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Jaundice in 
Pregnancy 
Dr.MSc. Raul Hernandez Canete
 Incidence: This occurs in about 1 in 1,000 
pregnancies and is most common due to viral 
hepatitis. 
 Etiology: Classification is traditionally into the 
following categories: Hemolytic, 
Hepatocellular, and Obstruction. 
 Causes may be consequential to, or 
independent of, the pregnancy
Jaundice in pregnancy: 
 Hemolytic: 
- Incompatible blood transfusion 
- Cl. Perfringens, E. coli/septicemia 
 Hepatocellular: 
- Viral hepatitis 
- Severe preeclampsia 
- Acute fatty liver of pregnancy 
- Alcohol and drugs (e.g. halothane) 
- Autoimmune chronic active hepatitis
Cont. of jaundice in pregnancy 
 Obstructive: 
- Cholestasis of pregnancy 
- Cholelithiasis 
- Drugs (e.g. Chlorpromazine) 
- Primary biliary cirrhosis 
- Pancreatic carcinoma
Diagnosis: 
 Careful history and examination 
 Biochemical test 
 Ultrasound 
Biochemical test will help to differentiate between 
hepatocellular damage and obstruction: 
- Hepatocellular: predominantly unconjugated bilirubin 
and hepatocellular enzymes (aspartate 
transaminase or alanine transaminase) 
- Cholestasis (intrahepatic or extrahepatic): 
predominantly conjugated bilirubin and alkaline 
phosphatase
Cholestasis of pregnancy: 
 Pathogenesis: is due to an estrogen sensitivity 
effect and exhibits a familial tendency. It is 
frequently recurrent in successive pregnancies or if 
the women is prescribed oral contraceptives. 
 Clinical features: mild jaundice, malaise, and itching 
of the skin. 
Liver function tests (alkaline phosphatase, urine 
urobilinogen) suggest biliary obstruction, cholic acid 
levels are typically elevated . 
Serum bilirubin is rarely more than 85 mmol/L
 Effect of Cholestasis on pregnancy: 
 Postpartum hemorrhage (reduced vitamin K 
absorption) 
 Premature labour (30%) 
 Stillbirth. 
 Management: Other causes of jaundice should be 
excluded, USG and CTG (fetal well-being), 
cholestyramine resin is effective for pruritus, 
Induction of labour is indicated at 37-38 weeks or 
earlier if there is fetal compromise. 
The condition resolves rapidly after pregnancy.
Acute fatty liver of pregnancy: 
 Is unique to pregnancy 
 More common in primigravidas 
 Extremely uncommon before the late second 
trimester 
 It may follow intravenous tetracycline 
administration or prolonged vomiting
Clinical features of AFL 
 The syndrome comprises malaise, fatigue, 
epigastric discomfort and vomiting. Jaundice soon 
follows. There may be hypertension and proteinuria. 
Risk of PPH. Hepatic encephalopathy may be 
develop 
 Laboratory studies reveal a significant leucocytosis, 
moderately disturbed liver function, hypoglycemia 
impaired renal function and often coagulopathy 
 The mortality may be 50% or more without energetic 
treatment.
Management of AFL: 
 Intensive Unit Care 
 Adequate intravenous fluids 
 Albumin, glucose and vitamin K 
 Correction of coagulation defects 
 The pregnancy should be terminated, usually 
by CS.
Severe Preeclampsia 
(including HELLP syndrome) 
 May be part of the spectrum of Acute fatty liver 
 Has a predisposition for late pregnancy and 
primigravidas 
 Widespread endothelial cell damage resulting in 
hemolysis and thrombocytopenia 
 The women needs to be stabilized and delivered 
regardless of gestational age 
 There are some reports of a beneficial effect of 
coticosteroids.

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Jaundice in pregnancy

  • 1. Jaundice in Pregnancy Dr.MSc. Raul Hernandez Canete
  • 2.  Incidence: This occurs in about 1 in 1,000 pregnancies and is most common due to viral hepatitis.  Etiology: Classification is traditionally into the following categories: Hemolytic, Hepatocellular, and Obstruction.  Causes may be consequential to, or independent of, the pregnancy
  • 3. Jaundice in pregnancy:  Hemolytic: - Incompatible blood transfusion - Cl. Perfringens, E. coli/septicemia  Hepatocellular: - Viral hepatitis - Severe preeclampsia - Acute fatty liver of pregnancy - Alcohol and drugs (e.g. halothane) - Autoimmune chronic active hepatitis
  • 4. Cont. of jaundice in pregnancy  Obstructive: - Cholestasis of pregnancy - Cholelithiasis - Drugs (e.g. Chlorpromazine) - Primary biliary cirrhosis - Pancreatic carcinoma
  • 5. Diagnosis:  Careful history and examination  Biochemical test  Ultrasound Biochemical test will help to differentiate between hepatocellular damage and obstruction: - Hepatocellular: predominantly unconjugated bilirubin and hepatocellular enzymes (aspartate transaminase or alanine transaminase) - Cholestasis (intrahepatic or extrahepatic): predominantly conjugated bilirubin and alkaline phosphatase
  • 6. Cholestasis of pregnancy:  Pathogenesis: is due to an estrogen sensitivity effect and exhibits a familial tendency. It is frequently recurrent in successive pregnancies or if the women is prescribed oral contraceptives.  Clinical features: mild jaundice, malaise, and itching of the skin. Liver function tests (alkaline phosphatase, urine urobilinogen) suggest biliary obstruction, cholic acid levels are typically elevated . Serum bilirubin is rarely more than 85 mmol/L
  • 7.  Effect of Cholestasis on pregnancy:  Postpartum hemorrhage (reduced vitamin K absorption)  Premature labour (30%)  Stillbirth.  Management: Other causes of jaundice should be excluded, USG and CTG (fetal well-being), cholestyramine resin is effective for pruritus, Induction of labour is indicated at 37-38 weeks or earlier if there is fetal compromise. The condition resolves rapidly after pregnancy.
  • 8. Acute fatty liver of pregnancy:  Is unique to pregnancy  More common in primigravidas  Extremely uncommon before the late second trimester  It may follow intravenous tetracycline administration or prolonged vomiting
  • 9. Clinical features of AFL  The syndrome comprises malaise, fatigue, epigastric discomfort and vomiting. Jaundice soon follows. There may be hypertension and proteinuria. Risk of PPH. Hepatic encephalopathy may be develop  Laboratory studies reveal a significant leucocytosis, moderately disturbed liver function, hypoglycemia impaired renal function and often coagulopathy  The mortality may be 50% or more without energetic treatment.
  • 10. Management of AFL:  Intensive Unit Care  Adequate intravenous fluids  Albumin, glucose and vitamin K  Correction of coagulation defects  The pregnancy should be terminated, usually by CS.
  • 11. Severe Preeclampsia (including HELLP syndrome)  May be part of the spectrum of Acute fatty liver  Has a predisposition for late pregnancy and primigravidas  Widespread endothelial cell damage resulting in hemolysis and thrombocytopenia  The women needs to be stabilized and delivered regardless of gestational age  There are some reports of a beneficial effect of coticosteroids.