Evidence map›Paper›PMID 36877058›Full record

ArticlemSphere2023

Molecular Mechanisms of Resistance to Ceftazidime/Avibactam in Clinical Isolates of

María Fernanda Mojica, Elsa De La Cadena, Juan Carlos García-Betancur, Jessica Porras, Isabella Novoa-Caicedo, Laura Páez-Zamora, Christian Pallares, Tobias Manuel Appel, Marcela A Radice, Paulo Castañeda-Méndez and 3 more

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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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

13 authors at 5 institutions in 6 countries.

María Fernanda MojicaGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.ORCID 0000-0002-1380-9824
Elsa De La CadenaGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Juan Carlos García-BetancurGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Jessica PorrasGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Isabella Novoa-CaicedoGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Laura Páez-ZamoraGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Christian PallaresGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Tobias Manuel AppelGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Marcela A RadiceDepartamento de Microbiología, Inmunología, Biotecnología y Genética, Cátedra de Microbiología, Universidad de Buenos Aires-CONICET, Buenos Aires, Argentina.
Paulo Castañeda-MéndezDepartment of Infectious Diseases, Hospital Médica Sur, Ciudad de México, México.
Ana C GalesDepartment of Internal Medicine, Division of Infectious Diseases, Universidade Federal de São Paulo, São Paulo, Brazil.
José M MunitaGenomics and Resistant Microbes (GeRM) Group, Millennium Initiative for Collaborative Research on Bacterial Resistance (MICROB-R), Santiago, Chile.
María Virginia VillegasGrupo de Investigación en Resistencia Antimicrobiana y Epidemiología Hospitalaria, Universidad El Bosque, Bogotá, Colombia.
Universidad El Bosque · COConsejo Nacional de Investigaciones Científicas y Técnicas · ARHospital Médica Sur · MXMillennium Initiative for Collaborative Research on Bacterial Resistance · CLUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceftazidime-avibactam (CZA) is the combination of a third-generation cephalosporin and a new non-β-lactam β-lactamase inhibitor capable of inactivating class A, C, and some D β-lactamases. From a collection of 2,727 clinical isolates of

Indexed as

CeftazidimePseudomonas InfectionsAnti-Bacterial AgentsAzabicyclo CompoundsDrug CombinationsHospitalsHumansLatin AmericaPseudomonas aeruginosaAnti-Bacterial Agentsavibactamavibactam, ceftazidime drug combinationAzabicyclo CompoundsCeftazidimeDrug Combinationsantimicrobial resistanceceftazidime/avibactamEnterobacteralesLatin AmericaPseudomonas aeruginosa

Identifiers

PMID36877058
PMCPMC10117078
OpenAlexW4323294869

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.