Evidence map›Paper›PMID 28369261›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Gastrointestinal Carriage Is a Major Reservoir of Klebsiella pneumoniae Infection in Intensive Care Patients.

Claire L Gorrie, Mirjana Mirceta, Ryan R Wick, David J Edwards, Nicholas R Thomson, Richard A Strugnell, Nigel F Pratt, Jill S Garlick, Kerri M Watson, David V Pilcher and 4 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 344 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
344citing papers in PubMed, 2 pooled it
–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

344 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  20. Expanding Threat of Carbapenemase-ProducingbioRxiv : the preprint server for biology · 2026
    Article

284 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Claire L GorrieDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute.
Mirjana MircetaMicrobiology Unit, Alfred Health, Melbourne, Victoria, Australia.
Ryan R WickDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute.
David J EdwardsDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute.
Nicholas R ThomsonWellcome Trust Sanger Institute, Hinxton, Cambridgeshire, United Kingdom.
Richard A StrugnellDepartment of Microbiology and Immunology at the Peter Doherty Institute for Infection and Immunity, The University of Melbourne.
Nigel F PrattInfectious Diseases Clinical Research Unit.
Jill S GarlickInfectious Diseases Clinical Research Unit.
Kerri M WatsonInfectious Diseases Clinical Research Unit.
David V PilcherIntensive Care Unit, The Alfred Hospital.
Steve A McGloughlinIntensive Care Unit, The Alfred Hospital.
Denis W SpelmanMicrobiology Unit & Department of Infectious Diseases, The Alfred Hospital, Melbourne, Victoria, Australia.
Adam W J JenneyMicrobiology Unit & Department of Infectious Diseases, The Alfred Hospital, Melbourne, Victoria, Australia.
Kathryn E HoltDepartment of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute.

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundKlebsiella pneumoniae is an opportunistic pathogen and leading cause of hospital-associated infections. Intensive care unit (ICU) patients are particularly at risk. Klebsiella pneumoniae is part of the healthy human microbiome, providing a potential reservoir for infection. However, the frequency of gut colonization and its contribution to infections are not well characterized.

methodsWe conducted a 1-year prospective cohort study in which 498 ICU patients were screened for rectal and throat carriage of K. pneumoniae shortly after admission. Klebsiella pneumoniae isolated from screening swabs and clinical diagnostic samples were characterized using whole genome sequencing and combined with epidemiological data to identify likely transmission events.

resultsKlebsiella pneumoniae carriage frequencies were estimated at 6% (95% confidence interval [CI], 3%-8%) among ICU patients admitted direct from the community, and 19% (95% CI, 14%-51%) among those with recent healthcare contact. Gut colonization on admission was significantly associated with subsequent infection (infection risk 16% vs 3%, odds ratio [OR] = 6.9, P < .001), and genome data indicated matching carriage and infection isolates in 80% of isolate pairs. Five likely transmission chains were identified, responsible for 12% of K. pneumoniae infections in ICU. In sum, 49% of K. pneumoniae infections were caused by the patients' own unique strain, and 48% of screened patients with infections were positive for prior colonization.

conclusionsThese data confirm K. pneumoniae colonization is a significant risk factor for infection in ICU, and indicate ~50% of K. pneumoniae infections result from patients' own microbiota. Screening for colonization on admission could limit risk of infection in the colonized patient and others.

Indexed as

Gastrointestinal MicrobiomeIntensive Care UnitsAdultAgedAnti-Bacterial AgentsCarrier StateCohort StudiesCross InfectionFemaleGastrointestinal TractGenetic VariationHumansKlebsiella InfectionsKlebsiella pneumoniaeMaleMicrobial Sensitivity TestsAnti-Bacterial Agentsgastrointestinal colonizationgenomic epidemiologyhospital acquired infectionintensive careKlebsiella pneumoniae

Identifiers

PMID28369261
PMCPMC5850561

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Registered trials

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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.