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. 2015 Feb 27;8(1):18–25. doi: 10.1177/1753495X14568055

Table 1.

Maternal cardiovascular risk based on World Health Organization (WHO) classifications (from Thorne et al.10).

Conditions in which pregnancy risk is WHO class I: risk not significantly higher than the general population  • Uncomplicated small or mild pulmonary stenosis, patent ductus arteriosus or mitral valve prolapse  • Successfully repaired simple lesions (atrial or ventricular septal defect, patent ductus arteriosus, anomalous pulmonary venous connection)  • Isolated atrial and ventricular ectopic beats
Conditions in which pregnancy risk is WHO class II (low to moderate risk compared with the general population) – III (significantly higher risk compared with the general population) depending on the individual  • Mild left ventricular impairment  • Hypertrophic cardiomyopathy  • Native or tissue valvular heart disease not considered WHO class I or WHO class IV  • Marfan syndrome without aortic dilatation (aortic size < 40 mm)  • Aorta < 45 mm in association with bicuspid aortic valve disease  • Repaired coarctation of the aorta
Conditions in which pregnancy risk is WHO class III: significantly increased risk of maternal morbidity and mortality compared with the general population  • Mechanical heart valve  • Systemic right ventricle  • Fontan circulation  • Unrepaired cyanotic heart disease  • Other complex congenital heart disease  • Aortic dilatation 40–45 mm in Marfan syndrome  • Aortic dilatation 45–50 mm in bicuspid aortic valve disease
Condititions in which pregnancy risk is WHO class IV: extremely high risk of maternal morbidity and mortality; patients should be counselled against pregnancy  • Pulmonary arterial hypertension from any cause  • Severe systemic ventricular dysfunction from any cause (ejection fraction < 30%, New York Heart Association class II–IV symptoms)  • Previous peripartum cardiomyopathy with any residual impariment of systemic ventricular function  • Severe mitral stenosis  • Severe symptomatic aortic stenosis  • Marfan syndrome with dilated aorta >45 mm  • Bisucspid aortic valve disease with dilated aorta >50 mm  • Native severe coarctation of the aorta