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Investigation in a case of Obstructive
jaundice and Approach
Dr uttam Laudari
2014/12/12
Aims of Investigation
• Detection of disease
• Assessment of severity
• Assess prognosis
• Assess effect of therapy/ recurrence/ follow up
Questions faced
• Is it obstructive jaundice?
• Where is the obstruction?
• What is the cause of obstrution? ( benign/ malignant)
Liver Function Test
• Bilirubin
• Aspartate Transaminase
• Alanine Transanaminae
• Alkaline Phosphatase
• Albumin
• PT/INR
Bilirubin
• Hallmark of obstructive jaundice
• Measured Direct and indirect bilirubin level at same time
• Van Den Berg test- assess direct
• these days both fraction calculated separately by
spetrophotometry
• Conjugated hyperbilirubinemia  hall mark of obstructive
jaundice
• Differentiates hemolytic cause from other hepatic and post
hepatic causes of jaundice
• D/D- viral hepatitis/ Dubin-johnson’s Syndrome
• Presence of bilirubin on urine analysis is also marker of
conjugated hyperbilirubinemia
AST/ALT
• AST( SGOT)- is intracellular enzyme
responsible for amino acid metabolism
• Two isoenzymes
– Type 1- cytosolic
– Type 2- mitochodrial  more specific to liver
• AST is found in liver, cardiac muscles, skeletal
muscles, RBCs, kidney and brain
• I.E less specific than ALT
ALT(SGPT)
• Intracellular enzyme
• Responsible of amino acid metabolism
• Primarily present in liver cells
ALT/AST elevation is marker of cellular damage
Isolated elevation of AST non hepatic cause for jaundice
( muscle injury, MI)
• AST/ALT ratio indicator in alc. Liver disease 2:1
• Wilsons Disease- Ratio 4:1
• Raise AST and ALT indicates liver cellular injury liberating
intracellular enzymes
– Liver trauma
– Hepatitis
– Liver ischemia ( right hepatic artery clipped during Lap. Chole)
• raise in obstructive jaundice too
• Marked rise suspicious of Cholangitis
• AST > 10 times the normal
• Hepatic hypoxia
• CBD calculi
• Glutathione-S- Transferase (GST-a) more sensitive to
liver injury in assessing injury
• Has short half life (90min)
Alkaline phosphatase (ALP)
• Canaliucular enzyme
• Normally expressed by apical parts of hepatocytes
• Cleaved and secreted in space of Disse and then in bile
• Bile flow obstruction ALP overflow in vascular channels
• ALP also produced by osteoblasts, kidney and salivary glands
• also raised in bone metastasis
• GGT and 5’ nucleotidase estimation required to confirm its
elevation due to obstructive jaundice
Serum albumin
• Marker of chronic liver disease
• Half life -21 days
• Reduced value idicated malnutrition >3 weeks
• Prealbumin estimation
– Short half life (7 days)
– Low value indicated recent loss of synthetic function of liver
Prothrombin timed Raito (PTI)
• Factors I, II, V, VII, and X synthesized in liver
• Factors II,VII,IX and X vitamin K dependent factors
• PTI measures the extrinsic pathway of coagulation
• Bile flow obstruction
• Vit k cannot be absorbed from intestine
• hence II, VII, IX, X deficent
• PTI/INR is an indicator of liver function
• If PTI doesn’t Improve with parenteral Vit. K supplementaiton-
 likely liver cell damage
Tumor markers
• Value is suspicion of HCC, Ca. GB or pancreatic cancer
• AFP, Ca 19-9, Ca-125
• Monitoring response and follow up
Imaging modalities
• Ultrasound
– Detection of GB stones, possiblleCBD calculi
– CBD diameter
– Presence of intrahepatic biliary dilatation
– GB massses, liver metastasis,
– Not accurate for pancreatic lesion
• Intrahepatic bile duct – 2mm
• Common heaptic duct-<4mm
• CBD <5-7mm
Ultrasound
• Advantage- noninvasive, portable, least expensive
• disadvantage-
– bowel gas may boscure CBD
– diffcult in obese person
CT scan
• Indicated in malignant lesions of GB, liver or pancreas
• Not good for GB stone, usg more accurate than CT
• Good for liver, nodes
• MRCP good for biliary tree
CT - Scan
• Advantage
– Noninvasive
– Higher resolution than USG
– Not operator dependent
• Disadvantage
– IV contrast ( potential nephrotoxicity)
MRCP/MRI
• Defines structural abnormalities in jaudice
• Very accurate for CBD calculi,mural disease of CBD (
strictures, sclerosing cholangitis, choledochal cyst)
• Drawback
– Gadolinium contrast nephrogenic fibrosis later
– In presnce of gross ascitis image quality will be poor
MRCP
• Advantage
– Noninvasive
• Disadvantage
– Requires breath holding
– May miss small caliber bile duct disease
Endoscopic Ultrasound
• Has miniature ultrasound transducer mounted on its tip
• As sensitive as ERCP in detecting stone and strictures
• Sensitivity and accuracy of endoscopic USG for
choledocholithiasis is > 90%
• More accurate than transabdominal USG
ERCP
• Not be used as diagnostic modality
• Definite morbidity and mortality has been reported
• Combined with therapeutic procedures such as stent
placement or extraction
• Diagnostic and interventional procedures such as biopsy or
stone extraction is useful to the union of right and left hepatic
ducts
• Proximal to that PTC is helpful
ERCP
• Advantage
– Provides direct imaging of bile ducts
– Permits direct visualization of periampullary region and
acquisition of tissue distal to bifurcation of hepatic duct
– Potential for simultaneous therapeutic intervention
– Useful in lesion distal to bifurcation of hepatic ducts
ERCP
• Disadvantage
– Cannot be performed if altered anatomy precluded
endoscopy access to ampulla
– Morbidity 3%
– Mortality 0.2%
NBD-gram
• Nasobiliary drainage for external drainage
• Advantages
• Sample for culture in purulent cholangitis
• Injection of radio opaque dye  delineate CBD without need for
repeated ERCP
PTC/PTBD
• PTC
– Indicated to image proximal biliary tree
– Replaced by MRCP
– PTC alone rarely indicated
– Performed with PTBD
– PTBD- relief of cholangitis
PTC
• Advantages
– Provides direct imaging of bile ducts
– Potential for simulataneous therapeutic intervention
– Useful for lesion proximal to common hepatic duct
– Disadvantages
– more difficult with non-dilated intrahepatic bile duct
– Morbidity- 3%
– Mortality 0.2%
HIDA Scan
• No role in evaluation of jaundice
• Since it is not taken up by liver once bilirubin levels exceeds 7-
9gm%
• Value in diagnosis of acute Cholecystitis and
• For follow up after bilio-enteric anastomosis to confirm
patency of anastomosis
Comparison of different imaging
modalities
Test Sensitivity % Specificity %
Ultrasound 55-91 82-95
CT scan 63-96 93-100
MRCP 82-100 92-98
ERCP 89-98 89-100
PTC 98-100 89-100
Approach
• First step is to detemine if jaundice is medical or surgical
• Commonest disease is viral hepatitis in which there is
prodrome of malaise, anorexia
• Sensistivitiy of history, physical examination, blood test alone
range from 70-90%
• Specificity approx. 75%
Obstructive janudice VS Viral hepatitis
Obstructive jaundice Viral hepatitis
History RUQ pain
Fever, rigors
Prior biliary surgery
Older age
Anorexia, malaise, myalgis
Known infectious exposure
Receipt of blood
products/iv drugs
Jaundice in family/locality
Examination Abdominal tenderness
Fever
Abdominal masses
Scar of previous surgery
Ascitis
Stigmata of Liver disease
Investigations Elevated ALP
PTI normalizes with VIT K
Positive imaging
Elevated AST/ALT
PTI does not normalizes
with Vit K
Positive serological tests
Approach
• Clinical impression confirmed with investigations  LFT
• Provisional Dx obstructive jaundice
• Investigations are directed towards the casue
• USG good modality gives provisional DX in most cases
– And guides what future investigations should be done
• MRCP is done in next step
• Tumor markers are required only if imaging suggests a malignancy
Child Pugh Score
• Most widely used and best validated prognostic index
• Correlated with individual survival
• predicts the operative risk
• Applicable for all intervention
• Elective surgery should not be done in grade B or C
Variable 1 2 3
Encephalopathy Nil Slight to moderate Mod - severe
Ascites Nil Slight Mod- severe
Bilirubin mg.dl <2 2-3 >3
Albumin g/dl >3.5 2.8-3.5 <2.8
Prothrombin index >70% 40-70% <40%
Grade A 5 0r 6
Grade B 7-9
Grade C 10-15

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Investigation in a case of obstructive jaundice and

  • 1. Investigation in a case of Obstructive jaundice and Approach Dr uttam Laudari 2014/12/12
  • 2. Aims of Investigation • Detection of disease • Assessment of severity • Assess prognosis • Assess effect of therapy/ recurrence/ follow up
  • 3. Questions faced • Is it obstructive jaundice? • Where is the obstruction? • What is the cause of obstrution? ( benign/ malignant)
  • 4. Liver Function Test • Bilirubin • Aspartate Transaminase • Alanine Transanaminae • Alkaline Phosphatase • Albumin • PT/INR
  • 5. Bilirubin • Hallmark of obstructive jaundice • Measured Direct and indirect bilirubin level at same time • Van Den Berg test- assess direct • these days both fraction calculated separately by spetrophotometry
  • 6. • Conjugated hyperbilirubinemia  hall mark of obstructive jaundice • Differentiates hemolytic cause from other hepatic and post hepatic causes of jaundice • D/D- viral hepatitis/ Dubin-johnson’s Syndrome • Presence of bilirubin on urine analysis is also marker of conjugated hyperbilirubinemia
  • 7. AST/ALT • AST( SGOT)- is intracellular enzyme responsible for amino acid metabolism • Two isoenzymes – Type 1- cytosolic – Type 2- mitochodrial  more specific to liver • AST is found in liver, cardiac muscles, skeletal muscles, RBCs, kidney and brain • I.E less specific than ALT
  • 8. ALT(SGPT) • Intracellular enzyme • Responsible of amino acid metabolism • Primarily present in liver cells ALT/AST elevation is marker of cellular damage Isolated elevation of AST non hepatic cause for jaundice ( muscle injury, MI)
  • 9. • AST/ALT ratio indicator in alc. Liver disease 2:1 • Wilsons Disease- Ratio 4:1 • Raise AST and ALT indicates liver cellular injury liberating intracellular enzymes – Liver trauma – Hepatitis – Liver ischemia ( right hepatic artery clipped during Lap. Chole) • raise in obstructive jaundice too • Marked rise suspicious of Cholangitis
  • 10. • AST > 10 times the normal • Hepatic hypoxia • CBD calculi • Glutathione-S- Transferase (GST-a) more sensitive to liver injury in assessing injury • Has short half life (90min)
  • 11. Alkaline phosphatase (ALP) • Canaliucular enzyme • Normally expressed by apical parts of hepatocytes • Cleaved and secreted in space of Disse and then in bile • Bile flow obstruction ALP overflow in vascular channels
  • 12. • ALP also produced by osteoblasts, kidney and salivary glands • also raised in bone metastasis • GGT and 5’ nucleotidase estimation required to confirm its elevation due to obstructive jaundice
  • 13. Serum albumin • Marker of chronic liver disease • Half life -21 days • Reduced value idicated malnutrition >3 weeks • Prealbumin estimation – Short half life (7 days) – Low value indicated recent loss of synthetic function of liver
  • 14. Prothrombin timed Raito (PTI) • Factors I, II, V, VII, and X synthesized in liver • Factors II,VII,IX and X vitamin K dependent factors • PTI measures the extrinsic pathway of coagulation
  • 15. • Bile flow obstruction • Vit k cannot be absorbed from intestine • hence II, VII, IX, X deficent • PTI/INR is an indicator of liver function • If PTI doesn’t Improve with parenteral Vit. K supplementaiton-  likely liver cell damage
  • 16. Tumor markers • Value is suspicion of HCC, Ca. GB or pancreatic cancer • AFP, Ca 19-9, Ca-125 • Monitoring response and follow up
  • 17. Imaging modalities • Ultrasound – Detection of GB stones, possiblleCBD calculi – CBD diameter – Presence of intrahepatic biliary dilatation – GB massses, liver metastasis, – Not accurate for pancreatic lesion • Intrahepatic bile duct – 2mm • Common heaptic duct-<4mm • CBD <5-7mm
  • 18. Ultrasound • Advantage- noninvasive, portable, least expensive • disadvantage- – bowel gas may boscure CBD – diffcult in obese person
  • 19. CT scan • Indicated in malignant lesions of GB, liver or pancreas • Not good for GB stone, usg more accurate than CT • Good for liver, nodes • MRCP good for biliary tree
  • 20. CT - Scan • Advantage – Noninvasive – Higher resolution than USG – Not operator dependent • Disadvantage – IV contrast ( potential nephrotoxicity)
  • 21. MRCP/MRI • Defines structural abnormalities in jaudice • Very accurate for CBD calculi,mural disease of CBD ( strictures, sclerosing cholangitis, choledochal cyst) • Drawback – Gadolinium contrast nephrogenic fibrosis later – In presnce of gross ascitis image quality will be poor
  • 22. MRCP • Advantage – Noninvasive • Disadvantage – Requires breath holding – May miss small caliber bile duct disease
  • 23. Endoscopic Ultrasound • Has miniature ultrasound transducer mounted on its tip • As sensitive as ERCP in detecting stone and strictures • Sensitivity and accuracy of endoscopic USG for choledocholithiasis is > 90% • More accurate than transabdominal USG
  • 24. ERCP • Not be used as diagnostic modality • Definite morbidity and mortality has been reported • Combined with therapeutic procedures such as stent placement or extraction • Diagnostic and interventional procedures such as biopsy or stone extraction is useful to the union of right and left hepatic ducts • Proximal to that PTC is helpful
  • 25. ERCP • Advantage – Provides direct imaging of bile ducts – Permits direct visualization of periampullary region and acquisition of tissue distal to bifurcation of hepatic duct – Potential for simultaneous therapeutic intervention – Useful in lesion distal to bifurcation of hepatic ducts
  • 26. ERCP • Disadvantage – Cannot be performed if altered anatomy precluded endoscopy access to ampulla – Morbidity 3% – Mortality 0.2%
  • 27. NBD-gram • Nasobiliary drainage for external drainage • Advantages • Sample for culture in purulent cholangitis • Injection of radio opaque dye  delineate CBD without need for repeated ERCP
  • 28. PTC/PTBD • PTC – Indicated to image proximal biliary tree – Replaced by MRCP – PTC alone rarely indicated – Performed with PTBD – PTBD- relief of cholangitis
  • 29. PTC • Advantages – Provides direct imaging of bile ducts – Potential for simulataneous therapeutic intervention – Useful for lesion proximal to common hepatic duct – Disadvantages – more difficult with non-dilated intrahepatic bile duct – Morbidity- 3% – Mortality 0.2%
  • 30. HIDA Scan • No role in evaluation of jaundice • Since it is not taken up by liver once bilirubin levels exceeds 7- 9gm% • Value in diagnosis of acute Cholecystitis and • For follow up after bilio-enteric anastomosis to confirm patency of anastomosis
  • 31. Comparison of different imaging modalities Test Sensitivity % Specificity % Ultrasound 55-91 82-95 CT scan 63-96 93-100 MRCP 82-100 92-98 ERCP 89-98 89-100 PTC 98-100 89-100
  • 32. Approach • First step is to detemine if jaundice is medical or surgical • Commonest disease is viral hepatitis in which there is prodrome of malaise, anorexia • Sensistivitiy of history, physical examination, blood test alone range from 70-90% • Specificity approx. 75%
  • 33. Obstructive janudice VS Viral hepatitis Obstructive jaundice Viral hepatitis History RUQ pain Fever, rigors Prior biliary surgery Older age Anorexia, malaise, myalgis Known infectious exposure Receipt of blood products/iv drugs Jaundice in family/locality Examination Abdominal tenderness Fever Abdominal masses Scar of previous surgery Ascitis Stigmata of Liver disease Investigations Elevated ALP PTI normalizes with VIT K Positive imaging Elevated AST/ALT PTI does not normalizes with Vit K Positive serological tests
  • 34. Approach • Clinical impression confirmed with investigations  LFT • Provisional Dx obstructive jaundice • Investigations are directed towards the casue • USG good modality gives provisional DX in most cases – And guides what future investigations should be done • MRCP is done in next step • Tumor markers are required only if imaging suggests a malignancy
  • 35. Child Pugh Score • Most widely used and best validated prognostic index • Correlated with individual survival • predicts the operative risk • Applicable for all intervention • Elective surgery should not be done in grade B or C
  • 36. Variable 1 2 3 Encephalopathy Nil Slight to moderate Mod - severe Ascites Nil Slight Mod- severe Bilirubin mg.dl <2 2-3 >3 Albumin g/dl >3.5 2.8-3.5 <2.8 Prothrombin index >70% 40-70% <40% Grade A 5 0r 6 Grade B 7-9 Grade C 10-15