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Valvular disease may be unmasked in pregnancy when physiological changes increase demands on the heart. Women with valvular heart disease require close follow-up during pregnancy, delivery, and postpartum
Valvular heart disease in pregnancy is rare, but it significantly increases maternal and fetal risk. Despite an overall decline in the incidence of rheumatic heart disease in Europe and North America,1 worldwide rheumatic mitral stenosis is the most common valvular lesion in pregnancy.w1 With changing patterns of immigration, rheumatic heart disease may well become a serious problem in the United Kingdom. Advances in cardiac medication and surgery mean that more women with congenital valvular disease survive into adulthood and reproductive maturity.
Valvular heart disease may present for the first time in pregnancy as the increasing demands on the heart lead to decompensation and cardiac failure. However, the diagnosis is not always easy as the symptoms of pregnancy (tiredness, shortness of breath, and palpitations) can mask those of deteriorating disease. Moreover, in the United Kingdom, a decline in rheumatic fever means that valvular heart disease is now rare, and doctors—particularly general practitioners and obstetricians, to whom these patients present—are less aware of and less familiar with the condition. The scenario box highlights the complexities of the management of valvular heart disease in pregnancy.
Changes that occur in pregnancy pose a substantial demand on cardiac function in women with valvular disease. By eight weeks' gestation, systemic vascular resistance falls by 30-70% of its preconception value, initiating a 30-50% increase in cardiac output, an increase of 10-20 beats/min in heart rate, and a 30-50% increase in blood volume. Systemic vascular resistance falls by 30-70% of its preconception value. Labour, particularly the second stage, is associated with a further increase in cardiac output. Pain induces a sympathetic response causing an increase in heart rate. Stroke volume is augmented by autotransfusion during contractions. After delivery, the return of uterine blood into the systemic circulation results in a further increase in cardiac output. Stroke volume, heart rate, and cardiac output remain high for 24 hours after delivery, with rapid intravascular volume shifts in the first two weeks postpartum.
In mitral stenosis, the increase in cardiac output is limited by the amount of blood that can flow through the narrowed valve during diastole. The pregnancy induced increase in the maternal heart rate shortens diastole, reducing left ventricular filling.2 In some cases, this leads to reduced cardiac output, increased left atrial pressure, and overt cardiac failure. About 40% of women with mitral stenosis experience some symptomatic decline in cardiac function in pregnancy.3 Typically, patients develop shortness of breath with exertion in the second trimester, progressing to orthopnoea and paroxysmal nocturnal dyspnoea as pregnancy advances. Often the deterioration is acute, typically due to an arrhythmia, usually atrial fibrillation secondary to stretch of the left atrium.
Several reports have highlighted the dangers to the mother of pregnancy in the presence of mitral stenosis.2 3 4w2 Maternal outcomes are favourable in women with mild mitral stenosis, but not in women with moderate or severe mitral stenosis, who have a high rate of morbidity (such as pulmonary oedema, arrhythmias, the need to start or increase cardiac medication, and the need for admission to hospital). Predictors of adverse maternal outcome include the severity of mitral stenosis (valve area <1.5 cm2) and New York Health Association (NYHA) functional class (box 1).5 The prepregnancy risk of maternal mortality in the presence of severe mitral stenosis has been quoted at 1-5%6 and is also associated with NYHA functional class.7 No data are available on the long term effects of pregnancy on maternal cardiac function in mitral stenosis.
In young women aortic stenosis is usually congenital. The limited ability of the left ventricle to augment cardiac output results in an abnormal rise in left ventricular systolic and filling pressures, leading to a compensatory left ventricular hypertrophy. In pregnancy the increase in stroke volume and fall in systemic vascular resistance lead to an increase in the gradient across the aortic valve.2 The clinical consequences of the increased aortic gradient depend on the degree of pre-existing left ventricular hypertrophy and left ventricular systolic function. When compensatory changes in the left ventricle are inadequate to meet the demands imposed by the need for increased cardiac output late in pregnancy, symptoms develop.
Moderate to severe aortic stenosis (valve area <1.5 cm2) substantially affects pregnancy outcome. Studies from the 1970s show a high incidence (17.4%) of maternal mortality.w3 More recent studies report no maternal or neonatal deaths; however, moderate to severe aortic stenosis is associated with significant maternal morbidity, including heart failure, arrhythmia, and syncope.4 8w4 Pregnancy seems to have a long term effect on the clinical course of aortic stenosis, with a 31% rate of cardiac surgery reported within a three year follow-up period.4
Pregnancy is usually well tolerated in women with chronic left sided valve regurgitation without left ventricular dysfunction. This tolerance is due to the fall in systemic vascular resistance and reduced left ventricular afterload. Symptoms may occur in women with severe lesions, particularly in labour, delivery, and the early postpartum period and include dyspnoea on exertion, orthopnoea, and paroxysmal nocturnal dyspnoea.2
The fixed narrowing of left sided stenotic lesions limit the pregnancy induced increase in cardiac output, restricting uteroplacental perfusion and limiting fetal growth. When cardiac decompensation is superimposed on this background—whether this is the result of pulmonary oedema causing hypoxia or an arrhythmia acutely reducing the relatively low cardiac output still further—the prognosis for the fetus may be compromised.
Moderate and severe mitral stenosis have a clear effect on fetal outcomes. A case-control study comparing women who had mitral stenosis with well matched controls found an increased incidence of preterm delivery (28% in moderate stenosis v 6% in controls, 44% in severe stenosis v 11% in controls) and intrauterine growth restriction (27% in moderate stenosis v 0% in controls, 33% severe stenosis v 0% in controls). Overall, birth weight in the mitral stenosis group was also significantly reduced (3427 g in controls v 2706 g in moderate mitral stenosis (P=0.02) and 3332 g v 2558 g (P=0.05) in severe mitral stenosis).4 Fetal mortality is increased in women with mitral stenosis and is dependent on maternal functional capacity; a fetal mortality of 30% has been reported with NYHA class IV disease in the mother.5
Severe aortic stenosis is associated with a higher incidence of preterm delivery (44%), intrauterine growth restriction (22%), and lower birth weight (2650 g v 3391 g) compared with well matched controls.4 In a recent case series, disorders related to hypertension were observed slightly more often than reported in the general population (11.3% v 8%).w5 The authors suggest this may be the result of reduced cardiac output leading to abnormal placental bed vascular remodelling and reduced placental perfusion.
The management of women with valvular heart disease should ideally take place before conception. In women with congenital lesions this process should begin during adolescence with discussions about family planning, contraception, and pregnancy.
Women with valvular heart disease contemplating pregnancy should be assessed in a multidisciplinary prepregnancy clinic (staffed by an obstetrician, cardiologist, anaesthetist, and midwife). A full cardiac assessment should be performed. The history should focus on the patients' exercise capacity and past cardiac events. Echocardiography should assess cardiac haemodynamics including valve area and pulmonary pressures. In patients with impaired functional capacity an exercise test with maximum oxygen uptake refines risk stratification for pregnancy (box 2). These risks should be discussed with the woman and her family. However, when English is a barrier to communication, family members should not be used as interpreters for women, either in preconception counselling or for care during pregnancy.w6
Valve repair or replacement is recommended before pregnancy in women with severe mitral stenosis (valve area <1.0 cm2),2 3w1 symptomatic aortic stenosis,w7 and symptomatic mitral regurgitation.w8 Any medications contraindicated in pregnancy (such as angiotensin converting enzyme inhibitors, angiotensin receptor blockers, amiodarone, and sodium nitroprusside) should be changed to avoid any adverse fetal effects.
As valvular heart disease may present for the first time during pregnancy, clinicians should be watchful. The normal flow murmur of pregnancy is typically soft (grade 1 or 2), located at the pulmonary region, associated with a normal first and second heart sound, and is not accompanied by a diastolic murmur (box 3). Always bear in mind the possibility of valvular heart disease, particularly in women from developing countries.w9 Investigation with echocardiography is indicated in women with a history of resting or worsening dyspnoea, any signs of heart failure, a grade 3 or greater systolic murmur, or any diastolic murmur.
During pregnancy, women with valvular heart disease require regular review by the multidisciplinary team. The frequency of antenatal visits is determined by the type and severity of the valve lesion and the clinical course. In general, antenatal visits should be every month in women with mild disease and every two weeks in women with moderate and severe disease until 28 weeks then weekly thereafter until delivery. This allows the detection of any deterioration in maternal cardiac state and prompt intervention if needed. Women who miss appointments should be immediately contacted and followed up.w6
Cardiac function may worsen simply because of the increased workload of pregnancy or as a result of an arrhythmia, anaemia, or infection. Interventions such as bed rest and avoidance of the supine position may be useful. Medical treatment aims to reduce the heart rate and improve loading conditions. Cardiac drugs that are often used and are relatively safe in pregnancy include β blockers, hydralazine, diuretics, and digoxin. Atrial arrhythmia requires prompt treatment, including cardioversion.w7 Alternatively β blockers and digoxin can be used for rate control. Thromboprophylaxis with unfractionated heparin is indicated during bed rest and in the presence of atrial arrhythmia, particularly if the left atrium is dilated.
Patients who remain symptomatic despite adequate drug treatment may require repair or replacement of the diseased valve, particularly if prematurity means the fetus cannot be safely delivered. Balloon mitral valvuloplasty is the treatment of choice in mitral stenosis.w10 The reported results in several studies have been excellent, with few maternal or fetal complications.w11w12 Reported rates of maternal complications are small but include cardiac tamponade, excessive blood loss, transient atrial fibrillation, worsening of mitral regurgitation, systemic embolisation, uterine contractions, and labour.w11 Favourable long term results for both mother and baby have recently been reported.w13 In symptomatic aortic stenosis, aortic balloon valvuloplasty is useful as a palliative procedure, allowing deferral of valve replacement until after birth.w14
At the beginning of pregnancy women should be counselled about potentially worrying symptoms and advised to attend the labour ward if such symptoms develop. They should be given information about the available options during their care and be involved in all decision making.
Labour and delivery are an additional burden on the maternal cardiovascular system. Timing and mode of delivery should be carefully planned by the multidisciplinary team. Vaginal delivery with epidural anaesthesia is the preferred delivery mode unless surgical delivery is obstetrically indicated.3 4 9w7 w14 Invasive monitoring may be required in symptomatic women and those with severe disease,w15 and the length of the second stage should be shortened by elective assisted delivery to avoid excessive maternal effort.10 Antibiotic prophylaxis should be considered for all valvular lesions irrespective of delivery mode (box 4).9 10 During the third stage, a bolus dose of oxytocin can result in hypotension and should therefore be given slowly or as an infusion. During caesarean section a prophylactic compression suture may also be placed to reduce the risk of postpartum haemorrhage.
Immediately after delivery the venous return to the heart is greatly increased, which may precipitate pulmonary oedema. Consequently, haemodynamic monitoring should continue for 12 to 24 hours after delivery. Women should be discharged only when clinically stable.
Women should be reviewed six weeks postpartum by the multidisciplinary team. This appointment should include a full cardiac assessment and postnatal check. Appropriate advice on contraception should be givenw16 and follow-up with a cardiologist arranged.
Valvular heart disease may manifest itself for the first time during pregnancy, particularly in women from developing countries. Overall, risk during pregnancy is dependent on the valve lesion, its severity, and maternal prepregnancy functional capacity. Women with valvular heart disease require close follow-up during pregnancy, delivery, and postpartum so that any deterioration in cardiac state can be detected early and managed in a timely way.
A 32 year old woman from Iran was referred to the joint cardiac obstetric team at 28 weeks of pregnancy. She had a history of severe rheumatic mitral stenosis. This was her fourth pregnancy—her previous three children had been delivered at term by caesarean section. During this pregnancy she had had two episodes of pulmonary oedema, which were treated with bed rest, diuretics, and a β blocker. As her symptoms persisted despite medical treatment, a mitral valvuloplasty was carried out at 32 weeks of pregnancy. The procedure was uncomplicated, increasing the mean mitral valve area from 0.8 cm2 to 2.6 cm2. Four hours after the procedure, preterm labour was diagnosed, and a live male infant weighing 2345 g was delivered by emergency caesarean section. The operation was done under general anaesthesia with invasive cardiac monitoring. The estimated blood loss was 650 ml; to prevent further blood loss a prophylactic compression suture was sited. The patient had requested sterilisation, which was performed during the caesarean section. The postoperative period was uncomplicated, and the patient was discharged nine days after delivery.
This is one of a series of occasional articles about how to manage a pre-existing medical condition during pregnancy. If you would like to suggest a topic for this series please email Amy Davis (email@example.com).
Contributors: EG did the literature search and drafted the initial manuscript. MJ and Philip Steer revised this manuscript, and MJ edited the final manuscript. MG gave a cardiac opinion and helped to edit the paper. EG is guarantor.
Competing interests: None declared.
Provenance and peer review: Commissioned; externally peer reviewed.