Prevention of Ischaemic Heart Disease and Atherosclerosis
Prevention of Ischaemic Heart Disease and Atherosclerosis
ICD 10 code: I20.0-1/I20.8-9/I21.0-4/I21.9/I22.0-1/I22.8-9/I24.0-1/I24.8-9/I25.0-6/I25.8-9/I63.0-6/I63.8-9/I64/I65.0-3/I65.8-9/I73.8-9/G45.0-2/G45.8-9
- Patients at risk for cardiovascular diseases (such as stroke or myocardial infarction) may benefit from lifestyle modification and lipid-lowering medicine therapy
- Patients should be managed according to their level of risk, and lipid lowering medicines should be given to those with a high risk of CVD even if cholesterol is within the desirable range
Indications for lipid lowering medicine therapy
Patients with any of the following factors are at a relatively high risk for a cardiovascular event and should receive lipid lowering therapy:
- Established atherosclerotic disease:
- Ischaemic heart disease
- Peripheral vascular disease
- Atherothrombotic stroke
- Type 2 diabetes with age > 40 years
- Diabetes for > 10 years
- Diabetes with chronic kidney disease (eGFR < 60 mL/min)
LoE:IIa1
Patients with any of the following factors are also potentially at risk for cardiovascular disease (other than the categories above)
- Diabetes mellitus
- Hypertension
- Central obesity: waist circumference ≥ 94 cm (men) and ≥ 80 cm (women)
- Smoking
- Age: men > 55 years of age, women > 65 years of age
- Psychological stress
LoE:IIb2
These patients should be managed according to their 10-year risk of a cardiovascular event (See Appendix III: Cardiovascular risk assessment) as calculated using either:
- a) BMI - based risk assessment, or
- b) Framingham risk score (cholesterol-based assessment)
Management is based on the patient’s 10-year risk of a cardiovascular event as follows:
- < 10% risk: lifestyle modification and risk assess patient every 5 years
- 10–20% risk: lifestyle modification and risk assess patient annually
- ≥ 20% risk: lifestyle modification and start statin treatment
Screening for familial hypercholesteraemia
In addition to the above cardiovascular risk assessment, measure random total cholesterol in patients with the following features (suggestive of familial hypercholesterolaemia or other heritable dyslipidaemias), regardless of their cardiovascular risk:
- Cardiovascular event < 55 years in men or < 65 years in women
- Family history of early onset cardiovascular disease in male relatives < 55 years of age and in female relatives < 65 years of age
- Skin or tendon xanthomata in patient or first degree relative
- Family history of familial hyperlipidaemia
Refer patients with random total cholesterol > 7.5 mmol/L for further investigation.
GENERAL MEASURES
All people with any risk factors for cardiovascular disease should be encouraged to make the following lifestyle changes as appropriate.
- Maintain ideal weight, i.e. BMI 18 to 25 kg/m2. Weight reduction in the overweight patient
- Reduce alcohol intake to no more than 2 standard drinks per day for males and 1 for females (1 standard drink = a can of beer = a glass of wine = a shot of spirits).
- Follow a prudent eating plan i.e. low fat, high fibre and unrefined carbohydrates, with fresh fruit and vegetables
- Regular moderate aerobic exercise, e.g. 30 minutes brisk walking 5-7 times/week (150 minutes/week)
- Stop smoking
LoE:IIIb3
MEDICINE TREATMENT
- Lipid lowering medicines should be given to those with a high risk of CVD even if cholesterol is within the desirable range
- When lipid-lowering medicines are used, this is ALWAYS in conjunction with ongoing lifestyle modification
HMGCoA reductase inhibitors (statins), according to table below:
|
Indication
|
HMGCOA Reductase Inhibitor (Statin) Dose
|
|
A: Primary Prevention - No Existing CVD
|
|
|
- Type 2 diabetes with age > 40 years |
HMGCoA reductase inhibitors (statins), e.g.: Simvastatin, oral, 10 mg at night. |
|
- Patients on protease inhibitors |
- Atorvastatin, oral, 10 mg at night |
|
B: Secondary Prevention – Existing CVD |
|
|
- Ischaemic heart disease |
HMGCoA reductase inhibitors (statins), e.g.: - Rosuvastatin, 10 mg at night. LoE:Ia4 |
|
|
LoE:Ia5 |
|
- Patients on amlodipine (and not on protease inhibitor) |
- Simvastatin, oral, 10-20 mg at night LoE:IIIb6 |
|
|
Reduce dose: HMGCoA reductase inhibitors (statins), e.g.: - Simvastatin, oral, 20 mg at night OR - Consult specialist for further management. LoE:IIIb7 |
Table 4.1: Management with HMGCoA reductase inhibitors
Protease inhibitor-induced dyslipidaemia
- Certain antiretroviral medication, particularly protease inhibitors, can cause dyslipidaemia. Fasting lipid levels should be done 3 months after starting lopinavir/ ritonavir. Lopinavir/ritonavir is associated with a higher risk of dyslipidaemia (specifically hypertriglyceraemia) than atazanavir/ ritonavir
- Patients at high risk (> 20% risk of developing a CV event in 10 years) should switch to atazanavir/ ritonavir and repeat the fasting lipid profile in 3 months
- Patients with persistent dyslipidaemia despite switching, qualify for lipid lowering therapy. Criteria for initiating lipid lowering therapy are the same as for HIV-uninfected patients. Many statins (including simvastatin) cannot be used with protease inhibitors, as protease inhibitors inhibit the metabolism of the statin resulting in extremely high blood levels
- Patients who fail to respond to lifestyle modification and have dyslipidaemia treat with:
- Atorvastatin, oral, 10 mg at night
REFERRAL
- Random cholesterol > 7.5 mmol/L (to be evaluated for genetic disorders), after excluding secondary causes such as uncontrolled diabetes, hypothyroidism, or protease inhibitor use
- Tendon or skin xanthomata (except xanthelasma around the eyes)
- Statins not tolerated by patients, despite lower dose (for consideration of alternative treatment)
Standard Treatment Guidelines and Essential Medicines List for South Africa, Primary Healthcare, 2020-2024_Version 1.0_1 November 2024
Chapter 4: Cardiovascular Conditions_4.1 Prevention of Ischaemic Heart Disease and Atherosclerosis
Drugs mentioned
ICD-10 codes
- G45.0Vertebro-basilar artery syndrome
- G45.1Carotid artery syndrome (hemispheric)
- G45.2Multiple and bilateral precerebral artery syndromes
- G45.8Other transient cerebral ischaemic attacks and related syndromes
- G45.9Transient cerebral ischaemic attack, unspecified
- I20.0Unstable angina
- I20.1Angina pectoris with documented spasm
- I20.8Other forms of angina pectoris
- I20.9Angina pectoris, unspecified
- I21.0Acute transmural myocardial infarction of anterior wall
- I21.1Acute transmural myocardial infarction of inferior wall
- I21.2Acute transmural myocardial infarction of other sites
- I21.3Acute transmural myocardial infarction of unspecified site
- I21.4Acute subendocardial myocardial infarction
- I21.9Acute myocardial infarction, unspecified
- I22.0Subsequent myocardial infarction of anterior wall
- I22.1Subsequent myocardial infarction of inferior wall
- I22.8Subsequent myocardial infarction of other sites
- I22.9Subsequent myocardial infarction of unspecified site
- I24.0Coronary thrombosis not resulting in myocardial infarction
- I24.1Dressler's syndrome
- I24.8Other forms of acute ischaemic heart disease
- I24.9Acute ischaemic heart disease, unspecified
- I25.0Atherosclerotic cardiovascular disease, so described
- I25.1Atherosclerotic heart disease
- I25.2Old myocardial infarction
- I25.3Aneurysm of heart
- I25.4Coronary artery aneurysm
- I25.5Ischaemic cardiomyopathy
- I25.6Silent myocardial ischaemia
- I25.8Other forms of chronic ischaemic heart disease
- I25.9Chronic ischaemic heart disease, unspecified
- I63.0Cerebral infarction due to thrombosis of precerebral arteries
- I63.1Cerebral infarction due to embolism of precerebral arteries
- I63.2Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries
- I63.3Cerebral infarction due to thrombosis of cerebral arteries
- I63.4Cerebral infarction due to embolism of cerebral arteries
- I63.5Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries
- I63.6Cerebral infarction due to cerebral venous thrombosis, nonpyogenic
- I63.8Other cerebral infarction
- I63.9Cerebral infarction, unspecified
- I64Stroke, not specified as haemorrhage or infarction
- I65.0Occlusion and stenosis of vertebral artery
- I65.1Occlusion and stenosis of basilar artery
- I65.2Occlusion and stenosis of carotid artery
- I65.3Occlusion and stenosis of multiple and bilateral precerebral arteries
- I65.8Occlusion and stenosis of other precerebral artery
- I65.9Occlusion and stenosis of unspecified precerebral artery
- I73.8Other specified peripheral vascular diseases
- I73.9Peripheral vascular disease, unspecified