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Table 4. AHA/ACC Secondary Prevention for
Patients With Coronary and Other Vascular Disease*: 2006 Update
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Goals |
Intervention
Recommendations |
Smoking:
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Goal
Complete cessation. No exposure to environmental tobacco smoke. |
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• |
Ask about tobacco use status at every
visit. |
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• |
Advise every tobacco user to quit. |
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• |
Assess the tobacco user’s willingness
to quit. |
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• |
Assist by counseling and developing
a plan for quitting. |
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Arrange follow-up, referral to special
programs, or pharmacotherapy (including nicotine replacement and bupropion). |
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• |
Urge avoidance of exposure to environmental
tobacco smoke at work and home. |
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BP control:
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Goal
<140/90 mm Hg
or
<130/80 mm Hg if patient has diabetes or chronic kidney disease
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For all patients:
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• |
Initiate or maintain lifestyle modification—weight
control; increased physical activity; alcohol moderation; sodium reduction; and
emphasis on increased consumption of fresh fruits, vegetables, and low-fat dairy
products. |
For patients with blood pressure
> 140/90 mm Hg (or > 130/80 mm Hg for individuals with chronic kidney
disease or diabetes):
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• |
As tolerated, add blood pressure
medication, treating initially with ß-blockers and/or ACE inhibitors, with
addition of other drugs such as thiazides as needed to achieve goal blood pressure. |
For compelling indications for individual
drug classes in specific vascular diseases, see Seventh Report of the Joint National
Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure
(JNC 7). |
Lipid management:
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Goal
LDL-C <100 mg/dL
If triglycerides are > 200 mg/dL, non–HDL-C should be <130 mg/dL†
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For all patients:
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• |
Start dietary therapy. Reduce intake
of saturated fats (to <7% of total calories), trans-fatty acids, and cholesterol
(to <200 mg/d). |
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• |
Adding plant stanol/sterols (2 g/d)
and viscous fiber (>10 g/d) will further lower LDL-C. |
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• |
Promote daily physical activity and
weight management. |
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• |
Encourage increased consumption of
omega-3 fatty acids in the form of fish‡ or in
capsule form (1 g/d) for risk reduction. For treatment of elevated triglycerides,
higher doses are usually necessary for risk reduction. |
For lipid management:
Assess fasting lipid profile in all patients, and within 24 hours of hospitalization
for those with an acute cardiovascular or coronary event. For hospitalized patients,
initiate lipid-lowering medication as recommended below before discharge according
to the following schedule:
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• |
LDL-C should be <100 mg/dL,
and |
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• |
Further reduction of LDL-C to <70
mg/dL is reasonable. |
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• |
If baseline LDL-C is > 100
mg/dL, initiate LDL-lowering drug therapy.§ |
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• |
If on-treatment LDL-C is >
100 mg/dL, intensify LDL-lowering drug therapy (may require LDL-lowering drug combinationll). |
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• |
If baseline LDL-C is 70 to 100 mg/dL,
it is reasonable to treat to LDL-C <70 mg/dL |
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If triglycerides are 200 to 499 mg/dL,
non–HDL-C should be <130 mg/dL, and |
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• |
Further reduction of non–HDL-C to
<100 mg/dL is reasonable. |
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• |
Therapeutic options to reduce non–HDL-C
are:
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More intense LDL-C–lowering therapy, or |
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Niacin¶ (after LDL-C–lowering therapy),
or |
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Fibrate therapy# (after LDL-C–lowering
therapy) |
|
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• |
If triglycerides are > 500
mg/dL#, therapeutic options to prevent pancreatitis
are fibrate¶ or niacin¶
before LDL-lowering therapy; and treat LDL-C to goal after triglyceride-lowering
therapy. Achieve non–HDL-C <130 mg/dL if possible. |
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Physical activity:
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Goal
30 minutes, 7 days per week
(minimum 5 days per week) |
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• |
For all patients, assess risk with
a physical activity history and/or an exercise test, to guide prescription |
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• |
For all patients, encourage 30 to
60 minutes of moderate-intensity aerobic activity, such as brisk walking, on most,
preferably all, days of the week, supplemented by an increase in daily lifestyle
activities (eg walking breaks at work, gardening, household work). |
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• |
Encourage resistance training 2 days
per week. |
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• |
Advise medically supervised programs
(ie cardiac rehabilitation) for high-risk patients (eg recent acute coronary syndrome
or revascularization, heart failure). |
|
Weight management:
 |
Goal
Body mass index: 18.5 to 24.9 kg/m2
Waist circumference:
men <40 inches
women <35 inches |
|
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• |
Assess body mass index and/or waist
circumference on each visit and consistently encourage weight maintenance/reduction
through an appropriate balance of physical activity, caloric intake, and formal
behavioral programs when indicated to maintain/achieve a body mass index between
18.5 and 24.9 kg/m2. |
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• |
If waist circumference (measured
horizontally at the iliac crest) is > 35 inches in women and > 40
inches in men, initiate lifestyle changes and consider treatment strategies for
metabolic syndrome as indicated. |
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• |
The initial goal of weight loss therapy
should be to reduce body weight by approximately 10% from baseline. With success,
further weight loss can be attempted if indicated through further assessment. |
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Diabetes management:
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Goal
HbA1c <7% |
|
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• |
Initiate lifestyle and pharmacotherapy
to achieve near-normal HbA1c. |
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• |
Begin vigorous modification of other
risk factors (eg physical activity, weight management, blood pressure control, and
cholesterol management as recommended above). |
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• |
Coordinate diabetic care with patient’s
primary care physician or endocrinologist. |
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Antiplatelet agents/anticoagulants: |
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• |
Start aspirin 75 to 162 mg/d and
continue indefinitely in all patients unless contraindicated.
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For patients undergoing coronary artery bypass grafting, aspirin should
be started within 48 hours after surgery to reduce saphenous vein graft closure.
Dosing regimens ranging from 100 to 325 mg/d appear to be efficacious. Doses higher
than 162 mg/d can be continued for up to 1 year. |
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• |
Start and continue clopidogrel 75
mg/d in combination with aspirin for up to 12 months in patients after acute coronary
syndrome or percutaneous coronary intervention with stent placement (> 1
month for bare metal stent, > 3 months for sirolimus-eluting stent, and >
6 months for paclitaxel-eluting stent).
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Patients who have undergone percutaneous coronary intervention with stent
placement should initially receive higher-dose aspirin at 325 mg/d for 1 month for
bare metal stent, 3 months for sirolimus-eluting stent, and 6 months for paclitaxel-eluting
stent. |
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• |
Manage warfarin to international
normalized ratio=2.0 to 3.0 for paroxysmal or chronic atrial fibrillation or flutter,
and in post–myocardial infarction patients when clinically indicated (eg atrial
fibrillation, left ventricular thrombus). |
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• |
Use of warfarin in conjunction with
aspirin and/or clopidogrel is associated with increased risk of bleeding and should
be monitored closely. |
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Renin-angiotensin-aldosterone system
blockers: |
ACE inhibitors:
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• |
Start and continue indefinitely in
all patients with left ventricular ejection fraction (LVEF) < 40% and in
those with hypertension, diabetes, or chronic kidney disease, unless contraindicated. |
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Consider for all other patients. |
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Among lower-risk patients with normal
LVEF in whom cardiovascular risk factors are well controlled and revascularization
has been performed, use of ACE inhibitors may be considered optional. |
Angiotensin receptor blockers:
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• |
Use in patients who are intolerant
of ACE inhibitors and have heart failure or have had a myocardial infarction with
LVEF < 40%. |
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Consider in other patients who are
ACE inhibitor intolerant. |
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Consider use in combination with
ACE inhibitors in systolic-dysfunction heart failure. |
Aldosterone blockade:
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• |
Use in post–myocardial infarction
patients, without significant renal dysfunction** or hyperkalemia††,
who are already receiving therapeutic doses of an ACE inhibitor and ß-blocker,
have a LVEF < 40%, and have either diabetes or heart failure. |
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ß-blockers: |
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• |
Start and continue indefinitely in
all patients who have had myocardial infarction, acute coronary syndrome, or left
ventricular dysfunction with or without heart failure symptoms, unless contraindicated.
Consider chronic therapy for all other patients with coronary or other vascular
disease or diabetes unless contraindicated. |
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Influenza vaccination: |
Patients with cardiovascular disease
should have an influenza vaccination. |
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*Patients covered by these guidelines
include those with established coronary and other atherosclerotic vascular disease,
including peripheral arterial disease, atherosclerotic aortic disease, and carotid
artery disease. Treatment of patients whose only manifestation of cardiovascular
risk is diabetes will be the topic of a separate AHA scientific statement. ACE indicates
angiotensin-converting enzyme.
†Non–HDL-C=total cholesterol minus HDL-C.
‡Pregnant and lactating women should limit their intake of fish to minimize
exposure to methylmercury.
§When LDL-lowering medications are used, obtain at least a 30% to 40%
reduction in LDL-C levels. If LDL-C <70 mg/dL is the chosen target, consider drug
titration to achieve this level to minimize side effects and cost. When LDL-C <70
mg/dL is not achievable because of high baseline LDL-C levels, it generally is possible
to achieve reductions of >50% in LDL-C levels by either statins or LDL-C–lowering
drug combinations.
llStandard dose of statin with ezetimibe, bile acid sequestrant, or niacin.
¶The combination of high-dose statin+fibrate can increase risk
for severe myopathy. Statin doses should be kept relatively low with this combination.
Dietary supplement niacin must not be used as a substitute for prescription niacin.
#Patients with very high triglycerides should not consume alcohol. The
use of bile acid sequestrant is relatively contraindicated when triglycerides are
>200 mg/dL.
**Creatinine should be <2.5 mg/dL in men and <2.0 mg/dL in women.
††Potassium should be <5.0 mEq/L.
Chobanian AV, Bakris GL, Black HR, et al, for the Joint National Committee on Prevention,
Detection, Evaluation, and Treatment of High Blood Pressure. Seventh Report of the
Joint National Committee on Prevention, Detection, Evaluation, and Treatment of
High Blood Pressure. Hypertension. 2003;42:1206-1252.
Smith SC Jr, Allen J, Blair SN, et al. AHA/ACC Guidelines for Secondary Prevention
for Patients With Coronary and Other Atherosclerotic Vascular Disease: 2006 Update.
Circulation. 2006;113:2363-2372.

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