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Liver Disease In
Pregnancy
Gopisankar.M.G
2008MBBS
Physiologicalchangesin pregnancy
• Palmar Erythema, vascular spiders
• Placenta  Alkaline Phosphatase in last trimester
• Bilirubin and Transaminase levels are normal
Liver diseases
1. Pregnancy Induced Liver disease
• Hyperemesis Gravidarum
• Obstetric Cholestasis
• AFLP
• Pre- eclampsia and HEELP syndrome
2. Coincidental Liver Disease
• Viral Hepatitis
• Drug Induced Jaundice
3. Pregnancy superimposed on Chronic Liver Disease
• Congenital hyperbilirubinaemia
• Cirrhosis
• Chronic Hepatitis
Obstetric Cholestasis
• Intra hepatic cholestasis of pregnancy / icterus gravidarum
Aetiology
• Normal pregnancy –mildly cholestatic/retarded biliary flow
• Due to estrogen
• Also genetic basis
• 50% family history
• Inc bile acids in circulation
• h/o pruritis on OCP anticipate tendency for cholestasis in
pregnancy
Clinical features
• Generalised severe Pruritis in third trimester
• More in palms , soles, trunk
• Rarely jaundice may follow the pruritis after 2-4weeks
• Significant hepatosplenomegaly is unlikely
• Investigations
• Abnormal LFT
• Elevated s.bile acids ,Alkaline Phosphatase ,SGOT ,SGPT-mild
• If very high SGOT/PT(>250) think of hepatitis
• Elev. S.bilirubin –but not > 5g/dL
• USG –exclude Gall stones
Management
• LFT frequently
• Antepartum Fetal surveillance and Induction at 38 weeks is
ideal
• Continuous CTG at time of labour
• Vitamin K administration –reduce chance of PPH and Fetal
intracranial haemorrhage
• Pruritus  Ursodeoxycholic acid -300mg BD hydrophilic bile
acid
• Releives symptoms ,normalise LFT – reduce the proportion of
hydrophobic and hepatotoxic bile acids
• Another option is Cholestyramine  but won’t corrects LFT
Maternal and Perinatal Prognosis
• Inc perinatal mortality and morbidity
• Fetal distress
• Unexplained IUD – due to acute anoxia
• No IUGR /Oligamnios so USG and Doppler are not helpful
• Fetal coagulopathy
• IC bleed - Vit K deff.
• Maternal morbidity  Malbsorption and Vitamin K deff. 
prolongation of clotting time and PPH
• Jaundice usually disappears after 1-2 weeks of delivery
• Recurrence – may happens , and with use of OCP with
estrogen
Liver disease in pregnancy

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Liver disease in pregnancy

  • 2. Physiologicalchangesin pregnancy • Palmar Erythema, vascular spiders • Placenta  Alkaline Phosphatase in last trimester • Bilirubin and Transaminase levels are normal
  • 3. Liver diseases 1. Pregnancy Induced Liver disease • Hyperemesis Gravidarum • Obstetric Cholestasis • AFLP • Pre- eclampsia and HEELP syndrome 2. Coincidental Liver Disease • Viral Hepatitis • Drug Induced Jaundice 3. Pregnancy superimposed on Chronic Liver Disease • Congenital hyperbilirubinaemia • Cirrhosis • Chronic Hepatitis
  • 4. Obstetric Cholestasis • Intra hepatic cholestasis of pregnancy / icterus gravidarum Aetiology • Normal pregnancy –mildly cholestatic/retarded biliary flow • Due to estrogen • Also genetic basis • 50% family history • Inc bile acids in circulation • h/o pruritis on OCP anticipate tendency for cholestasis in pregnancy
  • 5. Clinical features • Generalised severe Pruritis in third trimester • More in palms , soles, trunk • Rarely jaundice may follow the pruritis after 2-4weeks • Significant hepatosplenomegaly is unlikely • Investigations • Abnormal LFT • Elevated s.bile acids ,Alkaline Phosphatase ,SGOT ,SGPT-mild • If very high SGOT/PT(>250) think of hepatitis • Elev. S.bilirubin –but not > 5g/dL • USG –exclude Gall stones
  • 6. Management • LFT frequently • Antepartum Fetal surveillance and Induction at 38 weeks is ideal • Continuous CTG at time of labour • Vitamin K administration –reduce chance of PPH and Fetal intracranial haemorrhage • Pruritus  Ursodeoxycholic acid -300mg BD hydrophilic bile acid • Releives symptoms ,normalise LFT – reduce the proportion of hydrophobic and hepatotoxic bile acids • Another option is Cholestyramine  but won’t corrects LFT
  • 7. Maternal and Perinatal Prognosis • Inc perinatal mortality and morbidity • Fetal distress • Unexplained IUD – due to acute anoxia • No IUGR /Oligamnios so USG and Doppler are not helpful • Fetal coagulopathy • IC bleed - Vit K deff. • Maternal morbidity  Malbsorption and Vitamin K deff.  prolongation of clotting time and PPH • Jaundice usually disappears after 1-2 weeks of delivery • Recurrence – may happens , and with use of OCP with estrogen