Liver disease and Cirrhosis Flashcards

1
Q

What are the general functions of the liver?

A

Storage,
Breakdown (drugs, toxins, ammonia)
Synthesis (bile, cholesterol, coagulation factors),
Immune function.

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2
Q

What are some causes of chronic liver disease/cirrhosis?

A

Alcohol
Viral hepatitis,
Inherited - Alpha-1 antitrypsin deficiency, Wilson’s disease, Haemochromatosis.
Autoimmune hepatitis,
Metabolic - NAFLD
Biliary - PSC, PBC,
Vascular,
Medication
Think pre-hepatic, hepatic and post hepatic

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3
Q

What is the result of long standing liver disease?

A

Cirrhosis (often synonymous with end stage liver disease) Presents with two clinical states:
Compensated liver disease - Asymptomatic.
Decompensated liver disease - Present with coagulopathy, jaundice, encephalopathy, ascites, GI bleeding

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4
Q

What is a scorring system to determine severity of cirrhosis?

A

Child-Pugh score. It looks at encephalopathy, ascites, bilirubin, albumin and INR

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5
Q

What is the clinical presentation of chronic liver disease>

A

Caput medusa,
Splenomegaly,
Palmar erythema,
Dupytren’s contracture,
Leuconychia (sign of hypoalbuminaemia),
Gyaencomastia ( reduced hepatic clearance of androgens leads to conversion to oestrogen).
Spider naevi (due to excess oestrogen, found in distribution of SVC)

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6
Q

What are the features of hepatic decompensation?

A

A - altered mental state (hepatic encephalopathy)
B - Bleeding (coagulopathy and GI bleeding)
C - colour change (jaundice),
D - distension (ascites)
Ascites,
Encephalopathy,
Jaundice,
GI bleeding,
Coagulopathy.

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7
Q

What are the investigations for liver disease/cirrhosis?

A

Non-invasive liver screen: LFTs, FBC, U&Es, virology, alpha1 antitrypsin, iron studies, AFP, serum copper and caeruloplasmin, auto-antibodies
Imaging: transient elastography to look at fibrosis, ultrasound, endoscopy

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8
Q

What antibodies are seen in autoimmune hepatitis?

A

Antismooth muscle antibodies and ANA

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9
Q

What can be seen on imaging in liver cirrhosis?

A

Nodular liver surface, small liver, ascites, splenomegaly, dilation of portal vein

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10
Q

What are the investigations for cirrhosis?

A

Transient elastrography (fibroscan), measures how stiff the liver is.
Endoscopy,
Liver ultrasound every 6 months to check for hepatocellular cancer.
And if unsure of underlying cause then do liver screen.

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11
Q

What are the different classifications of ascites?

A

By serum ascites albumin gradient. This looks at the albumin concentration in the ascitic fluid vs albumin conc in serum.
Either
< 11 = low SAAG (means peritoneum vessels are more permeable then normal as albumin can pass through).
or > 11= High SAAG (fluid pushed out of vessel, leaving high conc of albumin in blood)

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12
Q

What are the causes of a high SAAG ascites?

A
  1. Portal hypertension (pushes fluid our of vessels)
  2. Right heart failure or constrictive pericarditis,
  3. Cirrhosis,
  4. Liver mets,
  5. Budd-chiari syndrome
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13
Q

What are the causes of a low SAAG ascites?

A
  1. Hypoalbuminaemia (nephrotic syndrome or malnutrition)
  2. Peritoneal malignancy,
  3. Infections - TB,
  4. Pancreatitis,
  5. Bowel obstruction,
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14
Q

What is the treatment of ascites?

A
  1. Reduce dietary sodium,
  2. Aldosterone antagonists +/- loop diuretic
  3. Large volume paracentesis if tense ascites + albumin cover
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15
Q

How do you diagnose spontaneous bacterial peritonitis?

A

Clinical features - fever, diffuse abdominal pain, diarrhoea and cirrhosis.
Ultrasound to detect ascites
Do paracentesis - Neutrophil count > 250cells /ul or WCC > 0.5
Culture - often shows e.coli

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16
Q

What is the management and prophylaxis of SBP?

A

Treat - IV cefotaxime.
Prophylaxis - Patients with previous episode, patients with fluid protein < 15g/l andchild push score >9 or hepatorenal syndrome (continued until ascites has resolved). give cipro

17
Q

What are the haemochromatosis symptoms?

A

Early features = faitgue, erectile dysfuncction and arthralgia.
Bronze pigmentation (reversible),
Diabetes mellitus (irreversible),
Liver disease - hepatomegaly, cirrhosis (irreversible),
Cardiac failure (due to dilated cardiomyopathy - myopathy can be reversible)
Hypogonadism (irreversible),
Arthritis (irreversible),

18
Q

What are the investigations for haemochromatosis?

A

Transferrin saturation will be high (most useful) but also measure ferritin.
Test family members by testing for the HFE mutation

19
Q

What are some other investigations which should be done once haemochromatosis is confirmed?

A

LFTs,
Molecular genetic testing,
MRI - quantify liver/cardiac iron.
Liver biopsy if you suspect hepatic cirrhosis

20
Q

What is the management of haemochromatosis?

A

First line - venesection. Aim to keep transferrin saturation < 50% and ferritin conc <50 ug/l.
Second line - Desferrioxamine

21
Q

Describe features of hepatocellular carcinoma, investigations and treatment?

A

Most commonly occurs due to cirrhotic liver disease of Hep B.
Investigations - CT/MRI, CT PET, alpha fetoprotein and biopsy
Treatment - surgical rescection is mainstay

22
Q

Describe features of cholangiocarcinoma, investigations and treatment?

A

Can present with jaundice, often late stage at this point.
Investigations - obstructive LFTs, positive CA 19-9, CEA and Ca 123. CT/MRI and MRCP for imaging.
Treatment - Surgical resection

23
Q

How can you determine the difference between alcoholic or non alcoholic fatty liver disease

A

In alcoholic liver disease the AST is raised and so the AST/ALT ratio is above 1.5.
In NAFLD the AST is normal and the ALT can be raised so ratio is below 0.8

24
Q

What is a cause of renal failure in cirrhosis?

A

Hepatorenal syndrome - AKI diagnosis of exclusion.
Type1 - Rapidly progressive, Cr doubles to > 221 in less than 2 weeks. Poor prognosis.
Type 2 - slowly progressive

25
Q

What is the management of a liver abscess?

A

Drainage and antibiotics (amox, met and cipro)

26
Q

What is the management of hepatorenal syndrome?

A

Vasopressin analogues (terlipressin).
Large volume expansion with 20% albumin.
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