Liver Flashcards

1
Q

What is the most common cause of chronic liver disease

A

Non Alcoholic fatty liver disease - hepatic steatosis

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2
Q

What are the risk factors for NAFLD

A
  • Dyslipidaemia
  • Insulin resistant DM
  • HTN
  • Obesity
  • TPN
  • Hepatotoxic meds
  • Rapid weight loss
  • Metabolic syndrome
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3
Q

What are the Sx of NAFLD

A
  • RUQ pain
  • Jaundice
  • Puritis
  • Truncal obesity
  • Fatigue
  • Organomegaly
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4
Q

What is the management of NAFLD

A
  • Diet and exercise
  • Insulin sensitizer
  • Vit E
  • Lipid lowering drugs
  • Liver transplant
  • gastric bypass
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5
Q

What are the 3 stages of alcoholic liver disease

A
  1. steatosis
  2. alcoholic hepatitis - inflamation and necrosis
  3. Alcoholic citthosis
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6
Q

What is the management for Alcoholic liver disease

A
  • STOP DRINKING
  • corticosteroids
  • Sodium restriction
  • Nutrition and multivit
  • lower weight and stop smoking
  • Liver transplant
  • Immunisations
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7
Q

What are the complications of Alcoholic liver disease

A
  • Hepatocellular Ca
  • Hepatic encephalopathy
  • Sepsis
  • Hepatorenal syndrome
  • coagulopathy
  • GI bleed
  • Portal HTN
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8
Q

What are the Sx of alcoholic liver disease

A
  • abdo pain
  • anorexia
  • fatigue
  • confusion
  • puritis
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9
Q

What are the signs of alcoholic liver disease

A
  • Ascites
  • Weight loss/gain
  • Muscle wasting/malnutrition
    Haematemesis/malaena
  • Jaundice
  • venous collaterals
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10
Q

What drugs can cause hepatocellular insult

A
  • Statins
  • Epilepsy meds
  • paracetamol
  • Amiodarone
  • TB meds
  • Nitrofurantoin
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11
Q

What is given in a paraccetamol overdose

A

Acetlycysteine

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12
Q

What are the causes of liver ischaemia

A
  • Hypoperfusion
  • Heat stroke
  • burns
  • clots
  • vasculitus
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13
Q

What types of hypoperfusion may lead to liver Ischaemia

A
  • HF
  • arrythmias
  • Sepsis
  • GI bleed
  • Dehydration
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14
Q

What are the signs and Sc of liver ischaemia

A
  • Decrease in appetite
  • Jaundice
  • general discomfort
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15
Q

What serum marker do you look for in Liver Ca

A

AFP

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16
Q

Where does hepatocellular ca arise from

A

Hepatocytes

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17
Q

What are the risk factors for hepatocellular CA

A
  • Hep B/C
  • chronic heavy alcohol
  • cirrhosis
  • FH
  • Obesity
  • DM
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18
Q

What are the signs and symptoms of Cirrhosis

A
  • Peripheral oedema
  • consitutional symptoms
  • Hepatic fator
  • mm wasting
  • Jaundice and puritis
  • distention - ascites/hepatomegaly
  • malaena
  • Hand and nail signs
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19
Q

What does ascites indicate in liver disease

A

Portal HTN

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20
Q

What are the RF of cirrhosis

A
  • IVDU
  • Unprotected sex
  • Obesity
  • Blood transfusion
  • tattoos
  • Alcohol
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21
Q

What is the management of Cirrhosis of the liver

A
  • treat underlying cause
  • liver transplant
  • sodium restriction
  • monitor for complications
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22
Q

What are the complications of liver cirrhosis

A
  • Portopulmonary HTN
  • Gastro-oesophageal varcies
  • Hepatic hydrothorax
  • Hepatocellular Ca
  • Hepatopulmonary syndrome
  • Ascites
  • hepatorenal syndrome
  • Spontaneous bacterial peritonitis
  • portosystemic encephalopathy
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23
Q

What are the precipitating factors for portosystemic encephalopathy?

A
  • Constipation
  • GI bleed
  • Hypocalcaemia
  • drugs
  • electrolyte imbalances
  • excess protein intake
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24
Q

what % of people with cirrhosis will develop portosystemic encephalopathy per year

A

2-3%

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25
Q

What signs/symptoms may indicate portosystemic encephalopathy

A
  • increased drowsiness
  • changes in personality - aggression
  • disorientation/confusion
  • asterixis
  • slurred speech
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26
Q

What investigation should be done if suspecting portosystemic encephalopathy

A
  • serum ammonia - usually raised
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27
Q

What is the management of portosystemic encephalopathy

A
  • treat underlying cause

- May require rifaxmin - Abx

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28
Q

What is portosystemic encephalopathy

A

neuropsychiatric syndrome associated with hepatocellular failure or portosystemic venous shunting

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29
Q

What is spontaneous bacterial peritonitis

A

infection of ascitic fluid that cannot be attributed to any intra-abdominal, ongoing inflammatory, or surgically correctable condition

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30
Q

What are the symptoms of SBP

A
  • abdominal pain & tenderness
  • fever
  • malaise
  • D&V
  • altered mental state
  • GI bleed
  • hyperthermia
  • tachycardia
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31
Q

RF for SBP

A
  • cirrhosis
  • low ascitic protein complement
  • GI bleeding
  • sclerosis/oesophageal varices
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32
Q

Investigations for SBP

A
  • FBC
  • CRP
  • ascitic tap
  • blood cultures
  • LFTs
  • INR and Coags
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33
Q

What may you see in an ascitic tap in SBP

A
  • polymorphonuclear count >250
  • hazy/cloudy/blood stained
  • pH <7.35
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34
Q

What is the management of SBP

A
  • IV cefotaxime/quinolone
  • Lifelong secondary prophylactic Abx
  • IV albumin if renal dysfunction
  • large volume paracentesis if large amounts of fluid
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35
Q

What is hepatopulmonary syndome

A

Complication from portal HTN whereby the vessels in the lungs vasolidate causing hypoxaemia

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36
Q

How to you manage hepatopulmonaary syndrome

A

liver transplant - 5-10% of patients awaiting liver transplant have this

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37
Q

What is hepatorenal syndrome

A

progressive kidney failure seen in people with severe liver damage, most often caused by cirrhosis

38
Q

What is type 1 hepatorenal syndrome

A
  • rapidly progressive

- createnine doubles within 2 wks

39
Q

What is the management of type 1 hepatorenal syndrome

A
  • Albumin infusion
  • Abx
  • octreotide
  • list for transplant
40
Q

What is type 2 hepatorenal syndrome

A
  • slowly progressive renal failure

- refractory ascites

41
Q

What medication MUST be avoided in hepatorenal syndrome

42
Q

What hand and nail signs can be seen in liver problems

A
  • leuconychia
  • Palmar erythema
  • duputryns contracture
  • Clubbing
  • hepatic failure
43
Q

What facial signs can be seen in liver problems

A
  • Jaundiced sclera
  • Xanthalasma
  • telangectasia
  • Spider angiomata
  • bruising
  • Parotid gland swellign
44
Q

What signs can be seen on viewing the abdomen in liver problems

A
  • distention
  • bruising
  • caput medussa
  • testicular atrophy
  • loss of secondary sexual hair
45
Q

What signs can be felt/heard on abdominal examination in liver problems

A
  • shifting dullness
  • organomegaly
  • hepatic bruit
46
Q

What are common causes of chronic liver problems

A
  • chronic infection
  • NAFLD
  • Alcoholic fatty liver disease
  • CIrrhosis
  • Primary billiary cirrhosis
47
Q

What are some uncommon causes of chronic liver problems

A
  • alpha 1 antitrypsin defiency
  • Wilson’s disease
  • Haemochromatosis
48
Q

What causes acute hepatocellular injury

A
  • Poisoning
  • Infection
  • Liver ischaemia
49
Q

What are the functions of the liver

A
  • Synthesis of albumin
  • Synthesis of coagulation factors
  • Gluconeogenesis
  • conjugate and eliminate billirubin
50
Q

What LFTs may indicate a hepatocellular injury

A

raised ALT and AST

51
Q

In acute hepatocellular injury what may the LFTs show

52
Q

In chronic hepatocellular injury what may the LFTs show

53
Q

what colour is unconjugated billirubin in the urine

A

Unconjugated is water soluble so doesn’t change the colour of the urine

54
Q

What colour is conjugated billirubin in the urine

A

conjugated billirubin passes to the urine as urobilogen causing dark urine

55
Q

What impact does pre hepatic jaundice have on urine and stool

A

Normal urine and stool

56
Q

What impact does hepatic jaundice have on urine and stool

A

Dark urine

Normal stool

57
Q

What impact does post hepatic jaundice on urine and stools

A

Dark urine

Pale stools

58
Q

What causes prehepatic jaundice - unconjugated hyperbillirubinaemia

A
  • Gilberts
  • Haemolysis: haemolytic anaemia
  • Impaired hepatic uptake: Drugs
59
Q

What causes post-hepatic jaundice

A
  • obstruction: cholestasis, head of panc ca
60
Q

What is hepatitis A

A
  • Most common viral infection worldwide (rare UK)
  • RNA virus
  • Faecal-oral route: contaminated food or water
61
Q

What is the presentation of hepatitis A

A
  • Nausea and vomiting
  • Anorexia
  • Jaundice
  • Cholestasis
  • dark urine, pale stools
  • hepatomegaly
62
Q

What is the treatment of hepatitis A

A
  • Resolves on own in 1-3 months
  • analgesia
  • vaccination
  • notifiable disease
63
Q

What is hepatitis B

A
  • DNA virus

- Transmitted via direct contact with bodily fluids, toothbrush, pregnancy

64
Q

Why do people become chronic hepatitis B carriers

A
  • the virus DNA has integrated into their own DNA and so they will continue to produce the viral proteins. (10%)
  • most people recover in 1-2 months
65
Q

What does a Surface antigen (HBsAg) mean

A

active infection

66
Q

what does E antigen (HBeAg) mean

A

marker of viral replication and implies high infectivity

67
Q

What do Core antibodies (HBcAb) suggest?

A

implies past or current infection

68
Q

what do Surface antibody (HBsAb) suggest

A

implies vaccination or past or current infection

69
Q

What isHepatitis B virus DNA (HBV DNA)

A

Direct count of viral load

70
Q

What investigations should you do for suspected viral hepatitis

A
  • test HBcAb (for previous infection) and HBsAg (for active infection)
  • If these are positive then do further testing for HBeAg and viral load.
71
Q

How can you distinguish between acute, chronic or past infection?

A
  • IgM and IgG versions of the HBcAb.
  • IgM: active infection, high titre = acute infection and a low titre = chronic infection
  • IgG indicates a past infection where the HBsAg is negative.
72
Q

Wha tis the Hep B vaccination

A
  • injects the hepatitis B surface antigen
  • tested for HBsAb to confirm their response
  • 3 doses at different intervals
  • Included as part of the UK routine vaccination schedule (as part of the 6 in 1 vaccine).
73
Q

What is the management of hepatitis B or C

A
  • low threshold for screening those at risk of hepatitis B.
  • Screen for other blood born viruses & STIs
  • Refer to gastroenterology, hepatology or infectious diseases for specialist management
  • Notify Public Health (it is a notifiable disease)
  • Stop smoking and alcohol
  • Education about reducing transmission and informing potential at risk contacts
  • Testing for complications
  • Antiviral medication
  • Liver transplantation for end-stage liver disease
74
Q

What is the invstigations for complications of hepatitis B

A

FibroScan for cirrhosis and ultrasound for hepatocellular carcinoma

75
Q

What is the role of antiviral medication in hepatitis B

A

slow the progression of the disease and reduce infectivity

76
Q

What is hepatitis C

A
  • RNA virus
  • spread by blood and body fluids
  • No vaccine is available
77
Q

What is the disease course of hepatitis C

A

1 in 4 fights off the virus and makes a full recovery

3 in 4 it becomes chronic

78
Q

What are the complications of hepatitis C

A
  • liver cirrhosis

- hepatocelluar carcinoma

79
Q

What investigations are done for ? hepatitis C

A
  • Hepatitis C antibody is the screening test
  • Hepatitis C RNA testing: confirm the diagnosis of hepatitis C, calculate viral load and assess for the individual genotype
80
Q

What is hepatitis D

A
  • RNA virus
  • Requires hepatitis B co-infection
  • low rates in the UK
  • Increases the complications and disease severity of hepatitis B.
  • No treatment
  • Notifiable disease
81
Q

What is hepatitis E

A
  • RNA virus
  • faecal oral rout
  • Very rare in the UK.
  • mild illness, the virus is cleared within a month and no treatment is required.
  • Rarely it can progress to chronic hepatitis and liver failure, if immunocompromised
  • no vaccination.
  • Notifiable disease
82
Q

What is auto-immune hepatitis

A
  • Rare cause of chronic hepatitis, not sure of cause
  • genetic predisposition
  • triggered by environmental factors such as a viral infection that causes a T cell-mediated response against the liver cells
  • T cells of the immune system recognise the liver cells as being harmful and alert the rest of the immune system to attack these cells.
83
Q

What is type 1 autoimmune hepatitis

A
  • women in late 40s-50.
  • It presents around or after the menopause with fatigue and features of liver disease on examination
  • less acute course than type 2.
84
Q

What is type 1 autoimmune hepatitis

A

patients in their teenage or early twenties present with acute hepatitis with high transaminases and jaundice.

85
Q

What auto-antibodies are associated with type 1

A

Anti-nuclear antibodies (ANA)
Anti-smooth muscle antibodies (anti-actin)
Anti-soluble liver antigen (anti-SLA/LP)

86
Q

What auto-antibodies are associated with type 2

A

Anti-liver kidney microsomes-1 (anti-LKM1)

Anti-liver cytosol antigen type 1 (anti-LC1)

87
Q

How do you confirm diagnosis of autoimmune hepatitis

A

liver biopsy

88
Q

What is the treatment of autoimmune hepatitis

A
  • high dose steroids (prednisolone)
  • immunosuppression: azothiaprine (usually life long)
  • Liver transplants ( can still recur)
89
Q

What factors make you unsuitable for a liver transplant

A

Significant co-morbidities (e.g. severe kidney or heart disease)
Excessive weight loss and malnutrition
Active hep B or C or other infection
End stage HIV
Active alcohol use (generally 6 months of abstinence is required)

90
Q

How do you monitor for evidence of liver rejection

A

Abnormal LFTs
Fatigue
Fever
Jaundice

91
Q

What advice is given to patients post organ donation

A

Avoid alcohol and smoking
Treating opportunistic infections
Monitoring for disease recurrence (i.e. of hepatitis or primary biliary cirrhosis)
Monitoring for cancer as there is a significantly higher risk in immunosuppressed patients

92
Q

Common Causes of hepatomegaly

A
Cirrhosis (in early stages)
Malignancy
Right heart failure
Viral hepatitis
Haematological malignancies
Glandular fever
Malaria