Chapter 15 Cardiovascular, respiratory, haematological, neurological and gastrointestinal disorders in pregnancy
CARDIOVASCULAR COMPLICATIONS IN PREGNANCY
Management during childbirth
The risks and management of specific cardiac conditions are summarized in Table 15.1.
Condition | Pregnancy Risks | Management |
---|---|---|
Atrial septal defect | Rarely causes problems | Nil specific after exclusion of other secondary complications |
Ventricular septal defect | Small defects rarely cause problems | Avoid hypertension, endocarditis prophylaxis |
Patent ductus arteriosus | Small shunts rarely problematic | Exclude pulmonary hypertension |
Coarctation of aorta | Corrected, few problems; uncorrected, maternal mortality (15%) | Prevent hypertension, use epidural in labour |
Primary pulmonary hypertension | Maternal mortality of 50% | |
Eisenmenger’s syndrome | Maternal mortality 30%, termination mortality 10% | As for pulmonary hypertension |
Fallot’s tetralogy | Avoid hypotension which can cause shunt reversal, assisted vaginal delivery | |
Mitral stenosis | Uncorrected – IUGR and prematurity, maternal mortality 5–15% | Control heart rate with β-blockers, use epidural, assisted delivery not mandatory, endocarditis prophylaxis |
Aortic stenosis | Endocarditis. Severe – IUGR, maternal mortality 5–15% | Avoid hypo- and hypervolaemia, endocarditis prophylaxis |
Prosthetic heart valves | Pregnancy accelerates need for replacement, thromboembolism | Careful anticoagulation throughout pregnancy |
Marfan syndrome | β-Blockers, serial echocardiography, avoid hypertension, epidural and assisted vaginal delivery |
VENOUS THROMBOEMBOLISM IN PREGNANCY
Treatment of a pulmonary embolus during pregnancy consists of unfractionated heparin (UH), initially intravenously (40 000 U/day by continuous infusion in normal saline) to obtain a concentration of 0.6–1.0 U/mL. Once full heparinization has been obtained for 3–7 days, the infusion may be replaced by calcium heparin given subcutaneously. A deep vein thrombosis (DVT) is treated either with UH if delivery or surgery is imminent, or low molecular weight heparin (LWMH) given subcutaneously. UH is substituted for LMWH 24–36 hours prior to delivery. UH is suspended once labour is established or 6 hours before surgery, and recommenced 2–6 hours after vaginal or caesarean delivery. If the woman has a high risk of VTE antenatally (includes recurrent VTE, previous idiopathic VTE or previous VTE and a strong family history of VTE) she may be given LMWH prophylaxis throughout pregnancy and for 6 weeks postpartum (see also postpartum thromboembolism, p. 186).
ANTIPHOSPHOLIPID SYNDROME
Antiphospholipid syndrome (APS) is associated with early-onset pre-eclampsia, intrauterine fetal growth restriction, preterm birth, miscarriage, fetal death and venous thromboembolism. Diagnosis requires at least one of the clinical criteria and one of the laboratory criteria (see Box 15.1). Women who have suffered from clinical complications should be screened and referred for specialist evaluation.