Evidence map›Paper›PMID 27788691›Full record

ArticleEpidemiology and infection2017

Outbreak of KPC-3-producing ST15 and ST348 Klebsiella pneumoniae in a Portuguese hospital.

D Vubil, R Figueiredo, T Reis, C Canha, L Boaventura, G J DA Silva

Abstract read
In one paragraph

Article in Epidemiology and infection, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Prevalence and features of hypervirulentInfection and immunity · 2025
    Review
  5. Article
  6. Molecular and virulence differences ofFrontiers in microbiology · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Genomic Analysis of Carbapenem-Resistant HypervirulentInfection and drug resistance · 2023
    Article
  11. Article
  12. TEM,CTX-M,SHV Genes in ESBL-ProducingAntibiotics (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Treatment for carbapenem-resistant Enterobacterales infections: recent advances and future directions.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Characterization of Carbapenem-ResistantInfection and drug resistance · 2021
    Article
  19. Article
  20. An Emerging Clone, Klebsiellapneumoniae Carbapenemase 2-Producing K. pneumoniae Sequence Type 16, Associated With High Mortality Rates in a CC258-Endemic Setting.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    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

6 authors.

D VubilFaculdade de Farmácia,Universidade de Coimbra,Portugal.
R FigueiredoFaculdade de Farmácia,Universidade de Coimbra,Portugal.
T ReisCentro Hospitalar e Universitário de Coimbra,Portugal.
C CanhaCentro Hospitalar e Universitário de Coimbra,Portugal.
L BoaventuraCentro Hospitalar e Universitário de Coimbra,Portugal.
G J DA SilvaFaculdade de Farmácia,Universidade de Coimbra,Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To date, only a few sporadic cases of infections due to Klebsiella pneumoniae carbapenemase (KPC) producers have been reported in Portugal. Here, we report for the first time an outbreak of K. pneumoniae KPC-3 producers in a tertiary-care hospital during 2013. Twenty-seven ertapenem-resistant K. pneumoniae were identified in patients at a tertiary-care hospital during 2013 isolated predominantly from urine (48·1%) and blood (25·9%) cultures. All isolates were highly resistant to β-lactam antibiotics and most showed intermediate resistance to imipenem. The more frequent β-lactamases were TEM- (77·7%), CTX-M- (70·3%) and KPC-type (66·6%). KPC-3 was identified by sequencing. The bla KPC-3 gene was associated with an IncF plasmid, and efficiently transferred to E. coli J53. Pulsed-field gel electrophoresis typing revealed three clusters of isolates which were further characterized by multi-locus sequence typing as ST11, ST15 and ST348. Ertapenem-resistant ST15 was already in circulation in the hospital, related to expression of OmpK36 modified porin, but the other two sequence types had not been previously found in the hospital. We conclude that the IncF plasmid mediated transfer of KPC-3 in the outbreak and that implementation of carbapenemase gene screening in isolates from patients on admission to hospital is advisable in order to control dissemination of these antimicrobial resistance elements.

Indexed as

Disease OutbreaksGenotypeAnti-Bacterial AgentsBacterial Proteinsbeta-Lactamasesbeta-Lactam ResistanceBloodCluster AnalysisCross InfectionElectrophoresis, Gel, Pulsed-FieldEscherichia coliGene Transfer, HorizontalHumansKlebsiella InfectionsKlebsiella pneumoniaeMultilocus Sequence TypingAnti-Bacterial AgentsBacterial Proteinsbeta-lactamase KPC-3, Klebsiella pneumoniaebeta-LactamasesAntimicrobial resistancecarbapenemaseepidemiologyoutbreakβ-lactamase KPC-3

Identifiers

PMID27788691
PMCPMC9507641

What OpenQuestion holds

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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.