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Approach to liver disease
in pregnancy
Dr. charles panackel
Introduction
 3% of pregnancy
 Mild to severe
 Coincidental A/c hepatobiliary disease
 Preexisting Hepatobiliary disease
exacerbated by pregnancy
 Hepatobiliary disease specific to pregnancy
 Vital to make etiologic diagnosis
Physiologic changes
 Decrease is serum albumin
 Increase in S.alkaline Phosphatase
 S. bil, AST/ALT, LDH, GGT, PT, remain normal
 Palmar erythema, spider naevi
 Liver span
 Increased blood volume, decreased peripheral
resistance, increased cardiac output, increased
splanchenic circulation, increased IVC pressure
Viral Hepatitis
 Most common cause of jaundice in
pregnancy
 HEV, HSV – Mortality is increased
 HAV –
 Same course
 Maternal fetal transmission
 No fetal loss or developmental anomalies
 No CI for breast feeding
Viral Hepatitis
 Hepatitis B
 A/c HBV Course not altered
 C/c HBV
 Risk of transmission
 HBeAg positive- 90%
 HBeAg Negative – 10-40%
 Risk more if infection occurs in 3rd trimester
 HBV Ig + Vaccination
 Lamivudine
Viral Hepatitis
 HCV
 Does not interfere with normal pregnancy
 Vertical transmission of HCV - 0-36%
 HIV co infection, HCV RNA levels more than 1
million copies/ml, IV drug abuse
 No contraindication for breast feeding
 A/c infection less chance for transmission
 Interferon and Ribavarin - CI
Viral Hepatitis
 HEV
 Females in child bearing age group
 58% can develop fulminant hepatitis
 Mortality 1st -1.5%, 2nd -8.5%, 3rd -21%
 Increased risk of abortions
 No CI for breast feeding
 HDV
 No vertical transmission reported
Viral hepatitis
 HSV, VZ
 2nd and 3rd trimester
 50% mucocutaneous lesions
 Liver biopsy, cultures and serology
 MMR – 40%
 Acyclovir
 CMV
 Rare
 Hepatitis
 Gancyclovir- teratogenic
Cholelithiasis
 6% of pregnancy
 Decreased bile acid pool
 Increased bile cholesterol
 Impaired contraction of GB
 Cholecystitis, Cholangitis and gall stone
pancreatitis
 Gall stone pancreatitis has 15%MMR and 60%
fetal mortality
 Laparoscopic cholecystectomy can safely be
done in 1st and2nd
 ERCP
Portal Hypertension
 Cirrhosis V/s NCPHT
 Cirrhosis – pregnancy is rare
 NCPHT – Liver function and fertility
 Increased portal pressure - Maximum in
2nd trimester
 Increased risk of variceal bleed in 2nd
trimester and 2nd stage of labor
Portal hypertension
 Fetal wastage –
 cirrhotics – 9.6% - 66%,
 NCPHT- 7.9% - 20%
 Spontaneous abortions –
 cirrhotics – 15-20%,
 EHPVO- 3-6%
 Most spontaneous abortions occur in first
trimester
 Portal decompression surgery/endoscopic
obliteration of varices prior to conception
decreases risk
 Perinatal mortality increased 11-18%
Portal hypertension
 30-50% pregnant women develop complication
 Variceal hemorrhage occurs in 19-45%
 Maternal mortality from variceal hemorrhage
 - cirrhotics- 18-89%,
 Non cirrhotics- 2-6%
 PPH occurs in 2-6%
 A/c on C/c hepatic failure 24% - 1/3rd die in 48
hours
 Overall maternal mortality –
 EHPVO- 4-7% and
 cirrhosis- 10-18%
Portal hypertension
 Preconception counseling
 Planned pregnancy
 Liver transplantation
 Medications optimized
 Screened with endoscopy
 Primary prophylaxis
 Antenatal monitoring
 Management of bleed
Portal hypertension
 Delivery closely monitored
 Sedation
 Second stage kept short
 Avoid overzealous IVF
 Caesarian section
Hyperemesis gravidarum
 2% of pregnancies
 Severe dehydration, electrolyte imbalance
 Young age, obese, non smokers,
hyperthyroidism
 50% have elevated transaminases
 Mild hyperbilirubinemia
 IVF, antiemetics
 Good outcome
 Low birth weight
Budd chiari syndrome
 20%
 2nd trimester to 3 months after pregnancy
 Hypercoagulable state
 Ascites
 A/C v/s C/C
 Anticoagulation
 TIPS
 Transplant
Wilsons disease
 Decreased fertility
 Treatment same as non pregnant
 D Pencillamine- micrognathia, low set
ears, inguinal hernia and cutis laxa
 Trientene and oral Zinc also safe
Autoimmune hepatitis
 Course is augmented
 Maternal mortality and morbidity increased
 Fetal loss is 13-44%
 Steroids / azathioprin
Liver Transplant and Pregnancy
 High risk pregnancy
 Conception delayed up to 6 months
 Increased risk of preecclampsia
 Well tolerated provided graft function and
renal function are normal
Dengue and pregnancy
 Can mimic HELLP/AFLP
 Vertical transmission
 Fever, thrombocytopenia, hepatomegaly,
circulatory failure
 Severe thrombocytopenia can lead to PPH
Leptospirosis and pregnancy
 Fetal wastage, premature delivery
 Vertical transmission
 No congenital infection
 Mimic HELLP syndrome
Dengue and Pregnancy
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt
Approach to liver disease in pregnancy 1.ppt

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Approach to liver disease in pregnancy 1.ppt

  • 1. Approach to liver disease in pregnancy Dr. charles panackel
  • 2. Introduction  3% of pregnancy  Mild to severe  Coincidental A/c hepatobiliary disease  Preexisting Hepatobiliary disease exacerbated by pregnancy  Hepatobiliary disease specific to pregnancy  Vital to make etiologic diagnosis
  • 3. Physiologic changes  Decrease is serum albumin  Increase in S.alkaline Phosphatase  S. bil, AST/ALT, LDH, GGT, PT, remain normal  Palmar erythema, spider naevi  Liver span  Increased blood volume, decreased peripheral resistance, increased cardiac output, increased splanchenic circulation, increased IVC pressure
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  • 6. Viral Hepatitis  Most common cause of jaundice in pregnancy  HEV, HSV – Mortality is increased  HAV –  Same course  Maternal fetal transmission  No fetal loss or developmental anomalies  No CI for breast feeding
  • 7. Viral Hepatitis  Hepatitis B  A/c HBV Course not altered  C/c HBV  Risk of transmission  HBeAg positive- 90%  HBeAg Negative – 10-40%  Risk more if infection occurs in 3rd trimester  HBV Ig + Vaccination  Lamivudine
  • 8. Viral Hepatitis  HCV  Does not interfere with normal pregnancy  Vertical transmission of HCV - 0-36%  HIV co infection, HCV RNA levels more than 1 million copies/ml, IV drug abuse  No contraindication for breast feeding  A/c infection less chance for transmission  Interferon and Ribavarin - CI
  • 9. Viral Hepatitis  HEV  Females in child bearing age group  58% can develop fulminant hepatitis  Mortality 1st -1.5%, 2nd -8.5%, 3rd -21%  Increased risk of abortions  No CI for breast feeding  HDV  No vertical transmission reported
  • 10. Viral hepatitis  HSV, VZ  2nd and 3rd trimester  50% mucocutaneous lesions  Liver biopsy, cultures and serology  MMR – 40%  Acyclovir  CMV  Rare  Hepatitis  Gancyclovir- teratogenic
  • 11. Cholelithiasis  6% of pregnancy  Decreased bile acid pool  Increased bile cholesterol  Impaired contraction of GB  Cholecystitis, Cholangitis and gall stone pancreatitis  Gall stone pancreatitis has 15%MMR and 60% fetal mortality  Laparoscopic cholecystectomy can safely be done in 1st and2nd  ERCP
  • 12. Portal Hypertension  Cirrhosis V/s NCPHT  Cirrhosis – pregnancy is rare  NCPHT – Liver function and fertility  Increased portal pressure - Maximum in 2nd trimester  Increased risk of variceal bleed in 2nd trimester and 2nd stage of labor
  • 13. Portal hypertension  Fetal wastage –  cirrhotics – 9.6% - 66%,  NCPHT- 7.9% - 20%  Spontaneous abortions –  cirrhotics – 15-20%,  EHPVO- 3-6%  Most spontaneous abortions occur in first trimester  Portal decompression surgery/endoscopic obliteration of varices prior to conception decreases risk  Perinatal mortality increased 11-18%
  • 14. Portal hypertension  30-50% pregnant women develop complication  Variceal hemorrhage occurs in 19-45%  Maternal mortality from variceal hemorrhage  - cirrhotics- 18-89%,  Non cirrhotics- 2-6%  PPH occurs in 2-6%  A/c on C/c hepatic failure 24% - 1/3rd die in 48 hours  Overall maternal mortality –  EHPVO- 4-7% and  cirrhosis- 10-18%
  • 15. Portal hypertension  Preconception counseling  Planned pregnancy  Liver transplantation  Medications optimized  Screened with endoscopy  Primary prophylaxis  Antenatal monitoring  Management of bleed
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  • 17. Portal hypertension  Delivery closely monitored  Sedation  Second stage kept short  Avoid overzealous IVF  Caesarian section
  • 18. Hyperemesis gravidarum  2% of pregnancies  Severe dehydration, electrolyte imbalance  Young age, obese, non smokers, hyperthyroidism  50% have elevated transaminases  Mild hyperbilirubinemia  IVF, antiemetics  Good outcome  Low birth weight
  • 19. Budd chiari syndrome  20%  2nd trimester to 3 months after pregnancy  Hypercoagulable state  Ascites  A/C v/s C/C  Anticoagulation  TIPS  Transplant
  • 20. Wilsons disease  Decreased fertility  Treatment same as non pregnant  D Pencillamine- micrognathia, low set ears, inguinal hernia and cutis laxa  Trientene and oral Zinc also safe
  • 21. Autoimmune hepatitis  Course is augmented  Maternal mortality and morbidity increased  Fetal loss is 13-44%  Steroids / azathioprin
  • 22. Liver Transplant and Pregnancy  High risk pregnancy  Conception delayed up to 6 months  Increased risk of preecclampsia  Well tolerated provided graft function and renal function are normal
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  • 24. Dengue and pregnancy  Can mimic HELLP/AFLP  Vertical transmission  Fever, thrombocytopenia, hepatomegaly, circulatory failure  Severe thrombocytopenia can lead to PPH
  • 25. Leptospirosis and pregnancy  Fetal wastage, premature delivery  Vertical transmission  No congenital infection  Mimic HELLP syndrome
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