Diseases Of The Liver And Biliary System IM Plat Flashcards
Basic patterns of liver disease
Hepatocellular
Cholestatic
Mixed
Hepatocellular examples
Viral hepatitis
Alcoholic liver disease
Cholestatic
Obstructive biliary diseases
Mixed
Drug induced liver diseases
Major risk factors for liver diseases
Alcohol use Medications - herbal compounds Birth control pills, OTC meds Personal habits Sexual activity Travel Exposure to jaundiced or other high-risk persons Injection drug use Recent surgery Remote or recent transfusion with blood and blood products Occupation Accidental exposure to blood or needle stick injury Familial history of liver disease
Most common and most characteristic symptom of liver disease
Fatigue
Hallmark of liver disease and the most reliable marker of severity
Jaundice
Constitutional symptoms of liver disease
Fatigue poor appetite Weakness Nausea Malaise
Liver-specific symptoms
Jaundice,dark urine, light stools, itching, abdominal pain
Bloating
Signs of hepatic disease(12)
Icterus Palmar erythema Spider angiomata Hepatomegaly Splenomegaly Ascites Peripheral edema Hepatic encephalopathy Fetor hepaticus Umbilical hernia Caput medusa Hyperestrogenemia (for males)- gynecomastia, testicular atrophy, loss of male pattern hair distribution
Superficial tortuous arterioles seen on the arms, face, upper torso, fill outwards from the center
Spider angiomata
Icterus can be noted on the
Sclerae, skin
Mucous membrane below the tongue
The most reliable physical finding in examining the liver
Hepatic tenderness
Hepatomegaly is seen in
Venoocclusive disease, infiltrative disorders, hepatic malignancy, alcohol hepatitis
Subtle significant finding in liver disease and portal hypertension
Splenomegaly
Ascites is best appreciated by
percussing for Shifting dullness
How much volume of ascitic fluid should be present before dullness is appreciated
~1500 mL
Contributing factors to peripheral edema in liver disease
Hypoalbuminemia, venous insufficiency
Heart failure
Medications
First signs of hepatic encephalopathy
Change in sleep patterns Change in personality Irritability Mental dullness Confusion Disorientation Stupor Eventually coma supervene
Acute liver failure neurologic signs
Excitability , mania
Slightly sweet, ammonia-like odor in patients especially if there is portovenous shunting of blood
Fetor hepaticus
Umbilical hernia develops in liver disease due to
Increased intraabdominal pressures from ascites
Appearance of distended and engorged superficial epgastric veins which are seen radiating from the umbilicus across the abdomen
Caput medusae
Golden-brown copper pigment deposited in the periphery of the cornea
Kayser-fleischer rings
Kayser-fleischer rings are found in
Wilson’s disease
Is a condition in which one or more fingers become permanently bent in a flexed position
Dupuytren’s contracture
Dupuytren’s contracture and parotiod enlargement is found in
Alcoholic liver disease
Slate-gray pigmentation of skin is found in
Hemochromatosis
Also called as bronze diabetes
Hemochromatosis - because it can lead to darkening of the skin and hyperglycemia
Tests based on detoxification and excretory functions
Serum bilirubin
Aminotransferases
Enzymes that reflect cholestatsis
Alkaline phosphatase (ALP)
5’ Nucleotidase (5NT)
Y- glutamyl transpeptidase (GGT)
Tests that measure biosynthetic function of the liver
Serum albumin
Serum globulins
presence of icterus
Total serum bilirubin is at least
3 mg/dL
Unconjugated bilirubinemia
Indirect
Conjugated bilirubinemia
Direct
Uncojugated bilirubinemia is seen in
INDIRECT
Hemolytic disorders
Crigler-Najjar
Gilbert’s syndrome
Conjugated bilirubinemia (DIRECT) is seen in
Liver or biliary tract disease
Enzymes that reflect damage to hepatocytes
Aminotransferases
Which is the more specific indicator of liver injury
ALT VS AST
ALT
Elevatins of >1000 U/L aminotransferases occur almost exclusively in
Viral hepatitis
Ischemic liver injury (prolonged hypotension or acute heart failure)
Toxin- or drug- induced liver injury
Autoimmune hepatitis
Acute phase of biliary obstruction caused by passage of gallstone into the CBD
ALP >4X UPPER LIMIT NORMAL
Indicates
Cholestatic liver disease
Infiltrative liver diseases
Rapid bone turnover
AST/ALT <1
Chronic viral hepatitis
Non-alcoholic fatty liver disease
AST/ALT >2
Alcoholic liver disease
Development of cirrhosis
Wilson disease
Low ALP may be seen in
Wilson disease (esp those presenting with
Fulminant hepatitis and hemolysis) - due to reduced activity of the enzyme from the displacement of the cofactor zinc by copper
(ALP : BILIRUBIN <4)
ALP/AST >3
Cholestatic conditions like primary biliary cirrhosis
ALP/AST <1.5
Autoimmune hepatitis
5NT is elevated in
Cholestatic liver disease Hepatitis Biliary cirrhosis Hepatotoxic drugs Metastasis
Primary use of GGT
Identify the source of an isolated elevation in ALP
GGT not elevated in bone disease
Half-life of serum albumin is
18-20 days
Thus not a good indicator of acute or mild hepatic dysfunction
Hypoalbuminemia is
<3g/dL
Hypoalbuminemia is more common in
Chronic liver disorders - cirrhosis, reflecting severe liver damage and decreased albumin synthesis
Y-globulins are increased in
Chronic liver disease (inc antibody synthesis to fight off intestinal bacteria that the cirrhotic liver failed to clear from the hepatic circulation
Single best acute measure of hepatic synthetic functio
Clotting factors
All clotting factors are synethesized in the liver except for factor
VIII (8)
PT measures clotting factors
II, V, VII, X
Prolongation of PT >5 s above the control not corrected by IV Vitamin K portends
Poor prognosis
Clotting factors have prognostic value in
Alcoholic hepatitis
Acute acetaminophen and non acetaminophen related liver injury
most commonly employed imaging of the liver
Ultrasound
CT
MRI
Is the first line if initial blood test suggest cholestasis
Ultrasound - to check for dilated ducts/ gallstones
Procedures of choice to visualize the biliary tree
ERCP
MRCP
Assessment of hepatic vasculature and hemodynamics
Doppler UTZ and MRI
Is the first test ordered if suspecting for Budd-Chiari syndrome
Doppler US
The criterion standard in the evaluation of patient with liver disease
Liver biopsy
Liver biopsy is subject to this error in focal infiltrative disorders
Sampling error
Contraindications to percutaneous approach are
Significant ascites Prolonged INR (may use transjugular approach instead)
Diagnostic tests for autoimmune hepatitis
ANA or SMA
Anti-LKM1
Elevated IgG levels
Diagnostic tests for Primary Biliary Cirrhosis
AMA (anti-mitochondrial antibody)
Elevated IgM
Diagnostic tests for primary sclerosing cholangitis
Cholangiography
p-ANCA
Diagnostic tests for Wilson’s disease
Decreased serum ceruloplasmin and increased urinary copper
Increased hepatic copper level
Diagnostic tests for hepatocellular cancer
Elevated alpha-fetoprotein level >500
US or CT image of mass
Stratifies liver disease patients into risk groups
CHILD-PUGH SCORE
Predicts the likelihood of major complications of cirrhosis (e.g. variceal bleeding, spontaneous bacterial peritonitis)
CHILD-PUGH SCORE
What are the parameters needed to evaluate for Child-Pugh score
Serum bilirubin Serum albumin Prothrombin time Ascites and Hepatic encephalopathy
Child-Pugh score of 5-6
Class A
Child Pugh score of 7-9
Class B
Child-Pugh score of 10-15
Class C
Decompensation indicates
CIRRHOSIS, with a score of >/= 7
Has been the accepted criterion for listing a patient for liver transplant
Decompensation
Score of >/=7
Maximum score of Child-Pugh score
15
Minimum score of Child-pugh score
5
Child Pugh score of 1
Per parameter
SERUM BILIRUBIN: <2 mg/dL SERUM ALBUMIN >3.5 g/dL PT 0-4 INR <1.7 No ascites No hepatic encephalopathy
Child Pugh score of 2
Per parameter
SERUM BILIRUBIN: 2-3 mg/dL SERUM ALBUMIN 2.8-3.5 g/dL PT 4-6 INR 1.7-2.3 ASCITES - easily controlled HEPATIC ENCEPHALOPATHY - minimal
Child Pugh score of 3
Per parameter
SERUM BILIRUBIN: >3mg/dL SERUM ALBUMIN <2.8 g/dL PT >6 seconds INR >2.3 ASCITES - poorly controlled HEPATIC ENCEPHALOPATHY - advanced
MELD SCORE stands for
Model for end-stage liver disease score
scoring system to predict prognosis of patients with liver disease and portal hypertension
Model of End-Stage Liver disease (MELD SCORE)
MELD SCORE is calculated using three non-invasive variables
PT-INR
Serum bilirubin
Serum creatinine
Budd-Chiari syndrome is caused by
Occlusion of the hepatic veins that drain the liver
Classical triad of Budd-chiari syndrome
Abndominal pain
Ascites
Liver enlargement
Complications of cirrhosis
Variceal bleeding
Spontaneous bacterial peritonitis