Jaundice and Chronic Liver Disease Flashcards

1
Q

what is the synthetic function of the liver?

what does it produce?

A

bile salts, bile acids, bilirubin
carbohydrates
clotting factors
protein - albumin
lipids - cholesterol, lipoprotein and triglycerides
hormones - angiotensin and insulin like growth factor

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2
Q

what vitamins does the liver store?

A

vitamin A, D, B12 and K

copper and iron

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3
Q

what is billirubin elevated as a result of?

A

pre hepatic haemolysis
hepatic parenchymal damage
post hepatic obstruction

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4
Q

where is alkaline phosphate found?

A

present in the bile ducts

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5
Q

Alkaline phosphate can be elevated as a result of?

A

obstruction of biliary system or liver infiltration

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6
Q

when is Gamma GT elevated?

A

when their is history of alcohol consumption

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7
Q

other than alcohol, what can gamma GT also be raised due to?

A

drugs such as NSAIDS

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8
Q

does low or high levels of albumin indicate liver disease?

A

low levels

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9
Q

why is prothrombin time included in liver function tests?

A

all clotting factors are produced from the liver

it is also a good measurement of the extent of liver dysfunction

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10
Q

what tests is a critical assessment for need for transplant?

A

creatine

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11
Q

what information does a platelet count give you in regards to liver disease and why is it carried out?

A

the liver produces thrombopoetin which is a regulates production of platelets.
in cirrhosis the liver produces less thrombopoetin = low platelets.
cirrhosis = splenomagely ad the spleen holds on to as many platelets as it can therefore there are less circulating platelets
–> thrombocytopenia is an indicator of CLD

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12
Q

what are the signs of decompensated liver disease?

A
jaundice
ascites
hepatic encephalopathy
variceal bleeding 
infection
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13
Q

jaundice is detectable when bilirubin reaches what levels?

A

> 34umol/l

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14
Q

what is a differential diagnosis of jaundice and what can differentiate the two?

A

carotenemia

in carotenemia you don’t get yellowing of the sclera

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15
Q

what are the signs which suggest that the jaundice is pre hepatic?

A

anaemia
aucholoric jaundice - pale coloured urine
pallor
splenomegaly

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16
Q

what are the signs that suggests that the jaundice is hepatic?

A

ascites, vatical bleeding and encephalopathy

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17
Q

what signs suggest that the jaundice is post hepatic?

A

abdominal pain
cholestasis (pale stool, dark urine, pruritus)
palpable gallbladder

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18
Q

what are the main investigations for chronic liver diseases?

A

ultrasound / endoscopic USS
ERCP/MRCP
percutaneous transhepatic cholangiogram (PTC)

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19
Q

what are the complications of ERCP?

A

respiratory and CV risks with sedation
pancreatitis
cholangitis, sphincterotomy

20
Q

what is defined as chronic liver disease?

A

liver disease persistent for > 6 months

21
Q

ascites can be detected and confirmed on ultrasound when there is a minimum of what volume of fluid?

A

100cc/100ml

22
Q

what is defined as low and high albumin/protein ascites?

A

high >1.1g/dl

low <1.1g/dl

23
Q

what is the difference in the causes of ascites depending on the albumin content?

A

albumin >1.1g/dl caused by portal hypertension

albumin <1.1g/dl cause is not portal hypertension related

24
Q

what are the treatments for ascites?

A
diuretics 
large volume paracentesis (drainage)
TIPS - transjugular intrahepatic portosystemic shunt
aquaretic 
liver transplant
25
Q

where are the different portosystemic anastomoses ?

A
skin (caputmedusae)
oesophageal
rectal
posterior abdominal wall
stomal
26
Q

what are the treatments for vatical haemorrhage?

A

endoscopic band ligation + terlipressin for bleeding control
sengstaken blakemore tube for controlled bleeding
TIPS to prevent re-bleeding after banding

27
Q

hepatocellular carcinoma is associated with what type(s) of hepatitis?

A

hep B and C

28
Q

what is the presentation of hepatocellular carcinoma?

A
decompensated liver disease i.e. ascites, variceal haemorrhage, encephalopathy
abdominal mall
abdominal pain
weight loss 
bleeding from tumour
29
Q

what investigations are used in the diagnosis of hepatocellular carcinoma?

A
tumour marker - AFP
USS
CT
MRI 
Liver biopsy
30
Q

what is the treatment for hepatocellular carcinoma?

A

hepatic resection
liver transplant

palliative:
chemotherapy
locally ablative treatments - alcohol injection or radio frequency ablation

sorafenib (tyrosine kinase inhibitor) or tamoxifen (hormone therapy) - last resorts

31
Q

what can precipitate encephalopathy?

A
GI bleed
infection
dehydration 
constipation
medication i.e. sedatives
32
Q

how do you treat encephalopathy?

A

treat the underlying cause i.e.
if infection = antibiotics
if constipation = laxatives (lactulose), enema, aquatics
if dehydration = iv fluids

33
Q

what is acholuric jaundice?

A

jaundice with pale urine

causes pale urine due to conjugated bilirubin - it is insoluble so isn’t secreted in the urine

34
Q

what are the causes of ascites with an albumin content of 1 g/dl?

A
non portal hypertensive related;
pancreatitis 
malignancy 
biliary ascites
tuberculosis 
nephrotic syndrome
chylous ascites 
seositis
35
Q

what are the causes of ascites with an albumin content of 2.1 g/dl?

A
portal hypertensive related i.e.
congestive heart failure
constrictive pericarditis 
masive liver metastasis
budd chiarri
myxedema
36
Q

what are the advantages of carrying out an endoscopic ultrasound scan for suspected LD?

A

staging of tumours
fine needle aspiration (FNA) of cysts or tumours
excluding biliary microcalculi

37
Q

why might a percutaneous transhepatic cholangiogram (PTC) be carried out?

A

ERCP not possible due to previous surgery or duodenal obstruction

38
Q

what is the disadvantage of percutaneous transhepatic cholangiogram?

A

more invasive than ERCP

it is used instead of ERCP

39
Q

what is the most useful investigation for LD and why?

A

abdominal USS

  • differentiates intrahepatic from extra hepatic obstruction
  • identifies site and cause of obstruction
  • documents evidence of portal hypertension
  • early staging of extent of disease e.g. cancer spread
40
Q

how does hepatic encephalopathy occur due to CLD?

A

bacteria in our gut break down proteins and release ammonia.
this ammonia is broken down in urea by the liver
ammonia is toxic to our brains therefore if the liver cannot break it down = encephalopathy

41
Q

what are other features might you find which confirms ascites caused by liver failure? (apart from fluid thrill and shifting dullness)

A
spider naevi 
gynaecomastia 
palmar erythema
umbilical nodule
elevated JVP
flank haematoma
abdominal veins (caput medusae)
fetor hepaticus
42
Q

what are the causes of liver cirrhosis?

A
alcohol 
autoimmune (PSC, PBC)
drugs i.e. TMX (antimetabolites), amiodarone 
NAFLD
cystic fibrosis
vascular problems i.e portal hypertension
chronic viral hepatitis B &amp; C
haemochromatosis, wilsons disease 
cryptogenic 
others: sarcoidosis, amyloidosis
43
Q

What drugs can cause liver cirrhosis?

A

MTX (anti metabolites)

amiadorone

44
Q

what is the clinical presentation of hepatic cirrhosis?

A

compensated liver disease (abnormal LFT’s)

decompensated liver disease (ascites, vatical haemorrhage, encephalopathy)

45
Q

what does cirrhosis put you at risk of?

A

hepatocellular carcinoma