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Walkerton Health Study (post-infectious IBS)

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Design notes & limitations. One of the strongest post-infectious cohorts in the database: a whole-community denominator with a within-town unexposed comparator, quantifying post-infectious IBS after bacterial gastroenteritis (36.2% after clinically suspected GE vs 10.1% without). Non-fatigue outcome (IBS), broadening the syndrome coverage. Exposure was ascertained by self-reported acute illness rather than culture, the main limitation.

Identity & trigger

Cohort id
walkerton-health-study
Aliases
WHS
Outbreak / event
Walkerton waterborne gastroenteritis outbreak, May 2000 (Ontario, Canada)
Pathogen
Campylobacter jejuni / E. coli O157:H7 (Walkerton outbreak) (Mixed)
Exposure ascertainment
clinical diagnosis

Design

Design
Retrospective cohort
Denominator defined
Yes
Denominator method
Adult Walkerton residents with no prior chronic GI disorder, classified by whether they had acute gastroenteritis during the May 2000 municipal water contamination; residents without acute GE form the unexposed comparison.
Recruitment
community
Time zero
May 2000 waterborne gastroenteritis outbreak (Campylobacter jejuni / E. coli O157:H7) (month)
Control group
Unexposed (unmatched)

Size & attrition

Enrolled
2069
Analysed / enrolled
2069/2069 (100%)
Max follow-up (months)
96

Biospecimens

Specimens
No
Types
none
Acute-phase specimens
No
Biobank
N/A
External access
Unknown

Observations (1)

Symptoms

36.2% Proportion

Measure
Irritable bowel syndrome (post-infectious) sym:irritable-bowel-syndrome
As worded
“post-infectious irritable bowel syndrome 2 years after outbreak in those with clinically suspected gastroenteritis vs those without acute gastroenteritis”
Population
whole cohort · denominator Unclear · N=measured, not reported
Timing
24 mo (12-24 mo) · ref Not reported
Method
Unclear · Rome criteria for irritable bowel syndrome
Comparator
Unexposed (unmatched): 10.1%
Comparability signature
42693faea9 — measure sym:irritable-bowel-syndrome · Unclear · ref Not reported · denom Unclear · 12-24 mo · Proportion
Provenance
Results/Abstract (36.2% with suspected GE vs 10.1% without) · Manual · verified OSMF research-tracker (web-verified against source) on 2026-07-20

Publications

Provenance & verification

Registration
n/r
Funders
Ontario Ministry of Health and Long-Term Care, Canadian Institutes of Health Research
Related cohorts
none
Symptom-inventory scope
Single domain
Last verified
2026-07-20 — OSMF research-tracker (web-verified against source)