Table 2.
Patient group | Statin intensitya |
---|---|
Secondary prevention (history of coronary heart disease, vascular brain disease or peripheral arterial disease) | Start high-intensity statin therapy |
Primary prevention | |
(a) Diabetes mellitus | Start moderate/high-intensity statin therapyb |
(b) Severe hypercholesterolemia (LDL-C > 190 mg/dl or familial hypercholesterolemia) | Start high-intensity statin therapy |
(c) Moderate to severe chronic renal insufficiency without hemodialysis (eGFR between 30 and 59 ml/min/1.73 m2 or < 30 ml/min/1.73 m2, respectively) | Start moderate statin therapy |
(d) High cardiovascular risk score (after adjusting for the multiplier factor) | Start high-intensity statin therapy |
(e) Moderate risk score (after adjusting for the multiplier factor) with some associated cardiovascular risk factor | Start moderate intensity statin therapy |
(f) Subclinical atheromatosis | Start moderate/high-intensity statin therapy |
aHigh-intensity statins: when reducing the LDL-C level ≥ 50% (atorvastatin 40–80 mg/day, rosuvastatin 20–40 mg/day). Moderate intensity statins: when reducing the LDL-C level 30–50% (atorvastatin 10–20 mg/day, rosuvastatin 5–10 mg/day, simvastatin 20–40 mg/day, fluvastatin 80 mg/day, pitavastatin 2–4 mg/day)
bIn patients with more risk, with associated cardiovascular risk factors or white organ damage, it is reasonable to administer high doses of statins