Reduced outflow of bile acids from the liver which resolves after delivery of the baby
Aetiology
- Underlying cause not known, thought to be the result of increased oestrogen and progesterone levels
- There seems to be a genetic component
Risk factors
- More common in women of South Asian ethnicity
- Past history of obstetric cholestasis
- Family history of obstetric cholestasis
Clinical presentation
- Usually develops later in pregnancy, particularly in the third trimester
- Itching (pruritis)) is the main symptom, particularly affecting the palms of the hands and soles of the feet
- Rarely - dark urine, anorexia, steatorrhoea
Investigations
- Abnormal LFTs, mainly ALT, AST and GGT
- Diagnosis of exclusion - other tests used to rule out other causes (should be normal)
- Liver USS
- Viral serology
- Liver autoantibodies
Management
- Ursodeoxycholic acid improves LFTs, bile acids, and symptoms
- Symptoms of itching can be managed with:
- Emollients e.g. calamine lotion to soothe the skin
- Antihistamines e.g. chlorphenamine can help sleeping
- Water-soluble vitamin K can be given if PT is deranged
- Monitoring of LFTs is required weekly during pregnancy and for at least 10 days after delivery
- Planned delivery after 37 weeks may be considered, particularly when the LFTs and bile acids are severely deranged
- Stillbirth in obstetric cholestasis is difficult to predict, and early delivery aims to reduce the risk
Complications
- Increased risk of fetal distress at term
- Amniotic fluid meconium aspiration
- Need for preterm delivery (and risks of preterm delivery)