Medical Management of Atherosclerotic Cardiovascular Disease (ASCVD)
For patients with established ASCVD, initiate high-intensity statin therapy targeting LDL-C <70 mg/dL (<1.8 mmol/L), combined with ACE inhibitor or ARB therapy, antiplatelet therapy with aspirin 75-162 mg daily, and comprehensive lifestyle modifications including Mediterranean or DASH diet, regular aerobic exercise, smoking cessation, and weight management. 1, 2
Pharmacological Management
Lipid-Lowering Therapy
High-intensity statin therapy is the cornerstone for all patients with established ASCVD, targeting LDL-C reduction of ≥50% from baseline and achieving LDL-C <70 mg/dL (<1.8 mmol/L). 1, 2
Add ezetimibe if LDL-C remains ≥70 mg/dL on maximally tolerated statin therapy, particularly in patients with multiple ASCVD risk factors. 1
Consider PCSK9 inhibitors (evolocumab, alirocumab) for very high-risk patients who fail to achieve LDL-C targets despite statin plus ezetimibe combination. 1, 2
For statin-intolerant patients, bempedoic acid is recommended as an alternative cholesterol-lowering agent to reduce cardiovascular event rates. 1
Blood Pressure Management
Target blood pressure <130/80 mmHg in all patients with ASCVD to reduce cardiovascular morbidity and mortality. 3, 4
Initiate ACE inhibitor or ARB as first-line therapy, particularly beneficial in patients with coronary artery disease, diabetic kidney disease, or hypertension. 1
Add a dihydropyridine calcium channel blocker as second-line therapy if blood pressure remains uncontrolled on ACE inhibitor/ARB monotherapy. 3, 4
Thiazide-like diuretics (chlorthalidone or indapamide) are preferred over thiazide diuretics when a third agent is needed, as they afford superior cardioprotection. 1, 3
β-blockers are specifically indicated in patients with prior myocardial infarction, active angina, or heart failure with reduced ejection fraction (HFrEF), and should be continued for at least 3 years post-MI in those with preserved left ventricular function. 1
Avoid combination therapy with both ACE inhibitors and ARBs, or ACE inhibitor/ARB with direct renin inhibitors, due to increased risk of hyperkalemia, syncope, and acute kidney injury without added ASCVD benefit. 1
Antiplatelet Therapy
Aspirin 75-162 mg daily should be initiated and continued indefinitely in all patients with established ASCVD unless contraindicated. 2
Dual antiplatelet therapy (DAPT) with aspirin plus clopidogrel 75 mg is recommended for up to 12 months following acute coronary syndrome or percutaneous coronary intervention with stent placement. 2
Consider rivaroxaban 2.5 mg twice daily plus aspirin 100 mg once daily as an alternative to DAPT or single antiplatelet therapy for enhanced cardiovascular protection, though this increases bleeding risk. 1
Glucose-Lowering Therapy (for patients with diabetes)
SGLT2 inhibitors (empagliflozin, canagliflozin) are recommended for patients with type 2 diabetes and established ASCVD, as they reduce cardiovascular death, myocardial infarction, stroke, and hospitalization for heart failure. 1
Target HbA1c close to normal (<7%) through lifestyle modifications and pharmacotherapy, coordinating care with primary care physician or endocrinologist. 2
Avoid thiazolidinediones in patients with symptomatic heart failure due to increased risk of heart failure exacerbation. 1
Lifestyle Modifications
Dietary Interventions
Adopt a Mediterranean or DASH eating pattern with 8-10 servings of fruits and vegetables daily and 2-3 servings of low-fat dairy products. 1, 3, 2
Reduce saturated fat to <7% of total calories and eliminate trans fats to <1% of energy intake. 2
Limit sodium intake to <2,300 mg/day (equivalent to 3,000-6,000 mg/day of sodium chloride). 3, 2, 4
Increase dietary n-3 fatty acids, viscous fiber (oats, legumes, citrus), and plant stanols/sterols to improve lipid profile. 1
Limit cholesterol intake to <200 mg/day and increase dietary fiber to 14 g per 1,000 calories consumed. 2
Physical Activity
Engage in 30-60 minutes of moderate-intensity aerobic activity (such as brisk walking) on most days, preferably daily. 2, 4
Add resistance training 2 days per week to complement aerobic exercise. 2
High-risk patients (recent acute coronary syndrome, revascularization, heart failure) should participate in medically supervised cardiac rehabilitation programs. 2
Weight Management
Target BMI 18.5-24.9 kg/m² and waist circumference <94 cm in men, <80 cm in women. 2, 4
Initial weight loss goal should be approximately 10% of baseline body weight for those with overweight or obesity. 2
Smoking Cessation
Complete smoking cessation is mandatory, with counseling, pharmacological therapy (nicotine replacement, bupropion), and formal cessation programs offered at each visit. 2
Avoid secondhand smoke exposure at work and home. 2
Alcohol Consumption
- Limit alcohol to maximum 100 g/week, with complete avoidance preferred for optimal cardiovascular risk reduction. 2
Monitoring and Follow-Up
Obtain lipid panel 4-12 weeks after initiating or changing statin therapy, then annually to monitor response and medication adherence. 1
Monitor serum creatinine and potassium 7-14 days after initiating or changing doses of ACE inhibitors, ARBs, or mineralocorticoid receptor antagonists. 3
Reassess blood pressure within 1-3 months to ensure target <130/80 mmHg is achieved, evaluating medication adherence and tolerability. 4
Continue annual cardiovascular risk factor assessment and blood pressure monitoring once control is established. 4
Common Pitfalls to Avoid
Therapeutic inertia in blood pressure management: Titrate and add medications in a timely fashion to achieve blood pressure targets rather than accepting suboptimal control. 1
Poor medication adherence: Use once-daily dosing and single-pill combinations to improve compliance, as this is the most common cause of resistant hypertension. 3, 4
Bedtime dosing of antihypertensives is not superior: Medications can be taken at the most convenient time of day to improve adherence, as evening dosing shows no benefit over morning dosing. 1, 3
Screening asymptomatic high-risk patients is not recommended: These patients should already receive intensive medical therapy, which provides similar benefit to invasive revascularization. 1
Combination ACE inhibitor plus ARB therapy is contraindicated: This increases adverse events (hyperkalemia, syncope, acute kidney injury) without added cardiovascular benefit. 1