Tad Kim, M.D. UF Surgery [email protected] (c) 682-3793; (p) 413-3222
Transcript of Tad Kim, M.D. UF Surgery [email protected] (c) 682-3793; (p) 413-3222
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Jaundice
Jaundice
Tad Kim, M.D.
UF Surgery
(c) 682-3793; (p) 413-3222
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Jaundice
Overview
Normal Physiology
Pathophysiology
Broad Differential Diagnosis DDx of Obstructive Jaundice
Work-up for Medical Jaundice
Work-up if Obstructive Jaundice Treatment of Obstructive Jaundice
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Jaundice
Normal Physiology
Bilirubin is from breakdown of hemoglobin Unconjugated bilirubin transported to liver
Bound to albumin because insoluble in water
Transported into hepatocyte & conjugated With glucuronic acid now water soluble
Secreted into bile
In ileum & colon, converted to urobilinogen
10-20% reabsorbed into portal circulation and
re-excreted into bile or into urine by kidneys
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Jaundice
Pathophysiology
Jaundice = bilirubin staining of tissue @ lvlgreater than ~2
Mechanisms:
production of bilirubin hepatocyte transport or conjugation
Impaired excretion of bilirubin
Impaired delivery of bilirubin into intestine
surgically relevant jaundice or obstructivejaundice
Cholestasis refers to the latter two, impairedexcretion and obstructive jaundice
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Jaundice
Broad Differential Diagnosisproduction transport or
conjugationImpairedexcretion
Biliaryobstruction
Unconjugate Unconjugate Conjugated Conjugated
Hemolysis Gilberts Rotors CH/CBD stone
Transfusions Crigler-Najarr DubinJohnson Stricture
Txfusion rxn Neonatal Cancer Cancer
Sepsis Cirrhosis Cirrhosis Chronic
pancreatitisBurns Hepatitis Hepatitis PSC
Hgb-opathies Drug inhibition Amyloidosis
Pregnancy
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Jaundice
DDx: Unconjugated bilirubinemia
production Extravascular hemolysis
Extravasation of blood into tissues
Intravascular hemolysis Errors in production of red blood cells
Impaired hepatic bilirubin uptake(trnsport)
CHF Portosystemic shunts
Drug inhibition: rifampin, probenecid
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Jaundice
DDx: Unconjugated bilirubinemia
Impaired bilirubin conjugation Gilberts disease
Crigler-Najarr syndrome
Neonatal jaundice (this is physiologic) Hyperthyroidism
Estrogens
Liver diseases chronic hepatitis, cirrhosis, Wilsons disease
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Jaundice
DDx: Conjugated Bilirubinemia
Intrahepatic cholestasis/impaired excretion Hepatitis (viral, alcoholic, and non-alcoholic)
Any cause of hepatocellular injury
Primary biliary cirrhosis or end-stage liver dz
Sepsis and hypoperfusion states TPN
Pregnancy
Infiltrative dz: TB, amyloid, sarcoid, lymphoma Drugs/toxins i.e. chlorpromazine, arsenic
Post-op patient or post-organ transplantation
Hepatic crisis in sickle cell disease
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Jaundice
DDx: Obstructive Jaundice
This is the slide to remember for surgeons
Obstructive Jaundice extrahepaticcholestasis Choledocholithiasis (CBD or CHD stone)
Cancer(peri-ampullary or cholangioCA) Strictures after invasive procedures
Acute and chronic pancreatitis
Primary sclerosing cholangitis (PSC) Parasitic infections
Ascaris lumbricoides, liver flukes
Just remember top 5 (not parasites)
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Jaundice
Initial Evaluation: History
Jaundice, acholic stools, tea-colored urine
Fever/chills, RUQ pain (cholangitis)
Could lead to life-threatening septic shock
Reasons to have hepatitis or cirrhosis?
Alcohol, Viral, risk factors for viral hepatitis
Exposure to toxins or offending drugs
Inherited disorders or hemolytic conditions Recent blood transfusions or blood loss?
Is patient septic or on TPN?
Recent gallbladder surgery? (CBD injury)
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Jaundice
Initial Evaluation: Physical Exam
Signs of end stage liver disease (cirrhosis)
Ascites, splenomegaly, spider angiomata, and
gynecomastia
Jaundice evident first underneath the
tongue, also evident in sclerae or skin
Courvoisiers sign = painless, but palpable
or distended gallbladder on exam
Could indicate malignant obstruction
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Jaundice
Screening Labs
NL LFT r/o hepatic injury or biliary tract dz Consider inherited disorders or hemolysis
Alk Phos moreso than AST/ALT implies
cholestasis (intrahepatic vs obstruction) Alk Phos also seen in sarcoid, TB, bone
In this case, GGT is specific for biliary origin
Predominant AST/ALT implies intrinsichepatocellular disease
AST/ALT ratio > 2 in alcoholic hepatitis
albumin or INR c/w advanced liver dz
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Jaundice
Subsequent Labs
If no concern for obstructive jaundice:
Viral (Hep B&C) serologies for viral hepatitis
anti-mitochondrial Ab (PBC)
anti-smooth muscle Ab (Auto-immune)
iron studies (hemochromatosis)
ceruloplasmin (Wilsons)
Alpha-1 anti-trypsin activity (for deficiency)
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Imaging for Obstructive Jaundice
RUQ Ultrasound See stones, CBD diameter
CT scan
Identify both type & level of obstruction ERCP
Direct visualization of biliary tree/panc ducts
Procedure of choice for choledocholithiasis Diagnostic AND- therapeutic (unlike MRCP)
PTC useul of obstruction is prox to CHD
Endoscopic Ultrasound or EUS
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Jaundice
Treatment
If Medical, then treat the etiology If Obstructive Jaundice: Should r/o ascending cholangitis, ABC/resusc
For cholangitis: IVF, IV Antibiotics, Decompression
Stones (remove stones vs stent vs drainage) Done via ERCP or PTC or open (surgery)
Benign stricture (stent vs drainage catheter)
Cancer (Stent vs drainage +/- resect the CA) The key principle is decompression, either
externally(drainage) or internally(stenting)the duct open to allow better drainage
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Jaundice
Take Home Points
Above is a comprehensive approach
For surgery clerkship, all you need toknow is: 1. Broad categories (no specific diagnoses)
2. The four DDx ofobstructive jaundice
3. H&P (ask about fevers/chills, jaundice,acholic stools, dark urine, weight loss for CA),r/o ascending cholangitis = emergency
4. Labs (LFT: ?cholestatic, CBC w diff, BMP)
5. Imaging (U/S, CT, MRCP, EUS)
6. Therapy (ERCP vs PTC vs surgery)