Evidence map›Paper›PMID 41886423›Full record

ArticlePloS one2026

Population-based incidence and antimicrobial susceptibility patterns of shigellosis among children and adults from rural and urban Kenya, 2010-2019.

Richard Omore, Billy Ogwel, John B Ochieng, Jane Juma, Victor Omballa, Alice Ouma, George Aol, Allan Audi, George O Agogo, George Odongo and 14 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Richard OmoreKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.ORCID https://orcid.org/0000-0003-3702-3030
Billy OgwelKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
John B OchiengKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Jane JumaKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Victor OmballaKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Alice OumaKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
George AolKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Allan AudiKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
George O AgogoDivision of Global Health Protection (DGHP), Kenya Office of the US Centers for Disease Control and Prevention, Nairobi, Kenya.
George OdongoDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Clayton OnyangoDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Newton WamolaKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Terry KomoKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Daisy ChepkemoiKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Elizabeth HunspergerDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Daniel R FeikinDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Joel M MontgomeryDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Marc-Alain WiddowsonDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Graeme Prentice-MottDivision of Foodborne, Waterborne, and Environmental Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Eric D MintzDivision of Foodborne, Waterborne, and Environmental Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Robert F BreimanDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Patrick K MunywokiDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Godfrey M BigogoKenya Medical Research Institute-Center for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
Jennifer R VeraniDivision of Global Health Protection, Centre for Global Health, US Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0001-5267-1883

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgrounShigella is an important cause of diarrheal morbidity and mortality globally. Data on disease burden across age groups, in different epidemiologic settings, and over time are needed to guide preventive strategies. We examined shigellosis in two sites in Kenya over a 10-year period.

methodsWe used data from the Population-Based Infectious Disease Surveillance (PBIDS) platform in a rural (Asembo, population ~35,000) and urban (Kibera, population ~23,000) setting. PBIDS participants presenting to surveillance clinics with diarrhea (≥3 loose stools in 24-hour period) had stool collected and cultured; Shigella isolates underwent antimicrobial susceptibility testing. We estimated incidence by dividing Shigella cases by person-years- observation, adjusting for the proportion of diarrhea cases with stool collected and for care-seeking outside surveillance clinics.

resultsFrom January 1, 2010 to December 31, 2019, we isolated Shigella from 23% and 15% of 2,017 and 4,074 stool specimens collected in Asembo and Kibera, respectively; S. flexneri accounted for 61% and 67%, respectively. In Asembo, the adjusted shigellosis incidence was 684/100,000; it was highest in ages 12-23 months (1,873/100,000) and ≥50 years (1,502/100,000). In Kibera, the adjusted incidence was 647/100,000, highest in ages 12-23 (2,828/100,000) and 24-59 months (936/100,000). Incidence declined significantly in Asembo (p = 0.009), but not in Kibera (p = 0.53). Overall, ≥ 97% of isolates were susceptible to ciprofloxacin and ceftriaxone.

conclusionThe shigellosis burden was greatest among young toddlers in both urban and rural areas and was high among older adults in the rural setting. Although resistance to first-line antibiotics was infrequent, continued susceptibility monitoring is warranted.

Indexed as

Anti-Bacterial AgentsDysentery, BacillaryShigellaAdolescentAdultChildChild, PreschoolFecesFemaleHumansIncidenceInfantKenyaMaleMicrobial Sensitivity TestsMiddle AgedAnti-Bacterial Agents

Identifiers

PMID41886423
PMCPMC13020798

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.