Gastrointestinal Flashcards

(177 cards)

1
Q

Name 2 main forms of chronic autoimmune inflammatory bowel diseases

A

Ulcerative Colitis - Only affects the colon (mucosa)

Crohn’s Disease - Can affect any part of the gut from mouth to anus

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2
Q

Define ulcerative colitis

A

Describes a relapsing remitting inflammatory bowel disease characterised by diffuse, continuous superficial inflammation of the colonic mucosa

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3
Q

Where does ulcerative colitis mainly affect?

A

Most commonly affects the rectum, but may extend into the sigmoid colon, beyond the sigmoid or include the entire colon.

US never spreads proximal to the ileocecal valve.

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4
Q

Give 4 risk factors for Ulcerative Colitis

A

Positive Family History

HLA-B27

Infection (50% of relapses are associated with enteritis)

NSAIDS (may exacerbate UC)

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5
Q

Describe the epidemiology of Ulcerative Colitis (3)

A

Age of onset = 20-40 years old

Slight female predominance

3x more common in NON smokers

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6
Q

Describe the macroscopic pathophysiology of ulcerative colitis

A

Most cases arise from the rectum. Mucosal inflammation leads to oedema, ulcers, bleeding and electrolyte loss.

Mucosal inflammation progresses in a continuous uninterrupted fashion to the proximal colon.

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7
Q

Describe the microscopic pathophysiology of ulcerative colitis (4)

A

Never extends further than the submucosa.

Neutrophils invade crypts of Lieberkuhn, forming crypt abscesses (UC hallmark)

Depletion of goblet cells and mucin

Ulcerated areas become covered by granulomatous tissue, forming polyps (pseudocysts)

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8
Q

How does Ulcerative Colitis appear on a barium enema

A

Lead pipe appearance of colon

(loss of haustral markings)

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9
Q

Give 5 intestinal symptoms of ulcerative colitis

A

Diarrhoea (episodic or persistent) +/- Blood (blood more associated with UC than Crohn’s)

Faecal urgence and/or incontinence

PR bleeding +/- mucus

Abdominal pain (lower left quadrant)

Tenesmus (painful urge to pass stool)

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10
Q

Give 6 extraintestinal symptoms of Ulcerative Colitis

A

Uveitis

Primary Sclerosing Cholangitis

Colorectal cancer

Pallor, clubbing, mouth ulcers

Erythema nodosum

Pyoderma gangrenosum

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11
Q

What tests are performed to diagnosed Ulcerative Collitis? (5)

A

Colonoscopy + Biopsy

Barium enema (lead pipe appearance)

Abdominal x-ray (megacolon)

Faecal calprotectin (elevated - intestinal inflammatory marker)

Stool sample (to exclude infections - c.diff, E.coli, Shigella ect)

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12
Q

What additional tests would be useful to conduct in ? Ulcerative Colitis to exclude other pathologies? (4)

A

Upper intestinal endoscopy (exclude Crohn’s)

Coeliac serology (exclude coeliac)

Thyroid function tests (exclude hyperthyroidism)

U&Es (to assess dehydration/electrolyte disturbance)

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13
Q

What criteria is used to classify Ulcerative Colitis?

A

Truelove and Witts Criteria

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14
Q

Describe the Truelove and Witts Criteria for mild Ulcerative Colitis

A

Motions - <4
PR bleed - Small
Temp - Apyrexic
HR - <70
Hb >11
ESR <30

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15
Q

Describe the Truelove and Witts Criteria for Moderate Ulcerative Colitis

A

Motions - 4-6
PR bleed - Moderate
Temp - 37.1-37.8
HR - 70-90
Hb - 10.5-11

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16
Q

Describe the Truelove and Witts Criteria for Severe Ulcerative Colitis

A

Motions - >6
PR bleed - Large
Temp - >37.8
HR - >90
Hb - <10.5
ESR - >30

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17
Q

What type of surveillance is it important for Ulcerative Colitis patients to have?

A

Colonoscopic Surveillance for colorectal cancer

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18
Q

What is the goal of treatment for Ulcerative Colitis?

A

To induce and maintain remission

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19
Q

Describe the treatment for Mild-Moderate Proctitis (Ulcerative Colitis localised to the rectum) (1st, 2nd, 3rd line and maintaining remission)

A

1st line - Topical Aminosalicylate (Mesalazine)
2nd line - Oral Aminosalicylate (Sulfasalazine)
(If remission not achieved within 4 weeks)
3rd line - Topical Hydrocortisone or Oral Prednisolone

Maintain remission - Oral/Topical aminosalicylate

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20
Q

Describe the treatment for mild-moderate proctosigmoiditis/left sided Ulcerative Colitis (1st, 2nd, 3rd line and maintaining remission)

A

1st line - Topical Aminosalicylate (mesalzine)
2nd line - High dose oral aminosalicylate (sulfasalazine) (if remission not achieved in 4 weeks)
3rd line - Oral Aminosalicylate (sulfasalazine) + Oral Prednisolone (Stop topical aminosalicylate)

Maintain remission - Oral/topical aminosalicylates

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21
Q

Describe the treatment for mild-moderate extensive Ulcerative Colitis (1st, 2nd line and maintaining remission)

A

1st line - Topical aminosalicylate (mesalazine) + High dose oral aminosalicylate (sulfasalazine)
2nd line - Oral aminosalicylate (sulfasalazine) + Oral Prednisolone

Maintain remission - Oral aminosalicylate (sulfasalazine)

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22
Q

Describe the treatment for severe ulcerative colitis

A

1st line - Anti- TNFa monoclonal antibody - Infliximab
2nd line - Monoclonal antibody - Ustekinumab

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23
Q

What is the treatment for Acute Severe Ulcerative Colitis requiring hospitalisation? (1st, 2nd, 3rd line)

A

1st line - IV corticosteroids +/- Surgery
2nd line - IV Ciclosporin
3rd line - Infliximab

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24
Q

Patients with acute severe ulcerative colitis may need surgery if? (5)

A

Passing stool >8x per day

Pyrexic

Tachycardic

Abdominal X-ray showing megacolon

Low albumin, low Hb, High platelet count or CRP >46mg/L

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25
What medication should ulcerative colitis patients receive following a severe relapse or >=2 exacerbations in the past year?
Oral azathioprine or oral mercaptopurine
26
What do Oral thiopruines (azathioprine or mercaptopurine) increase the risk of developing?
Non-melanoma skin cancer
27
Describe Crohn's Disease
Describes a chronic, relapsing-remitting inflammatory disease of the gastrointestinal tract. Unlike UC which is continuous, Crohn's inflammation involves discrete parts (skip lesions) of the GI tract, anywhere from the mouth to the anus. Additionally, the full thickness of the intestinal wall is inflamed (unlike UC which is just the mucosa)
28
Where in the GI tract is usually most affected in Crohn's disease?
Terminal ileum
29
Give 5 risk factors for Crohn's Disease
Positive Family History Smoking Infectious gastroenteritis (caused by rota/norovirus) Appendicectomy Drugs (NSAIDs increase risk of relapse and exacerbation)
30
Give 6 pathophysiological features of Crohn's Disease
Can occur anywhere from mouth to anus Involves all 4 layers of the intestinal wall Skip lesions Cobblestone appearance Granuloma formation (non-caseating) Increase in goblet cells
31
What are the 4 layers of the intestinal wall?
Mucosa Submucosa Muscularis propria Serosa
32
Give 5 complications of Crohn's Disease
Fistula formation (Abnormal connections) Intestinal strictures (obstruction) Perianal disease (fistulas, fissures, abscesses) Osteoporosis Anaemia (iron, vitamin B12, folate deficiency)
33
Give 5 clinical features of Crohn's Disease
Non-bloody diarrhoea (unexplained and persistent) Lower right quadrant abdominal pain/tenderness/mass Weight loss/failure to thrive in children Perianal disease (fissures, fistulas, abscesses) Bowel obstruction (strictures)
34
What eye problem can occur in Crohn's disease?
Episcleritis
35
What investigations are required for diagnosis of Crohn's disease? (3)
Colonoscopy (Shows deep ulcers, skip lesions, cobblestone appearance, rectal sparing) Histology (biopsy showing inflammation across all intestinal layers, also shows increased goblet cells and granulomas) Small bowel enema (may show Kantor's String sign or Rose Thorn Ulcers in terminal ileum)
36
What may be seen on a small bowel enema for a patient with Crohn's Disease? (2)
Kantor's String Sign (severe narrowing) Rose Thorn Ulcers in terminal ileum.
37
What is the goal of treatment for Crohn's Disease?
To induce and maintain remission
38
Describe the treatment used to induce remission in Crohn's Disease (1st, 2nd and 3rd line)
1st line - Glucocorticoids (Prednisolone, methylprednisolone, IV hydrocortisone) 2nd line - Aminosalicylates (mesalazine or sulfasalazine) 3rd line - TNF-a inhibitor monoclonal antibodies (Infliximab/Adalimumab)
39
Describe the treatment used to maintain remission in Crohn's disease (1st and 2nd line)
1st line - Thiopurines (Azathiopurine and Mercaptopurine) 2nd line - DMARD (methotrexate)
40
When should Crohn's patients be considered for surgery? (3)
Failure to respond to medical treatment Intestinal Obstruction or Perforation (fistula) Massive haemorrhage
41
What treatment should Crohn's patients whom have undergone surgery be offered to maintain remission?
Azathioprine + Metronidazole (antibiotic) for up to 3 months.
42
Describe the differences between Ulcerative Colitis and Crohn's with regards to diarrhoea
UC - Bloody diarrhoea Crohn's - Not usually bloody
43
Describe the differences between Ulcerative Colitis and Crohn's with regards to pathology and location
UC; Inflammations always starts at the rectum and never spreads beyond the ileocecal valve. Inflammation is continuous. Crohns; Lesions may be anywhere from the mouth to the anus. Inflammation is discontinuous (skip lesions are usually present)
44
Describe the differences between Ulcerative Colitis and Crohn's with regards to histological features.
UC; Inflammation never spans beyond the submucosa. Goblet cells and mucin become depleted Neutrophils invade crypts of Lieberkuhn forming crypt abscesses Crohns; Inflammation spans through all intestinal layers (mucosa to serosa) Increase in goblet cells Formation of granulomas
45
Describe the differences between Ulcerative Colitis and Crohn's with regards to what may be seen on endoscopy
UC; Widespread ulceration with preservation of of adjacent mucosa - Pseudopolyps Crohns; Deep ulcers, skip lesion giving the lumen a cobblestone appearance
46
Describe the differences between Ulcerative Colitis and Crohn's with regards to complications
UC - Colorectal cancer Crohn's - Obstruction (structure), Perianal disease, colorectal cancer
47
Describe the differences between Ulcerative Colitis and Crohn's with regards to associations
UC - Primary Sclerosing Cholangitis Crohns - Gallstones (secondary to reduced bile acid reabsorption)
48
Define coeliac disease
Aka gluten sensitive enteropathy. Coeliac disease describes a T cell mediated, chronic autoimmune disorder triggered by exposure to ingested gluten
49
What foods components will you find gluten?
Wheat, Barley and Rye
50
How and Where does coeliac disease commonly manifest?
Commonly manifests in the duodenum as villous atrophy and malabsorption.
51
Give 3 associations for Coeliac Disease
HLA-DQ2 and HLA-DQ8 Autoimmune disorders (T1DM, Hashimotos, IgA deficiency) Herpetiformis (a vesicular pruritic skin eruption)
52
Describe the pathophysiology of coeliac disease
Gluten is ingested < Gliadin (component of gluten) interacts with interstitial cells > triggers uptake of gliadin into lamina propria. Within, gliadin is delaminated by tissue transglutaminase (tTG) > gliadin binds HLA-DQ2/8 receptors and presents on surface of CD4+ T cells > production of anti-gliadin and anti-tissueglutaminase antibodies. Triggers immune response > villous atrophy
53
What antibodies are present in coeliac disease
Anti-gliadin and Anti-transglutaminase antibodies
54
Give 3 complications of coeliac disease
Depression, anxiety, eating disorders Delayed growth/puberty in children Nutritional deficiencies (iron, B12, folate, osteoporosis)
55
Give 5 gastrointestinal symptoms of coeliac disease
Diarrhoea Steatorrhoea + foul smelling stools Abdominal pain Weight loss/Failure to therive Aphathous ulceration
56
Give 4 non-GI features of coeliac disease
Dermatitis herpetiformis (blisters on elbows, knees, buttocks and scalp) Ataxia/Peripheral neuropathy Infertility or recurrent miscarriage Symptoms of anaemia
57
What is the gold standard test used to confirm diagnosis of coeliac disease? What will this show?
Small Bowel Endoscopy and Histology Endoscopy shows; flat mucosa with no villi, very smooth intestinal mucosa Histology shows; Villous atrophy, Crypt Hyperplasia, Increased intraepithelial lymphocytes
58
What features are present on histology for coeliac disease? (3)
Villous atrophy Crypt hyperplasia Increased intraepithelial lymphocytes
59
What a the first line investigation for ? coeliac disease? Describe this (4)
Coeliac serology; 1st line - IgA-tTG (Tissue Transglutaminase) - Raised 2nd line - Endomyseal antibody (IgA-EMA) - Raised 3rd line - IgA deficiency (conduct if both IgA-tTG and IgA-EMA are negative) 4th line - If IgA deficiency is present, test for IgG GDP (deaminated gliadin peptide)
60
What additional blood tests would be important to consider in coeliac disease? (3)
FBC/Ferritin - Screen for anaemia and iron deficiency TFTs - Screen for Hashimoto's thyroiditis LFTs - Screen for autoimmune hepatitis, PBS, PSC
61
How is coeliac disease managed? (3)
Long term adherence to gluten free diet Assess osteoporosis risk with DEXA inform 10% risk for 1st degree family members
62
Why is it important for coeliac patients to receive vaccinations? What vaccinations should they recieve?
Coeliac patients often have a degree of functional hyposplenism. Recommended all patients have the pneumococcal vaccine and has a booster every 5 years.
63
Define appendicitis
Describes an acute inflammation of the appendix and is the most common surgical emergency.
64
How does appendicitis commonly present
Umbilical pain that moves to the lower right quadrant (McBurney's Point)
65
What is the appendix anatomically connected to?
Caecum
66
What is the most common cause of appendicitis?
Luminal obstruction by faecolith
67
Give 5 complications of appendicitis
Abscess formation Peritonitis Sepsis Intra-abdominal adhesions Bowel obstruction
68
Between what ages does appendicitis most commonly present?
Between 10-20 years old
69
Give 5 clinical features of appendicitis
Umbilical pain that moves to the lower right quadrant (McBurney's point tenderness) Abdominal guarding and rebound tenderness (peritonitis) Low grade fever, pyrexia, malaise and anorexia Nausea and vomiting Constipation
70
Name and describe 3 signs associated with appendicitis
Rovsing's sign - Pain greater in the RIF when LIF is pressed Psoas sign - Pain on extending the hip (retrocaecal appendix) Copes sign - Pain on flexion and internal rotation of right hip (pelvic appendix)
71
Give 4 differentials for appendicitis
Intestinal obstruction Gastroenteritis Incarcerated inguinal hernia Perforated peptic ulcer
72
What are the 2 main histological types of oesophageal cancer? Which is most common?
Adenocarcinoma (most common) - linked to Barrett's oesophagus and GORD (lower) Squamous cell carcinoma (linked to smoking, alcohol, achalasia and Plummer-Vinson syndrome) (upper)
73
Give 4 risk factors for oesophageal cancer
Low Socioeconomic status Alcohol, Obesity, Smoking Barrett's oesophagus (GORD) Plummer Vinson Sundrome
74
What form of metaplasia is seen in Barrett's Oesophagus?
Metaplasia of lower oesophageal squamous epithelial cells to columnar epithelial cells
75
What triad is seen in Plummer Vinson Syndrome? What type of oesophageal cancer is it associated with?
Triad; Dysphagia Iron deficiency anaemia Oesophageal webs Associated with squamous cell carcinomas (upper oesophageal cancers)
76
Give 5 clinical features of oesophageal cancer
*Usually advanced at presentation Dysphagia (difficulty swallowing), Odynophagia (pain when swallowing), Reflux Weight loss (unexplained) Retrosternal chest pain Nausea and vomiting Hoarseness, Hiccups, postprandial/paroxysmal cough
77
What is the 1st line investigation for oesophageal cancer?
Upper GI endoscopy with biopsy
78
When should an urgent referral be made for a patient with ? oesophageal cancer? (2)
Dysphagia Are >55 with weight loss and Reflux, Upper abdominal pain or dyspepsia
79
What test is used for the initial staging of oesophageal cancer?
Chest CT
80
What test is used for locoregional staging of oesophageal cancer?
Endoscopic ultrasound
81
What is the most common procedure used to treat oesophageal cancer?
Ivor-Lewis type oesophagectomy
82
Define GORD
Gastro-oesophageal reflux disease Describes symptoms or complications resulting from reflux of gastric contents into the oesophagus, oral cavity or lung.
83
Give 5 causes of GORD
Lower oesophageal sphincter hypotension Hiatus hernia Abdominal obesity/over eating Alcohol, fat, chocolate, coffee, smoking Defective oesophageal peristalsis
84
Name 3 classes of drug that can cause GORD
Tricyclics Anticholinergics Nitrates
85
Give 5 oesophageal symptoms of GORD
Heart burn (retrosternal pain aggravated by bending, stooping or laying down) Belching Acid brash (acid/bile regurgitation) Odynophagia (painful swallowing) Water brash (increased salivation)
86
Give 4 extra-oesophageal symptoms of GORD
Asthma (nocturnal) Chronic cough Laryngitis (hoarsness, throat clearing) Sinusitis
87
Give 4 complications of GORD
Barrett's oesophagus (increased risk of adenocarcinoma) Oesophagitis Duodenal or gastric ulceration Benign strictures (causing dysphagia)
88
Name 2 factors that can aggravate heartburn (retrosternal pain) in patients with GORD
Bending, stooping or lying down Drinking hot drinks or alcohol
89
Give 3 red flag symptoms for a patient with GORD
Weight loss Haemoptysis Dysphagia
90
How is GORD diagnosed? (2)
No red flag symptoms - Clinically Red flag symptoms - Endoscopy
91
When should an endoscopy be performed on a patient with GORD? (4)
Symptoms for >4 weeks >55 years old Red flag symptoms (weight loss, haematemesis, dysphagia) Persistent symptoms despite treatment
92
How should GORD that has NOT been investigated with endoscopy be managed? (3)
Treat as dyspepsia; 1. Review medications for possible cause of dyspepsia 2. Lifestyle advice (weight loss, smoking cessation, small/regular meals, avoid hot drinks, eating before bed) 3. Trial of PPI (lansoprazole/omeprazole) for 1 month OR a 'test and treat' approach for H.pylori
93
How should GORD with endoscopically proven oesophagitis be managed? (3)
1. Full dose proton pump inhibitor for 1-2 months 2. If responds well then low dose treatment as required. 3. If doesn't respond well, double-dose PPI for 1 months.
94
When should a patient be seen for an urgent cancer referral?
Within 2 weeks
95
What would warrant an urgent referral for ? oesophageal/stomach cancer? (3)
Patient has dysphagia Patient has upper abdominal mass consistent with stomach cancer Patient is >=55 with weight loss AND one of the following; Upper abdominal pain Reflux Dyspepsia
96
What would warrant a non-urgent referral for ? oesophageal/stomach cancer?
Patient has haematemesis Patient is aged >=55 with; Treatment-resistant dyspepsia OR Upper abdominal pain with low Hb levels OR Raised platelet count with nausea, vomiting, weight loss, dyspepsia, upper abdominal pain
97
What test is used to test for H.pylori?
Carbon-13 urea breath test
98
What type of cancer are the majority of stomach cancers?
Adenocarcinomas
99
Give 4 risk factors for stomach cancer
H.pylori infection Smoking High salt/nitrate diet Pernicious anaemia
100
How does H.Pylori cause stomach cancer?
Causes chronic gastritis > atrophic gastritis and pre-malignant intestinal metaplasia > dysplasia and gastric cancer
101
Give 5 clinical features of stomach cancer
Presents similar to oesophageal cancer Dysphagia, Odynophagia (pain when swallowing), reflux Weight loss - red flag Nausea and vomiting Upper abdominal mass Constant and severe epigastric pain
102
How may advanced (metastatic) stomach cancer present? (2)
Jaundice (liver metastasis) Virchow's node (palpable lymph node in the subclavicular fossa - left side)
103
What clinical sign is distinctively linked to stomach cancer?
Virchow's node (palpable lymph node usually in left subclavicular fossa)
104
How is stomach cancer diagnosed? (3)
Gastroscopy with biopsy Endoscopic ultrasound - evaluate depth and invasion CT/MRI - for staging
105
What is the most common type of colorectal cancer?
Adenocarcinoma
106
Where do the majority of colorectal cancers arise?
Distal colon (sigmoid and rectum)
107
Give 4 risk factors for colorectal cancer
Genetic factors (loss of APC gene) Ulcerative Colitis Crohn's disease (particularly if ileocecal region affected) Smoking, alcohol, diet (low fibre, red/processed meats)
108
What 2 inherited syndromes are strongly linked to colorectal cancer?
Familial adenomatous polyposis (mutation in APC) Lynch syndrome (hereditary non-polyposis colorectal cancer)
109
Describe the pattern of inheritance for familial adenomatous polyposis
Autosomal dominant
110
Describe the pattern of inheritance for lynch syndrome
Autosomal dominant
111
Familial adenomatous polyposis occurs due to a mutation in what gene?
APC - Adenomatous Polyposis Coli
112
Give 5 clinical features of colorectal cancer
Abdominal pain Abdominal/rectal mass Change in bowel habit (constipation, diarrhoea) Unexplained weight loss Rectal bleeding +/- tenesmus
113
How may colorectal cancer present in an emergency? Give 4 signs of this
May present with signs of obstruction; Signs; Absolute constipation Colicky abdominal pain Abdominal distension Vomiting (faeculent - vomit contents is faecal in origin)
114
Give 3 red flag features of colorectal cancer
>40 with unexplained weight loss and abdominal pain >50 with unexplained rectal bleeding >60 with iron deficiency anaemia or changes in bowel habit
115
How should patients with red flag symptoms be investigated for colorectal cancer?
Do NOT offer Faecal Immunochemical Test (FIT). Go straight to colonoscopy.
116
What test is used to screen for colorectal cancer?
Faecal Immunochemical Test (FIT test)
117
Describe how the NHS screen for colorectal cancer.
FIT test Conducted every 2 years for all men and women aged 60-74
118
What is the gold standard diagnostic test for colorectal cancer?
Colonoscopy
119
Describe how FIT test results dictate the next steps in a ? colorectal cancer patient
If positive - Arrange urgent 2 week referral for colonoscopy If negative - Consider IBD/IBS
120
What is the main tumour marker for colorectal cancer?
Carcinoembryonic antigen (CEA)
121
What classification is used to stage colorectal cancer? Describe this (4)
Dukes Classification; A - Limited to muscularis mucosae (95%) B - Extends through the muscularis mucosae (not lymph) C - Involvement of regional lymph nodes D - Distal metstases
122
Describe peptic ulcer disease (2)
Includes both gastric and duodenal ulceration. Characterised by a breach in the epithelium of the gastric/duodenal mucosa
123
What is the most common form of peptic ulcer?
Duodenal ulcers (more common by gastric ulcers) (duodenal ulcer epigastric pain may be relieved by eating)
124
What are the 2 most common causes of peptic ulcers?
H.pylori infection NSAIDs
125
How do NSAIDs contribute to peptic ulcer formation?
Inhibit COX1 enzyme > Blocking prostaglandin synthesis > decrease in gastric mucus and bicarbonate > decrease in mucosal blood supply > ulcer formation
126
Name 4 drug classes that commonly cause peptic ulcers
NSAIDs Bisphosphonates Corticosteroids SSRIs
127
Give 2 complications associated with peptic ulcers
Gastric outlet obstruction (abdo pain and postprandial vomiting) Gastro-intestinal perforation and haemorrhage (of gastro-duodenal artery)
128
Give 3 clinical features of peptic ulcers
Can be asymptomatic Upper abdominal/epigastric pain relieved by antacids
129
With regards to pain, what in a patients history helps distinguish between a gastric ulcer and a duodenal ulcer?
Gastric ulcer associated with postprandial pain Duodenal ulcer associated with relief of pain after eating.
130
How should an uncomplicated peptic ulcer be investigated?
Test for H.pylori Carbon-13 (urea) breath test or Stool Antigen Test *Conduct in patients without dysphagia or <55 with no red flag symptoms
131
Give 2 clinical features that may suggest a peptic ulcer has perforated
Acute onset epigastric pain (later becoming more generalised) Syncope
132
What investigations should be performed in a patient with ? perforated peptic ulcer?
Upright (erect) chest x ray (shows free air under the diaphragm)
133
What artery is a common source for gastrointestinal bleeding in patients with peptic ulcers?
Gastroduodenal artery (branch of common hepatic artery)
134
Give 3 clinical features of gastrointestinal haemorrhage secondary to peptic ulcer
Haematemesis (most common) Melaena Hypotension/tachycardia
135
How is GI haemorrhage secondary to peptic ulcer managed? (3)
ABCDE IV proton pump inhibitor Endoscopic Intervention (1st line)
136
Describe the general management of an uncomplicated peptic ulcer (2)
Lifestyle changes - reduce/stop smoking and alcohol intake Stop inducing drugs (NSAIDs, Bisphosphonates, Corticosteroids, SSRIs)
137
How should peptic ulcer disease with a positive H.pylori test be managed?
1st line: PPI (lansoprazole) + Amoxicillin + Clarithromycin/Metronidazole 2nd line: PPI + Clarithromycin + Metronidazole (if penicillin allergy)
138
How should a patient with a pencillin allergy with H.pylori positive peptic ulcer be managed?
PPI + Clarithromycin + Metronidazole
139
How should a patient with H.pylori negative peptic ulcer be managed?
PPI or H2 receptor antagonist (ranitidine)
140
How should patients with gastric ulcers and H.pylori be followed up?
Repeat endoscopy and H.pylori testing in 6-8 weeks.
141
When should a diagnosis if IBS be considered? (3)
If a patient has had the following for at least 6 months (ABC); Abdominal Pain and/or Bloating and/or Change in bowel habit
142
What may exacerbate symptoms of IBS? (4)
Ingestion of food Stress Menstruation Gastroenteritis (post-infectious IB)
143
Name 3 types of IBS
IBS-C - IBS with constipation IBS-D - IBS with diarrhoea IBS-M - IBS with constipation and diarrhoea
144
When should a diagnosis of IBS be made?
If a patient has; Abdominal pain either related to defecation and/or associated with altered stool form/frequency AND at least 2 of the following; o Alternative conditions with similar symptoms have been excluded. o Passage of the rectal mucus o Symptoms worsened by eating o Abdominal bloating (more common in women than men), distension or hardness o Altered stool passage (straining, urgency, incomplete evacuation)
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IBS is a diagnosis of exclusion, what investigations should be arranged to exclude other pathologies? (4)
FBC - Assess anaemia or raised platelet count (inflammation) Inflammatory markers - ESR/CRP (inflammation) Coeliac serology (exclude IgA-tTG and IgA-EMA) Ovarian cancer screen (Ca-125 elevated)
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Differentials for IBS - Give 2 other possible causes of constipation
Hypothyroidism Drug induced (codine)
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Differentials for IBS - Give 5 other possible causes of diarrhoea
IBD (Ulcerative colitis, Crohn's) Coeliac Disease GI infection Antibiotics Hyperthyroidism
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Differentials for IBS - Give 4 other possible causes for abdominal pain/discomfort
Diverticulitis Chronic pancreatitis Gallstones Peptic Ulcer Disease
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Describe the first-line pharmacological management of IBS according to the predominant symptom(3)
Pain - Antispasmodic agents - Mebeverine Constipation - Laxatives - Linaclotide, Ispaghula hust, methylcellulose (but avoid lactulose) Diarrhoea - Loperamide
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What is the 2nd line pharmacological medication for the treatment of pain in IBS?
Tricyclic antidepressants - Amitriptyline (Consider SSRI - fluoxetine/citalopram if contraindicated)
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Describe the general management of IBS (3)
Balanced diet - Adjust fibre intake according to symptoms (good for constipation, bad for diarrhoea) Consider reducing caffeine, alcohol, fizzy drinks Reduce FODMAP carbohydrates (these contribute to symptoms)
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What are the FODMAP carbohydrates that can contribute to IBS symptoms?
F - Fermentable O - Oligosaccharides (fructans) D - Diasaccharsides MAP - Monosaccharides And Polyols (One of the main foods to avoid is wheat)
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Name an antispasmodic used to treat abdominal pain/bloating in IBS
Mebeverine
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Name an anti-motility agent used to treat diarrhoea in IBS
Loperamide
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Name 2 bulk-forming laxatives used to treat constipation in IBS. In who are these contraindicated?
Ispaghula Husk and Methylcellulose Contraindicated in IBD, Intestinal Obstruction and Toxic Megacolon
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Name one mediation used to pharmaceutically treat constipation in IBS
Linaclotide
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Describe diverticulitis
Describes an infection of a diverticulum (an out-pouching of the intestinal mucosa)
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Describe diverticular disease
Describes the presence of diverticula (diverticulosis). A common surgical problem consisting of herniation of colonic mucosa through the muscular wall of the colon.
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What is thought to drive the formation of diverticula?
Increased intra-colonic pressure along weaker areas of the wall.
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Where is the usual site (in the colon wall) for diverticular disease to manifest?
Between the taenia coli where vessels pierce the muscle to supply the mucosa. (rectum is often spared as it doesn't contain taenia)
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Where are diverticula most commonly found?
Sigmoid colon
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Give 4 risk factors for diverticulitis
Age Lack of dietary fibre Obesity: especially in younger patients Sedentary lifestyle
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Patients presenting with diverticular disease typically present with a chronic history of what? (3)
Intermittent abdominal pain (lower left quadrant) Bloating Change in bowel habit: Constipation or diarrhoea
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Give 5 features of acute diverticulitis
Severe lower left quadrant pain Nausea and vomiting Diarrhoea/Constipation Urinary frequency, urgency or dysuria PR bleeding
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Give 4 complications (and their symptoms) of acute diverticulitis
Colovesical fistula (pneumaturia or faecaluria) Colovaginal fistula (vaginal passage of faeces or flatus) Abscess (tender abdominal mass, ongoing fever despite antibiotics) Sepsis (tachycardia, tachypnoea, hypotension, altered GCS)
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Give 4 clinical signs on examination of diverticulitis
Low grade pyrexia Tender Lower left Quadrant Guarding (may suggest complicated diverticulitis with perforation) Tachycardia
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What investigation should be avoided in diverticulitis and why?
Colonoscopy Due to increased risk of perforation
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Give 3 bedside investigations that would be useful to perform when ? diverticulitis (exclude other pathologies)
Vital signs (ensure patient is haemodynamically stable) Urinalysis (to exclude urological cause - UTI) Urine pregnancy test (exclude ectopic pregnancy in females of childbearing age)
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What imaging may be used to investigate diverticulitis?
CT abdomen and pelvis (If AKI then non-contrast CT scan)
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Describe the management of complicated diverticulitis
1st line - 5 days Co-amoxiclav + Fluids + Analgesia 2nd line - Co-trimoxazole or Metronidazole
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Name 2 types of peritonitis
Purulent and Faeculant
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How is purulent peritonitis managed?
Laparoscopic lavage or resection
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How is faeculant peritonitis managed?
Colonic resection
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Describe Hartmann's procedure and state when it is used. (3)
Used in severe cases of complicated diverticulitis. Involves removing the sigmoid colon (sigmoid colectomy) and forming an end colostomy. An anastomosis and colostomy reversal can be performed once the patient has recovered from the acute illness.
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What drug class should be avoided in diverticular disease and why?
NSAIDs Due to risk of perforation
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Describe and name the classification system used for diverticular disease
Hinchey classification; I - Para-colonic abscess II - Pelvic Abscess III - Purulent peritonitis IV - Faecal peritonitis
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