Gastroenterology (medical) Flashcards

1
Q

UC classification

A

Mild (<4 stools, little blood)
Moderate (4-6 stools)
Severe (>6 blood stools, systemic upset)

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2
Q

IBD investigation

A

Bloods: faecal calprotectin
Stool cultures and C diff toxin
AXR
MR enterography with oral contrast

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3
Q

UC features

A

Mucosa and submucosa
Decreased goblet cells
Cryst abscesses
Rectum common
Lead-pipe
Thumb-printing
Tenesmus
Nocturnal incontinence
Surgery curative

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4
Q

CD features

A

Transmural
Increased goblet cells
Terminal ileum common
Abscesses and fissues
String sign
Surgery not curative

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5
Q

Crohn’s management (induce remission, maintain remission)

A

Induce remission
1) Glucocorticoids

Maintain remission
1) Glucocorticoids
2) Azathioprine or mercaptopurine
3) Methotrexate

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6
Q

Crohn’s management (strictural terminal ileal disease, perianal fistulae (including investigation))

A

STID: ileocecal resection
Perianal fistula: MRI -> oral metronidazole

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7
Q

UC management (induce remission, maintain remission)

A

Induce remission
1) Topical rectal 5-ASA
2) Oral 5-ASA
3) Oral corticosteroid

Maintain remission
1) Topital/oral 5-ASA
2) Azathioprine or mercaptopurine

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8
Q

UC management (severe colitis)

A

IV steroids or ciclosporin

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9
Q

Internal haemorrhoids grading

A

1) No prolapse
2) Prolapse on defecation (reduces spontaneously)
3) Prolapse on defecation (reduces manually)
4) Can’t reduce prolapse

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10
Q

Haemorrhoids management

A

1) Conservative
2) Sclerotherapy
3) Rubber band ligation
4) Surgical haemorrhoidectomy

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11
Q

Management of anal fissure present for < 1 week

A

Conservative
Laxatives (bulk-forming)
Analgesia (including topical anaesthetics)

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12
Q

Management of anal fissure present for >6 weeks (chronic)

A

Topical GTN
Sphincterotomy/botox

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13
Q

Cause of perianal abscess

A

E. coli (most common)
Staph. aureus (from skin)

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14
Q

Perianal abscess investigations

A

Clinical
MRI gold standard but used for complications

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15
Q

Perianal abscess management

A

Incision and drainage
Abx if systemic

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16
Q

Skin sign and deficiencies in coeliac disease in order of prevalence

A

Dermatitis herpetiformis

Irond deficiency anaemia > folate > B12

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17
Q

Coeliac management

A

Replace B12 then folate
Gluten-free diet
Refer to dietician or gastro - annual review

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18
Q

Autoimmune hepatitis antibodies

A

ANA
SMA
LKM1

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19
Q

Autoimmune hepatitis biopsy findings

A

Piecemeal necrosis
Bridging necrosis

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20
Q

Autoimmune hepatitis management

A

Steroids, immunosuppressants
Liver transplant

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21
Q

Primary biliary cholangitis presentation

A

Pruritus before jaundice
Fatigue
May have RUQ pain

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22
Q

What is PBC?

A

Intrahepatic inflammation of bile ducts causing cholestasis

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23
Q

PBC antibodies

24
Q

PBC treatment

A

1) Ursodeoxycholic acid
2) Liver transplant

25
What is primary sclerosing cholangitis?
Inflammation and fibrosis of intra and extrahepatic bile ducts
26
PSC antibodies
pANCA
27
PSC MRCP finding
Beaded
28
PSC management
1) Cholestyramine / immunsuppresants 2) Liver transplant
29
Acute decompensation of liver disease signs
Splenomegaly Ascites Encephalopathy Varices Failed liver function e.g. poor clotting
30
Ascites management
Restrict fluids Spironolacton SBP prophylaxis (ciprofloxacin + propranolol) TIPSS shunt between hepatic portal vein and hepatic vein Paracentesis if tense
31
SBP investigation
USS Ascitic tap PMNL >250
32
SBP management
Piptazobactam
33
Haemochromatosis transferrin, ferritin, iron, and TIBC
Transferrin: high Ferritin: high (late) Iron: high TIBC: low
34
Stain for liver biopsy and finding in joint xray in haemochromatosis
Perl's stain Chondrocalcinosis
35
Haemochromatosis management
1) Venesection 2) Desferrioxamine
36
Alcoholic hepatitis LFT findings
Very high GGT AST 2 or 3x ALT
37
Alcoholic hepatitis management
Prednisolone (Maddrey's discriminant function) Pentoxyphilline
38
T1 and T2 in Budd-Chiari syndrome (blockage of hepatic vein: liver to vena cava)
T1: thrombosis T2: tumour
39
Budd-Chiari investigation
USS with doppler flow
40
Cause of achalasia
Loss of ganglia from Auerbach's plexus - lower oesophageal sphincter contracted
41
Achalasia gold standard investigation
Manometry
42
How to exclude malignancy if achalasia symptoms
Endoscopy
43
Achalasia medication whilst waiting for surgery
CCB
44
Surgical achalasia management
Pneumatic dilatation Laparoscopic cardiomyotomy / peroral endoscopic myotomy
45
Carcinoid syndrome investigation
Urinary 5-HIAA
46
Carcinoid syndrome management
Somatostatin analogue e.g. octreotide
47
C. difficile complication
Severe megacolon
48
C. difficile diagnosis
Toxin in stool Antigen shows exposure, not current infection
49
C. difficile management
1) Oral vancomycin 2) Oral fidaxomicin (or first if recurrence) 3) Oral vancomycin + IV metronidazole
50
Small bowel overgrowth investigations
Hydrogen breath test High folate Culture Abx trial
51
Small bowel overgrowth management
Rifaximin
52
Boerhaave's syndrome presentation (rupture of oesophagus from vomiting)
Chest pain Subcutaneous emphysema
53
Boerhaave's syndrome investigation
CT contrast swallow
54
Boerhaave's syndrome management
< 12 hours: thoracotomy and lavage > 12 hours: T tube (fistula between oesophagus and skin)
55
Basal ganglia degeneration, renal tubular acidosis, blue nails - which eye signs would you expect?
Kayser-Fleischer rings (Wilson's disease)
56
Wilson's disease investigations
Slit lamp Low serum caeruloplasmin Low total serum copper High free serum copper
57
Wilson's disease management
1) Penicillamine 2) Trientine hydrochloride