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Liver Disease In Pregnancy
Dr Amita Suneja
Professor, OB & GYN
UCMS & GTBH
Challenging disease to manage
• Because of physiology of pregnancy
certain disorders take more ominous
course in pregnancy than in non pregnant
state and some are unique to pregnancy
• May have severe maternal & fetal effects
Therefore it is important to have accurate
diagnosis
Physiological changes in hepatic
parameters
NO CHANGE
• Hepatic blood flow
• Hepatic & splenic size
• Liver histopathology
• Bilirubin- direct or
indirect, AST, ALT,
GGTP, TBA
• PT/INR
WITH CHANGE
• Albumin - ↓ 20%-50%
• Globulin -↑
• Fibrinogen - ↑50%
• Ceruloplasmin & transerrin - ↑
• ALP - ↑2-4 fold
• LDH - ↑slight
• Cholesterol & TGL - ↑2fold
↑ AST, ALT,S Bb, TBA during
pregnancy indicate liver disease
Classification
Unique to pregnancy
• Hyperemesis Gravidarum
• Intrahepatic cholestasis of pregnancy
• Preeclampsia & liver - HELLP, INFARCTION & RUPTURE
• Acute fatty liver of pregnancy
concurrent with pregnancy
• Viral hepatitis A,B,C,E, herpes simplex
• Drug hepato toxicity
• Budd chiari syndrome
Pregnancy on Preexisting ch liver disease
• Cirrhosis & Portal HT
• Ch Hepatitis B, Ch Hepatitis C, Autoimmune hepatitis
• Primary biliary cirrhosis
• FNH & Hepatic adenoma
• Liver transplantation
Case report
• 36yrs, G2P1+0+0+1, 36wks, prev LSCS,↓FM
• c/o nausea, malaise & jaundice
• Treated as viral hepatitis x 3days in NH
• ANC - normal
• GPE – conscious, vitals & BP-n
icterus ++, no edema
• P/A–36wks, Vx, mild contractions, FHS-128/m
• P/V-early labor, unclotted blood in vagina
Investigations
Hb-10g%, TLC-11000/mm,
platelet-110,000/ul
Bb-11.8mg%: D-8mg%
AST-144U/L
ALT-197U/L
ALP-578U/L
PT,PTTK,TT ↑↑
INR 3.25
BUN-6mg/dl
Creatinine-1.5mg%
Co2-13mEq/L
Blood glucose- Normal
Viral markers-negative
Urine-normal
USG-normal
AFLP or HELLP
• AFLP
Normal BP
No haemolysis
Less thrombocytopenia
Marked coagulopathy
• HELLP
Can occur in normal BP
Had EL & LP
No hypoglycemia
Treatment
• 19U FFP & 10U cryoprecipitate
• LSCS 5hrs later for AFD, Male baby A&H
• Hysterectomy for PPH
• D2- moderate ascitis, thrombocytopenia,
coagulopathy, jaundice
• D3- marked icterus, semicomatose,
hypoglycemia, metabolic acidosis
- waiting list: cadaveric liver transplant
- deep coma, convulsions, cerebral edema
• D11- patient died, liver bx taken
Acute Fatty Liver Of Pregnancy
• Rare & fatal disorder
• 50% mortality, with early diagnosis & T/t
mortality is 20%
• More common in primi gravida & multiple
pregnancy
• Mildly raised enzymes, -ve viral markers,
dominantly hypoglycemia & coagulopathy,
• Normal USG
• Treatment is supportive management &
termination of pregnancy.
• Ac fulminant failure – liver transplant,
• If starts improving- full recovery
• LCHAD (long chain 3-hydroxyacyl-coenzyme A
dehydrogenase) deficiency in fetus →no
oxidation of Fatty acids in fetus
→maternal liver gets overwhelmed with
FA in heterzygous mother →AFLP
• Both parents r heterozygous for this defect
Case History II
• 24yrs,G2P1+0+0+1, 34 wks, intense pruritis
H/O pruritis & jaundice in previous pregnacy
ANC in this preg – N, no nausea or vomiting
• Examination
No icterus or hepatosplenomegaly or tenderness
scratch marks +ve, no evidence of scabies
Obstetric exam – uneventful
• Investigations
S Bb – 3mg%, Direct – 2mg%
AST – 200U/L, ALT 104 U/L, ALP – 400IU/L
PT - normal
Differential diagnosis
• IHCP
• Anicteric viral hepatitis
• Obstructive jaundice
Further investigations
• USG liver to rule out obsruction of the
biliary tract - normal
• Viral markers – normal
• If diagnosis is still in doubt due to unusual
features – confirmatory serum tests should
be total bile acids (TBA) which are raised
IHCP
• IIIrd trimester, Recurrent, Mild icterus (Bb is
not > 5 mg%)
• No prodrome, itching, ↑ALP, ↑TBA, n USG
• Counselling – maternal & fetal risk
• Relief of maternal symptoms- phenobarbitone
• Ursodeoxycholic acid – 300mg bd
• Addition of SAMe (S adnosylmethionine) to
UDCA – ? benefit;
• VIT K
• Terminate pregnancy at 37 weeks
• Etiology:
genetic – mutation of MDR3 gene
- hypersensitivity to oestrogens
Environmental
• Future pregnancy
Recurrence
No OCP
No progesterone in next pregnancy
IgM HAV +ve
• Similar course, ↑PTL, ↑
PPH, No perinatal
transmission
• IG to baby 0.02ml/kg IM if
infection within 2 weeks
of delivery or immediate
postpartum
• Vaccination to mother
when she moves to
endemic area
• IG to mother 0.02ml/kg
deep IM within 2 weeks of
exposure to index case
Anti HEV +ve
• Severe course in preg
• 20% fatal
• 50% of fulminant hepatitis
• No vaccine for it
• Supportive T/t
• Maternal outcome fatal if
fetus dies of hepatitis
• No carrier stage
Positive HBsAg, IgM anti HBc, HBeAg
• Course = non preg
• 10% carrier rate: 25%
have ch active hepatitis
& CA
• With HBeAg – highrisk
for ca
• PNT-20%
+ve HBeAg-90%
anti HBe ab-no
transmission
• Transplacental - 5%
vertical at TOD – 95%
& Breast Feeding
Infants born with HB are generally asymptomatic but
become carrier in 85%
Immunoprophylaxis for HBV
Neonate of HBsAg +ve
mother
• HBIG-0.5ml(250IU)
IM
TOD and 6 weeks
• HBV vaccine-different
site, IM
0,6,10,14, weeks vs.
0,1,6 months
Unimmunised Mother
• PEP within 48hrs
HBIG-500IU, IM
HBV vaccine 0,1,6
months at different
site
Hepatitis C & D & G
Hepatitis C
• IgM anti HCV +ve
• Course = non preg
• 85% develop ch
hepatitis
• Vertical transmission
only IgM +ve – 10%
PCR +ve - 30%
or HIV +ve
• No immunoprophylaxis
Hepatitis D
• Co infects with HBV
• Course = HB
• HC+HB is more severe
than HB alone
• 75% develop cirrhosis
• HB vaccine prevents
delta hepatitis
Hepatitis G
• HC coinfection
• Does not cause hepatitis
Fulminant hepatitis
• HE is commonest cause
• Jaundice, encephalopathy, coagulopathy, ARF
• Multiple organ failure
• DD: APLP,HELLP, Eclampsia
• Serological markers r helpful
• ICU care, supportive care, liver transplant facility
• Poor predictors: Bb>18mg%,INR>3.5,III-IV Enceph
• Vit K should be given, replacement of clotting factors
in absence of bleeding should not be done.
• Termination of pregnancy – role is doubtful. Should
be done id diagnosis is in doubt or for fetal survival
in 3rd trimester
• Chronic hepatitis
• Liver cirrhosis & portal hypertension
• Cholelithiasis in pregnancy
• Budd-Chiari syndrome
• Post liver transplantation pregnancy
Liver Disease In Pregnancy2

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Liver Disease In Pregnancy2

  • 1. Liver Disease In Pregnancy Dr Amita Suneja Professor, OB & GYN UCMS & GTBH
  • 2. Challenging disease to manage • Because of physiology of pregnancy certain disorders take more ominous course in pregnancy than in non pregnant state and some are unique to pregnancy • May have severe maternal & fetal effects Therefore it is important to have accurate diagnosis
  • 3. Physiological changes in hepatic parameters NO CHANGE • Hepatic blood flow • Hepatic & splenic size • Liver histopathology • Bilirubin- direct or indirect, AST, ALT, GGTP, TBA • PT/INR WITH CHANGE • Albumin - ↓ 20%-50% • Globulin -↑ • Fibrinogen - ↑50% • Ceruloplasmin & transerrin - ↑ • ALP - ↑2-4 fold • LDH - ↑slight • Cholesterol & TGL - ↑2fold ↑ AST, ALT,S Bb, TBA during pregnancy indicate liver disease
  • 4. Classification Unique to pregnancy • Hyperemesis Gravidarum • Intrahepatic cholestasis of pregnancy • Preeclampsia & liver - HELLP, INFARCTION & RUPTURE • Acute fatty liver of pregnancy concurrent with pregnancy • Viral hepatitis A,B,C,E, herpes simplex • Drug hepato toxicity • Budd chiari syndrome Pregnancy on Preexisting ch liver disease • Cirrhosis & Portal HT • Ch Hepatitis B, Ch Hepatitis C, Autoimmune hepatitis • Primary biliary cirrhosis • FNH & Hepatic adenoma • Liver transplantation
  • 5. Case report • 36yrs, G2P1+0+0+1, 36wks, prev LSCS,↓FM • c/o nausea, malaise & jaundice • Treated as viral hepatitis x 3days in NH • ANC - normal • GPE – conscious, vitals & BP-n icterus ++, no edema • P/A–36wks, Vx, mild contractions, FHS-128/m • P/V-early labor, unclotted blood in vagina
  • 6. Investigations Hb-10g%, TLC-11000/mm, platelet-110,000/ul Bb-11.8mg%: D-8mg% AST-144U/L ALT-197U/L ALP-578U/L PT,PTTK,TT ↑↑ INR 3.25 BUN-6mg/dl Creatinine-1.5mg% Co2-13mEq/L Blood glucose- Normal Viral markers-negative Urine-normal USG-normal
  • 7. AFLP or HELLP • AFLP Normal BP No haemolysis Less thrombocytopenia Marked coagulopathy • HELLP Can occur in normal BP Had EL & LP No hypoglycemia
  • 8. Treatment • 19U FFP & 10U cryoprecipitate • LSCS 5hrs later for AFD, Male baby A&H • Hysterectomy for PPH • D2- moderate ascitis, thrombocytopenia, coagulopathy, jaundice • D3- marked icterus, semicomatose, hypoglycemia, metabolic acidosis - waiting list: cadaveric liver transplant - deep coma, convulsions, cerebral edema • D11- patient died, liver bx taken
  • 9. Acute Fatty Liver Of Pregnancy • Rare & fatal disorder • 50% mortality, with early diagnosis & T/t mortality is 20% • More common in primi gravida & multiple pregnancy • Mildly raised enzymes, -ve viral markers, dominantly hypoglycemia & coagulopathy, • Normal USG • Treatment is supportive management & termination of pregnancy. • Ac fulminant failure – liver transplant,
  • 10. • If starts improving- full recovery • LCHAD (long chain 3-hydroxyacyl-coenzyme A dehydrogenase) deficiency in fetus →no oxidation of Fatty acids in fetus →maternal liver gets overwhelmed with FA in heterzygous mother →AFLP • Both parents r heterozygous for this defect
  • 11. Case History II • 24yrs,G2P1+0+0+1, 34 wks, intense pruritis H/O pruritis & jaundice in previous pregnacy ANC in this preg – N, no nausea or vomiting • Examination No icterus or hepatosplenomegaly or tenderness scratch marks +ve, no evidence of scabies Obstetric exam – uneventful • Investigations S Bb – 3mg%, Direct – 2mg% AST – 200U/L, ALT 104 U/L, ALP – 400IU/L PT - normal
  • 12. Differential diagnosis • IHCP • Anicteric viral hepatitis • Obstructive jaundice
  • 13. Further investigations • USG liver to rule out obsruction of the biliary tract - normal • Viral markers – normal • If diagnosis is still in doubt due to unusual features – confirmatory serum tests should be total bile acids (TBA) which are raised
  • 14. IHCP • IIIrd trimester, Recurrent, Mild icterus (Bb is not > 5 mg%) • No prodrome, itching, ↑ALP, ↑TBA, n USG • Counselling – maternal & fetal risk • Relief of maternal symptoms- phenobarbitone • Ursodeoxycholic acid – 300mg bd • Addition of SAMe (S adnosylmethionine) to UDCA – ? benefit; • VIT K • Terminate pregnancy at 37 weeks
  • 15. • Etiology: genetic – mutation of MDR3 gene - hypersensitivity to oestrogens Environmental • Future pregnancy Recurrence No OCP No progesterone in next pregnancy
  • 16. IgM HAV +ve • Similar course, ↑PTL, ↑ PPH, No perinatal transmission • IG to baby 0.02ml/kg IM if infection within 2 weeks of delivery or immediate postpartum • Vaccination to mother when she moves to endemic area • IG to mother 0.02ml/kg deep IM within 2 weeks of exposure to index case Anti HEV +ve • Severe course in preg • 20% fatal • 50% of fulminant hepatitis • No vaccine for it • Supportive T/t • Maternal outcome fatal if fetus dies of hepatitis • No carrier stage
  • 17. Positive HBsAg, IgM anti HBc, HBeAg • Course = non preg • 10% carrier rate: 25% have ch active hepatitis & CA • With HBeAg – highrisk for ca • PNT-20% +ve HBeAg-90% anti HBe ab-no transmission • Transplacental - 5% vertical at TOD – 95% & Breast Feeding Infants born with HB are generally asymptomatic but become carrier in 85%
  • 18. Immunoprophylaxis for HBV Neonate of HBsAg +ve mother • HBIG-0.5ml(250IU) IM TOD and 6 weeks • HBV vaccine-different site, IM 0,6,10,14, weeks vs. 0,1,6 months Unimmunised Mother • PEP within 48hrs HBIG-500IU, IM HBV vaccine 0,1,6 months at different site
  • 19. Hepatitis C & D & G Hepatitis C • IgM anti HCV +ve • Course = non preg • 85% develop ch hepatitis • Vertical transmission only IgM +ve – 10% PCR +ve - 30% or HIV +ve • No immunoprophylaxis Hepatitis D • Co infects with HBV • Course = HB • HC+HB is more severe than HB alone • 75% develop cirrhosis • HB vaccine prevents delta hepatitis Hepatitis G • HC coinfection • Does not cause hepatitis
  • 20. Fulminant hepatitis • HE is commonest cause • Jaundice, encephalopathy, coagulopathy, ARF • Multiple organ failure • DD: APLP,HELLP, Eclampsia • Serological markers r helpful • ICU care, supportive care, liver transplant facility • Poor predictors: Bb>18mg%,INR>3.5,III-IV Enceph • Vit K should be given, replacement of clotting factors in absence of bleeding should not be done. • Termination of pregnancy – role is doubtful. Should be done id diagnosis is in doubt or for fetal survival in 3rd trimester
  • 21. • Chronic hepatitis • Liver cirrhosis & portal hypertension • Cholelithiasis in pregnancy • Budd-Chiari syndrome • Post liver transplantation pregnancy