Evidence map›Paper›PMID 35625189›Full record

ArticleAntibiotics (Basel, Switzerland)2022

German Multicenter Study Analyzing Antimicrobial Activity of Ceftazidime-Avibactam of Clinical Meropenem-Resistant

Jana Manzke, Raphael Stauf, Bernd Neumann, Ernst Molitor, Gunnar Hischebeth, Michaela Simon, Jonathan Jantsch, Jürgen Rödel, Sören L Becker, Alexander Halfmann and 9 more

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 61% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

19 authors at 11 institutions in 1 country.

Jana ManzkeInstitute of Clinical Hygiene, Medical Microbiology and Infectiology, Paracelsus Medical University, Klinikum Nürnberg, 90419 Nuremberg, Germany.
Raphael StaufInstitute of Clinical Hygiene, Medical Microbiology and Infectiology, Paracelsus Medical University, Klinikum Nürnberg, 90419 Nuremberg, Germany.
Bernd NeumannInstitute of Clinical Hygiene, Medical Microbiology and Infectiology, Paracelsus Medical University, Klinikum Nürnberg, 90419 Nuremberg, Germany.ORCID 0000-0002-3580-2105
Ernst MolitorInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, 53127 Bonn, Germany.
Gunnar HischebethInstitute of Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, 53127 Bonn, Germany.
Michaela SimonInstitute of Clinical Microbiology and Hygiene, Regensburg University Hospital, 93053 Regensburg, Germany.
Jonathan JantschInstitute of Clinical Microbiology and Hygiene, Regensburg University Hospital, 93053 Regensburg, Germany.
Jürgen RödelInstitute of Medical Microbiology, Jena University Hospital, 07743 Jena, Germany.
Sören L BeckerInstitute of Medical Microbiology and Hygiene, Saarland University, 66421 Homburg, Germany.ORCID 0000-0003-3634-8802
Alexander HalfmannInstitute of Medical Microbiology and Hygiene, Saarland University, 66421 Homburg, Germany.
Thomas A WichelhausGerman National Consiliary Laboratory on Cystic Fibrosis Bacteriology, Institute of Medical Microbiology and Infection Control, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.ORCID 0000-0002-4029-2955
Michael HogardtGerman National Consiliary Laboratory on Cystic Fibrosis Bacteriology, Institute of Medical Microbiology and Infection Control, University Hospital Frankfurt, Goethe University, 60590 Frankfurt am Main, Germany.
Annerose SerrDepartment for Medical Microbiology and Hygiene, University Hospital Freiburg, 79106 Freiburg, Germany.
Christina HessDepartment for Medical Microbiology and Hygiene, University Hospital Freiburg, 79106 Freiburg, Germany.
Andreas F WendelInstitute of Hygiene, Cologne Merheim Medical Centre, University Hospital of Witten/Herdecke, 51058 Cologne, Germany.
Ekkehard SiegelInstitute for Medical Microbiology, University Medical Center, Johannes Gutenberg University Mainz, 55131 Mainz, Germany.
Holger RohdeInstitute for Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.ORCID 0000-0001-8587-4433
Stefan ZimmermannDepartment of Infectious Diseases, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Jörg SteinmannInstitute of Clinical Hygiene, Medical Microbiology and Infectiology, Paracelsus Medical University, Klinikum Nürnberg, 90419 Nuremberg, Germany.
Nuremberg Hospital · DEGoethe University Frankfurt · DEInstitute of Medical Microbiology and Hygiene · DEUniversity Hospital Bonn · DEUniversity Medical Center Freiburg · DEHeidelberg University · DEJena University Hospital · DEJohannes Gutenberg University Mainz · DEUniversität Hamburg · DEUniversity Hospital Regensburg · DEUniversity of Cologne · DE

Funding

Merlin Diagnostika not applicablePfizer (Germany) not applicable
6 · The paper itself

Abstract

Multidrug resistance is an emerging healthcare issue, especially concerning Pseudomonas aeruginosa. In this multicenter study, P. aeruginosa isolates with resistance against meropenem detected by routine methods were collected and tested for carbapenemase production and susceptibility against ceftazidime-avibactam. Meropenem-resistant isolates of P. aeruginosa from various clinical materials were collected at 11 tertiary care hospitals in Germany from 2017−2019. Minimum inhibitory concentrations (MICs) were determined via microdilution plates (MICRONAUT-S) of ceftazidime-avibactam and meropenem at each center. Detection of the presence of carbapenemases was performed by PCR or immunochromatography. For meropenem-resistant isolates (n = 448), the MIC range of ceftazidime-avibactam was 0.25−128 mg/L, MIC90 was 128 mg/L and MIC50 was 16 mg/L. According to EUCAST clinical breakpoints, 213 of all meropenem-resistant P. aeruginosa isolates were categorized as susceptible (47.5%) to ceftazidime-avibactam. Metallo-β-lactamases (MBL) could be detected in 122 isolates (27.3%). The MIC range of ceftazidime-avibactam in MBL-positive isolates was 4−128 mg/L, MIC90 was >128 mg/L and MIC50 was 32 mg/L. There was strong variation in the prevalence of MBL-positive isolates among centers. Our in vitro results support ceftazidime-avibactam as a treatment option against infections caused by meropenem-resistant, MBL-negative P. aeruginosa.

Indexed as

carbapenemasesceftazidime-avibactamsusceptibility testing

Identifiers

PMID35625189
PMCPMC9137722
OpenAlexW4224302300

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.