Acute and Chronic Liver Failure Flashcards

1
Q

Jaundice

A

Failure to clear bilirubin, accumulates in blood

Red cells broken down after 3 months, turned over, iron containing haem metabolised and excreted as bilirubin

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2
Q

Encephalopathy

A

Failure to clear gut-derived toxins (NH3)

Colon packed with bacteria, by products into bloodstream

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3
Q

Detoxification diseases

A

Jaundice

Encephalopathy

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4
Q

Protein synthesis diseases

A
  • Failure to produce clotting factors= coagulopathy on blood tests
  • Failure to produce clotting inhibitors= balance in practice?
  • Failure to produce albumin= oedema, impaired binding of drugs
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5
Q

Energy storage diseases

A

Hypoglycaemia

Muscle breakdown

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6
Q

Hypoglycaemia

A

Failure to store or release glucose

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7
Q

Muscle breakdown

A

Failure to utilise carbohydrate

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8
Q

Factors of acute vs chronic

A

 Time scale (<2-3 months vs >2-3 months)
 Different aetiologies
 Different clinical presentations

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9
Q

Describe Acute Liver Failure

A

Rapid onset; no underlying chronic liver disease
 Acute liver injury = high ALT COMMON (an enzyme produced by liver)
 Severe acute liver injury = high ALT
+ jaundice / coagulopathy UNCOMMON
 Acute liver failure = high ALT
+ jaundice / coagulopathy
+ encephalopathy RARE

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10
Q

Causes of ALF

A

-Common= paracetamol
-Less common
=Other drugs
=antibiotics esp. anti-TB meds
=antiepileptics
=herbal remedies
=ecstasy
=Acute viral infections
-hepatitis B (and A, E)
=Autoimmune hepatitis
=Seronegative (non-A to E)= causes extensive necrosis
hepatitis
-Rare
Vascular diseases
=Budd-Chiari
Metabolic diseases
=Wilson’s
=acute fatty liver of
pregnancy
Cancer
Ischaemia
=hypotension
Toxins
=Amanita phalloides
mushroom
=carbon tetrachloride

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11
Q

Treatments of Acute Liver Failure (Correction of coagulopathy)

A

-N-acetyl cysteine infusion
-Vitamin K
=substrate required for certain clotting factor synthesis
(II, VII, IX, X)
=if dietary deficiency, clotting will look worse than liver
function really is, so give
=replacement will not “mask” liver dysfunction
-FFP (fresh frozen plasma)
=blood product containing clotting factors
=replacement will prevent use of clotting times as a
marker of liver function, so try to avoid giving
-Liver transplant unit

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12
Q

Prognosis in paracetamol ALF

A
-Unlikely to recover spontaneously if:
= PT>100 AND
= Anuric / creatinine >300 AND
= Grade 3-4 encephalopathy (stupor/coma)
-Contraindications:
= Alcohol?
= Previous overdoses?
= Depressed?
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13
Q

Outcomes of seronegative hepatitis (extensive necrosis of liver)

A
  • Liver regenerates and recovers fully

- Liver fails to regenerate and needs transplant

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14
Q

Prognosis in non-paracetamol ALF

A

 Age (<10 or >40 worse)
 Aetiology (drug/seronegative worse than viral)
 PT >50 or INR >3.5
 Bilirubin >300
 Time from jaundice to encephalopathy <7d
 3 out of 5 = unlikely to recover spontaneously

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15
Q

Paracetamol vs non-paracetamol ALF

A

Paracetamol causes hyper acute liver failure
 Rapid progression of coagulopathy over hours, rather
than days
 Usually encephalopathy in less than 1 week

Other causes usually more gradual onset
 Progression over several weeks

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16
Q

General management of ALF

A

Identify and treat underlying cause
 NAC for paracetamol
 Antivirals for hepatitis B
 Steroids for autoimmune hepatitis

 Supportive care
 Close monitoring (especially paracetamol)
 Liver transplantation if appropriate

17
Q

What is Chronic Liver Failure?

A

Less well-defined terminology
 “chronic liver failure”
 “decompensated cirrhosis”

Impaired hepatocyte function
 Jaundice
 Coagulopathy
 Low albumin

18
Q

Hepatic Encephalopathy

A

 Failure of hepatocyte function (NH3 clearance)

 Portosystemic shunting

19
Q

What is Hepatic Encephalopathy triggered by?

A
  • Constipation
  • Drugs (opiates, sedatives)
  • Dehydration (diuretics)
  • Infections
  • GI bleeding
20
Q

Ascites

A

 Low albumin
 Portal hypertension
 Renal hypoperfusion

21
Q

Causes of CLF

A
Any cause of cirrhosis:
 Alcohol
 Non-alcoholic fatty liver disease
 Hepatitis B or C
 Haemochromatosis
 Wilson’s disease
 Primary biliary cholangitis
 Primary sclerosing cholangitis
 Autoimmune hepatitis
22
Q

Management of CLF

A

Identify and treat underlying cause
 Abstinence for alcohol (Diazepam)
 Antivirals for hepatitis B/C
 Steroids for autoimmune hepatitis

 No treatment for jaundice
 Low salt diet and diuretics for ascites
 Laxatives and antbiotics for encephalopathy
=Vitamin B supplements (Pabrinex/ thiamine)
=Oesophageal varices treated with beta-blocker to reduce pressure/ risk of bleeding, band ligation

 Liver transplantation if appropriate