Gastrointestinal Flashcards
Name 2 main forms of chronic autoimmune inflammatory bowel diseases
Ulcerative Colitis - Only affects the colon (mucosa)
Crohn’s Disease - Can affect any part of the gut from mouth to anus
Define ulcerative colitis
Describes a relapsing remitting inflammatory bowel disease characterised by diffuse, continuous superficial inflammation of the colonic mucosa
Where does ulcerative colitis mainly affect?
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.
Give 4 risk factors for Ulcerative Colitis
Positive Family History
HLA-B27
Infection (50% of relapses are associated with enteritis)
NSAIDS (may exacerbate UC)
Describe the epidemiology of Ulcerative Colitis (3)
Age of onset = 20-40 years old
Slight female predominance
3x more common in NON smokers
Describe the macroscopic pathophysiology of ulcerative colitis
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.
Describe the microscopic pathophysiology of ulcerative colitis (4)
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)
How does Ulcerative Colitis appear on a barium enema
Lead pipe appearance of colon
(loss of haustral markings)
Give 5 intestinal symptoms of ulcerative colitis
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)
Give 6 extraintestinal symptoms of Ulcerative Colitis
Uveitis
Primary Sclerosing Cholangitis
Colorectal cancer
Pallor, clubbing, mouth ulcers
Erythema nodosum
Pyoderma gangrenosum
What tests are performed to diagnosed Ulcerative Collitis? (5)
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)
What additional tests would be useful to conduct in ? Ulcerative Colitis to exclude other pathologies? (4)
Upper intestinal endoscopy (exclude Crohn’s)
Coeliac serology (exclude coeliac)
Thyroid function tests (exclude hyperthyroidism)
U&Es (to assess dehydration/electrolyte disturbance)
What criteria is used to classify Ulcerative Colitis?
Truelove and Witts Criteria
Describe the Truelove and Witts Criteria for mild Ulcerative Colitis
Motions - <4
PR bleed - Small
Temp - Apyrexic
HR - <70
Hb >11
ESR <30
Describe the Truelove and Witts Criteria for Moderate Ulcerative Colitis
Motions - 4-6
PR bleed - Moderate
Temp - 37.1-37.8
HR - 70-90
Hb - 10.5-11
Describe the Truelove and Witts Criteria for Severe Ulcerative Colitis
Motions - >6
PR bleed - Large
Temp - >37.8
HR - >90
Hb - <10.5
ESR - >30
What type of surveillance is it important for Ulcerative Colitis patients to have?
Colonoscopic Surveillance for colorectal cancer
What is the goal of treatment for Ulcerative Colitis?
To induce and maintain remission
Describe the treatment for Mild-Moderate Proctitis (Ulcerative Colitis localised to the rectum) (1st, 2nd, 3rd line and maintaining remission)
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
Describe the treatment for mild-moderate proctosigmoiditis/left sided Ulcerative Colitis (1st, 2nd, 3rd line and maintaining remission)
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
Describe the treatment for mild-moderate extensive Ulcerative Colitis (1st, 2nd line and maintaining remission)
1st line - Topical aminosalicylate (mesalazine) + High dose oral aminosalicylate (sulfasalazine)
2nd line - Oral aminosalicylate (sulfasalazine) + Oral Prednisolone
Maintain remission - Oral aminosalicylate (sulfasalazine)
Describe the treatment for severe ulcerative colitis
1st line - Anti- TNFa monoclonal antibody - Infliximab
2nd line - Monoclonal antibody - Ustekinumab
What is the treatment for Acute Severe Ulcerative Colitis requiring hospitalisation? (1st, 2nd, 3rd line)
1st line - IV corticosteroids +/- Surgery
2nd line - IV Ciclosporin
3rd line - Infliximab
Patients with acute severe ulcerative colitis may need surgery if? (5)
Passing stool >8x per day
Pyrexic
Tachycardic
Abdominal X-ray showing megacolon
Low albumin, low Hb, High platelet count or CRP >46mg/L
What medication should ulcerative colitis patients receive following a severe relapse or >=2 exacerbations in the past year?
Oral azathioprine or oral mercaptopurine
What do Oral thiopruines (azathioprine or mercaptopurine) increase the risk of developing?
Non-melanoma skin cancer
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)
Where in the GI tract is usually most affected in Crohn’s disease?
Terminal ileum
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)
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
What are the 4 layers of the intestinal wall?
Mucosa
Submucosa
Muscularis propria
Serosa
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)
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)
What eye problem can occur in Crohn’s disease?
Episcleritis
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)
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.
What is the goal of treatment for Crohn’s Disease?
To induce and maintain remission
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)
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)
When should Crohn’s patients be considered for surgery? (3)
Failure to respond to medical treatment
Intestinal Obstruction or Perforation (fistula)
Massive haemorrhage
What treatment should Crohn’s patients whom have undergone surgery be offered to maintain remission?
Azathioprine + Metronidazole (antibiotic) for up to 3 months.
Describe the differences between Ulcerative Colitis and Crohn’s with regards to diarrhoea
UC - Bloody diarrhoea
Crohn’s - Not usually bloody
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)
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
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
Describe the differences between Ulcerative Colitis and Crohn’s with regards to complications
UC - Colorectal cancer
Crohn’s - Obstruction (structure), Perianal disease, colorectal cancer
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)
Define coeliac disease
Aka gluten sensitive enteropathy.
Coeliac disease describes a T cell mediated, chronic autoimmune disorder triggered by exposure to ingested gluten
What foods components will you find gluten?
Wheat, Barley and Rye
How and Where does coeliac disease commonly manifest?
Commonly manifests in the duodenum as villous atrophy and malabsorption.
Give 3 associations for Coeliac Disease
HLA-DQ2 and HLA-DQ8
Autoimmune disorders (T1DM, Hashimotos, IgA deficiency)
Herpetiformis (a vesicular pruritic skin eruption)
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
What antibodies are present in coeliac disease
Anti-gliadin and Anti-transglutaminase antibodies
Give 3 complications of coeliac disease
Depression, anxiety, eating disorders
Delayed growth/puberty in children
Nutritional deficiencies (iron, B12, folate, osteoporosis)
Give 5 gastrointestinal symptoms of coeliac disease
Diarrhoea
Steatorrhoea + foul smelling stools
Abdominal pain
Weight loss/Failure to therive
Aphathous ulceration
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
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
What features are present on histology for coeliac disease? (3)
Villous atrophy
Crypt hyperplasia
Increased intraepithelial lymphocytes
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)
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
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
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.
Define appendicitis
Describes an acute inflammation of the appendix and is the most common surgical emergency.
How does appendicitis commonly present
Umbilical pain that moves to the lower right quadrant (McBurney’s Point)
What is the appendix anatomically connected to?
Caecum
What is the most common cause of appendicitis?
Luminal obstruction by faecolith
Give 5 complications of appendicitis
Abscess formation
Peritonitis
Sepsis
Intra-abdominal adhesions
Bowel obstruction
Between what ages does appendicitis most commonly present?
Between 10-20 years old
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
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)