IBS Flashcards

1
Q

Irritable Bowel Syndrome
Diagnostic Criteria*

A

◦ Recurrent abdominal pain, on average, at least 1
day per week in the last 3 months, associated with
two or more of the following:
 1. Related to defecation
 2. Associated with a change in frequency of stool
 3. Associated with a change in form (appearance) of stool
 * Criterion fulfilled for the last 3 months with symptom
onset at least 6 months prior to diagnosis

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2
Q

Irritable Bowel Syndrome
Subjects with IBS can be subdivided by their
symptoms into subtypes

A

◦ Constipation-predominant (C-IBS)
◦ Diarrhoea-predominant (D-IBS)
◦ Mixed IBS (M-IBS or DA-IBS)
◦ Unsubtyped IBS

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3
Q

Irritable Bowel Syndrome
Aetiological Factors

A

Enhanced visceral perception –
 patients with IBS have been found to have increased visceral
sensation and visceral hyperalgaesia compared to healthy
controls (Delvaux, 2002)(Camilleri et al, 2002)

◦ Low-grade inflammation – (Camilleri et al, 2002)(Bercik et al, 2005)
 IBS patients show no identifiable inflammation on routine
colonic biopsies
 some do show increased expression of inflammatory
markers
 i.e., increased enterochromaffin and mast cell numbers, increased
intraepithelial T lymphocytes and increased mucosal interleukin-1 β
messenger RNA
 suggesting low-grade inflammation is present
 this mild mucosal inflammation is theorised to cause local
disruptions to neuromuscular function

◦ Altered GIT motility – (Coulis, 2001)(Serra et al, 2001)
 in C-IBS - significant delays in overall colonic transit
and decreased numbers of fast and propagated
colonic contractions compared to healthy controls
 in D-IBS – more rapid ileocolonic transit and colonic
transit
 impaired transit of intestinal gas

Altered GIT microflora (dysbiosis) –
 colonic fermentation studies have found patients with
IBS to produce significantly more colonic hydrogen
than healthy controls, as well as having altered faecal
short-chain fatty acid profiles (King et al, 1998)(Treem et al, 1996)
 lower faecal concentrations of bifidobacteria and
lactobacilli (Si et al, 2005)(Malinen et al, 2005)(Balsari et al, 1982)
 higher concentrations of Enterobacteriaceae

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4
Q

Irritable Bowel Syndrome
Risk Factors

A

◦ Familial disposition (Morris-Yates etal, 1995)(Locke et al, 1996)
 may contribute to the development of IBS in some patients
 this predisposition may not be disease specific but more
related to alterations in the responsiveness of the central
nervous system to stimuli

◦ Acute gastrointestinal infections (McKendrick and Read, 1994)(Gwee et al,
1999)(Mayer, 1999)(Rodriguez and Ruigomez, 1999)(Thabane et al, 2007)(Dai and Jiang, 2012)
 long-lasting alterations in mucosal function and structure
may be responsible for post-infective IBS
 increased intestinal permeability, increased expression of
inflammatory markers (such as interleukin-1β), and neuromuscular
dysfunction

◦ Antibiotic use (Mendall and Kumar, 1998)(Maxwell et al, 2002)(Villarreal et al, 2012)
 probably mediated via antibiotic-induced alterations in the
GIT microflora and/or enhanced visceral sensitivity

◦ Stressful and traumatic life events
 frequently reported to precede the initial onset of IBS
symptoms and symptom flare-ups in patients already
suffering from IBS (Bennett et al, 1998)(Whitehead et al, 1998)
 IBS has consistently been found to have a high degree of
psychiatric co-morbidities (Masand et al, 1995)(Hochstrasser and Angst, 1996)
 such as dysthymia, depression, panic disorder, and generalised
anxiety disorder

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5
Q

Irritable Bowel Syndrome
Consequences

A

◦ substantial impact on QOL
 Impacts physical functioning, mood, sexual functioning,
social functioning and even sleep
◦ economic
 absent 3-5% of work week
 report impaired productivity ~30% of the week
◦ substantial healthcare burden
 3.6 million visits annually in US due to IBS
 >$20 billion annually in direct and indirect expenditures

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6
Q

IBS –Treatment Aims

A

Optimise GIT microflora
‘Normalise’ bowel habit
Manage GIT symptoms
Support the nervous system
Decrease gut inflammation and diminish visceral
hypersensitivity
Improve liver function
Assess and manage food allergens and intolerances

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7
Q

How Optimise GIT Microflora

A

Prebiotics
Probiotics
Role for Antimicrobials?

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8
Q

Optimise GIT Microflora -
Prebiotics

A

Galactooligosaccharides (GOS)
◦ R, SB, PC, CO (Silk et al, 2009)
 3.5 g/day GOS or 7.0 g/day or placebo for 4 weeks to subjects
with IBS
 Results:
 3.5 g/day
 improvement in stool consistency, flatulence scores, bloating scores,
and overall IBS symptom scores compared to placebo (all P<0.05)
 7.0 g/day
 improvements in overall IBS symptom scores and a reduction in
anxiety levels compared to placebo (both P<0.05)
 increase in bloating scores relative to baseline (P<0.05

NB - FOS txt no better than placebo at end of trial

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9
Q

Optimise GIT Microflora - Probiotics

A

Lactobacillus plantarum 299v (Ducrotte et al, 2012)
◦ R, DB, PC; n=214
 all IBS sub-types included
◦ L.. plantarum 299v (1 x 1010 CFU/day) for 4 weeks
◦ Results:
 the frequency and severity of abdominal pain, bloating, and
feeling of incomplete evacuation scores were significantly
reduced in the 299v group compared to controls (all
P<0.05)
 stool frequency was significantly reduced in the 299v
group (P<0.05)
 78% of subjects in the 299v group scored the symptomatic
effect as excellent or good vs 8% of controls (P<0.01)

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10
Q

Manage GIT Symptoms
Three gastrointestinal symptoms have the
greatest negative impact upon quality of
life:

A

◦ straining at stool
◦ abdominal pain
◦ abdominal bloating

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