GI + Hepatology 27/7/20 Flashcards

1
Q

stages of hepatic encephalopathy

A

1) . altered mood and behaviour, disturbance of sleep pattern and dyspraxia
2) . drowsiness, confusion, slurring of speech and personality change
3) . incoherency, restlessness, asterixis
4) . coma

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2
Q

complications of liver failure

A
  • infection
  • cerebral oedema, hepatic encephalopathy
  • bleeding
  • hypoglycaemia (easily treated with glucose)
  • multi-organ failure, hepatorenal syndrome.
  • ascites, spontaneous bacterial peritonitis
  • portal hypertension, variceal bleeding
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3
Q

management of hepatic encephalopathy

A
  • treat underlying cause
  • lactulose (removes nitrogenous waste)
  • IV mannitol to reduce cerebral oedema
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4
Q

management of liver-related coagulopathy

A
  • vitamin K

- FFP

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5
Q

King’s college criteria for liver transplant (paracetamol overdose)

A
- arterial pH <7.3 24h after ingestion
OR
- pro-thrombin time >100s
AND creatinine >300µmol/L
AND grade III or IV encephalopathy
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6
Q

King’s college criteria for liver transplant (NON-paracetamol overdose)

A
- prothrombin time >100s 
OR any three of:
- drug-induced liver failure
- age under 10 or over 40 years
- 1 week from 1st jaundice to encephalopathy
- prothrombin time >50s
- bilirubin ≥300µmol/L
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7
Q

causes of liver cirrhosis

A
  • alcohol
  • hepatitis B and C (+autoimmune hep)
  • non-alcoholic fatty liver disease
  • biliary: primary biliary cirrhosis, primary sclerosing cholangitis
  • genetic: haemochromatosis, Wilson’s disease, alpha-1-antitrypsin deficiency
  • drugs: methotrexate, amiodarone, isoniazid
  • Budd-Chiari syndrome
  • heart failure
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8
Q

Child-Pugh score

A
used to assess severity of liver cirrhosis
score 
- bilirubin (umol/l)
- albumin (g/l)	
- prothrombin time (seconds prolonged) 
- encephalopathy 
- ascites

scores are added and the degree of cirrhosis is classified as

  • A (<7 points)
  • B (7-9 points)
  • C (>9 points)

Model for End-Stage Liver Disease (MELD) used increasingly in recent years, especially when considering liver transplant

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9
Q

management of ascites

A
  • fluid restriction + low Na diet
  • spironolactone (can add furosemide)
  • drainage if tense
  • albumin infusion may be required
  • prophylactic Abx if at increased risk of SBP
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10
Q

GI features of ulcerative colitis

A
  • diarrhoea ± blood
  • urgency/tenesmus
  • abdominal pain, particularly in the left lower quadrant
  • increased risk of colorectal cancer (UC higher risk than Crohn’s)
  • lead pipe sign on AXR, loss of haustra with no skips in barium enema
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11
Q

GI features of Crohn’s

A
  • diarrhoea ± blood
  • abdominal pain
  • perianal disease: e.g. skin tags or ulcers
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12
Q

extra-GI tract features of Crohn’s and UC

A
  • weight loss + absorption problems
  • arthritis
  • erythema nodosum, pyoderma gangrenosum
  • osteoporosis
  • uveitis (UC more commonly)/episcleritis (Crohn’s more commonly)
  • primary sclerosing cholangitis (UC more commonly)
  • clubbing
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13
Q

NICE classification of UC severity

A
  • mild: < 4 stools/day, only a small amount of blood
  • moderate: 4-6 stools/day, varying amounts of blood, no systemic upset
  • severe: >6 bloody stools per day + features of systemic upset (pyrexia, tachycardia, anaemia, raised inflammatory markers)
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14
Q

management of UC

A

MILD-MOD UC
- proctitis, proctosigmoiditis, left-sided UC = topical aminosalicylate (5-ASA eg. sulfasalazine), add oral 5-ASA if unresponsive after 4 wks/extensive

SEVERE UC

  • inpatient management
  • IV corticosteroids (IV ciclosporin if CI)
  • surgery may be required (panproctocolectomy with permanent end ileostomy )
  • following a severe relapse, PO azathioprine may be used for remission
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15
Q

triggers for UC flares

A
  • usually no identifiable trigger
  • stress
  • medications: NSAIDs, antibiotics
  • cessation of smoking
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16
Q

management of Crohn’s

A
- smoking cessation 
inducing remission:
- prednisolone
- 5-ASAs second line to glucocorticoids
maintaining remission:
- azathioprine
- methotrexate second line
surgery
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17
Q

features of coeliac disease

A
  • abdominal pain
  • bloating
  • nausea and vomiting
  • diarrhoea
  • steatorrhoea
  • fatigue
  • weight loss or failure to thrive in children
  • dermatitis herpetiformis
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18
Q

complications of coeliac and associated conditions

A
  • anaemia (folate/B12/iron deficiency)
  • osteoporosis
  • enteropathy associated T-cell lymphoma
  • autoimmune conditions: type 1 diabetes, thyroid disease eg. Graves’ disease or Hashimoto’s thyroiditis
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19
Q

investigations for coeliac disease

A
  • gluten diary
  • stool culture to rule out infection
  • serological markers
    > anti-TTG IgA
    > anti-endomysial antibody
    > IgA to prevent false negatives due to deficiency
  • diagnostic OGD with biopsy
    > histology shows: sub-total villous atrophy, crypt hyperplasia, intra-epithelial lymphocytes
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20
Q

diagnostic criteria for IBS

A

Manning criteria:

  • abdominal discomfort or pain that is relieved by defecation
  • associated with altered bowel frequency or stool form (diarrhoea or constipation)
  • bloating
  • symptoms made worse by eating
  • passage of mucus
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21
Q

lifestyle advice for IBS

A
  • regular mealtimes and take time to eat
  • reduce caffeine, fizzy drinks, alcohol
  • restrict fibre, porridge may be useful for people with wind/bloating
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22
Q

pharmacological management of IBS

A
  • IBS-C, laxative
  • IBS-D, loperamide
  • if ineffective, TCAs may be of use
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23
Q

screening tools for alcohol dependence

A
  • CAGE questionnaire
  • AUDIT (alcohol use disorders identification test)
  • SADQ (severity of alcohol dependence questionnaire)

also consider risk to others, eg. children, and associated psychosocial problems

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24
Q

CAGE questionnaire

A
  • have you ever felt you needed to CUT down on your drinking?
  • have people ANNOYED you by criticising your drinking?
  • have you felt GUILTY about your drinking?
  • have you ever felt you needed a drink first thing in the morning (EYE OPENER) to get rid of a hangover or steady your nerves?

2+ = likely alcohol dependence

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25
Q

management of alcohol withdrawal

A
  • CBT if appropriate (mild dependence/problem drinking)
  • assisted withdrawal required if >20 score in AUDIT or over 15units daily
    > pabrinex
    > chlordiazepoxide
    > acamprosate or naltrexone
    > PO lorazepam if delirium tremens
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26
Q

stages of alcohol withdrawal

A
6-12 hrs
- insomnia/anxiety/agitation
- sweating/palpitations/tremor
- nausea/vomiting
12-24hrs
- hallucinations (visual/tactile/auditory)
typically ~36-72 hrs
- delirium tremens
     > seizures
     > psychosis
     > confusion
27
Q

features of pancreatitis

A
ACUTE PANCREATITIS
- severe epigastric pain radiating to back
- vomiting
- possibly Cullen's/Gray-Turner's signs
- rarely ischaemic retinopathy
CHRONIC PANCREATITIS
- steatorrhoea
- epigastric pain, typically worse on eating, especially fatty foods
- endocrine dysfunction (eg. T1DM)
28
Q

investigations for pancreatitis

A
ACUTE
- serum lipase
- serum amylase
- USS for cause (can have contrast CT)
CHRONIC
- CT/AXR for pancreatic calcification
- faecal elastase for exocrine dysfunction
- OGTT for T1DM
lipase/amylase not typically raised in chronic
29
Q

causes of acute pancreatitis

A
I GET SMASHED
Idiopathic
Gallstones
Ethanol
Trauma
Steroids
Mumps (other viruses include Coxsackie B)
Autoimmune (e.g. polyarteritis nodosa)
Scorpion venom
Hypertriglyceridaemia, Hypercalcaemia
ERCP
Drugs (azathioprine, mesalazine, bendroflumethiazide, furosemide, sodium valproate)
30
Q

management of acute pancreatitis

A
  • fluid resuscitation
  • analgesia
  • surgery dependent on cause (eg. gallstone = cholecystectomy or ERCP)
  • treat underlying cause, eg. alcoholism, nutrition, change meds
31
Q

causes of chronic pancreatitis

A
  • alcohol dependence
  • genetic: CF, haemochromatosis
  • ductal obstruction: gallstone, tumour
32
Q

management of chronic pancreatitis

A
  • treat underlying cause, eg. alcohol abstinence
  • analgesia
  • pancreatic enzyme supplements
  • manage endocrine dysfunction if present, eg. give insulin
33
Q

management of variceal bleeding

A
  • ABCDE
  • vit K, FFP, platelets
  • terlipressin 2mg every 4-6 hrs until controlled (reduces portal hypertension)
  • IV Abx broad spec eg. co-amox
  • urgent endoscopy once haemodynamically stable (variceal banding done with endoscopy)
    > regular endoscopy in those with cirrhosis
  • prophylactic propranolol
    TIPS (trans-jugular intrahepatic portosystemic shunt) if recurrent, unresponsive)
34
Q

Glasgow-Blatchford Score

A

stratifies upper GI bleeding patients who are “low-risk” and candidates for outpatient management
- score of 1+ = high risk

35
Q

features of primary biliary cholangitis

A

autoimmune condition causing scarring and inflammation of the bile ducts, eventually leading to liver cirrhosis

  • symptoms of biliary disease: jaundice, itch, fatigue
  • anti-mitochondrial antibodies
  • increased risk of hepatocellular carcinoma
  • associated with other autoimmune conditions, particularly Sjogrens
36
Q

causes of pre-hepatic jaundice

A
  • conjugation disorders: Gilbert’s, Crigler-Naajjar
  • haemolysis
  • drugs: contrast, rifampicin
37
Q

causes of intra-hepatic jaundice

A
  • viruses (hepatitis, CMV, EBV)
  • drugs: paracetamol overdose, valproate, statins, TB antibiotics
  • cirrhosis
  • liver abscess or malignancy
  • haemochromatosis, Wilson’s disease
  • autoimmune hepatitis
  • alpha-1 antitrypsin deficiency
  • Budd-Chiari syndrome
  • failure to excrete conjugated bilirubin (Dubin-Johnson syndrome)
38
Q

causes of post-hepatic jaundice

A
  • cholestasis (dark urine, pale stools)
    > primary biliary cholangitis
    > primary sclerosing cholangitis
    > gallstones
  • drugs: coamoxiclav, flucloxacillin, nitrofurantoin, steroids, sulfonylureas
  • malignancy: pancreas adenocarcinoma, cholangiocarcinoma
39
Q

features of primary sclerosing cholangitis

A

inflammation and fibrosis of intra and extra-hepatic bile ducts

  • deranged LFTs
  • hepatomegaly
  • cholestatic jaundice
  • p-ANCA
  • multiple beaded biliary strictures seen on ERCP
  • increased risk of cholangiocarcinoma
40
Q

investigations for haemochromatosis

A
  • bloods: deranged LFTs, raised serum ferritin and transferrin saturation
  • genetic testing: HFE gene defects
  • liver biopsy: increased iron stores
41
Q

management of Barrett’s oesophagus

A

due to chronic GORD - squamous to columnar epithelium at lower oesophagus
- endoscopy classification:
> low-grade dysplasia = high dose PPI and 6 monthly endoscopy
> high-grade dysplasia = endoscopic resection

42
Q

management of H. pylori

A
  • triple therapy: amoxicillin (metronidazole if allergy), clarithromycin and a PPI twice daily for seven days
  • untreated H. pylori can lead to:
    > peptic ulcers
    > gastric cancer
    > B cell lymphoma of MALT tissue
43
Q

management of gastroenteritis

A
  • fluid replacement/oral rehydration sachets
  • Abx if systemic disease/immunocompromised
    > salmonella and shigella = ciprofloxacin
    > campylobacter = erythromycin
    > cholera = tetracycline
    food poisoning is a notifiable disease
44
Q

antibiotics with increased risk of facilitating Clostridium dificile infection

A
  • clindamycin
  • ciprofloxacin
  • cephalosporins
  • penicillins
45
Q

management of Clostridium dificile infection

A
  • PO metronidazole
  • PO vancomycin if severe
  • supportive treatment
  • faecal transplant in recurrence
46
Q

investigations for achalasia

A
  • oesophageal manometry: excessive LOS tone which doesn’t relax on swallowing
  • barium swallow: bird’s beak appearance
47
Q

management of achalasia

A
  • pneumatic balloon dilation (if low surgical risk - due to possible complications of procedure)
  • botox injection of LOS if high surgical risk
  • nitrates/CCBs
48
Q

features of achalasia

A
  • dysphagia of BOTH liquids and solids
  • heartburn
  • regurgitation
  • may lead to cough, aspiration pneumonia etc
  • malignant change in small number of patients
49
Q

features of pharyngeal pouch

A

typically in elderly men

  • dysphagia
  • regurgitation
  • aspiration
  • neck swelling which gurgles on palpation
  • halitosis
50
Q

features of oesophageal stricture

A
  • longer history of dysphagia, often not progressive
  • GORD
  • lack of systemic features seen with malignancy
51
Q

features of oesophageal cancer

A
BOTH
- progressive dysphagia
- weight loss
ADENOCARCINOMA
- may have previous symptoms of GORD or Barrett's oesophagus
SQUAMOUS CELL CARCINOMA
- usually no GORD history
- more linked with weight loss
52
Q

alcohol picture of LFTs

A
  • raised GGT

- AST:ALT > 2

53
Q

features of Budd-Chiari syndrome

A
triad of:
- abdominal pain: sudden onset, severe
- ascites
- tender hepatomegaly
doppler US diagnostic
54
Q

features of ascending cholangitis

A
usually follow gallstone obstruction/biliary stricture = severely septic and unwell
Charcot's triad:
- fever
- jaundice
- right upper quadrant pain
typically E. coli
55
Q

management of ascending cholangitis

A
  • fluid resuscitation
  • IV Abx
  • ERCP
56
Q

Hep B antigen testing

A

HBsAg = ongoing infection, either acute or chronic if present > 6 months

anti-HBc = caught, i.e. negative if immunized

57
Q

screening for hepatocellular carcinoma

A

USS and alpha fetoprotein in at risk groups, eg. current cirrhosis

58
Q

metabolic features of refeeding syndrome

A
  • hypophosphataemia
  • hypokalaemia
  • hypomagnesaemia: may predispose to torsades de pointes
  • abnormal fluid balance
    these may lead to organ failure
59
Q

management of SBP

A

ABCDE
- IV cefotaxime
> most common organism is E. coli
- prophylactic ciprofloxacin in those with ascites and cirrhosis

60
Q

features of Whipple’s disease

A
Tropheryma whippelii
- malabsorption: diarrhoea, weight loss
- arthralgia
- lymphadenopathy
- skin: hyperpigmentation and photosensitivity
treatment with PO co-trimoxazole
61
Q

features of Wilson’s disease

A

increased copper deposition, particularly in liver, brain and cornea

  • hepatitis/cirrhosis
  • basal ganglia degeneration (behaviour, speech, psychiatric features, later parkinsonism, dementia)
  • Kayser-Fleischer rings
  • Fanconi syndrome
62
Q

management of primary biliary cholangitis

A
  • ursodeoxycholic acid: slows disease progression and improves symptoms
  • pruritus: cholestyramine
  • fat-soluble vitamin supplementation (ADEK)
  • liver transplantation

no definitive treatment for primary SCLEROSING cholangitis besides liver transplant

63
Q

management of alcoholic liver disease

A

alongside pabrinex, alcohol withdrawal pathway, etc.

- prednisolone + NAC

64
Q

management of haemorrhoids

A
  • soften stools: increase dietary fibre and fluid intake
  • topical local anaesthetics and steroids
  • rubber band ligation
  • surgery is reserved for non-responsive, large, symptomatic haemorrhoids