Evidence map›Paper›PMID 37540701›Full record

ArticlePloS one2023

Testing the mutant selection window hypothesis with meropenem: In vitro model study with OXA-48-producing Klebsiella pneumoniae.

Kamilla N Alieva, Maria V Golikova, Svetlana A Dovzhenko, Mikhail B Kobrin, Elena N Strukova, Vladimir A Ageevets, Alisa A Avdeeva, Ofeliia S Sulian, Sergey V Sidorenko, Stephen H Zinner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Predicting the Effect of Meropenem AgainstAntibiotics (Basel, Switzerland) · 2025
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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

10 authors at 3 institutions in 2 countries.

Kamilla N AlievaDepartment of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, Moscow, Russia.ORCID 0000-0002-2107-8259
Maria V GolikovaDepartment of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, Moscow, Russia.ORCID 0000-0002-7588-1733
Svetlana A DovzhenkoDepartment of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, Moscow, Russia.
Mikhail B KobrinDepartment of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, Moscow, Russia.
Elena N StrukovaDepartment of Pharmacokinetics & Pharmacodynamics, Gause Institute of New Antibiotics, Moscow, Russia.
Vladimir A AgeevetsPediatric Research and Clinical Center for Infectious Diseases, St. Petersburg, Russia.
Alisa A AvdeevaPediatric Research and Clinical Center for Infectious Diseases, St. Petersburg, Russia.
Ofeliia S SulianPediatric Research and Clinical Center for Infectious Diseases, St. Petersburg, Russia.
Sergey V SidorenkoPediatric Research and Clinical Center for Infectious Diseases, St. Petersburg, Russia.
Stephen H ZinnerDepartment of Medicine, Harvard Medical School, Mount Auburn Hospital, Cambridge, MA, United States of America.
Gause Institute of New Antibiotics Russian Academy of Medical Sciences · RUMinistry of Health of the Russian Federation · RUMount Auburn Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OXA-48 carbapenemases are frequently expressed by Klebsiella pneumoniae clinical isolates; they decrease the effectiveness of carbapenem therapy, particularly with meropenem. Among these isolates, meropenem-susceptible carbapenemase-producers may show decreased meropenem effectiveness. However, the probability of the emergence of resistance in susceptible carbapenemase-producing isolates and its dependence on specific K. pneumoniae meropenem MICs is not completely known. It is also not completely clear what resistance patterns will be exhibited by these bacteria exposed to meropenem, if they would follow the patterns of non-beta-lactamase-producing bacteria and other than beta-lactams antibiotics. These issues might be clarified if patterns of meropenem resistance related to the mutant selection window (MSW) hypothesis. To test the applicability of the MSW hypothesis to meropenem, OXA-48-carbapenemase-producing K. pneumoniae clinical isolates with MICs in a 64-fold range (from susceptible to resistant) were exposed to meropenem in a hollow-fiber infection model; epithelial lining fluid meropenem pharmacokinetics were simulated following administration of 2 grams every 8 hours in a 3-hour infusion. Strong bell-shaped relationships between the meropenem daily dose infused to the model as related to the specific isolate MIC and both the antimicrobial effect and the emergence of resistance were observed. The applicability of the MSW hypothesis to meropenem and carbapenemase producing K. pneumoniae was confirmed. Low meropenem efficacy indicates very careful prescribing of meropenem to treat K. pneumoniae infections when the causative isolate is confirmed as an OXA-48-carbapenemase producer.

Indexed as

Anti-Bacterial AgentsKlebsiella InfectionsBacterial Proteinsbeta-LactamasesCarbapenemsHumansKlebsiella pneumoniaeMeropenemMicrobial Sensitivity TestsAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasesCarbapenemsMeropenem

Identifiers

PMID37540701
PMCPMC10403107
OpenAlexW4385567994

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.