Background prevalence of subclinical Shiga toxin-producing Escherichia coli in children attending childcare facilities in the Irish Midlands

Abstract Background Exclusion of asymptomatic shedders of Shiga toxin-producing Escherichia coli (STEC) from childcare facilities (CCFs) is a recognized measure to minimize risk of secondary transmission. This is predicated on factors including an assumption of low background prevalence of STEC amon...

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Veröffentlicht in:Journal of public health (Oxford, England) England), 2020-11, Vol.42 (4), p.766-771
Hauptverfasser: Burns, H, Fallon, U, Collins, A, Ni Shuilleabhain, C
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Sprache:eng
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Zusammenfassung:Abstract Background Exclusion of asymptomatic shedders of Shiga toxin-producing Escherichia coli (STEC) from childcare facilities (CCFs) is a recognized measure to minimize risk of secondary transmission. This is predicated on factors including an assumption of low background prevalence of STEC amongst CCF attendees. There is a paucity of scientific evidence regarding the true prevalence of STEC in paediatric populations. The study aimed to develop and test a methodology to estimate background prevalence of STEC amongst CCF attendees at regional level in Ireland. Methods Computerized Infectious Disease Reporting data were used to compile a list of outbreaks of STEC occurring in CCFs in the Irish Midlands since the introduction of polymerase chain reaction (PCR)-based testing. Laboratory data were used to determine background prevalence of STEC in screened children in each outbreak individually and across all outbreaks. Results A pooled summary prevalence estimate of 2.9% (95% confidence interval 1.4–5.5%) was determined for the entire screened cohort across all outbreaks. Sensitivity analysis supported the validity of the estimate. Conclusions The relatively high prevalence estimate of 2.9% suggests that a public health risk assessment approach to return of prolonged asymptomatic shedders to the CCF may be appropriate in peak STEC season in the Midlands.
ISSN:1741-3842
1741-3850
DOI:10.1093/pubmed/fdz166