LF & Cirrhosis Flashcards

1
Q

Symptoms of Portal HTN

A
  • spider naevi (subclavian distribution)
  • caput medusae
  • splenomegaly
  • ascites
  • haemorrhoids
  • haematemesis
  • melena
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2
Q

Wilson’s disease presentations

A

Liver - jaundice, Kayser-Fleischer rings, ascites/oedema, hepatomegaly
Neuro - tremor, dysphagia, dysarthria, spasticity, muscle rigidity
Cardiac - arrhythmias, cardiomyopathy
Bone - osteoporosis, osteophytes
Renal - renal calculi

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3
Q

What is the first sign of Acute liver disease?

A

Tender, smooth hepatomegaly

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4
Q

How to test ascites?

A

Ascitic tap - exudative/transudative
(<7, cancer etc)

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5
Q

Budd Chiari syndrome

A

Thrombosis of hepatic veins

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6
Q

What are the clinical features of compensated cirrhosis?

A
  • fatigue, anergia
  • anorexia, cachexia
  • nausea, abdo pain
  • spider naevi, gynaecomastia
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7
Q

What are the clinical features of decompensated cirrhosis?

A
  • ascites, oedema
  • jaundice
  • pruritus
  • palmar erythema
  • gynaecomastia, testicular atrophy
  • easy bruising
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8
Q

What are the most common causes of liver cirrhosis?

A
  • alcohol
  • hep B & C
  • NAFLD
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9
Q

What autoimmune conditions can cause cirrhosis?

A
  • AIH
  • PBC, PSC
  • sarcoid
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10
Q

What are the genetic causes of liver cirrhosis?

A
  • haemochromatosis
  • Wilson’s
  • a-1-antitrypsin deficiency (A1AD)
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11
Q

Which drugs can cause cirrhosis?

A
  • methotrexate
  • amiodarone
  • isoniazid
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12
Q

Which blood tests should be ordered for suspected cirrhosis?

A

FBC - leucocytosis, thrombocytopenia, anaemia
UE - baseline renal function, hepatorenal syndrome
LFTs
INR - coagulopathy
Causes:
- viral serology
- Fe studies, A1AD
- Caeruloplasmin
- autoantibodies

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13
Q

What imaging & invasive investigations can support z diagnosis of cirrhosis?

A
  • peritoneal tap (microscopy, culture for SBP)
  • Doppler USS (Budd-Chiari)
  • transient elastography/acoustic radiation force impulse imaging (ARFII) (NAFLD)
  • liver biopsy
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14
Q

What is the Child-Pugh score?

A

Calculate severity of liver cirrhosis (predictor of mortality, liver transplant)
- Br
- Alb
- PTT
- encephalopathy
- ascites

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15
Q

What are the common complications of cirrhosis?

A
  • ascites
  • SBP
  • LF
  • HCC
  • oesophageal varices (haemorrhage)
  • RF
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16
Q

How does liver cirrhosis cause ascites?

A
  • portal HTN
  • hypoalbuminaemia
17
Q

When should SBP be suspected?

A
  • ascites
  • oft no abd tenderness/guarding
  • sudden deterioration, no obvious cause
  • low ascitic albumin risk
18
Q

What result of an ascitic tap is indicative of SBP?

A

> 250mm³

19
Q

What are the features of liver failure?

A
  • hepatic encephalopathy (cerebral oedema > ICP > death)
  • coagulopathy (bleeds)
20
Q

How can oesophageal varices be a fatal complication of liver cirrhosis?

A
  • portal HTN > dilation of veins
  • varices rupture (acute blood loss may be fatal in coagulopathy)
21
Q

What is hepatorenal syndrome ?

A
  • cirrhosis
  • ascites
  • renal failure (renal vasoconstriction, susceptible to AKI)
22
Q

How is decompensated cirrhosis managed?

A
  • alcohol abstinence, good nutrition
  • avoid NSAIDs, sedatives, opiates
  • 6m: USS, serum a-fetoprotein (monitor HCC)
  • cholestyramine (pruritus)
  • manage ascites
  • prophylactic lactulose, rifaximin (encephalopathy)
  • prophylactic abx (SBP risk)
  • liver transplant
23
Q

How is ascites acutely managed?

A
  • fluid restriction <1.5L,
  • low salt diet
  • spironolactone (+/- furosemide)
  • therapeutic paracentesis
  • albumin infusions
24
Q

What scores are used for severity of chronic liver disease?

A

MELD
UKELD

25
Q

What is the criteria used to judge severity of acute liver failure?

A

King’s college criteria