IBS IBD Flashcards

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1
Q

Discuss epidemiology of IBD

A
  • Generally 1st world problem ,increasing 3rd world
  • Increasing incidence in Australia 29 per 100,000
    Prevalence 200 – 400 per 100,000 (65,000 Australians)
    Can occur at any age
    Peak age of onset between 15 and 30 years
    Affects males and females equally
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2
Q

Discuss theories of IBD aetiology

A

toxic response to luminal contents
* specific microbial pathogen
* abnormal luminal constituents
* increased absorption of luminal macromolecules
enhanced immune response to normal constituents
autoimmune response
* to epithelial cell or mucous glycoprotein
* molecular mimicry
* to immune cells

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3
Q

Discuss pathogenesis of IBD

A

Genetics
Infection
* Mycobacterium paratuberculosis
* measles virus
* microbiome
Smoking
Diet
Medications: aspirin, NSIADs, OCP
Stress

Evidence of genetic influence
Prevalence varies among different populations
Risk increased (5 - 20-fold) among first degree relatives
Child of a parent with IBD has 5% risk of developing IBD
Greater concordance among monozygotic (50 - 70%) than dizygotic (5 – 10%)
twins
Identification of “susceptibility genes” (NOD2/CARD 15)

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4
Q

Describe UC features and histology

A

Diffuse mucosal inflammation
Always involves rectum
Extend proximally in a continuous fashion
Limited to colon
Location/Extent not static

Mucosal / Submucosal
Lymphocytic infiltrate
Goblet cell depletion
Crypt distortion
Cryptitis
Crypt abscesses
No granulomas

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5
Q

Describe Crohns features and histology

A

Segmental transmural inflammation
Skip lesions separated by areas of normal bowel
May affect any part of GIT

Transmural inflammation
Infiltrate of lymphocytes
and macrophages
Granulomas in >50% of
cases

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6
Q

Compare and contrast UC and Crohn’s ant vs path, location, symptoms

anatomy and pathoglogy

A
  • UC 95% rectal, 75% lieft sided colitis, 15-25% pancolitis
  • Crohn’s: 40% only SI, 30% ileocolonic, 30% colon only

Pain more likely in cROHN;S
MALAISE in both, slighyly more common in UC
fever in both
Diarrhoea overwhelmingly in UC

Stools way more bloody in UC
More pus and mucusin Crohns’

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7
Q

Discuss how to establish a diagnosis of IBD and the role of biomarkers

A

History and examination
* Findings depend on disease location, extent and severity
Laboratory tests
* CRP, ESR, platelet count, faecal calprotectin
Endoscopy and histology
Imaging
* CT, MRI
Serology
* ASCA, ANCA generally unhelpful

Biomarkers can help: eg CFP, FCP
- diagnosis ie to distinguish from functional disease ie IBS
- evaluate dusease activity
- predict therapeutic effect at start of treatment
- predict remission/recurrence

Ala Mayo iscore and Crhon;’s index fro UC and Crhn’s

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8
Q

List systemic complications of IBD

A

Oral ulcers
Large joint arthritis and ankylosing spondylitis
Episcleritis, iritis and uveitis
Erythema nodosum
Pyoderma gangrenosum
Sclerosing cholangitis
Gallstones and renal stones

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9
Q

Discuss therapy goals for IBD

A

Short-term: Induce remission
* Relieve symptoms
* Improve quality of life
Long-term: Maintain remission
* Control inflammation (without need for steroids)
* Prevent recurrence of symptoms (flares)
* Prevent complications (of disease and treatment)
* Reduce need for hospitalisation and surgery
* Maintain quality of life

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10
Q

Discuss an optimised therapeutic approach

A

Early diagnosis
Rapid induction of remission
Clear definition of
* Goals of therapy
* Time frame required to achieve goals
Minimal side effects of treatment
Adherence and compliance
Recognising when therapy is ineffective
Escalating therapy in timely manner

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11
Q

List therapeutic options

A

5-ASAs - more for UC
FMT - mixed data, efficaicy aafety and patient acceptability
CS to induceNOT to maintain - in both
AZA/6-MP
anti TNF - require drug monitoring, switch out of class or escaate or switch to antohte
anti integrin
anti cytokin

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12
Q

Discuss surgical optioons

A

creating a pouch eg J , W, S

Stool frequency 6 to 8 per day
Reduced fertility
Pouchitis
* Affects 15 –50%
* Predictors include PSC, pANCA, non-smoking
* Treatment with Ciprofloxacin, metronidazole
* Prophylaxis with Probiotics (VSL#3

87% of patients (failed medical therapy, complications,
initial presentation)
Stricturoplasty
Resection
Treatment of fistulas/setons
Ileostomy

inevitably recurs after: resect, perforates, smoke

note risk of cancer with IBD

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13
Q

What are some other management issues in IBD

A

Smoking cessation
Nutrition
Osteoporosis
Psychological wellbeing
Vaccination
* COVID-19, flu, pneumococcus, HBV, HPV, VZV (live vaccine)
Cancer prevention
* Skin checks, Pap smears, colonoscopy

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14
Q

Discuss pregnancy and IBD

A

Increased rates of adverse outcomes (active disease)
* SGA, LBW, preterm birth, foetal loss
Conflicting data regarding rates of congenital anomalies
Most medications are safe
Best outcomes if remission prior to conception and during
pregnancy
all but MTX ruled in

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15
Q

Describe diagnostic criteria in IBS

A

Recurrent abdominal pain on average at least 1
day/week in the last 3 months, associated with two
or more of the following criteria:
* Related to defaecation
* Associated with a change in frequency of stool
* Associated with a change in form (appearance) of stool
* Criteria fulfilled for the last 3 months with symptom
onset at least 6 months prior to diagnosis

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16
Q

List and describe IBS subtypes

A

IBS with constipation—hard or lumpy stools ≥25% and
loose (mushy) or watery stools ≤25% of bowel
movements
* IBS with diarrhoea—loose (mushy) or watery stools
≥25% and hard or lumpy stool ≤25% of bowel
movements
* Mixed IBS—hard or lumpy stools ≥25% and loose
(mushy) or watery stools ≥25% of bowel movements
* Unsubtyped IBS—insufficient abnormality of stool
consistency to meet criteria for IBS with constipation,
diarrhea, or mixed

17
Q

Discuss the pathophysiology of IBS

A

Multi-factorial
Likely has biome/inflammatory components
- psychosical: mood disorders, lfie stress, personality, social suppport, eucation, abuse history
- env: gneetics, early breastfeed, GFODMAP, fibre or H20 intake, Gi infection
- Gut physiology: motility, sensation, infakmmatuoin, permaeability, brain response to afferent pain signals, dysbiosis, bile acid malabsorption and pancreatic insufficiency

Produce IBS symptopms, behaviour and QOL influence

18
Q

Discuss IBS therapeuti approach

A

Stepwise
- dietary modifications
- laxatives or diarrheals
- other supportive care

UP to
- cl channel activators, serotonin modulators, antibiotics, guantle cyclse agent

  • tricyclics, SNRUM SSERI

Psychodynamic, stress recutiion etc

Depends on impact on QOL, patient comorbs, etc

Mainly symptomatic relief