Gastrointestinal Flashcards

1
Q

What is the triple therapy for H.pylori eradication?

A

A PPI and 2 antibiotic combination- usually Lansoprazole, Clarithromycin and Amoxicillin

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2
Q

What is the mechanism of action of ranitidine?

A

Suppresses acid production by antagonising H2 receptors

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3
Q

What is the mechanism of action of Misoprostol and what is its common indication in terms of GI disease?

A

It is a synthetic prostaglandin analogue that has antisecretory and protective properties, promoting healing of gastric and duodenal ulcers.

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4
Q

Give some signs seen in chronic iron-deficiency anaemia

A

Koilonychia, conjunctival pallor, atrophic glossitis, angular chelitis

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5
Q

Run through the terminology used in diverticular disease and the differences between the terms: diverticulosis, diverticula disease and diverticulitis.

A

Diverticulosis = the presence of diverticula
Diverticular disease = implies they are symptomatic
Diverticulitis = refers to inflammation of a diverticulum (potentially by an infection)

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6
Q

What type of surgical procedure might be performed in the case of a perforated diverticula?

A

Hartmann’s procedure. The most common indication for a Hartmann procedure is complicated diverticulitis. It involves surgical resection of the rectosigmoid colon with closure of the anorectal stump and formation of an end colostomy.

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7
Q

Name three familial polyposis syndromes

A

FAP, HNPCC, Peutz-Jegher’s syndrome

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8
Q

What is the risk of colon cancer in untreated FAP?

A

100% by 40 years (needs prophylactic total colectomy)

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9
Q

Why do colonic polyps form in normal individuals?

A

For unknown reasons, but are increasingly common with age.

The adenoma-adenocarcinoma sequence is thought to be due to a ‘double-hit’ of the APC tumour suppressor gene

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10
Q

Tell me briefly about FAP

A

FAP = familial adenomatous polyposis. Due to APC gene mutation causing thousands of polyps to form in teenage years.

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11
Q

Tell me briefly about HNPCC

A

HNPCC = hereditary non-polyposis colon cancer. Aka lynch syndrome. Autosomal dominant mutation in DNA mismatch repair mechanism -> carries high risk of colon cancer amongst others (e.g. endometrial)

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12
Q

Tell me briefly about Peutz-Jegher’s syndrome (PJS)

A

PJS is due to STK11 gene mutation which causes the development of benign hamartomatous polyps + hyperpigmentation of lips/ oral mucosa.

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13
Q

What conditions does the term ‘gallstone disease’ encompass?

A

Biliary colic, cholecystitis, ascending cholangitis and pancreatitis

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14
Q

Which type of drug class (that can be used in the treatment of diabetes) suppresses appetite and can aid weight loss?

A

GLP1 agonists e.g. liraglutide

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15
Q

What are the three types of enteric infection?

A

Type 1 = non-inflammatory watery diarrhoea
Type 2 = inflammatory dysentery (blood, mucus, leukocytes in stool)
Type 3 = penetrating enteric fever (where you get systemic infection)

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16
Q

What is the first line investigation for oesophageal reflux?

A

PPI trial

17
Q

What are Grey-turner’s and Cullen’s signs and when might they be seen?

A

Grey-turner’s sign = abdominal bruising on flanks.
Cullen’s sign = abdominal bruising in paraumbilical area
Both may be seen in acute pancreatitis

18
Q

What are the causes of acute pancreatitis and how can they be remembered?

A

I GET SMASHED

Idiopathic, Gallstones, Ethanol, Trauma, Steroids, Mumps, Autoimmune, Scorpion stings, ERCP, Drugs

19
Q

What are the signs of volvulus on an abdominal x-ray?

A

Coffee-bean sign.
Sigmoid volvulus (more common) the ‘coffee bean’ typically points towards the RUQ.
Caecal volvulus the ‘coffee bean’ points more horizontally.
Tend to lose haustrations more with sigmoid volvulus than caecal.

20
Q

What is the most common cause of peritonitis?

A

A perforated viscus

21
Q

What is Rovsing’s sign and what is it associated with?

A

Can be seen in acute appendicitis. It is when the left lower quadrant is pressed and it elicits pain on the right side.