03.05 Jaundice in Adults Flashcards

1
Q

Scleral icterus, presence of at least ____

A

3mg/dl serum bilirubin

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2
Q

Most visible manifestation of liver and biliary tract disease

A

Jaundice

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3
Q

D/dx for yellowing of skin

A

Jaundice
Carotenoderma/carotenemia
Quinacrine use
Excessive exposure to phenols

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4
Q

Becomes clinically evident when total serum bilirubin ____

A

> 3mg/dL

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5
Q

Helps in determining cause of jaundice or hyperbilirubinemia

A

Fractionation of bilirubin

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6
Q

Most commonly available technique of bilirubin measurement

A

Spectrophotometeric method (van der Bergh reaction)

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7
Q

Bilirubin reaction that directly reacts wth diazotized sulfanilic acid that is initially added (even in the absence of alcohol)

A

Direct bilirubin (conjugated)

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8
Q

Suspect liver disease or injury if conjugated bilirubin ____

A

> 0.3 mg/dL

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9
Q

The difference between the total and the direct bilirubin levels measured

A

Indirect bilirubin

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10
Q

Bilirubin formation occurs in ____

A

Reticuloendothelial system

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11
Q

Focus of history

A

Exposure to any chemicals or medications
Parenteral exposure
Risk-taking behaviour
Recent travel history
Exposure to people with jaundice and contaminated foods
Alcohol
Accompanying s/sx (antralgia, myalgia, rash, anorexia, weight loss, abdominal pain, fever, pruritus, urine or stool changes)

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12
Q

PE in assessing jaundice

A

Nutritional status
Muscle wasting (long-standing)
Stigmata of chronic liver disease: spider nevi, palmar erythema, gynecomastia, caput medusa, testicular atrophy
Abdominal examination: size and consistency of liver, palpation of the spleen for enlargement, presence or absence of ascites

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13
Q

Initial steps in evaluation

A

Liver-associated tests (total bilirubin, direct bilirubin, indirect bilirubin, alkaline phosphatase, ALT, AST, albumin, prothrombin time)
Determine if hyperbilirubinemia is direct or indirect
Other tests

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14
Q

Three main causes of jaundice

A
Isolated disorders of bilirubin metabolism
Liver diseases (hepatic disorder with prominent cholestasis, hepatocellular dysfunction)
Obstruction of the bile ducts
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15
Q

Both liver disease and obstruction of the bile ducts manifest with:

A

Elevated bilirubin
Abnormal liver test
Jaundice

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16
Q

Isolated elevation in bilirubin

Other liver tests are normal

A

Isolated disorder of bilirubin metabolism

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17
Q

Causes of IDBM

A

Hemolysis
Drugs (rifampicin)
Inherited disorders of metabolism

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18
Q

Unconjugated hyperbilirubinemia

A

Gilbert’s syndrome

Crigler-Najjar syndrome

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19
Q

Due to impairment in the conjugation of bilirubin

A

Gilbert’s syndrome

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20
Q

Not compatible with life

A

Crigler-Najjar syndrome

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21
Q

Conjugated hyperbilirubinemia

A

Dublin-Johnson syndrome

Rotor syndrome

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22
Q

Due to impairment in the export of bilirubin from the hepatocyte

A

Rotor syndrome

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23
Q

Decrease in bile flow due to impaired secretion by hepatocytes

A

Cholestasis

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24
Q

Clinical manifestations of cholestasis

A

Scleral icterus
Dark urine
Cutaenous jaundice (5 mg/dL)
Severe pruritus (inc. bile acids)

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25
Lab tests of choletastic jaundice
Inc bilirubin Abnormal ALT, AST, AlkPhos, albumin, PT) ALP>ALT
26
In obstruction (extrahepatic cholestasis), the biliary tree is ____
Dilated
27
In hepatic disorder with prominent cholestasis (intrahepatic cholestasis), the biliary tree is ___
Not dilated
28
Causes of obstruction of bile duct
Choledocholithiasis Diseases of the bile duct Extrinsic compression of the bile ducts
29
Diseases of the bile duct
Primary sclerosing cholangitis | Neoplasm
30
Extrinsic compression of bile ducts
Neoplasm Pancreatitis Lymph nodes Vascular engorgement
31
Most common cause of biliary obstruction
Choledocholithiasis
32
Dx of choledocholithiasis
``` Transabdominal UTZ CT scan Endoscopic retrograde pancreatography MR resonance cholangiopancreatography Endoscopic UTZ ```
33
Tx of choledocholithiasis
Urgent ERCP Percutaneous transhepatic procedure Sugery: laparoscopic, open
34
Bacterial infection superimposed on an obstruction of the biilary tree most commonly from a gallstone, but it may be associated with neoplasm or stricture
Acute cholangitis
35
Complications of choledocholithiasis
Charcot's triad: RUQ pain, fever, jaundice | Raynold's pentad: CT + hypotension + altered mental status
36
Choledocholithiasis may cause
Biliary obstruction Stasis of bile Infection
37
Tx of choledocholithiasis
Antibiotics and biliary drainage (ERCP with sphincterotomy)
38
Jaundice from bile duct obstruction (compression of a common hepatic duct by a stone impacted in cystic duct or neck of gallbladder) Uncommon complication of gallstone disease
MIrizzi syndrome
39
Tx of Mirizzi syndrome
Surgery (not ERCP)
40
16% of all TB cases in a 6-year period in Western INdia
Hepatobiliary tuberculosis
41
Most common clinical manifestation of HBtb
Hepatomegaly
42
Classification of HBtb
Miliary TB Granulomatous disease Localized TB
43
Part of generalized TB | Minimal liver-relevant s/sx
Miliary TB
44
Unexplained fever, with or without jaundice, abnormal liver tests, hepatomegaly Caseating granulomas
Granulomatous disease
45
Liver-relevant s/sx predominate - solitary or multiple nodules - tuberculomas - tuberculous hepatic abscess - bile duct dilation due to duct involvement or obstruction by lymph node
Localized TB
46
Important in those with obstructive jaundice for dx and therapy
ERCP
47
Findings of HBtb in ERCP
Bile duct stricture | Extraluminal narrowing
48
Dx of HBtb
Chronic RUQ pain | Chronic, recurrent obstructive jaundice
49
Tx of HBtb
No clear guidelines Standard quadruple anti-TB therapy Biliary decompression
50
Adjunct to those with obstructive jaundice whenever feasible
Biliary decompression
51
Hepatic disorder with prominent cholestasis are seen in patients with:
Infiltrative disease Diseases of the intrahepatic ducts Postoperative jaundice, sepsis, total intrahepatic cholestasis of pregnancy
52
Causes of intrahepatic cholestasis
``` Hepatitis Drugs Diseases of intrahepatic bile ducts Infiltrative disorders Sepsis Total parenteral nutrition Postoperative jaundice Cholestasis of pregnancy ```
53
Variant presentation: cholestatic instead of hepatocellular jaundice Anti-HAV IgM+ Benign, no tx
Acute HepA
54
Fibrosing cholestatic hepatitis Histology mimics obstruction of the extrahepatic ducts Seen in recipients of solid organ transplantation High mortality
Hepatic B and C
55
Syndrome of progressive inflammatory liver injury associated with long-term heavy intake of ethanol Hepatocellular jaundice Abdominal pain, leukocytosis, fever Biopsy
Alcoholic hepatitis
56
Usually develops between 5 and 50 days after drug ingestion Resolves when the drug is withdrawn Exclusion of other causes
Drug-induced cholestasis
57
Extrahepatic sepsis
Pneumonia, intraabdominal sepsis
58
Usually severe infection, often with multi-organ failure (renal or respiratory) Elevated serum bilirubin (80% conjugated)
Cholestasis of sepsis
59
Causing mainly hepatocellular dysfunction lead to hyperbilirubinemia by disrupting bilirubin metabolism at the level of hepatocyte
Liver diseases (hepatocellular dysfxn)
60
Causes of hepatocellular dysfxn
``` Viral hepatitis Alcoholic liver diseas Drug-induced liver injury Shock liver/ischemic hepatitis AI hepatitis Metabolic disorders (hemochromatosis, Wilson's disease, NAFLD, alpha-1 antitrypsin deficiency) Cirrhosis ```
61
Jaundice is due to cholestasis or impairment of bile flow Bilirubin/ALP >> ALT/AST Nondilated ducts
Cholestatic jaundice
62
Jaundice is due to global hepatocellular dysfunction ALT/AST >>>>>/= Bilirubin/ALP Nondialted ducts
Hepatocellular jaundice
63
Prevention of viral hepatitis
Vaccine HepA and B | Post-exposure prophylaxis with Ig for Hep A B
64
Liver injury following inhalation, ingestion or parenteral administration of pharmacologic or chemical agents ALT/AST > 1000u/L
Toxin/drug induced liver injury
65
Direct toxin examples
Paracetamol | Isoniazid
66
Idiosyncratic toxin examples
Isoniazid | Phenytoin
67
May result from hypotension or severe hypoxia | ALT/AST > 1000u/L
Ischemic hepatitis
68
Abdominal pain, tender, hepatomegaly, jaundice, fever Alcohol drinker AST/ALT < 300 AST/ALT ratio >2 u/L
Alcoholic hepatitis
69
Prognosis of alcoholic hepatitis
Discriminant function = [PT time - control] + serum bilirubin
70
Tx of alcoholic hepatitis
DF > 32: steroids, pentoxyphilline
71
More common in women Two types can only be distinguished serologically Gamma globulins are elevated
AI hepatitis
72
Type 1 AI hepatitis
ANA, ASMA
73
Type 2 AI hepatitis
Anti-LKM1
74
End stage of any chronic liver disease | Regenerative nodules surrounded by fibrous tissue
Cirrhosis
75
2 types of cirrhosis
Compensated | Decompensated
76
Liver is cirrhotic but somehow can still function
Compensated
77
With jaundice or complications of cirrhosis | Less than 30% of the liver is fxning
Decompenstaed
78
Dx of cirrhosis
Histological
79
PE findings of cirrhosis
``` Stigmata of CLD Palpable left lobe of the liver Small liver span Splenomegaly Signs of decompensation (jaundice, ascites, asterixis) ```
80
Lab findings of cirrhosis
Low albumin < 3.8 Prolonged albumin INR > 1.3 High bilirubin > 1.5 Low platelet count < 175
81
To score cirrhosis
Child-turcotte-pugh score
82
CTP 5-6
30% decompensated
83
CTP 10-15
Very much decompensated