Frequently asked questions — Cardiovascular risk stratification
1) What is absolute cardiovascular risk?
It corresponds to the probability of fatal or non-fatal cardiovascular events, such as myocardial infarction, stroke or sudden death, occurring over a defined period, usually 10 years. It is calculated based on blood pressure, classical risk factors, target-organ damage and established cardiovascular or renal disease.
2) What are the main classical risk factors?
Advanced age (≥55 years in men; ≥65 years in women), male sex, smoking, dyslipidaemia — total cholesterol ≥190 mg/dL, LDL >115 mg/dL, low HDL, triglycerides >150 mg/dL — elevated fasting glucose (102–125 mg/dL), obesity (BMI ≥30) or abdominal obesity (waist circumference ≥102 cm in men; ≥88 cm in women), and family history of premature cardiovascular disease.
3) What is HMOD?
HMOD means hypertension-mediated organ damage. It refers to early structural or functional changes in target organs, before overt clinical disease. Examples include left ventricular hypertrophy, carotid intima-media thickening or atherosclerotic plaques, ankle-brachial index <0.9, pulse wave velocity >10 m/s, eGFR 30–59 mL/min/1.73 m² or microalbuminuria (30–300 mg/24 h).
4) What do Stage 1, 2 and 3 mean in the ESC/ESH risk grid?
Stage 1: no organ damage, CVD or CKD, with risk factors only.
Stage 2: presence of HMOD, CKD G3 or diabetes without organ damage.
Stage 3: established cardiovascular disease, CKD ≥G4 or diabetes with organ damage.
5) How are blood pressure categories classified?
High-normal: SBP 130–139 or DBP 85–89 mmHg
Grade 1 hypertension: SBP 140–159 or DBP 90–99 mmHg
Grade 2 hypertension: SBP 160–179 or DBP 100–109 mmHg
Grade 3 hypertension: SBP ≥180 or DBP ≥110 mmHg
6) How should the risk stratification grid be interpreted?
The blood pressure category is combined with the disease stage and the number of risk factors. Each grid cell indicates absolute risk: low, moderate, high or very high. The presence of HMOD, CKD or clinically manifest CVD automatically reclassifies the patient into a higher risk category.
7) When is a patient considered to be at very high risk?
When there is clinical cardiovascular disease, such as myocardial infarction, stroke, angina, revascularisation, heart failure, atrial fibrillation or peripheral arterial disease; CKD G3b–G5 with eGFR <60; proteinuria >300 mg/day; or diabetes with organ damage, such as microalbuminuria, left ventricular hypertrophy or retinopathy.
8) What is the difference between “high” and “very high” risk?
High risk: multiple risk factors or grade 2–3 hypertension without HMOD/CVD. Very high risk: any target-organ damage, CKD ≥G3, diabetes with organ damage or established cardiovascular disease.
9) How does risk influence treatment?
It defines the intensity of antihypertensive therapy, blood pressure targets — the higher the risk, the stricter the target — and the need for additional preventive treatments, such as statins, antiplatelet therapy or intensive glycaemic control when indicated.
10) Which complementary tests help detect HMOD?
ECG/echocardiography for left ventricular hypertrophy, carotid Doppler ultrasound for intima-media thickening or plaques, ankle-brachial index, pulse wave velocity, eGFR and creatinine, urine albuminuria/proteinuria, and fundoscopy for hypertensive retinopathy.
11) How should risk be reassessed over time?
Risk should be reassessed annually or after therapeutic changes. Regression of HMOD, blood pressure control and reduction of risk factors, such as smoking, lipids, weight and glycaemia, may reclassify the patient into a lower risk category.
12) What is the final objective of stratification?
To allow a personalised and prognostic approach, adapting treatment to the severity of absolute cardiovascular risk, preventing fatal and non-fatal events and reducing overall mortality.