Basics
Description
- Ischemic heart disease (IHD) has been defined by the presence of atherosclerosis in the epicardial coronary arteries.
- Atherosclerosis forms plaque in coronary vessels, progressively impairing myocardial blood flow.
- Women have smaller coronary vessels.
- Plaque in women distributed diffusely with less areas of critical stenoses
- Women have symptoms despite less obstruction
- Other factors decrease flow in women > men
- Different mechanisms for IHD in symptomatic women
- Symptoms and signs of IHD in women may be due to significant obstruction (>50% obstruction in one or more vessels) alone or in combination with other recently identified mechanisms for impaired vascular flow.
- Persistent symptoms and signs of IHD in women without evidence of obstructive disease suggest the dominance of these other mechanisms in impaired vascular flow (see "Pathophysiology").
Epidemiology
- Women develop IHD 10-15 years later than men; at lower IHD risk until the seventh decade.
- Women with new onset IHD more likely to present with angina, followed by myocardial infarction (MI) (usually nontransmural).
- Less likely to have sudden death although increased rates in last 10 years
- Women are more likely to have silent MI.
- Women have a higher prevalence of congestive heart failure.
Incidence
- The lifetime risk of IHD for women aged 40 is 32% (49% in men of same age).
- Even women free from disease at age 70 have a lifetime risk of 24% (35% in men).
- 250,000 IHD deaths/year in women
- 38% women vs. 22% men will die in the year post-hospitalization for MI.
- IHD responsible for 38% of all deaths in women vs. 22% deaths from cancer.
Risk Factors
- Individual risk factors (RF) less predictive of IHD in women; clustering of RF more predictive
- Strongest predictors in women: Diabetes and low HDL cholesterol
Strongest risk/well established
- Diabetes (considered equivalent to having known IHD):
- Stronger predictor of IHD risk and prognosis in women than men
- Smoking:
- Seen in 50% of all acute IHD in women
- Risk elevated even with minimal use (1-4 cigs/day)
- Elevated cholesterol:
- Low HDL more important than high LDL
- Best estimate of risk: Total to HDL ratio
- Hypertension: Most common RF in women
- Family history premature IHD (first-degree male relative <55 or female relative <65)
- Peripheral vascular disease
- Chronic kidney disease
Moderate risk
- Hormones:
- Low endogenous estrogen levels seen in premenopausal women with signs and symptoms of IHD
- Increased risk of IHD postmenopause
- Elevated triglycerides: RF for women > men
- Obesity
- Sedentary lifestyle
- Metabolic syndrome: Consists of 3 or more of the following:
- Central obesity (waist >35 inches)
- Glucose intolerance (FBS >110 mg/dL)
- Elevated fasting triglycerides (>150 mg/dL)
- Low-serum HDL (<50 mg/dL)
- Elevated blood pressure (>130/85)
Other risk factors/less data available
- Inflammatory markers: CRP, WBC, amyloid A
- Hemostatic labs: Fibrinogen, Factor V Leiden
- Homocysteine
- Microalbuminuria
- Psychosocial (stress, depression, anxiety)
Assessing pretest risk
- Framingham risk score (FRS): Most used
- Incorporates age, gender, and traditional RF to estimate risk of developing coronary heart disease (CHD) within 10 years
- Validated and works well in black and white women (and men)
- Reynolds risk score: Developed on women with different variables (including hsCRP), adds discrimination to 40-50% of women with FRS intermediate score
Pathophysiology
Multiple gender differences contribute to the pathogenesis of IHD with women having:
- Smaller arterial size
- Increased inflammatory and immunologic factors
- Less focal and more diffuse distribution of atheroma
- Increased vascular stiffness
- Differences in hormone levels
- Endothelial dysfunction with decreased flow-mediated dilation
- Microvascular dysfunction
Diagnosis
History
- Women delay presentation despite having symptoms of longer duration than men.
- Signs and symptoms: Differ in women
- Chest pain may occur with or without exertion, in stressful situations, and may even awaken someone from sleep.
- Chest pain may be absent: May have pain in neck, jaw, or back only.
- Shortness of breath is common.
- Atypical symptoms more likely: Dizziness, weakness, fatigue
Physical Exam
- Vital signs:
- BP and heart rate are variable and may be normal.
- Cardiovascular exam: Assess for murmurs, extra heart sounds, point of maximum impulse (PMI)
- Lung exam: Listen for crackles
- Abdominal exam: Listen for bruits
- Peripheral vascular exam: Assess for peripheral vascular disease
Tests
Lab
- BUN, creatinine, electrolytes, fasting glucose, fasting lipid panel, CBC
- Troponin and MB-CPK in the acute setting
- CRP and homocysteine
- Urine microalbumin
Surgery
- EKG:
- Women have more baseline EKG changes due to heart size, axis, fluctuating hormone levels making diagnosis of acute IHD more difficult.
- Noninvasive testing:
- Duke Activity Status Index (DASI asks ability to perform 12 activities of daily living with MET score for each) to assess pretest exercise tolerance (1)[A].
- Knowledge of women's functional capacity determines appropriate cardiac testing.
- Consider pharmacologic stressors for women with low score on DASI/inability to exercise.
- Test characteristics vary by gender:
- Exercise stress test: Sensitivity 61%; specificity 70%
- Stress SPECT test: Sensitivity 78%; specificity 64%
- Stress echocardiogram: Sensitivity 86%; specificity 79%
- Coronary CT:
- Measures coronary calcification: Increased amount is associated with increased cardiac mortality in women.
- May be useful for women with abnormal EKG, symptoms and risk factors for CHD, and/or intermediate risk stress test.
- Coronary MRI:
- Evaluates: Coronary stenoses, coronary flow, myocardial perfusion, and wall motion abnormalities
- Particularly helpful in women with suspected impaired microvascular dysfunction
- Cardiac catheterization (CC):
- Women are more likely to have single vessel disease.
- Patients with nonobstructive disease (<50% stenosis) may have ongoing ischemia in the setting of vascular dysfunction.
- Acute MI 1/10,000 pregnancies:
- Increased risk due to:
- Hypercoagulable state
- Increased myocardial oxygen demand
- Risk factors:
- Age >33 years
- Multigravida
- Causes:
- Atherosclerosis with or without thrombosis: 43%
- Coronary thrombosis without atherosclerosis: 21%
- Coronary dissection: 16%
- Coronary aneurysm: 4%
Differential Diagnosis
Differential diagnosis for chest pain in women varies by age
- Young women: Costochondritis and GI causes predominate (gastroesophageal reflux disease, gastritis, irritable bowel syndrome)
- Middle-aged women: Menopause, GI causes predominate
- Older women: Aortic dissection, pulmonary (pulmonary embolism, pneumonia, cancer). May also include costochondritis and GI causes
Treatment
Medication
- Equal efficacy of medication for females as males (including beta blockers, angiotensin-converting enzyme inhibitors, and angiotensin receptor blockers) in post-MI patients or patients with active IHD (2)[A-B]
- Hormone therapy - no benefit and possible harm (2)[A]
- Aspirin:
- Effective as a secondary prevention of IHD events and stroke (2)[A]
- May be indicated as primary prevention in high-risk women and those >55
- Not shown to be effective as primary prevention in low-risk women <55
Additional Treatment
General Measures
- Initial care for acute coronary event (ACE)
- Identify ACE and hospitalize for additional evaluation and stabilization (not further addressed in this chapter)
- Identify the extent of CHD and the appropriate long-term treatment:
- Women with an abnormal catheterization are equally likely as men to be referred for revascularization.
- Women with no or nonobstructive atherosclerosis and persistent symptoms/signs could have vascular dysfunction and need additional studies/referral to a cardiologist.
- Address cardiovascular risk reduction (see below).
Issues for Referral
Referral to a cardiologist:
- Post-hospitalization for ACE for additional testing, medication adjustment, referral for cardiac rehabilitation.
- Post-CC with nonobstructive disease but persistent symptoms for testing for vascular dysfunction.
Additional Therapies
Goal: To reduce cardiovascular risk in women with recent ACE or at high risk for IHD
- Smoking cessation: Associated with rapid reduction in risk of MI (3)[B]
- Control of diabetes: Tight diabetic control reduces microvascular disease and improves other cardiac RF
- Control of hypertension: Reduces risk of IHD (2)[A]
- Treatment of elevated cholesterol: With diet and medication (2)[B]
- Cardiac rehab: Indicated for all women post-ACE (2)[A]
- Weight loss: Improves or prevents obesity-related RF for IHD
Ongoing Care
Diet
- Indicated for all patients post-ACE or at high risk of CHD
- Diet rich in vegetables and fruits, with whole grain, high-fiber foods, fish twice per week, saturated fat in very small amounts (<7% daily energy) and daily cholesterol intake <300 mg (2)[B]
Patient Education
- Education about IHD risk reduction should take place in office for women at all levels of risk.
- Weight loss for BMI >25 and waist >35 inches (2)[B]
- Exercise: 20-40 minutes of brisk exercise most days of week (2)[B]
- Cholesterol lowering:
- Dietary therapy: As above
- Primary prevention data support treatment in high-risk women with diabetes or chronic kidney disease or FRS >10% and elevated cholesterol (2)[B]
- Data less clear for medication for <55 women with no risk factors and elevated cholesterol
References
1Shaw LJ, Merz CNB, Pepine CJ. Insights from the NHLBI-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. Part I: Gender differences in traditional and novel risk factor, symptom evaluation and gender optimized diagnostic strategies. J Am Coll Cardiol. 2006;47:S4-S20. [View Abstract]2Mosca L, Benjamin EJ, Berra K Effectiveness-Based Guidelines for the Prevention of Cardiovascular Disease in Women-2011. Update: A Guideline from the American Heart Association. Circ. 2011;123:1243-1262.3Merz CNB, Shaw LJ, Reis SE. Insights from the NHLBI-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. Part II: gender differences in presentation, diagnosis, and outcome with regard to gender-based pathophysiology of atherosclerosis and macrovascular and microvascular coronary disease. J Am Coll Cardiol. 2006;47:S21-S29.
Additional Reading
- http://www.americanheart.org
- http://www.womenshealth.gov
- http://hp2010.nhlbihin.net/atpiii/calculator.asp (Framingham risk score)
- www.reynoldsriskscore.org (Reynolds risk score)
Codes
ICD9
- 413.9 Other and unspecified angina pectoris
- 414.01 Coronary atherosclerosis of native coronary artery
- 414.9 Chronic ischemic heart disease, unspecified
- 410.90 Acute myocardial infarction of unspecified site, episode of care unspecified
ICD10
- I20.9 Angina pectoris, unspecified
- I25.9 Chronic ischemic heart disease, unspecified
- I25.10 Athscl heart disease of native coronary artery w/o ang pctrs
- I25.119 Athscl heart disease of native cor art w unsp ang pctrs
- I21.3 ST elevation (STEMI) myocardial infarction of unsp site
SNOMED
- 414545008 ischemic heart disease (disorder)
- 53741008 coronary arteriosclerosis (disorder)
- 194828000 angina (disorder)
- 22298006 myocardial infarction (disorder)
Clinical Pearls
- Ischemic heart disease (IHD) is the leading cause of death in women of all ages.
- IHD is a disease of older women and more common in certain racial and ethnic minorities (African Americans, Native Americans).
- Mechanisms for IHD in women are different, necessitating new technologies for evaluation and potentially new treatment.
- Women continue to be under-represented in studies of the evaluation and treatment of IHD.