Liver tings Flashcards

1
Q

functions of the liver

A

Protein synthesis and metabolism- albumin, carrier proteins and coag factors, hepcidin and ferratins
Lipid and glucose metabolism
hormone and drug inactivation- converts to hydrophillic
conjugation of bilirubin to be excreted
bile synthesis
Immune function- consumes antigens
activation of Vit D

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Breakdown of RBCs

A

Haemoglobin in macrophage in spleen liver or bonemarrow- splits into globin (get reused) and haem.
haem broken into Fe and porphyrin which becomes biliverden then bilirubin that binds to albumin and leaves. Bilirubin goes ot the liver gets conjugated and secreted into bile where it becomes urobiliogen or sterobillin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

causes of acute liver disease

A
commonest: Drug induced liver disease usually paracetamol 
Hepatitis, AB????
Malignant cause
congestion due to heart
vascular ischaemic
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

symptoms of acute liver disease

A

Constitutional symptoms like malaise fever anorexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

signs of acute liver disease

A

usually non but can show jaundice or hepatomegally

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

symptoms of chronic liver disease

A
Prutius, earliest symptom
Fever Anorexia, Malaise 
lack of appetite
weakness 
Right hypochindriac pain- due to liver distension
abdominal distension
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

signs of chronic liver disease

A
Jaundice 
hepatomegally 
spleenomegally- indicates portal hypertension
ascites-due to cirrhosis or metastatic 
peripheral oedema 
dupytrens contracture- late
easy bruising and purpura
palmar erthyma 
clubbing 
leuconychia 
terrys nails 
parotid enlargement 
loss of body hair 
xanthosis, xantholilsma
spider naevi
enlarge breast- gyanecomastia
testicular atrophy 
amenhorrea 
confusion- encephalitis
grey skin if haemochromatosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

causes of chronic liver disease

A

Cirrhosis causes by alcoholism is commonest
Hep B C D
non alcoholic fatty liver disease
Metabolic causes, haemochromatosis, wilsons, alpha 1 antitrypsin deficiency
biliary tract diseases and stones
autoimmune-pcb, autoimmune hepatitis
drugs: methotrexate or amiodarone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

causes of jaundice

A

Haemolytic- increased turnover= increased unconjugated bilirubin. liver functional so there is no bilirubin in urine just very dark urine due to increased uobiliogen

congenital hyperalbuminuria- Gilbert disease

cholestatic- hepatic or extrahepatic- PCB, carcinoma cholangitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

natural progression of alcoholic liver disease

A

Alcoholic fatty liver- asymptomatic
alcoholic hepatitis- mild symptomatic or asymptomatic
Alcoholic cirrhosis- signs and symptoms of liver diease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
Alcoholic Fatty liver disease
symptoms signs
pathophysiology and damage 
investigation and results in serum 
Treatment
A

asymptomatic or nausea, vomiting diarrhoea- effect of excess alcohol
no liver damage and everything reversed on stopping alcohol. excess alcohol makes liver cells take up fat.
elevated MCV, anemia, serum Transaminase and Gamma glutymyl transpeptide
view by CT
Stop drinking and will return to normal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
alcohol hepatitis
symptoms signs
pathophysiology and damage 
investigation
Treatment
A

hepatic necrosis and presence of mallory bodies and giant mitochondria
mild signs and symptoms of chronic liver disease. the more severe the closer it is to cirrhosis
can be confirmed by biopsy
has increased serum bilirubin, Gamma Glytumal, ALT AST prothrombin time and decreased albumin
vitamin supplements and steroids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q
Alcohol cirrhosis
symptoms signs
pathophysiology and damage 
investigation
Treatment
A

Signs symptoms and makers of liver disease
seen on ultrasound and biopsy
stop alcohol and same treatment for cirrhosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

general management for alcoholic liver disease

A

stop drinking offer cessation
monitor for withdrawal delirium tremeus- treat with diaepan
offer vit B and other supplementary ADEK
bed rest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Haemochromatosis causes

A

Iron overload due to increased turnover like sickle cell or spherocytosis
or due to increased transfusions due to thalassemia
commonest cause is hereditary haemochromatosis- autosomal recessive- 1 in 10 carrier 1 in 400 affected

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Haemochromatosis Presnetation

A

present with Triad usually in 5th decade
bronze skin- becomes slated grey ove time
DM
hepatomegally

also: arrhythmia, hypogonadism, artrropathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

why does haemochromatosis present like this

A

iron deposition in liver, skin heart pancreas pituitary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Haemochromatosis investigation

A
Serum iron= elevated
serum ferratin= elevated
LFT- elevated
biposy- diagnostic and can stage level of damage
genetic test for HFE gene 

DEXA Glucose tolerence and Echo- Dilated C

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

haemochromatosis management conservative

A

screen family members
avoid excess iron and vit C D and alcohol
Vaccinate hep A and B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

haemochromatosis management disease modifying

A

venesection on a weekly bases for up to 2 years. montior serum iron ferratin and MCV
this will treat all symptoms except DM and testicular atrophy and arthropaty

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

haemochromatosis management disease modifying drug

A

Desferrioxamine- med for iron overdose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what is wilsons disease

A

Increased copper deposition in liver cornea and basal ganglia
autosomal Reseccive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

wilsons disease Presentation

A

children- hepatic problems

adults- neurological roblems- ataxia, dysarthia, tremou, dementia, dysdiadochokinesia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Investegation for Wilsons disease

A
Serum copper Low
urinary copper= Hifg
LFT= elevated 
DNA test
Kayser Fleisher sign in eyes
LIVER BIPOSY
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Treatment in wilsons disease

A

Trasnplant or Penicillamine (copper Clearer) and zinc

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Alpha 1 antitrypsin deficiency

What is it and what does it cause

A

Autosomal Recessive and it causes liver cirrhosis in children or emphysema in adults

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Alpha 1 antitrypsin deficiency

diagnoses and treatment

A

Serum Alpha 1 antitrypsin deficiency is low
dont smoke, screen relatives
same managmen for cirhossis and put on transplant if needed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

what is Primary Billiary Cirrhosis

A

chronic autoimmune disease which causes destruction of the bile ducts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Primary Billiary Cirrhosis

prevalence and risk factors and average onset

A

Assosiated with other autoimmune conditions (sjorgens, thyroid)
reoccuring UTIs, Smoking. family history. past pregnancy
90% are women and average onset is 40-50 YO
4 in 100,000

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

Presnetation of Primary Billiary Cirrhosis

A

first symptom is prutius and severe fatigue

can develop into more severe symptoms as disease progresses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

signs of Primary Billiary Cirrhosis

A
Hepatomegally, earliest sign
jaundice
skin pigmentation
xanthoma and xantholesma
can develop into other servre signs are cirrhosis occurs
32
Q

Investigations of Primary Billiary Cirrhosis

A

initally ALP is raised and Serum bilirubin
serology Presence of anti mitrochondial antibodies AMA and IgM -Diagnostic
increased cholesterol
Ultrasound excluded other causes
biopsy will show cirrhosis but not needed

33
Q

complications of Primary Billiary Cirrhosis

A

Liver cirrhosis and failure
osteoporosis
fat malabsorbtion- vit K deficient

34
Q

Managment of Primary Billiary Cirrhosis

A

bile acid analogue- ursodeoxycholic acid
fat soluble vitamins- adek
immunomodulatory therapy- prednisilone
treat prutius- Colestyramine
monitoring of LFTs and DEXA, transfer to liver transplant when failure occurs

35
Q

Bile acid analouge

A

Ursodeoxycholic acid

also used in gall stones

36
Q

Prutius Treatment - bile acid sequestrant

A

Colestyramine

37
Q

hand changes in liver dieases

A
Leuconychia- white nails due to hypoalbiminemia 
clubbing
dupytrens in alcoholic
xanthoma
Palmar erthyma
38
Q

complications of liver failure and cirrhosis

A
encephalopathy 
jaundice
Ascites - spontanous bacterial peritonitis 
sepsis 
portal hypertension - varices 
renal failure
Hepatiocell carcinoma
39
Q

signs that liver failures becoming decompensated

A

encephalopathy
jaundice
Ascites

40
Q

Investigations of liver failure

proving their is liver failure

A

increased bilirubin AST ALT ALP and prothrombin time
Decreased WCC and platelets
decreased albumin
serum creatinine increased and NA is low- indicator for severity

41
Q

investigations of liver failure

finding the cause (biochemically)

A

look for Gamma Glutamyl transaminase
serology- AMA (anti Mitochondrial) IgG- PBC
serology- ANA (anti nuclear) IgG - autoimmune hep
Viral markers- hep
Ferratin iron copper and Alpha antitrypsin

42
Q

investigations of liver failure

finding the cause (imagining and procedures)

A

Bloods
Ultrasound- hepatomegally , stones. obstructions
MRI- shows fibrosis
Liver Biposy diagnostic type and severity
ascites TAP

43
Q

Management of liver cirrhosis

A

diet, stop alcohol and reduced NSAIDS and Salt to minimum
Screen every 3-6 months via ultrasound and Alpha fetoprotein for HCC
treat pruritus by- colestyramine
put on transplant list if decompensated

44
Q

Management of Liver cirrhosis specific to causes

A

most of the time its supportive
PBC ursodeoxycholic acid
wilsons- penicillamne
ascites- diuretics

45
Q

what is ascites

A

fluid in the peritoneum

46
Q

causes of ascites

A

exudate- TB malignancy and peritonitis

Transudate- Cirrhosis (commonest cause), Fluid overload, CCF, portal hypertension, nephrotic syndrome

47
Q

pathophysiology of ascites

A

less albumin = less oncotic pressure

portal hypertension increased hydrosctatic pressure

48
Q

Investigations of ascites

A

Ascites Tap- analyses fluid
WCC- check if bacterial peritonitis
cultures and gram stain- identify pathogens
proteins and albumin- if exudate or transudate
cytology- if malignant
amylase- if pancreatic

49
Q

Presentation of Ascites

A
abd sweling and pain- can be sudden or gradulal
resp distress
peripheral oedema 
if painless- suspect malignancy
if painfull- suspect peritonitis
50
Q

signs of ascites

A

Umbilical hernia
shifting dullness
signs of liver disease or heart disease

51
Q

Investigations of Ascites

A

Ascitic tap

if unsure use X Ray- Ultrasound CT can detect small amounts of fluid

52
Q

Treatment of ascites

A

Rest
restict sodium (antacids, corticsteroids, some antibiotics) and fluids
spironolactone
Paracentesis- drain- not always do this

53
Q

pathogens in spontanous bacterial peritonitis
investigations
presentation
treatment

A

causes by ascites due to E.Coli, Klebestia and enterococi
increased WCC and bacteria on gram stain from ascites tap
ascites pain gets much more severe
cefotaximine

54
Q

causes of portal hypertension

A

prehepatic- congenital abnormality
hepatic- cirrhosis, commonest
post hepatic- heart failure and CCF

55
Q

What does portal hypertension cause

A

dilation of vessels causes collaterals to form. if these form in gastoesophageal junction they are called varices

56
Q

presentation of gastroesophageal varices bursting

A

Haematesis and Melaena

hypovolemic shock

57
Q

management of active gastroesophageal varices bleed

A

stabilise- IV plasma or blood transfusion, treat shock, prophylaxis antibiotics
endoscopy to confirm this was variceal bleed
injection sclerotherapy or variceal banding to stop bleeding

58
Q

Prevention of gastroesophageal varices bursting

A

B Blockers, proplanalol

variceal banding

59
Q

function of the gall bladder, how is it stimulated

A

stores and concentrates bile

stiumlated by CCK

60
Q

what are the different types of gall stones

A

cholesterol- commonest

calcium bilirubin

61
Q

what causes formation of cholesterol stones

A

cholesterol supersaturation-
less bile salts that twill bind to cholesterole- ileal resection or crohns
cholestatsis

62
Q

what will a stone stuck in the cystic ducts cause and present as

A

cholecystitis

billiray colic

63
Q

what is billiary colic

A

epigastric pain, with RUQ pain. radiating to right shoulder and scapula. colicky pain. sudden onset. usually comes on afternoon and stays until early hours of morning.
assosiated wit nausea and vomiting

64
Q

what is cholecystitis and its presentation/ signs and symptoms

A

once gall bladder is inflamed pain moves to RUQ
tenderness and palatable mass
murphys sign.
develops jaundice
fever
some guarding rebound tenderness if localised peritonitis

65
Q

what can cholecystitis develop into and what are the presentation

A

gets inflamed causing localised peritonitis or gangrenes and burst causing generalised peritonitis- rebound tenderness, guarding. fills with emphyma.
needs antibiotics.
sepsis

66
Q

acute cholecystitis and biliary colic investigations

A

bloods- serum bilirubin elevated, increased ALP,
increased WCC if infected, slight eleveated Aminotransferase

gold standard- ultrasound
can do Endocopic retrograde cholyangiopancreatic, ERCP prosedure

67
Q

Treatments for acute Cholecystitis

A

even if it clears, do laproscopic cholecystectomy incase reoccurance.
nil by mouth, IV fluids, analgesia and antiemetics and Antibiotics. once stabilised do cholecystectomy
monitor for signs of gangerine (ultrasound)

68
Q

what are the signs of cholecystitis gangerine and how to investigate

A

increased pyrexia and pain.

monitor via ultrasound

69
Q

Treatment for cholecystitis if stone isn’t passing

A

shock wave lithotripsy

70
Q

complication of reoccurring gall bladder stone

A

chronic cholecystitis or porcelain gall bladder.

71
Q

what happens if a stone moves from the cystic duct and gets stuck in the Common bile duct

A

biliray colic will still occur. however it will cause acute cholangitis- which can develop into ascending cholangitis and sepsis
and back pressure can go up and it can cause liver injury and jaundice

72
Q

what are the presentations of acute cholangitis

A

charcots triad- Biliary colic, fever, jaundice

reynolds pentad- biliary colic, fever jaundice and sepisi( tachycardia, hypo tension) and confusion (also sepsis)

73
Q

what are the presentations of ascending cholangitis

A

reynolds pentad, spesific to infection

74
Q

what infectious agents will cause ascending cholingitis

A

E. Coli, Klebestia, Enterococci

75
Q

what are the investigations in chlangitis, acute or ascending

A

Bloods, Increased WCC. MS&U cultures, bacteria
biochemistry, Increased bilirubin, ALP AST ALT. Increased CRP and ESR
Ultrasounds diagnostic
ERCP better first line for cholangitis

76
Q

Treatment of cholangitis

A

IV antbiotics- metraniazole and gentamycin
cholangitic decompression, ERCP or shock wave lithotrepsy.
cholecystectomy, once stabilised - to prevent reoccurance

77
Q

Why does PBC or liver cirrhosis cause Osteoporosis

A

Due to less production of Vit D so less absorption of calcium leading to increased bone resorption