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. 2016 Feb 26;8(2):201–210. doi: 10.4330/wjc.v8.i2.201

Table 2.

Target-level strategies

Strategy EAS/ESC 2011 CCS 2012 IAS 2013 NLA 2014 AACE 2012
Risk score SCORE chart to estimate 10-yr risk of fatal CVD Modified FRS to estimate 10-yr risk of non-fatal and fatal CVD Lifetime FRS to estimate lifetime risk of non-fatal and fatal CVD PCE or FRS or lifetime FRS FRS to determine 10-yr risk of non-fatal and fatal CVD
Step 1: Stratify CVD risk Very-high: ≥ 10% of fatal CVD risk; CHD equivalent risk; DM with microalbuminuria; CKD st. III High: 5%-9% of fatal CVD risk; DM; 1 markedly abnormal risk factor Moderate: 1%-4% of fatal CVD risk Low: < 1% of fatal CVD risk High: ≥ 20% risk of CVD; CHD risk equivalent; DM, age > 40 or > 30 with 15 yr DM history; CKD st. IIIb or IIIa with microalbuminuria; HTN with ≥ 3 CVD risk factors Intermediate: 10%-19% risk of CVD Low: < 10% risk of CVD (CVD risk factor: age > 55, smoker, TC/HDL-C > 6, LVH, abnormal ECG, microalbuminuria) High: ≥ 45% lifetime risk of CVD; DM with major risk factor; Familial hyperlipidemia; CKD Moderately-high: 30%-44% lifetime risk of CVD; DM alone; Metabolic syndrome; CKD Moderate: 15%-29% lifetime risk of CVD Low: < 15% lifetime risk of CVD [Major risk factor: high LDL-C, HDL-C < 40, HTN, smoker, family history of premature CAD, age (men > 55, women > 65)] Very-high: CHD risk equivalent; DM with ≥ 2 major risk factors or evidence of end organ damage High: DM with 0-1 major risk factor; CKD st. IIIb; LDL-C ≥ 190; ≥ 3 major risk factors; ≥ 1 secondary risk (marked major CVD risk, LDL-C > 160 or non-HDL-C > 190, CAC > 300, hsCRP > 2, Lp(a) > 50, microalbuminuria); High risk score (PCE > 15%, FRS > 10%, lifetime FRS > 45%) Intermediate: 2 major risk factors Low: 0-1 risk factor Very-high: CHD risk equivalent + ≥ 1 major risk factor High: CAD risk equivalent; ≥ 2 major risk factor + ≥ 20% risk of CVD Moderately-high: ≥ 2 major risk factor + 10%-19% risk of CVD Moderate: ≥ 2 major risk factor + < 10% risk of CVD Low: ≥ 1 major risk factor
Step 2: Determine target Very-high: LDL-C < 70; Alt: ApoB < 80, non-HDL-C < 100 High: LDL-C < 100; Alt: ApoB < 80, non-HDL-C < 130 Moderate-Low: LDL-C < 100-115 High: LDL-C < 77 or ≥ 50% ↓; Alt: ApoB < 80, Non-HDL-C < 100 Intermediate: LDL-C < 77 or ≥ 50% ↓ Alt: ApoB < 80, Non-HDL-C < 100 Low : ≥ 50% ↓ of LDL-C High to moderately-high: LDL-C < 100 or non-HDL-C < 130 (goal may be lower for very-high risk) Moderate to low: LDL-C < 130 or non-HDL-C < 160 Very-high: LDL-C < 70, non-HDL-C < 100 Alt: ApoB < 80 High-Moderate-Low: LDL-C < 100, non-HDL-C < 130 Very-high: LDL-C < 70, ApoB < 80 High: LDL-C < 100, ApoB < 90 Moderately-high: LDL-C < 130 Moderate: LDL-C < 130; Low: LDL-C < 160; All category: HDL-C > 40, TG < 150
Step 3: Treat according to risk Very-high or High: Lifestyle intervention + drug intervention Moderate: Lifestyle inter-vention; consider drug if uncontrolled with lifestyle Low: Life style intervention only High: Statin and lifestyle change Intermediate: LDL-C > 135: Statin if lifestyle change insufficient; LDL-C < 135: Get ApoB or non-HDL-C: # Apo B > 120 or Non-HDL-C > 165: Start statin if lifestyle change insufficient # Apo B< 120 or Non-HDL-C < 165: Lifestyle change Optional use of secondary test for further stratification Low: LDL-C > 190: Lifestyle change and statin; 5%-9% risk of CVD: Lifestyle change only optional use of secondary test for further stratification; < 5% risk of CVD: Lifestyle change only High: Statin and lifestyle change Moderately-high: Lifestyle change; Initiation of statin may be considered Moderate: Lifestyle change; initiation of statin may be considered if LDL-C > 160 Low: Lifestyle change only Very-high: Statin and lifestyle change; statin optional if baseline LDL-C, non-HDL-C and ApoB below target High: Concurrent statin and lifestyle change or statin after insufficient lifestyle change Moderate: Lifestyle change only; statin may be considered after 3 mo of optimal lifestyle change and LDL-C > 130 Low: Lifestyle change only; statin may be considered after 3 mo of optimal lifestyle change and LDL-C > 160 Exclude secondary cause of hyperlipidemia; Lifestyle change; Lipid lowering agent; Combination lipid lowering agent
Step 4: Follow-up lipids 1-12 wk after initiation; 1-3 mo after every change of dose or change of medication; Annually when target is achieved Every 3 mo until target is achieved; Every 4-12 mo when target is achieved 6 wk after initiation; Every 6-12 mo when target is achieved
Step 5: Options if target not reached Up-titration of statin dose; Add non-statin agent Add non-statin agent; Referral to lipid specialist

ESC: European Society of Cardiology; EAS: European Atherosclerosis Society; CCS: Canadian Cardiovascular Society; IAS: International Atherosclerosis Society; NLA: National Lipid Association; AACE: American Association of Clinical Endocrinologists; FRS: Framingham risk score; PCE: Pooled Cohort Equations; CVD: Cardiovascular disease; CHD: Coronary heart disease; CKD: Chronic kidney disease; DM: Diabetes mellitus; CAD: Coronary artery disease; LDL-C: Low density lipoprotein cholesterol; HDL-C: High density lipoprotein cholesterol; hsCRP: High sensitivity C-reactive protein; TG: Triglyceride; ApoB: Apolipoprotein B.