A. Low Maternal and Fetal Risk
- Asymptomatic Aortic Stenosis
- Low mean outflow gradient (<50 mmHg)
- Normal left ventricular (LV) systolic function
- Aortic Regurgitation
- New York Heart Association (NYHA) Class I or II
- Normal LV systolic function
- Mitral Regurgitation
- NYHA Class I or II
- Normal LV systolic function
- Mitral Valve Prolapse
- No mitral regurgitation (MR) OR
- Mild-to-moderate MR and normal LV systolic function
- Mild to moderate Mitral Stenosis
- Mitral valve area >1.5cm2, gradient <5 mmHg
- Absence of severe pulmonary hypertension (P-HTN)
- Mild to moderate pulmonary valve stenosis
B. High Maternal and Fetal Risk
- Severe Aortic Stenosis - with or without symptoms
- Aortic Regurgitation - NYHA Class III or IV
- Mitral Stenosis - NYHA Class II, III, or IV
- Mitral Regurgitation - NYHA Class III or IV
- Valve Associated P-HTN
- Severe P-HTN with pulmonary pressures >75% of systolic pressures
- Associated with aortic or mitral valve disease (or both)
- Valve Associated LV Systolic Dysfunction
- LV ejection fraction (EF) <40%
- Associated with aortic or mitral valve disease (or both)
- Maternal Cyanosis
- Any reduced functional status with NYHA Class III or IV
C. High Maternal Risk
- Reduced LV systolic function: LV EF <40%
- Previous congestive heart failure (CHF)
- Previous stroke or transient ischemic attack
D. High Neonatal Risk
- Maternal age <20 or >35 years with heart valve disease
- Use of anticogaulant therapy throughout pregnancy
- Smoking during pregnancy
- Multiple gestations
E. Evaluation
- Ideally, full cardiac evaluation should occur prior to conception
- Echocardiography is the cornerstone of cardiac valve and function evaluation
- Pulmonary pressures
- Full valve function evaluation
- Exercise testing - useful if functional capacity can be evaluated
- Full physical and echocardiographic evaluation at least every trimester
- Full evaluation whenever functional status changes
- Specialists must be involved and can guide individualized therapy
References
- Reimold SC and Rutherford JD. 2003. NEJM. 349(1):52