Evidence map›Paper›PMID 31931046›Full record

ArticleThe Journal of hospital infection2020

Risk factors for Klebsiella pneumoniae carbapenemase (KPC) gene acquisition and clinical outcomes across multiple bacterial species.

A J Mathers, K Vegesana, I German-Mesner, J Ainsworth, A Pannone, D W Crook, C D Sifri, A Sheppard, N Stoesser, T Peto and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of hospital infection, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Antimicrobial agents and chemotherapy · 2026
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  2. GenusMicroorganisms · 2026
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  8. Epidemiological data on the acquisition of carbapenem-resistantAntimicrobial stewardship & healthcare epidemiology : ASHE · 2025
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  9. [DISTRIBUTION OF CARBAPENEMASES IN TUNISIAN BURN PATIENTS].Annals of burns and fire disasters · 2024
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  13. Detection and Characterization of Carbapenemase-ProducingAntibiotics (Basel, Switzerland) · 2023
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  18. Carbapenem-ResistantAntibiotics (Basel, Switzerland) · 2021
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  19. Long-Term Carbapenems Antimicrobial Stewardship Program.Antibiotics (Basel, Switzerland) · 2020
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  20. Article
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

12 authors at 4 institutions in 2 countries.

A J MathersDivision of Infectious Disease and International Health, Department of Medicine, University of Virginia Health System, Charlottesville, VA, USA; Clinical Microbiology Laboratory, Department of Pathology, University of Virginia Health System, Charlottesville, VA, USA. Electronic address: ajm5b@virginia.edu.
K VegesanaHealth Information and Technology, University of Virginia Health System, Charlottesville, VA, USA.
I German-MesnerHealth Information and Technology, University of Virginia Health System, Charlottesville, VA, USA.
J AinsworthHealth Information and Technology, University of Virginia Health System, Charlottesville, VA, USA.
A PannoneDepartment of Public Health Sciences, University of Virginia, School of Medicine, Charlottesville, VA, USA.
D W CrookNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; National Institutes of Health Research, Health Protection Research Unit in Healthcare Associated Infection and Antimicrobial Resistance, University of Oxford, Oxford, UK.
C D SifriDivision of Infectious Disease and International Health, Department of Medicine, University of Virginia Health System, Charlottesville, VA, USA; Office of Hospital Epidemiology, University of Virginia Health System, Charlottesville, VA, USA.
A SheppardNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
N StoesserNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; National Institutes of Health Research, Health Protection Research Unit in Healthcare Associated Infection and Antimicrobial Resistance, University of Oxford, Oxford, UK.
T PetoNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
A S WalkerNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; National Institutes of Health Research, Health Protection Research Unit in Healthcare Associated Infection and Antimicrobial Resistance, University of Oxford, Oxford, UK.
D W EyreNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK; Big Data Institute, University of Oxford, Oxford, UK.
University of Virginia Health System · USUniversity of Oxford · GBNational Institute for Health Research · GBUniversity of Virginia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRisk factors for carbapenemase-producing Enterobacterales (CPE) acquisition/infection and associated clinical outcomes have been evaluated in the context of clonal, species-specific outbreaks. Equivalent analyses for complex, multi-species outbreaks, which are increasingly common, are lacking.

methodsBetween December 2010 and January 2017, a case-control study of Klebsiella pneumoniae carbapenemase (KPC)-producing organism (KPCO) acquisition was undertaken using electronic health records from inpatients in a US academic medical centre and long-term acute care hospital (LTACH) with ongoing multi-species KPCO transmission despite a robust CPE screening programme. Cases had a first KPCO-positive culture >48 h after admission, and included colonizations and infections (defined by clinical records). Controls had at least two negative perirectal screens and no positive cultures. Risk factors for KPCO acquisition, first infection following acquisition, and 14-day mortality following each episode of infection were identified using multi-variable logistic regression.

resultsIn 303 cases (89 with at least one infection) and 5929 controls, risk factors for KPCO acquisition included: longer inpatient stay, transfusion, complex thoracic pathology, mechanical ventilation, dialysis, and exposure to carbapenems and β-lactam/β-lactamase inhibitors. Exposure to other KPCO-colonized patients was only a risk factor for acquisition in a single unit, suggesting that direct patient-to-patient transmission did not play a major role. There were 15 species of KPCO; 61 (20%) cases were colonized/infected with more than one species. Fourteen-day mortality following non-urinary KPCO infection was 20% (20/97 episodes) and was associated with failure to achieve source control.

conclusionsHealthcare exposures, antimicrobials and invasive procedures increased the risk of KPCO colonization/infection, suggesting potential targets for infection control interventions in multi-species outbreaks. Evidence for patient-to-patient transmission was limited.

Indexed as

Academic Medical CentersAdultAgedAged, 80 and overBacterial Proteinsbeta-LactamasesCarbapenemsCase-Control StudiesCross InfectionFemaleHumansKlebsiella InfectionsKlebsiella pneumoniaeMaleMiddle AgedRisk FactorsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsRNF123 protein, humanUbiquitin-Protein LigasesCarbapenemase-producing Enterobacterales (CPE)Carbapenemase-producing organisms (CPO)Carbapenem-resistant Enterobacterales (CRE)Klebsiella pneumoniae carbapenemase (KPC)Multi-species clinical risk

Identifiers

PMID31931046
PMCPMC7193892
OpenAlexW2999396473

What OpenQuestion holds

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Registered trials

None linked

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.