liver Flashcards

liver failure: define liver failure, identify main types and underlying pathophysiology, recall aetiology, explain the clinical features and complications of liver failure and recall possible treatments

1
Q

commonest causes of liver disease in developed world

A

alcohol, non-alcoholic fatty liver disease

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2
Q

commonest causes of liver disease in developing world

A

chronic viral hep B or C

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3
Q

symptoms of liver disease

A

asymptomatic, with general lethargy, anorexia, malaise, pruritus (itchy skin), right upper quadrant pain

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4
Q

symptoms of progressive liver failure

A

peripheral swelling, abdominal bloating, bruising, vomiting of blood, confusion and somnolence

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5
Q

common signs of liver disease

A

jaundice; reduced ability to metabolise oestrogens: spider naevi, loss of body hair, gynaecomastia, testicular atrophy, palmar erythema

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6
Q

other signs of liver disease

A

xanthelasma (yellowish deposit of cholesterol underneath skin - normally around eyelids), finger clubbing, pruritus, Dupuytren’s contracture, ascites and dilated abdominal veins, hepatomegaly, hepatosplenomegaly, caput medusa (severe portal hypertension), oedema, weight loss and loss of musculature, bruising, hepatic encephalopathy, fetor hepaticus (musty sweet breath), hepatic flap (coarse hand tremor)

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7
Q

what 3 categoreis are signs split into

A

compensated (liver function compensated), general and decompensated (loss of function)

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8
Q

what is the final common pathway for liver disease

A

cirrhosis (confirmed by biopsy)

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9
Q

what is cirrhosis characterised by

A

necrosis of liver cells, followed by progressive fibrosis and nodule formation

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10
Q

what does cirrhosis lead to

A

impairment of function and gross distortion of architecture, leading to portal hypertension and deterioration of liver function

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11
Q

what does cirrhosis develop in response to

A

chronic liver injury

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12
Q

2 types of cirrhosis

A

micronodular, macronodular

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13
Q

feature of micronodular cirrhosis

A

uniform, small nodules up to 3mm diameter

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14
Q

2 causes of micronodular cirrhosis

A

ongoing alcohol damage, biliary tract disease

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15
Q

feature of macronodular cirrhosis

A

nodules of variable size

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16
Q

cause of macronodular cirrhosis

A

chronic viral hepatitis

17
Q

definition of acute liver failure

A

severe hepatic dysfunction occuring within 6 months of onset of liver disease, with clinical manifestation of hepatic encephalopathy (brain) or coagulopathy (blood), caused by massive loss of hepatocytes

18
Q

3 classifications of acute liver failure

A

hyperacute: encephalopathy occurs within 7 days of jaundice onset; acute: encephalopathy occurs after 8-28 days of jaundice onset; subacute: encephalopathy occurs 5-12 weeks after jaundice onset

19
Q

divisions of primary features of hepatic failure after jaundice

A

CNS complications, coagulopathy, renal failure, sepsis, cardiovascular complications, metabolic complications

20
Q

sepsis and liver failure

A

90% with bacteria, 32% with fungi; infection within 3 days of admission; fever and leucoytosis absent; reduced in acute liver failure by prophylactic IV antibiotic therapy

21
Q

cardiovascular: what does acute hepatic failure cause a reduction in

A

peripheral resistance, requiring reflex increase in cardiac output to maintain pressure

22
Q

cardiovascular outcome of acute liver failure in pre-existing heart disease

A

cardiac failure, hypotension

23
Q

2 common metabolic signs in liver failure

A

hypoglycaemia, hypoxia

24
Q

what induces cerebral oedema in hepatic encephalopathy caused by liver failure

A

accumulation of toxins from gut - leads to coma

25
Q

what is hepatorenal syndrome

A

occurence of unexplained renal failure in patients with liver disease/patients undergoing surgery for biliary tract obstruction (kidneys are morphologically normal)

26
Q

what is renal failure due to in hepatorenal syndrome

A

reduced renal blood flow (more in cortex) due to cortical vasoconstriction, resulting from endotoxin (vasoactive) cleared in liver

27
Q

when does resolution only occur for hepatorenal syndrome

A

dramatic improvement in liver function (transplant), otherwise 95% fatality

28
Q

what coagulation factors does liver synthesise

A

I, II, V, VII, IX, X

29
Q

what coagulation factors are affected first in liver disease

A

vitamin K-dependent factors (II, VII, IX, X) - liver absorbs vitamin K; VII is earliest as has shortest half-life; fibrinogen (I) synthesis only affected in severe disease

30
Q

what does the liver inhibit in its role with coagulation

A

fibrinolysis/coagulation (synthesises plasma anticoagulant proteins C, S and antithrombin III)

31
Q

role of liver in clearing activated clotting factors

A

fibrin, tPA removed from circulation by reticuloendothelial system

32
Q

what does impairment in any coagulation-associated liver role lead to

A

bleeding, oozing at venepuncture sites from excessive fibrinolysis, bruising

33
Q

when does chronic liver failure occure

A

when there is a deterioration in liver function superimposed on chronic liver disease causing decompensation

34
Q

pathological processes causing potentially rapid acute deterioration

A

underlying disease process, different process undermining functional reserve of liver (e.g. infection, haemorrhage, electrolyte imbalance)