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APPROACH TO A PATIENT WITH
JAUNDICE
Prepared by:
Kritika Jha
M.B.B.S Intern.
JAUNDICE
It is defined as yellowish discoloration of tissue
resulting from the deposition of bilirubin.
It is best appreciated by inspecting the sclera
under natural light. In dark skinned individuals,
mucous membrane below the tongue
demonstrates jaundice.
• Latent jaundice- when bilirubin<2.5mg/dl.
• Clinical jaundice-when bilirubin</=3mg/dl.
Production and metabolism of
bilirubin
Causes of hyperbilirubinemia
I. Unconjugated hyperbilirubinemia
A. Increased bilirubin production
1. Hemolytic disorder
• inherited: hereditary spherocytosis, sickle cell anemia,
thalassemia, enzyme deficiency: G6PD and pyruvate
kinase deficiency
• acquired: hemolytic uremic syndrome, immune
hemolysis, malaria.
2. Ineffective erythropoiesis
thalassemia;deficiency of iron, folate or vitamin
B12;lead poisoning.
B. Decreased hepatic bilirubin clearance
• decreased hepatic uptake: rifampicin,probenecid.
• Impaired conjugation:
physiological neonatal jaundice
acquired conjugation defects: advanced hepatitis or
cirrhosis; drugs-chloramphenicol, gentamycin; breast
milk jaundice.
C. Hereditary defects in conjugation
Crigler-najjar syndrome type I and II
Gilbert’s syndrome
Causes of conjugated hyperbilirubinemia
A. Inherited conditions: dubin johnson syndrome
rotor syndrome
B. Hepatocellular conditions:
• Viral hepatitis-hepatitis A,B,C,D,E; EBV; CMV;HSV
• Alcohol
• Drug- acetaminophen, isoniazid, halothane,
sodium valproate, amiodarone, phenytoin, statins,
cotrimoxazole,
• Toxins- wild mushroom, herbal tea, bee pollen,etc
• Wilson’s disease
• Autoimmune hepatitis.
C. Cholestatic jaundice
1. Intrahepatic
Viral hepatitis- hepatitis b and c
Alcoholic hepatitis
Drug: steroids, erythromycin, chlorpromazine
Primary biliary cirrhosis
Primary sclerosing cholangitis
Cholestasis of pregnancy
Infiltrative disease- TB, lymphoma
Venoocclusive disease
2. Extrahepatic : Cholangiocarcinoma, pancreatic, gall
bladder, ampullary cancer; choledocolithiasis.
CLINICAL HISTORY
• Duration of jaundice, dark urine, light stools, itching.
• Arthralgia, myalgia, rash, anorexia, weight loss,
abdominal pain, fever.
• Nausea may accompany fatigue, provoked by odors
of food or eating fatty foods; vomiting may occur.
• Diarrhea-in severe jaundice due to lack of bile acids.
• History of risk factors- blood transfusion, iv drug use,
tattoos and body piercing, sexual activity, use of any
chemical or medication, recent travel history, contact
history, alcohol consumption.
Physical examination
• Nutritional assesment-temporal and proximal muscle
wasting
• Icterus
• Stigmata of CLD-spider nevi, palmer erythema,
gynecomastia, caput medusae, dupuytren’s contractures,
parotid gland swelling, testicular atrophy.
• Virchow’s node and sister mary joseph’s node in abdominal
malignancy.
• Abdominal examination-
inspection- caput medusae, flank fullness
palpation- hepatomegaly ( tender- viral or alcoholic
hepatitis, right heart failure leading to hepatic congestion)
- Murphy’s sign- cholecystitis or cholangitis
percussion- for ascites.
Laboratory investigations
• Measurement of serum bilirubin
total serum bilirubin-0.2-0.9mg/dl
conjugated-0.2-0.7; unconjugated-0.1-0.4
• Serum albumin and globulin
• Alanine and aspartate aminotransferase[ALT and AST]-
AST:ALT >2:1 = alcoholic hepatitis
>500U/l in viral hepatitis,toxin or drug induced
liver injury
• Alkaline phosphatase and gamma glutamyl transferase.
• PT and INR
• Other diagnostic tests- USG= Gall stones, biliary
obstruction
Cholangiography-MRCP,ERCP
CT scan and MRI; Percutaneous liver biopsy.
• THANK YOU

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Approach to a patient with jaundice

  • 1. APPROACH TO A PATIENT WITH JAUNDICE Prepared by: Kritika Jha M.B.B.S Intern.
  • 2. JAUNDICE It is defined as yellowish discoloration of tissue resulting from the deposition of bilirubin. It is best appreciated by inspecting the sclera under natural light. In dark skinned individuals, mucous membrane below the tongue demonstrates jaundice. • Latent jaundice- when bilirubin<2.5mg/dl. • Clinical jaundice-when bilirubin</=3mg/dl.
  • 4. Causes of hyperbilirubinemia I. Unconjugated hyperbilirubinemia A. Increased bilirubin production 1. Hemolytic disorder • inherited: hereditary spherocytosis, sickle cell anemia, thalassemia, enzyme deficiency: G6PD and pyruvate kinase deficiency • acquired: hemolytic uremic syndrome, immune hemolysis, malaria. 2. Ineffective erythropoiesis thalassemia;deficiency of iron, folate or vitamin B12;lead poisoning.
  • 5. B. Decreased hepatic bilirubin clearance • decreased hepatic uptake: rifampicin,probenecid. • Impaired conjugation: physiological neonatal jaundice acquired conjugation defects: advanced hepatitis or cirrhosis; drugs-chloramphenicol, gentamycin; breast milk jaundice. C. Hereditary defects in conjugation Crigler-najjar syndrome type I and II Gilbert’s syndrome
  • 6. Causes of conjugated hyperbilirubinemia A. Inherited conditions: dubin johnson syndrome rotor syndrome B. Hepatocellular conditions: • Viral hepatitis-hepatitis A,B,C,D,E; EBV; CMV;HSV • Alcohol • Drug- acetaminophen, isoniazid, halothane, sodium valproate, amiodarone, phenytoin, statins, cotrimoxazole, • Toxins- wild mushroom, herbal tea, bee pollen,etc • Wilson’s disease • Autoimmune hepatitis.
  • 7. C. Cholestatic jaundice 1. Intrahepatic Viral hepatitis- hepatitis b and c Alcoholic hepatitis Drug: steroids, erythromycin, chlorpromazine Primary biliary cirrhosis Primary sclerosing cholangitis Cholestasis of pregnancy Infiltrative disease- TB, lymphoma Venoocclusive disease 2. Extrahepatic : Cholangiocarcinoma, pancreatic, gall bladder, ampullary cancer; choledocolithiasis.
  • 8. CLINICAL HISTORY • Duration of jaundice, dark urine, light stools, itching. • Arthralgia, myalgia, rash, anorexia, weight loss, abdominal pain, fever. • Nausea may accompany fatigue, provoked by odors of food or eating fatty foods; vomiting may occur. • Diarrhea-in severe jaundice due to lack of bile acids. • History of risk factors- blood transfusion, iv drug use, tattoos and body piercing, sexual activity, use of any chemical or medication, recent travel history, contact history, alcohol consumption.
  • 9. Physical examination • Nutritional assesment-temporal and proximal muscle wasting • Icterus • Stigmata of CLD-spider nevi, palmer erythema, gynecomastia, caput medusae, dupuytren’s contractures, parotid gland swelling, testicular atrophy. • Virchow’s node and sister mary joseph’s node in abdominal malignancy. • Abdominal examination- inspection- caput medusae, flank fullness palpation- hepatomegaly ( tender- viral or alcoholic hepatitis, right heart failure leading to hepatic congestion) - Murphy’s sign- cholecystitis or cholangitis percussion- for ascites.
  • 10. Laboratory investigations • Measurement of serum bilirubin total serum bilirubin-0.2-0.9mg/dl conjugated-0.2-0.7; unconjugated-0.1-0.4 • Serum albumin and globulin • Alanine and aspartate aminotransferase[ALT and AST]- AST:ALT >2:1 = alcoholic hepatitis >500U/l in viral hepatitis,toxin or drug induced liver injury • Alkaline phosphatase and gamma glutamyl transferase. • PT and INR • Other diagnostic tests- USG= Gall stones, biliary obstruction Cholangiography-MRCP,ERCP CT scan and MRI; Percutaneous liver biopsy.
  • 11.

Editor's Notes

  1. Vomiting rarely persistenrt. Fatigue increased on exercise-intermittent, variable in severity. Wt loss, lo appetote-acute liver dsz. Severe pain abdomen- gb dsz, liver abscess, venocllusive dsz.