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Brief Summary

GUIDELINE TITLE

Risk estimation and the prevention of cardiovascular disease. A national clinical guideline.

BIBLIOGRAPHIC SOURCE(S)

  • Scottish Intercollegiate Guidelines Network (SIGN). Risk estimation and the prevention of cardiovascular disease. A national clinical guideline. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network (SIGN); 2007 Feb. 71 p. (SIGN publication; no. 97). [315 references]

GUIDELINE STATUS

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

  • May 2, 2007, Antidepressant drugs: Update to the existing black box warning on the prescribing information on all antidepressant medications to include warnings about the increased risks of suicidal thinking and behavior in young adults ages 18 to 24 years old during the first one to two months of treatment.
  • March 2, 2005, Crestor (rosuvastatin calcium): Revisions to the WARNINGS, DOSAGE AND ADMINISTRATION, CLINICAL PHARMACOLOGY, and PRECAUTIONS sections of the labeling.

BRIEF SUMMARY CONTENT

 ** REGULATORY ALERT **
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Note from the Scottish Intercollegiate Guidelines Network (SIGN) and National Guideline Clearinghouse (NGC): In addition to these evidence-based recommendations, the guideline development group also identifies points of best clinical practice in the full-text guideline document.

The grades of recommendations (A–D) and levels of evidence (1++, 1+, 1-, 2++, 2+, 2-, 3, 4) are defined at the end of the "Major Recommendations" field.

Estimating Cardiovascular Risk

D - Individuals with symptoms of cardiovascular disease or who are over the age of 40 years and have diabetes (type 1 or 2) or familial hypercholesterolaemia should be considered at high risk (>20% risk over ten years) of cardiovascular events.

D - Cardiovascular risk should be estimated at least once every five years in adults over the age of 40 years with no history of cardiovascular disease, familial hypercholesterolaemia or diabetes and who are not being treated for blood pressure or lipid reduction.

D - Asymptomatic individuals should be considered at high risk if they are assessed as having >20% risk of a first cardiovascular event over ten years.

D - Individuals at high cardiovascular risk warrant intervention with lifestyle changes and consideration for drug therapy, to reduce their absolute risk.

Diet

A - Diets low in total and saturated fats should be recommended to all for the reduction of cardiovascular risk.

A - People with hypertension should be advised to reduce their salt intake as much as possible to lower blood pressure.

C - Increased fruit and vegetable consumption is recommended to reduce cardiovascular risk for the entire population.

A - Antioxidant vitamin supplementation is not recommended for the prevention or treatment of coronary heart disease.

B - Patients, and individuals at risk of cardiovascular disease, who are overweight, should be targeted with interventions designed to reduce weight, and to maintain this reduction.

Physical Activity

B - Physical activity of at least moderate intensity (e.g., makes person slightly out of breath) is recommended for the whole population (unless contraindicated by condition).

B - Physical activity should include occupational and/or leisure time activity and incorporate accumulated bouts of moderate intensity activities such as brisk walking.

B - Those who are moderately active and are able to increase their activity should be encouraged to do so. Activity can be increased through a combination of changes to intensity, duration or frequency.

Smoking

B - All people who smoke should be advised to stop and offered support to help facilitate this in order to minimise cardiovascular and general health risks.

B - Exposure to passive smoking increases cardiovascular risk and should be minimised.

A - Nicotine replacement therapies or bupropion should be used as part of a smoking cessation programme to augment professional advice and increase long term abstinence rates.

B - Smokers with coronary heart disease and comorbid clinical depression should have their depression treated both for alleviation of depressive symptoms and to increase the likelihood of stopping smoking.

Alcohol

B - Patients with no evidence of coronary heart disease may be advised that light to moderate alcohol consumption may be protective against the development of coronary heart disease.

C - Patients with established coronary heart disease may be advised that light to moderate alcohol consumption may be protective against further coronary events.

A - Brief multi-contact interventions should be used to encourage patients to reduce their levels of drinking if their current intake is hazardous to their health.

Antiplatelet Therapy

A - Individuals with established atherosclerotic disease should be treated with 75 mg aspirin daily.

A - Individuals with a history of stroke or transient ischaemic attack and who are in sinus rhythm should be considered for low dose aspirin (75 to 300 mg daily) and dipyridamole (200 mg twice daily) to prevent stroke recurrence and other vascular events. If aspirin is contraindicated, or there are side effects, clopidogrel 75 mg daily is an alternative.

A - Asymptomatic individuals without established atherosclerotic disease but with a calculated cardiovascular risk of >20% over ten years should be considered for treatment with aspirin 75 mg daily.

Lipid Lowering

A - All adults over the age of 40 years who are assessed as having a ten year risk of having a first cardiovascular event >20% should be considered for treatment with simvastatin 40 mg/day following an informed discussion of risks and benefits between the individual and responsible clinician.

B - All patients with established symptomatic atherosclerotic cardiovascular disease should be considered for more intensive statin therapy following an informed discussion of risks and benefits between the individual and responsible clinician.

A - Individuals with hypertriglyceridaemia (>1.7 mmol/l) and/or low high density lipoprotein cholesterol level (<1 mmol/l in men, or <1.2 mmol/l in women) should be considered for treatment with a fibrate or niconitic acid.

A - Statins are the drugs of choice in the management of diabetic subjects with mixed dyslipidaemia and elevated low density lipoprotein cholesterol.

Blood Pressure Lowering

A - Individuals with sustained systolic blood pressures >140 mm Hg systolic and/or diastolic blood pressures >90 mm Hg and clinical evidence of cardiovascular disease should be considered for blood pressure lowering drug therapy.

A - Individuals with established cardiovascular disease, who also have chronic renal disease or diabetes with complications, or target organ damage may be considered for treatment at the lower threshold of systolic >130 mm Hg and/or diastolic >80 mm Hg.

B - Individuals with blood pressure greater than 160/100 mm Hg should have drug treatment and specific lifestyle advice to lower their blood pressure and risk of cardiovascular disease.

Psychological Issues

B - Depression and social isolation or lack of quality social support are risk factors for the development of and prognosis with coronary heart disease and should be taken into account when assessing individual risk.

A - Stress management training is not recommended as a technique to reduce coronary heart disease mortality or morbidity or conventional risk factors. It may have a role in improving patients' mood, including depressed mood.

A - Cognitive behaviour therapy should be considered for increasing physical function and improving mood in patients with coronary heart disease.

A - Use of the stages of change model alone is not recommended as a method for changing the health behaviour of individuals with coronary heart disease.

B - Motivational interviewing should be considered in patients with cardiovascular disease who require to change health behaviours including diet, exercise, alcohol and compliance with treatment.

Definitions:

Grades of Recommendation

Note: The grade of recommendation relates to the strength of the evidence on which the recommendation is based. It does not reflect the clinical importance of the recommendation.

A: At least one meta-analysis, systematic review of randomized controlled trials (RCTs), or RCT rated as 1++ and directly applicable to the target population; or

A body of evidence consisting principally of studies rated as 1+, directly applicable to the target population, and demonstrating overall consistency of results

B: A body of evidence including studies rated as 2++, directly applicable to the target population, and demonstrating overall consistency of results; or

Extrapolated evidence from studies rated as 1++ or 1+

C: A body of evidence including studies rated as 2+, directly applicable to the target population and demonstrating overall consistency of results; or

Extrapolated evidence from studies rated as 2++

D: Evidence level 3 or 4; or

Extrapolated evidence from studies rated as 2+

Good Practice Points: Recommended best practice based on the clinical experience of the guideline development group

Levels of Evidence

1++: High quality meta-analyses, systematic reviews of randomised controlled trials (RCTs), or RCTs with a very low risk of bias

1+: Well-conducted meta-analyses, systematic reviews of RCTs, or RCTs with a low risk of bias

1-: Meta-analyses, systematic reviews of RCTs, or RCTs with a high risk of bias

2++: High quality systematic reviews of case control or cohort studies
High quality case control or cohort studies with a very low risk of confounding or bias and a high probability that the relationship is causal

2+: Well-conducted case control or cohort studies with a low risk of confounding or bias and a moderate probability that the relationship is causal

2-: Case control or cohort studies with a high risk of confounding or bias and a significant risk that the relationship is not causal

3: Non-analytic studies (e.g. case reports, case series)

4: Expert opinion

CLINICAL ALGORITHM(S)

An algorithm is provided in the original guideline document titled, "The British Hypertension Society A/CD algorithm for blood pressure."

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Scottish Intercollegiate Guidelines Network (SIGN). Risk estimation and the prevention of cardiovascular disease. A national clinical guideline. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network (SIGN); 2007 Feb. 71 p. (SIGN publication; no. 97). [315 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

1999 Sep (revised 2007 Feb)

GUIDELINE DEVELOPER(S)

Scottish Intercollegiate Guidelines Network - National Government Agency [Non-U.S.]

SOURCE(S) OF FUNDING

Scottish Executive Health Department

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Guideline Development Group: Dr James Grant (Chair) General Practitioner, Auchterarder; Mrs Brenda Anderson, Cardiac Rehabilitation Co-ordinator, Aberdeen Royal Infirmary; Mrs Mandy Andrew Tayside, Managed Clinical Network Manager, CHD, Dundee; Professor Christine Bond, Consultant in Pharmaceutical Public Health, University of Aberdeen; Dr Adrian Brady, Consultant Cardiologist, Glasgow Royal Infirmary; Dr Neil Campbell, Reader in General Practice, Department of General Practice and Primary Care, University of Aberdeen; Ms Joyce Craig, Senior Health Economist, NHS Quality Improvement Scotland; Dr John Dick, Consultant Physician, Ninewells Hospital, Dundee; Dr Penelope Fraser, Consultant Clinical Psychologist, Ninewells Hospital, Dundee; Mr James Grant, Lay Representative, Balerno; Ms Marianne Hayward, Managed Clinical Network Manager for diabetes, Greater Glasgow Health Board; Dr Matthew Lowther, Heart Health Network Co-ordinator, NHS Health Scotland; Dr Jill Murie, General Practitioner Principal, Forth; Dr Moray Nairn, Programme Manager, SIGN Executive; Professor Rudolph Riemersma, Consultant Biochemist, University of Edinburgh; Ms Ann Ross, Physiotherapist, Western Infirmary, Glasgow; Mr Duncan Service, Senior Information Officer, SIGN Executive; Dr Indrani Sinnak-Aruppan, Consultant Clinical (Neuro and Health) Psychologist, Ayrshire Central Hospital; Mr Roger Stableford, Lay Representative, Falkirk; Ms Nicola Stuckey, Consultant Clinical Psychologist, Astley Ainslie Hospital, Edinburgh; Ms Joan Thain, Cardiac Rehabilitation Health Visitor, Westburn Centre, Aberdeen; Dr Deborah Tinson, Consultant Clinical Psychologist, Astley Ainslie Hospital, Edinburgh; Dr Iain C Todd, Consultant in Cardiovascular Rehabilitation, Astley Ainslie Hospital, Edinburgh

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Declarations of interests were made by all members of the guideline development group. Further details are available from the Scottish Intercollegiate Guidelines Network (SIGN) Executive.

GUIDELINE STATUS

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

The following are available:

  • Quick reference guide: Heart disease. Scottish Intercollegiate Guidelines Network, 2007 Feb. 31 p. Available in Portable Document Format (PDF) from the SIGN Web site.
  • SIGN 50: A guideline developer's handbook. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network. (SIGN publication; no. 50). Available from the SIGN Web site.
  • Appraising the quality of clinical guidelines. The SIGN guide to the AGREE (Appraisal of Guidelines Research & Evaluation) guideline appraisal instrument. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network, 2001. Available from the SIGN Web site.
  • Management of coronary heart disease: A national clinical and resource impact assessment. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network, 2007 Feb. 120 p. Available in Portable Document Format (PDF) from the SIGN Web site.
  • Excel spreadsheets to assist health boards to estimate their local costs (used in conjunction with the national clinical and resource impact assessment). Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network, 2007 Feb. Available from the SIGN Web site.

PATIENT RESOURCES

The following is available:

  • Prevention of cardiovascular disease for patients. Edinburgh (Scotland): Scottish Intercollegiate Guidelines Network, 2007 Feb. 28 p.

Available in Portable Document Format (PDF) from the Scottish Intercollegiate Guidelines Network (SIGN) Web site. Urdu translation is also available from the SIGN Web site.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on January 3, 2002. The information was verified by the guideline developer as of February 4, 2002. This NGC summary was updated by ECRI Institute on April 24, 2007. This summary was updated by ECRI Institute on November 9, 2007, following the U.S. Food and Drug Administration advisory on Antidepressant drugs.

COPYRIGHT STATEMENT

DISCLAIMER

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Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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