Gastroenterology Flashcards

1
Q

Why do patients admitted with acute IBD need heparin?

A

Need prophylactic heparin as they are at high risk of VTE

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2
Q

What is main maintenance treatment in UC?

A

Mesalazine

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3
Q

What is maintenance treatment in Crohn’s?

A

Azathioprine and biologics

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4
Q

What are the first choice medications in perianal or fistulating Crohn’s?

A

Biologics

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5
Q

Which medications are generally used in acute IBD?

A

Steroids: topically, orally or IV

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6
Q

What different symptoms may a patient with coeliac disease present with?

A

None, loose stools, bloating, wind, abdominal cramps, weight loss, dermatitis herpetiformis

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7
Q

What are complications associated with coeliac disease?

A

Increased risk of: small bowel lymphoma, osteoporosis, gluten ataxia and neuropathy

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8
Q

What investigations should be done for coeliac disease?

A

Tissue transglutaminase (tTG) and OGD with duodenal biopsies

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9
Q

What can be see on histology with coeliac disease?

A

Villous atrophy and intra-epithelial lymphocytosis

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10
Q

If a young patient has liver disease with a low caeruloplasmin, what is the most likely pathology?

A

Wilson’s disease- abnormal copper storage

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11
Q

What screening do patient’s with cirrhosis have for hepatocellular carcinomas?

A

Alpha-fetoprotein and USS every 6 months

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12
Q

What imaging is best to diagnose cirrhosis?

A

Fibroscan

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13
Q

Through which lines can parenteral nutrition be given?

A

A dedicated central line

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14
Q

Do NG tubes or PEGs eliminate aspiration risk?

A

No as patients can still aspirate on saliva

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15
Q

Which two assessment scores are used for GI bleeding?

A

ROCKALL score: predicts risk of death and re bleeding of upper GI- done after endoscopy
Glasgow-Blatchford score: predicts need for intervention (inpatient Vs outpatient)

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16
Q

How do you initially manage variceal bleeding?

A
  1. Gain IV access, fluid resuscitation is haemodynamically unstable
  2. IV Terlipressin
  3. Refer to GI team
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17
Q

What are the definitive treatment options for variceal bleeding?

A

Oesophageal banding, Linton/Senstaken tube, TIPSS procedure

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18
Q

What is the management of non-variceal upper GI bleeding?

A

Fluid resus if haemodynamically unstable
Discuss with gastroenterology team
Investigate with endoscopy

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19
Q

What nutritional assessment tool can be used to help identify malnutrition of a patient?

A

MUST

Malnutrition universal screening tool

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20
Q

What form of management is indicated for a patient with ongoing acute GI bleeding despite repeated endoscopic therapy?

A

Emergency surgery or interventional radiology

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21
Q

What are some oesophageal causes of haematemesis?

A

Oesophageal varices, oesophagitis, cancer, Mallory Weiss tear

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22
Q

Is sudden weight loss associated with acute exacerbations of NAFLD?

A

Yes

It triggers importation of toxic lipids to the liver which trigger steatosis, inflammation and hepatocyte cell death

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23
Q

What is budd-chiara syndrome?

A

Hepatic vein thrombosis

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24
Q

What classic triad is associated with Budd-Chiara syndrome?

A

Abdo pain: sudden onset, severe
Ascites
Tender hepatomegaly

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25
What is the most sensitive and specific lab finding for diagnosing cirrhosis?
Thrombocytopenia (low platelets)
26
what are some common causes of mouth ulceration?
recurrent apthous ulcers, trauma, nutritional deficiencies (iron, B12, folate), viral/fungal infections, leukoplakia, crohn's
27
what are some early signs of HIV which can be seen in the mouth?
kaposi sarcoma (reddish-blue oral macule) oral hairy leukoplakia (white patches on lateral borders of tongue) secondary to EBV infection
28
intermittent dysphagia of both liquids and solids is likely due to what pathology?
oesophageal spasm
29
progressive dysphagia of liquids to solids is likely due to what pathology?
neurological disorder
30
progressive dysphagia affecting both solids and liquids with regurgitation that often relieves symptoms is likely due to what pathology?
achalasia
31
what is achalasia?
dysmotility where there is inadequate relaxation of the lower oesophageal sphincter and aperistalsis of the oesophagus
32
what is the first line imaging study done for patients with difficulty swallowing both liquids and solids indicating dysmotility?
barium swallow
33
what is seen on barium swallow with achalasia?
bird beak
34
what might be seen on an Xray with achalasia?
widened mediastinum from the dilated oesophagus
35
what is the gold standard investigation for achalasia? what is the diagnostic finding?
manometry high resting pressure of lower oesophageal sphincter is diagnostic
36
how might oesophageal spasm typically present?
transient retrosternal chest pain and intermittent dysphagia (can mimic angina)
37
what is seen on barium swallow with oesophageal spasm?
corkscrew oesophagus
38
why is barium swallow preferred in the investigation of suspected pharyngeal pouch compared to endoscopy?
risk of perforation with endoscopy
39
what is the M rule associated with primary biliary cholangitis?
IgM raised anti-Mitochondrial antibodies Middle aged female
40
What is the typical presentation of GORD?
Intermittent heartburn which gets worse after meals and on lying down, acid brash (metallic taste from acid regurgitation), dysphagia and atypical chest pain
41
How is GORD diagnosed?
Clinically, although if there are ALARM symptoms Ix can be done to rule out serious pathology
42
What are ALARM symptoms associated with dyspepsia that would warrant upper GI endoscopy?
A- anaemia L- loss of weight A- anorexia R- recent onset of progressive symptoms M- malaena/haematemesis S- swelling difficulty
43
What lifestyle advice can be given for GORD?
Smoking cessation, weight loss, less fatty/spicy/acidic foods, raise the head of the bed
44
How do we treat GORD pharmacologically?
PPI therapy for 4-8 weeks, over the counter antacids/alginates (not continuously but for symptomatic relief) If symptoms persist low dose PPI treatment or H2 antagonist can be trialled
45
What is fundoplication?
A surgery considered for GORD involving wrapping the gastric fundus around the oesophagus
46
What are some complications of GORD?
Barretts oesophagus, oesophagitis, oesophageal strictures, oesophageal carcinoma
47
What is a differential for GORD which may be considered in patients with atopic history presenting with dysphagia and vomiting?
Eosinophillic oesphagitis: diagnosed on biopsy and treated with aerosolised glucocorticoids
48
What investigations are done for suspected oesophageal cancer?
Bloods: FBC (GI blood loss), LFTs (liver mets?), U+Es (suitable for contrast CT?) OGD (oesophagogastroduodenoscopy) with biopsy Staging CT
49
What are immediate things to do when a patient has an upper GI bleed from varices?
A-E: oxygen, IV access, Bloods, fluid resuscitation. Assess for signs of shock Blatchford score Terlipressin and prophylactic antibiotics Transfusion of blood products as required
50
How is alcoholic ketoacidosis managed?
Infusion of saline and thiamine
51
How long must a patient be consuming gluten before serology tests are done for coeliac disease?
They must eat gluten for at least 6 weeks before they are tested
52
What dietary change is recommend to patients with ascites?
Low sodium diet
53
Why do patients with coeliac disease get offered the pneumococcal vaccine?
Hyposplenism (splenic reticuloendothelial atrophy)
54
What are common presenting symptoms of alcoholic hepatitis?
RUQ pain, anorexia, weight loss, jaundice, muscle wasting and fever
55
What LFT change is typical of alcoholic hepatitis?
AST/ALT>2 is characteristic of alcoholic hepatitis
56
if a patient tests positive for C diff antigen but not for c diff toxin A/B, are they likely to have an active c diff infection?
no these results suggest colonisation but no active infection
57
in which of the IBDs are pseudopolyps seen on colonoscopy?
ulcerative colitis
58
what are some side effects of mesalazine?
GI upset, agranulocytosis, interstitial nephritis, pancreatitis
59
what are first line investigations for a patient with suspected IBS which are expected to be normal?
FBC, ESR, CRP, coeliac screen
60
what are classic electrolyte disturbances seen with refeeding syndrome?
hypo: -kalaemia -magnesaemia -phophataemia
61
what is the management of baretts oesophagus?
lifestyle advice, high dose PPI therapy and endoscopic surveillance
62
how does pancreatic cancer typically present?
painless jaundice, pale stools, dark urine, cholestatic liver function tests
63
what effect can PPIs have on electrolytes?
hyponatraemia hypomagnesaemia
64
what is budd chiari syndrome?
hepatic vein thrombosis usually on background of hypercoaguable disease/state
65
what is the triad associated with budd chiari syndrome?
sudden onset severe abdo pain ascites tender hepatomegaly
66
what is initial Ix for suspected budd chiari syndrome?
USS abdo with doppler
67
what causes whipples disease?
tropheryma whippelii infection
68
what are common features of whipples disease?
diarrhoea, weight loss, fever, large joint arthralgia, lymphadenopathy
69
what will be seen on jejunal biopsy in whipples disease?
macrophages containing periodic acid schiff (PAS)
70
what gene mutations are associated with HNPCC?
MSH2/MLH1
71
what gene mutations are associated with FAP?
APC gene mutations
72
what is investigation of choice when investigating primary sclerosing cholangitis?
ERCP or MRCP
73
what is surgical management of achalasia?
pneumatic dilatation or heller cardiomyotomy
74
how is c.dif diagnosed?
stool culture looking at c dif toxin
75
what does c.diff antigen positivity show us?
shows exposure to the bacteria rather than current infection
76
what antibiotics are most associated with c.dif?
clindamycin and cephalosporins (start with cef)
77
should PPIs be given before endoscopy in suspected upper GI bleed?
no evidence this improves clinical outcomes and may obscure endoscopic findings
78
what is first line management of primary biliary cholangitis?
ursodeoxycholic acid
79