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Brief Summary

GUIDELINE TITLE

Evidence-based guidelines for cardiovascular disease prevention in women: 2007 update.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Mosca L, Appel LJ, Benjamin EJ, Berra K, Chandra-Strobos N, Fabunmi RP, Grady D, Haan CK, Hayes SN, Judelson DR, Keenan NL, McBride P, Oparil S, Ouyang P, Oz MC, Mendelsohn ME, Pasternak RC, Pinn VW, Robertson RM, Schenck-Gustafsson K, Sila CA, Smith SC Jr, Sopko G, Taylor AL, Walsh BW, Wenger NK, Williams CL. Evidence-based guidelines for cardiovascular disease prevention in women. Circulation 2004 Feb 10;109(5):672-93.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions of the strengths of the recommendations (I, IIa, IIb, III) and levels of the evidence (Levels A, B, C) are presented at the end of the "Major Recommendations" field.

Lifestyle Interventions

Cigarette Smoking

Women should not smoke and should avoid environmental tobacco smoke. Provide counseling, nicotine replacement, and other pharmacotherapy as indicated in conjunction with a behavioral program or formal smoking cessation program (Class I, Level B).

Physical Activity

Women should accumulate a minimum of 30 minutes of moderate-intensity physical activity (e.g., brisk walking) on most, and preferably all, days of the week. (Class I, Level B)

Women who need to lose weight or sustain weight loss should accumulate a minimum of 60 to 90 minutes of moderate-intensity physical activity (e.g., brisk walking) on most, and preferably all, days of the week (Class I, Level C).

Rehabilitation

A comprehensive risk-reduction regimen, such as cardiovascular or stroke rehabilitation or a physician-guided home- or community-based exercise training program, should be recommended to women with a recent acute coronary syndrome or coronary intervention, new-onset or chronic angina, recent cerebrovascular event, peripheral arterial disease (Class I, Level A), or current/prior symptoms of heart failure and a left ventricular ejection fraction (LVEF) <40% (Class I, Level B).

Dietary Intake

Women should consume a diet rich in fruits and vegetables; choose whole-grain, high-fiber foods; consume fish, especially oily fish,1 at least twice a week; limit intake of saturated fat to <10% of energy, and if possible to <7%, cholesterol to <300 mg/d, alcohol intake to no more than 1 drink per day,2 and sodium intake to <2.3 g/d (approximately 1 tsp salt). Consumption of trans-fatty acids should be as low as possible (e.g., <1% of energy) (Class I, Level B).

Weight Maintenance/Reduction

Women should maintain or lose weight through an appropriate balance of physical activity, caloric intake, and formal behavioral programs when indicated to maintain/achieve a body mass index (BMI) between 18.5 and 24.9 kg/m2 and a waist circumference <35 in. (Class I, Level B)

Omega-3 Fatty Acids

As an adjunct to diet, omega-3 fatty-acids in capsule form (approximately 850 to 1000 mg of eicosapentaenoic acid [EPA] and docosahexaenoic acid [DHA]) may be considered in women with coronary heart disease (CHD), and higher doses (2 to 4 g) may be used for treatment of women with high triglyceride levels. (Class IIb, Level B)

Depression

Consider screening women with CHD for depression and refer/treat when indicated (Class IIa, Level B)

Major Risk Factor Interventions

Blood Pressure — Optimal Level and Lifestyle

Encourage an optimal blood pressure of <120/80 mm Hg through lifestyle approaches such as weight control, increased physical activity, alcohol moderation, sodium restriction, and increased consumption of fresh fruits, vegetables, and low-fat dairy products. (Class I, Level B)

Blood Pressure — Pharmacotherapy

Pharmacotherapy is indicated when blood pressure is >140/90 mm Hg or an even lower blood pressure in the setting of chronic kidney disease or diabetes (>130/80 mm Hg). Thiazide diuretics should be part of the drug regimen for most patients unless contraindicated or if there are compelling indications for other agents in specific vascular diseases. Initial treatment of high-risk women3 should be with beta-blockers and/or angiotensin-converting enzyme (ACE) inhibitors/angiotensin receptor blockers (ARBs), with addition of other drugs such as thiazides as needed to achieve goal blood pressure. (Class I, Level A)

Lipid and Lipoprotein Levels – Optimal Levels and Lifestyle

The following levels of lipids and lipoproteins in women should be encouraged through lifestyle approaches: low-density lipoprotein cholesterol (LDL-C) <100 mg/dL, high-density lipoprotein cholesterol (HDL-C) >50 mg/dL, triglycerides <150 mg/dL, and non–HDL-C (total cholesterol minus HDL cholesterol) <130 mg/dL. (Class I, Level B) If a woman is at high risk3 or has hypercholesterolemia, intake of saturated fat should be <7% and cholesterol intake <200 mg/d (Class I, Level B)

Lipids — Pharmacotherapy for LDL Lowering, High Risk Women

Utilize LDL-C–lowering drug therapy simultaneously with lifestyle therapy in women with CHD to achieve an LDL-C <100 mg/dL (Class I, Level A) and similarly in women with other atherosclerotic cardiovascular disease (CVD) or diabetes mellitus or 10-year absolute risk >20% (Class I, Level B)

A reduction to <70 mg/dL is reasonable in very-high-risk women4 with CHD and may require an LDL-lowering drug combination (Class IIa, Level B).

Lipids — Pharmacotherapy for LDL Lowering, Other At-Risk Women

Utilize LDL-C–lowering therapy if LDL-C level is >130 mg/dL with lifestyle therapy, and there are multiple risk factors and 10-year absolute risk 10% to 20%. (Class I, Level B)

Utilize LDL-C–lowering therapy if LDL-C level is >160 mg/dL with lifestyle therapy and multiple risk factors even if 10-year absolute risk is <10% (Class I, Level B).

Utilize LDL-C–lowering therapy if LDL >190 mg/dL regardless of the presence or absence of other risk factors or CVD on lifestyle therapy (Class I, Level B).

Lipids — Pharmacotherapy for Low HDL or Elevated Non-HDL, High-Risk Women

Utilize niacin5 or fibrate therapy when HDL-C is low or non–HDL-C is elevated in high-risk women5 after LDL-C goal is reached (Class IIa, Level B).

Lipids — Pharmacotherapy for Low HDL or Elevated Non-HDL, Other At-Risk Women

Consider niacin5 or fibrate therapy when HDL-C is low or non–HDL-C is elevated after LDL-C goal is reached in women with multiple risk factors and a 10-year absolute risk 10% to 20% (Class IIb, Level B).

Diabetes Mellitus

Lifestyle and pharmacotherapy should be used as indicated in women with diabetes (Class I, Level B) to achieve glycosylated hemoglobin (HbA1C) <7% if this can be accomplished without significant hypoglycemia (Class I, Level C).

Preventive Drug Interventions

Aspirin — High Risk

Aspirin therapy (75 to 325 mg/d)6 should be used in high-risk3 women unless contraindicated. (Class I, Level A)

If a high-risk3 woman is intolerant of aspirin therapy, clopidogrel should be substituted (Class I, Level B).

Aspirin — Other At-Risk or Healthy Women

In women >65 years of age, consider aspirin therapy (81 mg daily or 100 mg every other day) if blood pressure is controlled and benefit for ischemic stroke and myocardial infarction (MI) prevention is likely to outweigh risk of gastrointestinal bleeding and hemorrhagic stroke (Class IIa, Level B) and in women <65 years of age when benefit for ischemic stroke prevention is likely to outweigh adverse effects of therapy (Class IIb, Level B).

Beta-Blockers

Beta-blockers should be used indefinitely in all women after MI, acute coronary syndrome, or left ventricular dysfunction with or without heart failure symptoms, unless contraindicated. (Class I, Level A)

ACE inhibitors/ARBs

ACE inhibitors should be used (unless contraindicated) in women after MI and in those with clinical evidence of heart failure or an LVEF <40% or with diabetes mellitus (Class I, Level A). In women after MI and in those with clinical evidence of heart failure or an LVEF <40% or with diabetes mellitus who are intolerant of ACE inhibitors, ARBs should be used instead. (Class I, Level B)

Aldosterone Blockade

Use aldosterone blockade after MI in women who do not have significant renal dysfunction or hyperkalemia who are already receiving therapeutic doses of an ACE inhibitor and beta-blocker, and have LVEF <40% with symptomatic heart failure (Class I, Level B).

1Pregnant and lactating women should avoid eating fish potentially high in methylmercury (e.g., shark, swordfish, king mackerel, or tile fish) and should eat up to 12 oz/wk of a variety of fish and shellfish low in mercury and check the Environmental Protection Agency and the US Food and Drug Administration's Web sites for updates and local advisories about safety of local catch.

2A drink equivalent is equal to a 12-oz bottle of beer, a 5-oz glass of wine, or a 1.5-oz shot of 80-proof spirit.

3Criteria for high risk include established CHD, cerebrovascular disease, peripheral arterial disease, abdominal aortic aneurysm, end-stage or chronic renal disease, diabetes mellitus, and 10-year Framingham risk >20%.

4Criteria for very high risk include established CVD plus any of the following: multiple major risk factors, severe and poorly controlled risk factors, diabetes mellitus.

5Dietary supplement niacin should not be used as a substitute for prescription niacin.

6After percutaneous intervention with stent placement or coronary artery bypass grafting within previous year and in women with noncoronary forms of CVD, use current guidelines for aspirin and clopidogrel.

Class III Interventions (Not Useful/Effective and May Be Harmful) for CVD or MI Prevention in Women

Menopausal Therapy

Hormone therapy and selective estrogen-receptor modulators (SERMs) should not be used for the primary or secondary prevention of CVD (Class III, Level A).

Antioxidant Supplements

Antioxidant vitamin supplements (e.g., vitamin E, C, and beta carotene) should not be used for the primary or secondary prevention of CVD (Class III, Level A)

Folic Acid1

Folic acid, with or without B6 and B12 supplementation, should not be used for the primary or secondary prevention of CVD (Class III, Level A).

Aspirin — for MI in Women <65 Years of Age2

Routine use of aspirin in healthy women <65 years of age is not recommended to prevent MI (Class III, Level B).

1Folic acid supplementation should be used in the childbearing years to prevent neural tube defects.

2For recommendation for aspirin to prevent CVD in women >65 years of age or stroke in women <65 years of age, please see Preventive Drug Interventions section above.

Definitions:

Strength of Recommendations

Classification:

Class I: Intervention is useful and effective.
Class IIa: Weight of evidence/opinion is in favor of usefulness/efficacy.
Class IIb: Usefulness/efficacy is less well established by evidence/opinion.
Class III: Intervention is not useful/effective and may be harmful.

Level of Evidence

  1. Sufficient evidence from multiple randomized trials
  2. Limited evidence from single randomized trial or other nonrandomized studies
  3. Based on expert opinion, case studies, or standard of care

CLINICAL ALGORITHM(S)

A clinical algorithm is provided in the original guideline document for cardiovascular disease (CVD) preventive care in women.

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2004 Feb (revised 2007 Mar 20)

GUIDELINE DEVELOPER(S)

American Heart Association - Professional Association

SOURCE(S) OF FUNDING

American Heart Association

GUIDELINE COMMITTEE

Expert Panel/Writing Group for Cardiovascular Disease Prevention in Women

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Expert Panel/Writing Group Members: Lori Mosca, MD, MPH, PhD, Chair; Carole L. Banka, PhD; Emelia J. Benjamin, MD; Kathy Berra, MSN, NP; Cheryl Bushnell, MD; Rowena J. Dolor, MD, MHS; Theodore G. Ganiats, MD; Antoinette S. Gomes, MD; Heather L. Gornik, MD, MHS; Clarissa Gracia, MD, MSCE; Martha Gulati, MD, MS; Constance K. Haan, MD; Debra R. Judelson, MD; Nora Keenan, PhD; Ellie Kelepouris, MD; Erin D. Michos, MD; L. Kristin Newby, MD, MHS; Suzanne Oparil, MD; Pamela Ouyang, MD; Mehmet C. Oz, MD; Diana Petitti, MD, MPH; Vivian W. Pinn, MD; Rita F. Redberg, MD, MSc; Rosalyn Scott, MD; Katherine Sherif, MD; Sidney C. Smith, Jr, MD; George Sopko, MD, MPH; Robin H. Steinhorn, MD; Neil J. Stone, MD; Kathryn A. Taubert, PhD; Barbara A. Todd, MSN, CRNP; Elaine Urbina, MD; Nanette K. Wenger, MD

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

The American Heart Association makes every effort to avoid any actual or potential conflicts of interest that may arise as a result of an outside relationship or a personal, professional, or business interest of a member of the writing panel. Specifically, all members of the writing group are required to complete and submit a Disclosure Questionnaire showing all such relationships that might be perceived as real or potential conflicts of interest.

Writing Group Disclosures

Writing Group Member Employment Research Grant Other Research Support Speakers' Bureau/ Honoraria Ownership Interest Consultant/ Advisory Board Other
Lori Mosca Columbia University NIH (Pfizer2) (no salary) Cholestech (in kind)1; Didexus (in kind)1; Lipo Science Inc (in kind)1 Abbott1 Fornier1; Kos1; Merck1; Schering-Plough1 None Eli Lilly2; McNeil1; NIH1; Novartis1; Pfizer1; Sanofi-Aventis1; Schering-Plough1; Unilever1; Waterfront Media1 Educational grants to Columbia University from Cholestech1; Fact Foundation2; Organon1; Pfizer2; Reliant2; Unilever1; Waterfront Media1
Carole L. Banka La Jolla Institute for Molecular Medicine None None None None None None
Emelia J. Benjamin Boston University School of Medicine None None None None None None
Kathy Berra Stanford Center for Research & Disease Prevention None Kos Pharmaceuticals1 None None None None
Cheryl Bushnell Duke University Medical Center None None None None None None
Rowena J. Dolor Duke University Medical Center None None None None Pfizer1; Wyeth1 None
Theodore G. Ganiats University of California, San Diego None None None None Pfizer None
Antoinete S. Gomes University of California at Los Angeles None None None None None None
Heather L. Gornik The Cleveland Clinic Foundation BMS-Sanofi1; Pfizer2 None None None None None
Clarissa Gracia University of Pennsylvania None None None None None None
Martha Gulati Northwestern University None None None None None None
Constane K. Haan University of Florida None None None None None None
Debra R. Judelson Cardiovascular Medical Group of Southern California None None Biovail1; Kos1; Novartis1; Pfizer1 None Novartis1; Pfizer1 Expert Witness1
Nora Keenan Centers for Disease Control and Prevention None None None None None None
Ellie Kelepouris Temple University School of Medicine None None None None None None
Erin D. Michos Johns Hopkins School of Medicine None None None None None None
L. Kristin Newby Duke University Medical Center BMS–Sanofi2; Millennium2; Schering-Plough2; Inverness Medical1; Roche Diagnostics2 None BMS–Sanofi1; Millennium1 None Biosite1; Eli Lilly1; Inverness Medical1; Proctor & Gamble1; Johnson & Johnson1 None
Suzanne Oparil University of Alabama, Birmingham Abbott Laboratories1; AstraZeneca1; Aventis1; Biovail1; Boehringer Ingelheim1; Bristol-Myers Squibb1; Forest Laboratories1; Glaxo-Smith Kline1; Novartis1; Merck & Co1; Pfizer1; Sankyo Pharma1; Sanofi-Synthelabo1; Schering-Plough1 None None None Bristol-Myers Squibb1; Merck & Co1; Pfizer1; Sanofi1; Novartis1; The Salt Institute1 Encysive Pharmaceuticals BOD1
Pamela Ouyang Johns Hopkins Bayview Medical Center None None None None CV Therapeutics1 None
Mehmet C. Oz Columbia University None None None None None None
Diana Petitti
Ad Hoc Member
Kaiser Permanente Southern California National Institutes of Health1 None None None None None
Vivian W. Pinn Department of Health and Human Services (NIH) None None None None None None
Rita F. Redberg University of California at San Francisco Medical Center None None Estrasorb1 None CV Therapeutics1 None
Rosalyn Scott Drew Medical Center, Los Angeles, Calif None None ABC Center for Women's Health Annual Symposium1 None ABC Center for Women's Health1 None
Katherine Sherif3 Drexel University College of Medicine Novartis2 None Novartis1 None None None
Sidney C. Smith, Jr University of North Carolina, Chapel Hill None None Bayer1; BMS1;Sanofi1 None Eli Lilly1; GlaxoSmith-Kline1; Merck1; Pfizer1; Sanofi-Aventis1 AstraZeneca (DSMB)1
George Sopko National Heart, Lung, and Blood Institute None None None None None None
Robin H. Steinhorn Children's Memorial Hospital, Chicago, Ill None None None None INO Therapeutics1 None
Neil J. Stone North-western University, Chicago, Ill None None Abbott1; Astra-Zeneca1; Merck1; Pfizer1; Sanofi1; Schering-Plough1 None Abbott1; Astra-Zeneca1 Merck1; Pfizer1; Reliant1; Schering-Plough1; Sonosite1 None
Kathryn A. Taubert American Heart Association None None None None None None
Barbara A. Todd University of Pennsylvania None None None None None None
Elaine Urbina Cincinnati Children's Hospital None None None None None None
Nanette K. Wenger Emory University School of Medicine Eli Lilly2; Astra-Zeneca1; Pfizer1 None Bristol-Myers Squibb1; Eli Lilly1; Merck1; NitroMed1; Novartis1; Pfizer1 None BMS1; CV Thera-peutics2; Eli Lilly1; GSK1; Kos Pharma-ceuticals1; Merck1; NitroMed1; Pfizer1; Sanofi-Aventis1; Schering-Plough1 None

This table represents the relationships of writing group members that may be perceived as actual or reasonably perceived conflicts of interest as reported on the Disclosure Questionnaire, which all members of the writing group are required to complete and submit. A relationship is considered to be "significant" if (1) the person receives $10,000 or more during any 12-month period, or 5% or more of the person's gross income; or (2) the person owns 5% or more of the voting stock or share of the entity, or owns $10,000 or more of the fair market value of the entity. A relationship is considered to be "modest" if it is less than "significant" under the preceding definition.

1Modest.

2Significant.

3Representation does not imply endorsement by the American College of Physicians.

ENDORSER(S)

American Academy of Physician Assistants - Professional Association
American Association for Clinical Chemistry, Inc.
American Association of Cardiovascular and Pulmonary Rehabilitation - Medical Specialty Society
American College of Chest Physicians - Medical Specialty Society
American College of Emergency Physicians - Medical Specialty Society
American Diabetes Association - Professional Association
American Geriatrics Society - Medical Specialty Society
American Society for Preventive Cardiology - Medical Specialty Society
American Society of Echocardiography - Professional Association
American Society of Nuclear Cardiology - Professional Association
Association of Women's Health, Obstetric, and Neonatal Nurses - Professional Association
Global Alliance for Women's Health - Professional Association
National Black Nurses Association, Inc - Professional Association
National Black Women's Health Initiative - Professional Association
National Women's Health Resource Center - Private Nonprofit Organization
Partnership for Gender-Specific Medicine - Professional Association
Preventive Cardiovascular Nurses Association - Medical Specialty Society
Society for Vascular Medicine and Biology - Medical Specialty Society
Society for Women's Health Research - Private Nonprofit Research Organization
Society of Geriatric Cardiology - Professional Association
The Mended Hearts Inc. - Private Nonprofit Organization
The North American Menopause Society - Private Nonprofit Organization
Women in Thoracic Surgery - Medical Specialty Society
WomenHeart the National Coalition for Women with Heart Disease - Private Nonprofit Organization

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Mosca L, Appel LJ, Benjamin EJ, Berra K, Chandra-Strobos N, Fabunmi RP, Grady D, Haan CK, Hayes SN, Judelson DR, Keenan NL, McBride P, Oparil S, Ouyang P, Oz MC, Mendelsohn ME, Pasternak RC, Pinn VW, Robertson RM, Schenck-Gustafsson K, Sila CA, Smith SC Jr, Sopko G, Taylor AL, Walsh BW, Wenger NK, Williams CL. Evidence-based guidelines for cardiovascular disease prevention in women. Circulation 2004 Feb 10;109(5):672-93.

GUIDELINE AVAILABILITY

Electronic copies: Available from the American Heart Association Web site.

Print copies: Available from the American Heart Association, Public Information, 7272 Greenville Ave, Dallas, TX 75231-4596; Phone: 800-242-8721

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

None available

NGC STATUS

This NGC summary was completed by ECRI on May 6, 2004. The information was verified by the guideline developer on June 4, 2004. This NGC summary was updated by ECRI Institute on June 4, 2007.

COPYRIGHT STATEMENT

DISCLAIMER

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