Evidence map›Paper›PMID 29730830›Full record

ReviewCurrent infectious disease reports2018

The Epidemiology, Evolution, and Treatment of KPC-Producing Organisms.

Ann Marie Porreca, Kaede V Sullivan, Jason C Gallagher

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current infectious disease reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. In vitro and in vivo antibacterial activity of oral tebipenem in combination with novel β-lactamase inhibitors (avibactam, relebactam, vaborbactam) against KPC-producing Enterobacterales.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
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  9. Genomic analysis of chromosomal cointegratedFrontiers in cellular and infection microbiology · 2023
    Article
  10. Rapid quantitative detection ofFrontiers in bioengineering and biotechnology · 2023
    Article
  11. MALDI-TOF mass spectrometry for direct KPC detection among Enterobacterales.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2022
    Article
  12. Article
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  15. Application Effect of Transparent Supervision Based on Informatization in Prevention and Control of Carbapenem-ResistantThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2022
    Article
  16. Article
  17. Safety and Efficacy of a Phage, kpssk3, in anFrontiers in microbiology · 2021
    Article
  18. Article
  19. Article
  20. Carbapenemases: TransformingBiomolecules · 2020
    Review
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

3 authors.

Ann Marie PorrecaTemple University School of Pharmacy, 3307 North Broad Street, Philadelphia, PA, USA.
Kaede V SullivanLewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
Jason C GallagherTemple University School of Pharmacy, 3307 North Broad Street, Philadelphia, PA, USA. Jason.gallagher@temple.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThe purpose of this review is to investigate the evolution and epidemiology of Klebsiella pneumoniae carbapenemase (KPC)-producing organisms and the current and future treatment options for infections caused by KPC-producing isolates. RECENT

findingsThe emergence of resistance in Enterobacteriaceae producing carbapenemases globally has increased the challenges in treating infections caused by these organisms. One of the prominent mechanisms of resistance is the production of KPC enzymes. Infections caused by organisms producing KPCs have limited treatment options and are associated with poor clinical outcomes. The rapid rise of KPC-producing organisms necessitated the use of drugs with pharmacokinetic and toxicity limitations, including polymyxins, tigecycline, fosfomycin, and aminoglycosides. The availability of new beta-lactamase inhibitor combinations that are effective against KPC-producing organisms represent an advance in safety and efficacy. Several agents are currently being studied that have activity against KPC-producing organisms and appear to represent promising additions to our armamentarium. KPC-producing organisms cause infections with high morbidity and mortality. Limited treatment options are available, though new therapies have been developed. Pipeline agents are likely to have a place in therapy for the treatment of infections caused by KPC-producing isolates.

Indexed as

CarbapenemasesKPCKPC epidemiologyKPC infectionsKPC treatmentMulti-drug resistance

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.