Gastroenterology Flashcards

1
Q

Inducing remission in UC

A

1)Proctitis
- topical (rectal) aminosalicylate
- after 4 weeks, add an oral aminosalicylate
- add topical or oral corticosteroid
2) proctosigmoiditis and left-sided ulcerative colitis
- topical (rectal) aminosalicylate
- after 4 weeks, add a high-dose oral aminosalicylate OR switch to a high-dose oral aminosalicylate and a topical corticosteroid
- stop topical treatments and offer an oral aminosalicylate and an oral corticosteroid
3) extensive disease
- topical (rectal) aminosalicylate and a high-dose oral aminosalicylate
- after 4 weeks, stop topical treatments and offer a high-dose oral aminosalicylate and an oral corticosteroid

4)SEVERE colitis
-admit
- IV steroids are usually given first-line
(IV ciclosporin may be used if steroids are contraindicated)
- after 72 hours add IV ciclosporin to IV corticosteroids or consider surgery

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2
Q

Maintenance of remission in UC

A

Following a mild-to-moderate ulcerative colitis flare:
1) proctitis and proctosigmoiditis
- topical (rectal) aminosalicylate alone (daily or intermittent) or
- an oral aminosalicylate plus a topical (rectal) aminosalicylate (daily or intermittent) or
- an oral aminosalicylate by itself: this may not be effective as the other two options
2)left-sided and extensive ulcerative colitis
- low maintenance dose of an oral aminosalicylate

3)Following a severe relapse or >=2 exacerbations in the past year
- oral azathioprine or oral mercaptopurine

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3
Q

Inducing remission in Crohn’s disease

A

1st line- glucocorticoids (PO, topical or IV)
2nd line- 5-ASA drugs e.g. mesalazine
3rd line- can add on azathioprine or mercaptopurine

NOTE: metro used for isolated peri-anal disease

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4
Q

Maintaining remission in Crohn’s disease

A

1st line- azathioprine or mercaptopurine (NOTE: TPMT activity should be assessed before starting)
2nd line- methotrexate is used second-line

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5
Q

What is the most useful investigations to monitor response to haemochromatosis management?

A

Ferritin and transferrin saturation

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6
Q

What are the possible adverse effects of metoclopramide?

A

1) extrapyramidal effects
-acute dystonia e.g. oculogyric crisis
2) diarrhoea
3) hyperprolactinaemia
4) tardive dyskinesia
5) parkinsonism

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7
Q

What are ALT, ALP and ALT/ALP ratio in hepatocellular disease (paracetamol OD)?

A

Raised (at least 2 fold) ALT, ALP normal, ALT/ALP high (5+)

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8
Q

What are ALT, ALP and ALT/ALP ratio in Cholestatic disease?

A

Normal ALT. Raised ALP (at least 2 fold), ALT/ALP <2

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9
Q

How do you treat bile acid malabsorption?

A

Cholestyramine

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10
Q

What are risk factors for small bowel bacterial overgrowth syndrome?

A

neonates
scleroderma
diabetes mellitus

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10
Q

What are both types of oesophageal cacner associated with?

A

Adenocarcinoma- Barrett’s oesophagus (US/UK)- lower third
Squamous cell carcinoma- Achalasia (third world)- upper two thirds

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11
Q

What is TIBC in IDA vs in Anaemia of Chronic disease?

A

IDA- high TIBC
Anaemia of Chronic Disease- low/normal

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12
Q

What is Peutz-Jeghers syndrome?

A
  • Autosomal dominant
    -Hamartomatous polpypis in GI tract (mainly small bowel)
    -Can present as small bowel obstruction or GI bleeding
    -Pigmented lesions on lips, oral mucosa, face, palms and soles
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13
Q

How do you treat a complex perianal abscess?

A

Seton placement

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14
Q

How do you treat someone with both vitamin B12 and folic acid deficiencies?

A

treat the B12 deficiency first to avoid precipitating subacute combined degeneration of the cord

Administer intramuscular vitamin B12 followed by oral folic acid

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15
Q

How does achalasia present?

A

dysphagia of BOTH liquids and solids

16
Q

What are the investigations for achalasia?

A

1) oesophageal manometry
- considered the most important diagnostic test

2) barium swallow
- ‘bird’s beak’ appearance

3) chest x-ray
- wide mediastinum
- fluid level

17
Q

What is the Glasgow-Blatchford score?

A

helps clinicians decide whether patients can be managed as outpatients or not in the context of GI bleeds

18
Q

What is the Rockall score?

A

used after endoscopy
provides a percentage risk of rebleeding and mortality

19
Q

Management of non-variceal bleeds?

A

PPIs then endoscopy

20
Q

Management of variceal bleeds?

A

1st: terlipressin and prophylactic antibiotics should be given to patients at presentation (i.e. before endoscopy)

2nd: band ligation should be used for oesophageal varices and injections of N-butyl-2-cyanoacrylate for patients with gastric varices

3rd: transjugular intrahepatic portosystemic shunts (TIPS) should be offered if bleeding from varices is not controlled with the above measures

21
Q

What is the management of alcoholic hepatitis?

A

1) glucocorticoids (e.g. prednisolone) during acute episodes

2) pentoxyphylline is also sometimes used

22
Q

What is angiodysplasia?

A

Angiodysplasia is a vascular deformity of the gastrointestinal tract which predisposes to bleeding and iron deficiency anaemia.

23
Q

How is angiodysplasia diagnosed?

A
  • colonoscopy
  • mesenteric angiography if acutely bleeding
24
Q

What is the management of angiodysplasia?

A
  • endoscopic cautery or argon plasma coagulation
  • antifibrinolytics e.g. Tranexamic acid
  • oestrogens may also be used
25
Q

What are the clinical features of Budd-Chiari syndrome?

A

TRIAD
1) abdominal pain: sudden onset, severe
2) ascites → abdominal distension
3) tender hepatomegaly

26
Q

What is the investigation for Budd-Chiari?

A

ultrasound with Doppler flow studies is very sensitive and should be the initial radiological investigation

27
Q

What are the investigations for carcinoid tumours?

A

1) urinary 5-HIAA
2) plasma chromogranin A y

28
Q

What is the management of carcinoid tumours?

A

1) somatostatin analogues e.g. octreotide
2) diarrhoea: cyproheptadine may help

29
Q

What is management of cyclical vomiting?

A

1) Avoidance of triggers
2) Prophylactic treatments e.g. amitriptyline, propranolol and topiramate.
3) Acute episodes: Ondansetron, prochlorperazine and triptans

30
Q

What is the mode of inheritance of haemochromatosis?

A

Autosomal recessive

31
Q

What are the complications of haemachromatosis?

A

Reversible:

Cardiomyopathy
Skin pigmentation

Irreversible:

Liver cirrhosis**
Diabetes mellitus
Hypogonadotrophic hypogonadism
Arthropathy

32
Q

What is the mode of inheritance in Gilbert’s syndrome?

A

Autosomal recessive

33
Q

What is the most common cause of hepatocellular carcinoma worldwide and in Europe?

A

Worldwide: Hep B
Europe: Hep C

34
Q

What is Whipple’s disease?

A
  • rare multi-system disorder caused by Tropheryma whippelii infection. - - - more common in those who are HLA-B27 positive and in middle-aged men.
35
Q

What is the investigation for Whipple’s disease and what do you expect to see?

A

jejunal biopsy: shows deposition of macrophages containing Periodic acid-Schiff (PAS) granules

36
Q

What is the management of Whipple’s disease?

A

oral co-trimoxazole for a year (lowest risk of relapse)

Sometimes preceded by course of IV penicillin

37
Q

What is the mode of inheritance of Wilson’s disease?

A

Autosomal recessive

38
Q

What is the management of Wilson’s disease?

A

penicillamine (chelates copper)