GI Medicine 5 Flashcards
1
Q
Pharyngeal Pouch
- What clinical features are seen?
- What investigations are done?
A
- dysphagia
- regurgitation
- aspiration
- neck swelling with gurgling on palpation
- halitosis
- barium swallow with dynamic fluoroscopy
2
Q
What are the SEs of PPIs?
A
- hyponatraemia / hypomagnasaemia
- osteoporosis
- microscopic colitis
- increased risk of c. difficile infection
3
Q
Pyogenic liver abscesses
- What is the most common cause in
a) children
b) adults - How is it managed?
A
- a) staph aureus
b) e. coli - drainage + ABx
amoxicillin + ciprofloxacin + metronidazole
if pen allergic: ciprofloxacin + clindamycin
4
Q
- What are the metabolic consequences of refeeding syndrome?
- What should be done if a patient is seen as high risk?
A
- hypophosphataemia
- hypokalaemia and hypomagnasaemia - can lead to torsades de pointes
- if a patient has not eaten for 5 days do not give more than 50% of requirements for next 2 days
5
Q
Small Bowel Bacterial Overgrowth Syndrome
- What are the RFs?
- What clinical features are seen?
- What investigations can be done?
- How is it managed?
A
- diabetes
- congenital GI abnormalities
- scleroderma
- chronic diarrhoea
- abdominal pain + bloating
- flatulence
- hydrogen breath test
- trial ABx
- rifaximin
6
Q
Spontaneous Bacterial Peritonitis
- What clinical features are seen?
- How is it diagnosed?
- How is it managed?
- When and what should prophylactic antibiotics be given?
- What is a marker of poor prognosis?
A
- ascites + abdo pain + fever
- paracentesis: neutrophil count >250
- IV cefotaxime
- previous SBP
- ascites fluid protein <15g/l and Child-Pugh score >9 or hepatorenal syndrome
give oral ciprofloxacin
- alcoholic liver disease
7
Q
What are villous adenomas?
A
colonic polyps with malignant potential secreting large amounts of mucous (possibly leading to electrolyte disturbances)
8
Q
Whipple’s Disease
- What is it?
- What clinical features are seen?
- What is seen on investigation?
A
- multi-system disorder caused by tropheryma whippelii infection
- weight loss + diarrhoea (due to malabsorption
- joint-pain (large joints)
- pleurisy
- pericarditis
- lymphadenopathy
mnemonic: Whipple’s (j looks like i)
3. jejunal biopsy shows deposition of macrophages containing periodic acid-Schiff granules
9
Q
Wilson’s Disease
- What is it?
- When is the typical onset of disease?
- What clinical features are seen?
- What is seen on investigation?
- How is it treated?
A
- autosomal recessive disorder causing increased copper in tissues
- 10-25
- liver: hepatitis, cirrhosis (presentations complaint in children)
- neuro: (presenting complaint in young adults)
basal ganglia degeneration - speech and psychiatric problems - Kayler-Fleischer rings (garen/brown deposits in outside of iris)
- blue nails
- hemolysis
- renal tubular necrosis
- decreased caeruloplasmin
- decreased total serum copper (as carried by caeruloplasmin)
- increased 24hr urine copper
- penicillamine (chelates copper)
10
Q
Zollinger-Ellison Syndrome
- What is it?
- What CFs are seen?
- How is it diagnosed?
A
- excessive gastrin (usually due to gastrin secreting duodenal or pancreatic tumour)
- > can occur as part of MEN 1 - ulcers (multiple)
- malabsorption
- diarrhoea
- fasting gastrin levels
- secretin stimulation test