Liver Disease and Cirrhosis Flashcards

1
Q

name a pattern on LFTs that could be used to differentiate between NAFLD and AFLD

A

AST in alcoholics is normally elevated 1.5 x ALT levels which normally remain normal
In NAFLD the AST is not normally elevated

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2
Q

name the characteristic features of alcoholic hepatitis

A

Hepatomegaly, fever, leucocytosis, hepatic bruit

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3
Q

name some clinical features of alcoholic liver disease

A
  • Malaise
  • Nausea
  • Hepatomegaly
  • Fever
  • Jaundice
  • Sepsis
  • Encephalopathy
  • Ascites
  • Renal Failure
  • Death
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4
Q

name some signs of chronic liver disease

A
•	Stigmata: spider naevi, 
•	Fœtor, 
•	Encephalopathy.
•	‘Synthetic dysfunction’:
o	Prolonged prothrombin time
o	Hypoalbuminaemia
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5
Q

name some signs of portal hypertension

A
  • Caput medusa
  • Hypersplenism:
  • Thrombocytopenia
  • (pancytopenia)
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6
Q

name three reasons that cirrhosis leads to fluid overload

A

back pressure created by the cirrhosis
Loss of albumin leads to a decline in the oncotic pressure of the blood
hyperaldosteronism results due to the reduced effective circulating volume, resulting in the body retaining even more fluid and sodium.

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7
Q

name some causes of acute liver failure

A
  • Infections e.g. viral hepatitis
  • Toxins e.g. ETOH, paracetamol
  • Vascular e.g. Budd-chiari
  • Others e.g. NAFLD, Wilson’s disease, Haemochromatosis, malignancy
  • Obstetrics – eclampsia acute fatty liver of pregnancy
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8
Q

Define acute liver failure

A

Defined by rapid decline in hepatic function – recognised by development of coagulopathy, new onset jaundice, and hepatic encephalopathy

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9
Q

how would you treat acute liver failure

A

• IV albumin and terlipressin
• Haemodialysis if renal failure develops
• Liver transplant
o Decide if candidate for a transplant

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10
Q

name some complications of acute liver failure

A
•	Bleeding 
o	Vitamin K, platelets, FFP, blood as needed 
•	Ascites 
o	Fluid restrict and use of diuretics 
•	Sepsis 
•	Hypoglycaemia 
o	Regular BMs, glucose solution if their glucose drops below 2
•	Encephalopathy 
o	Lactulose +/- enemas 
o	Lactulose if catabolised by gut bacteria to short chain fatty acids, decreasing colonic pH and reducing the ammonia in the colon by trapping it 
•	Seizures 
o	Lorazepam 
•	Cerebral oedema – major risk 
o	Mannitol
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11
Q

how do you treat acute liver failure and where should the patient be treated?

A
•	IV albumin  and terlipressin 
•	Haemodialysis if renal failure develops 
•	Liver transplant 
o	Decide if candidate for a transplant 
ITU
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12
Q

define hepatorenal syndrome

A

Cirrhosis + ascites + renal failure = Hepatorenal syndrome when all other causes of renal impairment have been excluded. The cirrhosis causes abnormal haemodynamics which leads to splanchnic arterial vasodilatation, increasing the effective circulatory volume. This activates RAS causing renal vasoconstriction. IF this leads to persistent underfilling of the renal vasculature it eventually leads to renal failure

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13
Q

define cirrhosis

A

Cirrhosis is a diffuse pathological process, characterised by fibrosis and loss of normal liver architecture with formation of nodules

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14
Q

name some signs you may see in the face of a person with cirrhosis

A

o Pallor: ACD
o Xanthelasma: PBC
o Parotid enlargement (esp. ̄c EtOH)

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15
Q

Name some abdominal signs of cirrhosis

A

o Striae
o Hepatomegaly (may be small in late disease)
o Splenomegaly
o Dilated superficial veins (Caput medusa)
o Testicular atrophy

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16
Q

name some hand signs of cirrhosis

A
o	Clubbing (± periostitis) 
o	Leuconychia (↓ albumin) 
o	Terry’s nails (white proximally, red distally) 
o	Palmer erythema 
o	Dupuytron’s contracture
17
Q

name some precipitating factors for hepatic encephalopathy

A
  1. Gastrointestinal bleeding
  2. Infections
  3. Constipation
  4. Electrolyte imbalance
18
Q

name four complications of portal hypertension

A

a. Splenomegaly
b. Ascites
c. Varices
d. Encephalopathy

19
Q

name some features of decompensated liver disease

A

a. Jaundice (conjugated)
b. Encephalopathy
c. Hypoglycaemia
d. Hypoalbuminemia

20
Q

if a patient has a conjugated jaundice what colour is their urine and stool likely to be

A

dark urine

pale stool.

21
Q

what could cause a conjugated jaundice

A

hepatocellular dysfunction - hepatocyte damage, likely with some level of cholestasis. Causes - viruses, drugs, live mets, cirrhosis
cholestasis - PBC, PSC, CBD gallstons, pancreatic cancer, compression

22
Q

what would cause an unconjugated jaundice

A

Unconjuagted - not water-soluble.

Causes: haemolysis, drugs (paracetamol), Gilbert’s