UKMLA: Gastroenterology

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95 Terms

1
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Alcohol Withdrawal: How do you manage the general symptoms?

Oral chlordiazepoxide

2
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Alcohol Withdrawal: How do you manage delirium tremens?

Oral or IV lorazepam → reduces seizures and hallucinations that occur 3 days after withdrawal

3
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Alcohol Withdrawal: What are the symptoms of the complication hepatic encephalitis?

  • Personality changes

  • Sleep-wake disturbances

  • Confusion

4
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Alcohol Withdrawal: How do you manage hepatic encephalitis?

Lactulose→ laxative drug to expel ammonia

5
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NAFLD: What are the symptoms?

  • Fatigue

  • RUQ pain

  • Hepatomegaly

  • Obese patient

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NAFLD: What are the expected serology findings?

ALT > AST in 2:1 ratio

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NAFLD: What is the gold standard investigation?

Liver biopsy

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NAFLD: Which tests are required every 6 months?

US and alpha fetoprotein test for hepatocellular carcinoma

9
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NAFLD: What is the management?

Pioglitazone

10
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NAFLD: Which imaging modalities are used?

  • Liver biopsy (gold standard)

  • US → shows hepatic echogenecity

  • Elastography→ stiff liver

  • Enhanced liver fibrosis test→ liver fibrosis

11
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Coeliac Disease: What are the symptoms?

  • Fatigue

  • Diarrhoea

  • Mouth ulcers

  • Weight loss

  • Dermatitis herpetiformis (itchy rash on elbows/knees/buttocks)

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Coeliac Disease: What are the expected serological findings?

  • Anti-TTG positive (check IgA deficiency if anti-TTG test is negative)

  • Anti-EMA positive

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Coeliac Disease: What is the gold standard investigation?

Gastroscopy and duodenal biopsy→ Howell—jolly bodies and duodenal villous atrophy

14
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Coeliac Disease: What foods are gluten-free friendly?

“CPR”:

  • Corn

  • Potato

  • Rice

15
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Coeliac Disease: Which genes are associated?

  • HLA-DQ2

  • HLA-DQ8

16
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GORD: What are the causes?

  • Defective lower oesophageal sphincter

  • Hiatus hernia

  • Reduced oesophageal motility

17
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GORD: What are the symptoms?

  • Hoarse voice

  • Reflux

  • Dyspepsia

  • Dysphagia

  • Nausea/vomiting

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GORD: What is the gold standard investigation?

OGD with carbon-13 urea breath test to rule out H.pylori

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GORD: What is the management?

PPI (omeprazole)

20
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Haemochromatosis: What is the epidemiology?

  • White Europeans

  • C282Y mutation

  • Co-morbidities include erectile dysfunction, amenorrhoea, mood disturbance, HF, diabetes, dilated cardiomyopathy, testicular atrophy

21
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Haemochromatosis: What are the symptoms?

  • Over 40 years old

  • Fatigue

  • Joint pain

  • Hepatomegaly

  • Darkened skin

22
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Haemochromatosis: What are the expected serological findings?

  • Increased ferritin

  • Increased transferritin saturation

  • Decreased iron binding capacity

23
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Haemochromatosis: What is the investigation?

  1. Transferrin saturation over 45%

  2. C282Y gene mutation test

  3. H63D gene mutation test

  4. Perl stain and liver biopsy

24
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Haemochromatosis: What is the management?

  • Venesection (removing blood, decreases iron levels)

  • Desferrioxamine

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Ascites: What is the pathophysiology?

Fluid leaks into the peritoneal cavity→ BP in kidneys decrease→ renin is activated→ aldosterone is secreted→ more H20 and Na is reabsorbed

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Ascites: What is the management?

  • Low sodium diet

  • Spironolactone

  • Ciprofloxacin

27
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Autoimmune Hepatitis: What are the symptoms?

  • Fatigue

  • Pain

  • Jaundice

  • Malaise

  • Hepatomegaly

  • Previous history of autoimmune disease (personally or in first-degree relative)

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Autoimmune Hepatitis: What are the different types?

  • Type 1→ typically affects older adults→ anti-smooth muscle antibody (ANA) positive

  • Type 2→ typically affects younger girls/teens→ anti-microsomial antibodies (AMA) positive, anti-liver cytosol antibodies (anti-LC1) positive

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Autoimmune Hepatitis: What is the management?

  • Initial management → prednisolone

  • Maintenance management→ azithioprine

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Hepatitis: What are the symptoms?

  • Vomiting

  • Severe abdominal pain

  • Jaundice

  • Pruitus

  • Flu-like symptoms

  • Signs of acute liver failure

  • Dark urine

  • Pale stools

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Hepatitis: What is hepatitis A?

  • Virus→ RNA piconovirus

  • Incubation period→ 2-6 weeks

  • Transmission→ faecal oral

  • Vaccine available?→ yes

  • Management→ supportive

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Hepatitis: What is hepatitis B?

  • Virus→ DNA hepadnivirdae

  • Incubation period→ 3-5 weeks

  • Transmission→ bodily fluids

  • Vaccine available?→ yes

  • Management→ supportive and anti-virals

  • Key information→ only managed medically in the vulnerable + is a major risk factor for hepatocellular carcinoma

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Hepatitis: What is hepatitis C?

  • Virus→ RNA flaviviridae

  • Incubation period→ 6-9 weeks

  • Transmission→ blood

  • Vaccine available?→ no

  • Management→ anti-virals

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Hepatitis: What is hepatitis D?

  • Virus→ RNA

  • Transmission→ with hepatitis B

  • Vaccine available?→ no

  • Management→ pegylated interferon alpha

  • Key information→ do a IgM, IgG test

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Hepatitis: What is hepatitis E?

  • Virus→ RNA

  • Incubation period→ 2-9 weeks

  • Transmission→ faecal-oral e.g. raw meat

  • Vaccine available?→ no

  • Management→ supportive

  • Key information→ common in pregnant women leading to fulminate hepatitis (death!!!)

36
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Hepatitis: What are the viral antibody and antigen markers?

  • Surface antigen HBsAg→ active infection

  • Surface antibodies HBsAb→ vaccination or past/current infection (immunity)

  • E antigen HBeAg→ high infectivity and viral replication

  • Core antibodies HBcAb→ past or current infection

  • IgM anti-HBc positive→ acute infection

  • IgG anti-HBc positive→ chronic infection

37
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IBD: What are the symptoms of Crohn’s?

  • Diarrhoea

  • Abdominal pain

  • Rectal bleeding

  • Fatigue

  • Weight loss

  • Mouth ulcers

  • Clubbing

  • RLQ tenderness

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IBD: What are the features of Crohn’s?

  • N→ no blood

  • E→ entire GI tract affected

  • S→ skip lesions seen on endoscopy

  • T→ terminal ileus and transmural inflammation

  • S→smoking history

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IBD: What are the risk factors?

  • FH

  • Smoking

  • Poor diet

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IBD: What is the onset?

  • 15-40 years old + 60-80 years old→ Crohn’s

  • 15-25 years old + 55-65 years old→ U.colitis

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IBD: What are the dermatological signs?

  • Pyoderma gangrenous

  • Erythema nodosum (painful, on shins)

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IBD: What are the ocular signs?

  • Uveitis (painful, blurry, photophobic, red eye)

  • Episcleritis (painless red eye)

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IBD: What is the investigation?

Faecal calprotectin and endoscopy

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IBD: What is the management?

  1. Stop smoking

  2. Oral prednisolone or IV hydrocortisone

  3. Azithioprine or mecaptopurine → only prescribe after testing thiopurine methyltransferase levels first! (alternative is methotrexate)

  4. Indiximab

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IBD: What is the management of peri-anal abscess?

Incision and drainage

46
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IBD: What is the management of peri-anal fistula?

  1. IV ceftriaxone and metronidazole

  2. Seton placement

47
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IBD: What are the symptoms of ulcerative colitis?

  • Tenesmus

  • Weight loss

  • Fever

  • Anorexia

  • Bloody diarrhoea

48
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IBD: What are the features of ulcerative colitis?

  • C→ continuous inflammation

  • L→ limited to colon

  • O→ only affects superficial mucosa

  • S→ smoking is NOT a risk factor

  • E→ excrete blood/mucus

  • U→ use aminosalicylates

  • P→primary sclerosing cholangitis

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IBD: What are the expected histological findings for ulcerative colitis?

  • Crypt abscesses

  • Loss of goblet cells

  • Inflammatory infiltrates

50
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IBS: What are the symptoms?

  • Intestinal discomfort worse after eating, improves after defecation

  • Bowel habit abnormalities

  • Stool abnormalities (watery, hard or mucusy)

51
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IBS: What are the investigations?

To rule out differentials:

  • FBC

  • ESR

  • CRP

  • Anti-TTG

  • CA125

  • Faecal calprotectin→ if normal = IBS, if raised = IBD

52
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IBS: What is the management?

  • Diarrhoea→ loperamide

  • Constipation→ 1) ispaghula husk 2) macrogol 3) chronic?= docusate

  • Cramps→ mebeverine

  • Anti-depressants→ amitriptyline

53
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Hepatocellular Carcinoma: What are the symptoms?

  • Jaundice

  • Pain

  • Ascites

  • Encephalopathy

  • Hepatomegaly

54
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Hepatocellular Carcinoma: What conditions are associated?

  • Liver cirrhosis

  • Hepatitis B

  • Do a 6-monthly US and AFP measurement

55
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Hepatocellular Carcinoma: What is the management?

Surgical resection

56
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Hepatocellular Carcinoma: What is the tumour marker?

Alpha fetoprotein

57
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Liver Cirrhosis: What are the causes?

  • Hepatitis B/C

  • Alcohol liver disease

  • Fatty liver disease

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Liver Cirrhosis: What are the clinical signs?

  • Hepatomegaly

  • Splenomegaly

  • Spider naevi

  • Bruising

  • Caput medusae (distended veins due to portal HTN)

  • Leukonychia (white nails)

  • Asterixis (flapping tremor)

  • Jaundice

  • Ascites

59
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Liver Cirrhosis: What are the expected serological findings?

LFT:

  • Increased bilirubin

  • Increased ALT

  • Increased AST

  • Increased ALP

  • Increased PT time

  • Decreased platelets

  • Decreased albumin

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Liver Cirrhosis: What is the management of stable oesophageal varices?

Propanolol

61
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Liver Cirrhosis: What is the management of unstable/bleeding oesophageal varices?

  • Terlinpressin and ceftraxione

  • TIPS

  • Fresh frozen plasma

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Liver Cirrhosis: What are the expected imaging findings?

US:

  • Liver modularity

  • Corkscrew artery appearance

  • Enlarged portal vein

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Liver Cirrhosis: Which scoring system is used for classification?

Child-Pugh cirrhosis severity score:

A→ albumin (increased)

B→ bilirubin (increased)

C→ clotting (decreased)

D→ dilation (ascites)

E→ encephalopathy

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Liver Transplant: Which scoring system is used for eligibility?

Kings College Criteria→ PT time over 100 OR any 3 of the following:

  • <10 years old or >40 years old

  • 1 week presentation

  • PT time over 50

  • Bilirubin over 300

  • Cr over 300

  • Grade 3 or 4 encephalopathy (incoherent, restless, asterixis)

65
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Liver Transplant: What is the criteria in patients with paracetamol overdose?

PH < 7.3 after 24 hours

66
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Liver Transplant: What is the management of acute transplant rejection?

High dose IV methylprednisolone

67
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Liver Transplant: What is the management of hyper-acute transplant rejection?

Remove graft

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Peptic Ulcers: What are the symptoms?

  • Dyspepsia

  • Relieved by eating

  • Pain restarts 2-3 hours after eating

  • Nausea

  • Vomiting

  • Epigastric pain

  • Usually duodenal

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Peptic Ulcers: What are the causes of peptic ulcer bleeds?

  • H.pylori

  • NSAIDS

  • SSRI’s

  • Aspirin

  • DOAC’s

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Peptic Ulcers: What are the symptoms of peptic ulcer bleeding?

  • Haematemesis

  • Coffee ground vomit

  • Malaena

  • Increased urea

  • Decreased Hb

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Peptic Ulcers: Which scoring system is used for classification of peptic ulcer bleeds?

Glasgow-blatchford GI bleed score

72
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Peptic Ulcers: What are the investigations?

  • Over 55 y/o, weight loss and dyspepsia→ 2 week referral for OGD

  • C-13 urea breath test for H.pylori

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Peptic Ulcers: What is the management?

  • PPI

  • Stop smoking

  • Improve diet

74
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Primary Biliary Cholangitis: What are the symptoms?

  • 40-60 y/o white woman (autoimmune condition)

  • Fatigue

  • Cholesterol deposits

  • Pale, greasy stools

  • Pruitus

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Primary Biliary Cholangitis: What are the expected serological findings?

  • Increased ALP

  • Increased IgM

  • AMA positive

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Primary Biliary Cholangitis: What is the management?

Ursodeoxycholic acid and colestyramine for pruitus

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Primary Sclerosing Cholangitis: Which condition is it associated with?

Ulcerative colitis

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Primary Sclerosing Cholangitis: What are the risk factors?

  • Male

  • 30-40 y/o

  • Ulcerative colitis

  • Family history

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Primary Sclerosing Cholangitis: What are the symptoms?

  • RUQ pain

  • Fatigue

  • Pruitus

  • Hepatomegaly

  • Splenomegaly

80
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Primary Sclerosing Cholangitis: What are the investigations?

  • Increased ALP

  • MRI scan (reveals hepatic strictures)

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Wilson’s Disease: What is the pathophysiology?

  • Autosomal recessive ATP7B gene mutation

  • Causes accumulation of copper in the liver and brain

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Wilson’s Disease: What are the symptoms?

  • Haemolytic uraemia

  • Jaundice

  • Ataxia

  • Drooling

  • Psychiatric manifestations

  • Kaiser-fleischer rings

83
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Wilson’s Disease: What are the investigations?

  1. Serum caeruloplasmin (<140mg)

  2. 24 hour urine collection

  3. ATP7B gene test

  4. MRI (shows ganglia deterioration)

  5. Biopsy

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Wilson’s Disease: What is the management?

  • Diet: no nuts or chocolate

  • D-penicillamine

  • Liver transplant

  • Zinc salts

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Pyloric Stenosis: What is the pathophysiology?

Pyloric sphincter hypertrophy causes obstruction

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Pyloric Stenosis: What are the symptoms?

  • Projectile vomiting

  • Palpable abdominal mass

  • Persistent hunger

  • Weight loss

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Pyloric Stenosis: What is the epidemiology?

Common in:

  • Infants aged 6-8 weeks

  • White males

  • Premature babies

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Pyloric Stenosis: What are the investigations?

  • US→ 16mm length, 3-4mm thickness

  • Low K+

  • Low Cl-

  • Metabolic alkalosis

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Pyloric Stenosis: What is the management?

  • NBM

  • IV fluids

  • Ramstead’s pylorotomy

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Hirschsprung’s Disease: What is the pathophysiology?

Absent ganglion cells in the myenteric and submucosal plexuses→ obstruction

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Hirschsprung’s Disease: What are the symptoms?

  • No meconium

  • Delayed meconium (>48 hours)

  • Distended bowel

  • Vomiting

  • Constipation

  • Poor weight gain

  • Failure to thrive

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Hirschsprung’s Disease: What is the management?

Rectal biopsy to confirm absence of ganglion cells→ remove this section

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Intussusception: What is the pathophysiology?

Ileum folds onto the caecum→ obstruction

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Intussusception: What are the symptoms?

  • < 2 y/o infant

  • Severe, colicky abdominal pain

  • Green vomit

  • Red-currant jelly stool

  • Sausage shaped mass on palpation

  • US→ donut or target sign

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Intussusception: What is the management?

  • Enema

  • Bowel resection