Table 4.
Purpose | Risk Category | LDL-C target | Non-HDL-C target | Threshold for initiating pharmacological therapya,b |
---|---|---|---|---|
Primary prevention | Low risk (0–1 CV risk factor and 10-year risk of hard CV events <10%) | <130 mg/dl | <160 mg/dl | Drug therapy required if LDL-C continues to remain elevated (>130 mg/dl) despite adequate TLC for 3 months |
Moderate risk (2 or more CV risk factors with 10-year risk of hard CV events <10%) | <100 mg/dl | <130 mg/dl | Drug therapy required if LDL-C continues to remain elevated (>100 mg/dl) despite adequate TLC for 3 months | |
Moderately high risk (2 or more CV risk factors with 10-year risk of hard CV events10-20%) | <100 mg/dl with at least 30–50% reduction from the baseline | <130 mg/dl | All patients should be on a statin | |
High risk (10-year risk of hard CV events ≥20% or long-standing diabetes or other high-risk categories as defined in section 3.2) | <70 mg/dl with at least 50% reduction from the baseline | <100 mg/dl | All patients should be on a statin | |
Secondary preventionc | Patients with established atherosclerotic vascular disease | <70 mg/dl with at least 50% reduction from the baseline | <100 mg/dl | All patients should be on a statin |
Whenever initiated, the aim of the statin therapy should be to lower LDL-C by at least 50% in those at high CV risk or those with established atherosclerotic vascular diseaseand by at least 30–50% in all the other subjects.
The treatment should begin with a statin dose expected to lower LDL-C by the desired margin. The dose can be up titrated if the initial dose fails to achieve the desired LDL-C reduction.
Does not include patients presenting with an acute CV event.