. J. 78: 269-272 [Abstract] [Full text]  
  • Roeters van Lennep, J. E, Westerveld, H.T., Erkelens, D.W., van der Wall, E. E (2002). Risk factors for coronary heart disease: implications of gender. Cardiovasc Res 53: 538-549 [Abstract] [Full text]  
  • Jackson, P. R., Ramsay, L. E. (2002). First-line treatment for hypertension. Eur Heart J 23: 179-182 [Full text]  
  • Garcia-Pena, C., Thorogood, M., Armstrong, B., Reyes-Frausto, S., Munoz, O. (2001). Pragmatic randomized trial of home visits by a nurse to elderly people with hypertension in Mexico. Int J Epidemiol 30: 1485-1491 [Abstract] [Full text]  
  • Black, H. R., Elliott, W. J., Weber, M. A., Frishman, W. H., Strom, J. A., Liebson, P. R., Hwang, C. T., Ruff, D. A., Montoro, R., DeQuattro, V., Zhang, D., Schleman, M. M., Klibaner, M. I. (2001). One-Year Study of Felodipine or Placebo for Stage 1 Isolated Systolic Hypertension. Hypertension 38: 1118-1123 [Abstract] [Full text]  
  • Ferrucci, L., Furberg, C. D., Penninx, B. W.J.H., DiBari, M., Williamson, J. D., Guralnik, J. M., Chen, J. G., Applegate, W. B., Pahor, M. (2001). Treatment of Isolated Systolic Hypertension Is Most Effective in Older Patients With High-Risk Profile. Circulation 104: 1923-1926 [Abstract] [Full text]  
  • Montgomery, A A, Fahey, T (2001). How do patients' treatment preferences compare with those of clinicians?. Qual Saf Health Care 10: i39-43 [Abstract] [Full text]  
  • Hippisley-Cox, J., Pringle, M. (2001). General practice workload implications of the national service framework for coronary heart disease: cross sectional survey. BMJ 323: 269-270 [Full text]  
  • Brown, M. J (2001). HYPERTENSION: Matching the right drug to the right patient in essential hypertension. Heart 86: 113-120 [Full text]  
  • Dix, P., Howell, S. (2001). Survey of cancellation rate of hypertensive patients undergoing anaesthesia and elective surgery. Br J Anaesth 86: 789-793 [Abstract] [Full text]  
  • Foggensteiner, L., Mulroy, S., Firth, J. (2001). Management of diabetic nephropathy. JRSM 94: 210-217 [Full text]  
  • Wahid, S. T., Baines, L. A., Savopoulos, L., Connolly, V. M., Kelly, W. F., Bilous, R. W. (2001). Longitudinal Analysis of Blood Pressure, Lipid, and Glycemic Control in Diabetic Patients With Nephropathy Attending a Hospital Outpatient Clinic and Their Relationship to Renal Function, Mortality, and Cardiovascular Morbidity. Diabetes Care 24: 789-790 [Full text]  
  • Sanmuganathan, P S, Ghahramani, P, Jackson, P R, Wallis, E J, Ramsay, L E (2001). Aspirin for primary prevention of coronary heart disease: safety and absolute benefit related to coronary risk derived from meta-analysis of randomised trials. Heart 85: 265-271 [Abstract] [Full text]  
  • British Cardiac Society Guidelines and Medical Pra, , Royal College of Physicians Clinical Effectiveness, (2001). Guideline for the management of patients with acute coronary syndromes without persistent ECG ST segment elevation. Heart 85: 133-142 [Full text]  
  • Meade, T W, Brennan, P J (2001). Authors' reply on aspirin for primary prevention. BMJ 322: 171-171 [Full text]  
  • , S. (2001). Recent advances: Geriatric. BMJ 322: 86-89 [Full text]  
  • Ashton, W.D, Nanchahal, K, Wood, D.A (2001). Body mass index and metabolic risk factors for coronary heart disease in women. Eur Heart J 22: 46-55 [Abstract]  
  • Pahor, M., Psaty, B. M., Alderman, M. H., Furberg, C. D. (2001). Meta-analysis of Hypertension Trials in Diabetic Patients: Response to Parving and Rossing. Diabetes Care 24: 178-180 [Full text]  
  • Jones, A F, Walker, J, Jewkes, C, Game, F L, Bartlett, W A, Marshall, T, Bayly, G R (2001). Comparative accuracy of cardiovascular risk prediction methods in primary care patients. Heart 85: 37-43 [Abstract] [Full text]  
  • Mogensen, C. E., Neldam, S., Tikkanen, I., Oren, S., Viskoper, R., Watts, R. W, Cooper, M. E (2000). Randomised controlled trial of dual blockade of renin-angiotensin system in patients with hypertension, microalbuminuria, and non-insulin dependent diabetes: the candesartan and lisinopril microalbuminuria (CALM) study. BMJ 321: 1440-1444 [Abstract] [Full text]  
  • Ramsay, L. E, Sanmuganathan, P. S, Wallis, E. J, Jackson, P. R, Alkhenizan, A. (2000). Aspirin for primary prevention. BMJ 321: 1472-1472 [Full text]  
  • Melville, A, Richardson, R, Lister-Sharp, D, McIntosh, A (2000). Complications of diabetes: renal disease and promotion of self-management. Qual Saf Health Care 9: 257-263 [Full text]  
  • Van den Hoogen, P.C.W., Seidell, J.C., Menotti, A., Kromhout, D. (2000). Blood pressure and long-term coronary heart disease mortality in the Seven Countries Study: implications for clinical practice and public health. Eur Heart J 21: 1639-1642  
  • Psaty, B. M., Furberg, C. D., Pahor, M., Alderman, M., Kuller, L. H. (2000). National Guidelines, Clinical Trials, and Quality of Evidence. Arch Intern Med 160: 2577-2580 [Full text]  
  • Malaviya, A N, Mourou, M (2000). Should low-dose aspirin also be a background therapy for all patients with systemic lupus erythematosus (SLE)?. Lupus 9: 561-562  
  • Meade, T W, Brennan, P J (2000). Determination of who may derive most benefit from aspirin in primary prevention: subgroup results from a randomised controlled trial. BMJ 321: 13-17 [Abstract] [Full text]  
  • Steel, N. (2000). Thresholds for taking antihypertensive drugs in different professional and lay groups: questionnaire survey. BMJ 320: 1446-1447 [Full text]  
  • O'Brien, E., Coats, A., Owens, P., Petrie, J., Padfield, P. L, Littler, W. A, de Swiet, M., Mee, F. (2000). Use and interpretation of ambulatory blood pressure monitoring: recommendations of the British Hypertension Society. BMJ 320: 1128-1134 [Full text]  
  • Bulpitt, C.J. (2000). Controlling hypertension in the elderly. QJM 93: 203-205 [Full text]  
  • Jackson, R. (2000). Guidelines on preventing cardiovascular disease in clinical practice. BMJ 320: 659-661 [Full text]  
  • Wallis, E. J, Ramsay, L. E, Haq, I. U., Ghahramani, P., Jackson, P. R, Rowland-Yeo, K., Yeo, W. W (2000). Coronary and cardiovascular risk estimation for primary prevention: validation of a new Sheffield table in the 1995 Scottish health survey population. BMJ 320: 671-676 [Abstract] [Full text]  
  • Baker, S., Priest, P., Jackson, R. (2000). Using thresholds based on risk of cardiovascular disease to target treatment for hypertension: modelling events averted and number treated. BMJ 320: 680-685 [Abstract] [Full text]  
  • Wilding, J., Williams, G., Drummond, G., Marshall, T., Rouse, A., Eisenberg, J., Hey, A., Chowdhury, T. A, Sandvik, H., Stewart, M., Sharvill, N J, Psaty, B. M, Furberg, C. D, Ramsay, L. E, Williams, B., Potter, J. F, Johnston, G D., MacGregor, G. A, Poston, L., Poulter, N. R, Russell, G. (2000). Management of hypertension. BMJ 320: 576-576 [Full text]  
  • Willis, C., Gaffney, B., Yarnell, J. (2000). Hypertension: what do people think? A survey in Northern Ireland of public knowledge and attitudes concerning high blood pressure. Health Education Journal 59: 308-314 [Abstract]  
  • Psaty, B. M, Furberg, C. D (1999). British guidelines on managing hypertension. BMJ 319: 589-590 [Full text]  

Rapid Responses:

Read all Rapid Responses

International community dispute BP targets
David Lewis
bmj.com, 4 Sep 1999 [Full text]
Guidelines-- of no benefit if they cannot be implemented
Robert Fleetcroft
bmj.com, 5 Sep 1999 [Full text]
Optimal target pressure not supported by strength A evidence
Hogne Sandvik
bmj.com, 4 Sep 1999 [Full text]
BRITISH HYPERTENSION SOCIETY GUIDELINES
Tahseen A Chowdhury
bmj.com, 7 Sep 1999 [Full text]
Role of the laboratory in disseminating and implementing guidelines
R Gama
bmj.com, 9 Sep 1999 [Full text]
Treating hypertension with lifestyle measures: Aim for modest weight loss, not ‘ideal body weight’
John Wilding, et al.
bmj.com, 8 Sep 1999 [Full text]
How many drugs is enough?
David Payne
bmj.com, 11 Sep 1999 [Full text]
BRITISH HYPERTENSION SOCIETY GUIDELINES
Gary Drybala
bmj.com, 16 Sep 1999 [Full text]
British Hypertension Society Guidelines
Garfield Drummond
bmj.com, 6 Oct 1999 [Full text]
Ownership and uptake of guidelines
Phil Taylor
bmj.com, 7 Oct 1999 [Full text]
British Guidelines on Hypertension Do not consider Workload Implications In Primary Care
John Eisenberg
bmj.com, 16 Oct 1999 [Full text]
Target organ assessment in nurse run clinics
Pam Sim
bmj.com, 2 Nov 1999 [Full text]
Guidelines do not address marginal cost benefit
Michael Moore
bmj.com, 17 Nov 1999 [Full text]
Management of Hypertension.
Tom Black
bmj.com, 16 Nov 1999 [Full text]



Student BMJ

Risk of surgery for inflammatory bowel disease: record linkage studies

What can you learn from this BMJ paper? Read Leanne Tite's Paper+

www.student.bmj.com

Listen to the latest BMJ Interview