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How to use the Coronary Risk Prediction Charts for Primary Prevention
Post your experienceRisk assessment tools estimating absolute coronary or cardiovascular risk should be used to identify high risk people for primary prevention. They are an aid to making clinical decisions about how intensively to intervene on lifestyle and whether to use antihypertensive and lipid lowering medication. A patient centred approach is essential, and the risk assessment should be documented in the record.1 Decisions on treatment should be made after full explanation and due note taken of the patient's needs and preferences.1
There is a Cardiovascular Risk Calculator programme and a separate article on Primary Prevention of Cardiovascular Disease (CVD).
- All charts are based on groups of people with untreated levels of blood pressure, total cholesterol and HDL cholesterol. The use of these charts is not appropriate for patients who have existing diseases which already put them at high risk, e.g. pre-existing cardiovascular disease, familial lipid disorders, renal dysfunction or established hypertension or diabetes with associated target organ damage.
- The charts should not be used to decide whether to introduce antihypertensive medication when blood pressure is persistently at or above 160/100 or when target organ damage due to hypertension is present. In both cases antihypertensive medication is recommended regardless of CVD risk.
- Risk assessment tools are likely to underestimate risk in people with a family history of premature CVD or in people from certain high-risk ethnic groups such as South Asians (modifications to the calculator are often available).
- Inaccuracies in estimating risk may also occur in people already taking antihypertensive treatment.
Risk assessment using calculators based on the Framingham heart study are the preferred method of assessment by JBS22 and NICE.1
- The Framingham Heart Study began in 1948 and more than 10,000 residents of Framingham, Massachusetts have been enrolled.
- The study has documented population characteristics such as blood pressure, diabetic status and smoking, together with causes of death for over 50 years. From these data, various risk factors for CHD, stroke and total CVD (including heart failure and peripheral vascular disease) have been defined and quantified.
- The Framingham study population was mainly Caucasian and people with pre-existing cardiovascular disease were excluded. The performance of the Framingham risk scores varies considerably between populations and evidence supporting the use of cardiovascular risk scores for primary prevention is scarce.3
However some studies have shown that the Framingham equations generally do give a reliable prediction of risk in northern European and UK populations.4 Work is continuing to develop further cardiovascular risk prevention tools, especially for specific groups, e.g. people with diabetes and people of Afro-Caribbean or Asian origin. - Although information taken from the Framingham Heart Study is based on observational data, this has mostly been supported by interventional studies that show the modification of defined risk factors is beneficial.
Considered to be the most accurate, the Joint British Societies Coronary Risk Prediction Chart is the preferred method for estimating CVD risk.4 The charts are printed at the back of the BNF but using computer calculators may be easier (for example our CVD calculator). Others are available on the internet sites below.
The use of these charts is not appropriate for patients with established cardiovascular disease, familial hypercholesterolaemia or other inherited dyslipidaemias, chronic renal dysfunction or type 1 or 2 diabetes mellitus.
Method
- To estimate an individual's absolute 10 year risk of developing CVD choose the table for his or her gender, diabetes (yes/no), smoking status (smoker/non-smoker) and age.
- Within this square define the level of risk according to the point where the coordinates for systolic blood pressure and the ratio of total cholesterol to high density lipoprotein (HDL) cholesterol meet.
- Higher risk individuals are defined as those whose 10 year CHD risk exceeds 15%, which is equivalent to a combined risk of CHD and stroke (cardiovascular risk) of >20% over the same period.
Patient data required is as follows
The initial blood pressure and the first random (non-fasting) total cholesterol and HDL cholesterol are used to estimate an individual's risk. However, the decision on using drug therapy should generally be based on repeat risk factor measurements over a period of time.
- Gender
- Age (years)
- Systolic BP (mmHg)
- Smoking status (yes/no): Smoking status should reflect lifetime exposure to tobacco and not simply tobacco use at the time of assessment (e.g. those who have given up smoking within 5 years should be regarded as current smokers for the purposes of the charts).
- Total cholesterol
- HDL cholesterol (if no HDL cholesterol result is available, then assume this is 1 mmol/l and the lipid scale can be used for total serum cholesterol alone).
Inaccuracies of the charts
CHD risk is also higher than indicated in the charts for:5
- Those with a family history of premature CHD (male first degree relatives aged less than 55 years and female first degree relatives aged less than 65 years) which increases the risk by a factor of approximately 1.5.
- Those with raised triglyceride levels.
- Women with premature menopause.
- Those who are not yet diabetic, but have impaired fasting glucose (6.1- 6.9 mmol/l).
- As the person approaches the next age category. Risk increases exponentially with age so the risk will be closer to the higher decennium for the last four years of each decade.
- In some ethnic minorities the risk charts underestimate CVD risk because they have not been validated in these populations. For example, in people originating from the Indian subcontinent it is safest to assume that the CVD risk is higher than predicted from the charts (1.4 - 1.5 times). ETHRISK calculator may be more appropriate.6
- In patients already receiving antihypertensive therapy in whom the decision is to be made about whether to introduce lipid-lowering medication or vice versa the charts can act as a guide, but unless recent pretreatment risk factor values are available it is generally safest to assume that CVD risk is higher than that predicted by current levels of blood pressure or lipids on treatment.
There are an increasing number of alternative risk prediction scores, particularly focused on specific groups, e.g. people with diabetes, ethnic populations.
- ASSIGN: developed in Scotland and includes an index of deprivation and also family history.7,8
- QRISK calculator - see separate article based on UK GP population.9
- Reynolds Risk Score: provides a greater accuracy for assessment of cardiovascular risk in women.10
- ETHRISK calculator for UK ethnic groups.6
- UK Prospective Diabetes Study Risk Engine for people with type 2 diabetes:11
- Provides risk estimates and 95% confidence intervals, in individuals with type 2 diabetes not known to have heart disease, for:
- Non-fatal and fatal coronary heart disease
- Non-fatal and fatal stroke
- These can be calculated for any given duration of type 2 diabetes based on current age, sex, ethnicity, smoking status, presence or absence of atrial fibrillation and levels of HbA1c, systolic blood pressure, total cholesterol and HDL cholesterol.
- Provides risk estimates and 95% confidence intervals, in individuals with type 2 diabetes not known to have heart disease, for:
- INDANA risk calculator:12 focuses on patients with raised blood pressure.13
- Other risk calculators include the older Sheffield Table for Primary Prevention of Cardiovascular Disease,14 the New Zealand tables and tables proposed by the European Society of Cardiology.15
Document references
- Lipid modification, NICE Clinical Guideline (May 2008); (Cardiovascular risk assessment and the modification of blood lipids for the primary and secondary prevention of cardiovascular disease.)
- No authors listed, JBS 2: Joint British Societies' guidelines on prevention of cardiovascular disease in clinical practice. Heart. 2005 Dec;91 Suppl 5:v1-52.
- Brindle P, Beswick A, Fahey T, et al; Accuracy and impact of risk assessment in the primary prevention of cardiovascular disease: a systematic review. Heart. 2006 Dec;92(12):1752-9. Epub 2006 Apr 18. [abstract]
- New JBS2 Cardiovascular Disease Risk Charts 2004. British Hypertension Society Website.
- Cardiovascular risk - assessment and management, Clinical Knowledge Summaries (2006)
- ETHRISK - Ethnic Group CHD risk Calculator (modified Framingham); A modified Framingham CHD and CVD risk calculator for British black and minority ethnic groups
- ASSIGN; cardiovascular risk assessment score for men and women aged 30-74 years
- Woodward M, Brindle P, Tunstall-Pedoe H; Adding social deprivation and family history to cardiovascular risk assessment: the ASSIGN score from the Scottish Heart Health Extended Cohort (SHHEC). Heart. 2007 Feb;93(2):172-6. Epub 2006 Nov 7. [abstract]
- QRISK Cardiovascular Risk Assessment Calculator
- Ridker PM, Buring JE, Rifai N, et al; Development and validation of improved algorithms for the assessment of global cardiovascular risk in women: the Reynolds Risk Score. JAMA. 2007 Feb 14;297(6):611-9. [abstract]
- UK Prospective Diabetes Study Risk Engine; Risk in people with type 2 diabetes.
- INDANA risk calculator
- Pocock SJ, McCormack V, Gueyffier F, et al; A score for predicting risk of death from cardiovascular disease in adults with raised blood pressure, based on individual patient data from randomised controlled trials. BMJ. 2001 Jul 14;323(7304):75-81. [abstract]
- Sheffield table for primary prevention of CHD (3rd edition, corrected)
- European Society of Cardiology; SCORE (Systematic COronary Risk Evaluation) Risk Charts
Internet and further reading
- Proposed Joint British Societies Cardiovascular Disease Risk Prediction Chart, British Hypertension Society Website
Document ID: 2274
Document Version: 24
Document Reference: bgp2451
Last Updated: 3 Jun 2008
Planned Review: 3 Jun 2010
The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.
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