Inflammatory bowel disease Flashcards

1
Q

What is ulcerative colitis and where does it affect?

A
  • UC is a relapsing + remitting inflammatory disorder of colonic mucosa
  • may affect:
    • just the rectum (proctitis ~30%)
    • extend to involve part of colon (left-sided colitis, in ~40%)
    • entire colon (pancolitis, in ~30%)
  • never’ spreads proximal to ileocaecal valve (except for backwash ileus)
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2
Q

What are the main risk factors for UC?

A
  • FHx of IBD → between 10-20% of pts have at least 1 family member w/ IBD
  • HLA-B27 → identified in most pts w/ UC
  • Infection → up to 50% of relapses of colitis are associated w/ enteritis due to recognised pathogens
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3
Q

What are the clinical features of UC?

A
  • Acute attacks alternate w/ asymptomatic intervals
  • Chronically active course (>2 relapses/year)
  • Incomplete remission despite adequate treatment
  • Diarrhoea w/ macroscopic visible blood + mucus
  • Abdominal pain, tenesmus
  • Tenderness (left lower abdo)
  • Extra-intestinal → anaemia, fever, weight loss, malaise, arthritis, sacroilitis, erythema nodosum, pyoderma gangraenosum, eye symptoms
  • Concomitant disease → PSC, amyloidosis, liver disease, ank spond
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4
Q

What is the pathophysiology of UC?

A
  • microscopically, UC usually involves ONLY THE MUCOSA
  • formation of crypt abscesses
  • coexisting depletion of goblet cell mucin
  • ulcerated areas soon covered by granulation tissue
  • undermining mucosa of XS of granulation tissue form polypoidal mucosal excrescences known as polyps or pseudopolyps
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5
Q

What are the investigations for UC?

A
  • Stool studies → faecal calprotectin
  • Bloods → FBC, LFTs, ESR, CRP
  • AXR → toxic megacolon
  • Flexi sigmoidoscopy
  • Colonoscopy + biopsies → widespread ulceration with preservation of adjacent mucosa which has appearance of polyps
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6
Q

How do you assess severity of a UC attack?

A
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7
Q

What is the management of UC?

A
  • Mild attackmesalazine (5-ASA) for remission-induction/maintenance; given PR for distal disease or PO For extensive disease, combine PO + PR if flare
  • Moderate attack → if 4-6 motions/day but otherwise well, induce remission w/ oral prednisolone 40mg/d for 1 wk, then taper by 5mg/week over 7 weeks → then maintain on 5-ASA
  • Severe attack → admit for: IV hydration/electrolyte replacement; IV steroids (hydrocortisone or methylprednisolone); rectal steroids (hydrocortisone); thromboembolism prophylaxis
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8
Q

What are the complications of UC?

A
  • Toxic megacolon → colon begins to widen (dilate), may be due to problems with muscle contraction or digestive reflexes; rare complication + occurs in 2.5% of those with UC
  • Colonic adenocarcinoma → develops in 3-5% pts w/ UC; risk increases with duration of disease
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9
Q

What is Crohn’s disease?

A
  • chronic inflammatory disease
  • characterised by transmural granulomatous inflammation
  • affecting any part of gut from mouth to anus (esp term ileum 70%)
  • unlike UC, there is unaffected bowel between areas of active disease (skip lesions)
  • age 15-40 or 60-80yrs → bimodal age distribution for onset
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10
Q

What are the clinical features of Crohn’s disease?

A
  • diarrhoeausually non-bloody
  • weight loss → Crohn’s > UC
  • systemic features → fatigue, fever, malaise, anorexia
  • abdo tenderness/mass → RIF
  • perianal abscess/fistulae/skin tags
  • mouth ulcers
  • clubbing
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11
Q

What is the pathophysiology of Crohn’s?

A
  • initial lesion starts as an inflammatory infiltrate around intestinal crypts
  • subsequently develops into ulceration of the superficial mucosa
  • inflammation progresses to involve deeper layers + forms non-caseating granulomas
  • granulomas involve ALL layers of intestinal wall + mesentry + regional lymph nodes
  • finding of these granulomas is highly suggestive of CD, yet absence does not exclude diagnosis
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12
Q

What investigations are done for Crohn’s?

A
  • stool MC+S → faecal calprotectin
  • bloods → FBC, iron studies, B12, folate, CRP, ESR
  • colonscopy + biopsy → cobble-stone appearance, histology to diagnose
  • CT/MRI → localises disease + diagnoses complications
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13
Q

What is the management of Crohn’s in terms of inducing remission?

A
  • conventional steroids (prednisolone, methylpred, IV hydrocortisone) to induce remission in people w/ a 1st presentation or single inflammatory exacerbation of CD in a 12 month period
  • in ppl w/ 1+ of distal ileal, ileocaecal or right-sided colonic disease who decline, cannot tolerate or in whom a conventional steroid is contraindicated → consider budesonide
  • consider adding azathioprine or mercaptopurine to conventional steroid or budesonide to induce remission in CD if:
    • 2+ inflammatory exacerbations in a 12-month period, OR
    • steroid dose cannot be tapered
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14
Q

What is the management of Crohn’s in terms of maintaining remission?

A
  • offer azathioprine or mercaptopurine as monotherapy to maintain remission
  • consider methotrexate to maintain remission only in people who
    • needed methotrexate to induce remission, OR
    • have tried but did not tolerate azathioprine or mercaptopurine
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15
Q

What are complications of Crohn’s?

A
  • intestinal obstruction → due to bowel wall thickening - presents w/ abdo pain, N+V, abdo distension + dilated bowel loops on AXR
  • malignancy → overall inc risk of cancer + inc risk of colon adenocarcinoma
  • kidney stones → develops in pt w/ severe disease due to inc absorption of oxalate, poor digestion of fats, acidosis + dehydration
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16
Q

Summary of differences between UC + CD?

A