Evidence map›Paper›PMID 38711045›Full record

ArticleAnnals of clinical microbiology and antimicrobials2024

Differences in clinical outcomes of bloodstream infections caused by Klebsiella aerogenes, Klebsiella pneumoniae and Enterobacter cloacae: a multicentre cohort study.

Mariana Guedes, David Gathara, Inmaculada López-Hernández, Pedro María Martínez Pérez-Crespo, María Teresa Pérez-Rodríguez, Adrian Sousa, Antonio Plata, Jose María Reguera-Iglesias, Lucía Boix-Palop, Beatriz Dietl and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

23 authors.

Mariana Guedes *Unidad Clínica de Enfermedades Infecciosas y Microbiología, Departamento de Medicina, Instituto de Biomedicina de Sevilla (IBiS)/CSIC, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Seville, Spain. mariananpguedes@gmail.com.
David Gathara *London School of Hygiene and Tropical Medicine, MARCH Centre, London, UK.
Inmaculada López-HernándezUnidad Clínica de Enfermedades Infecciosas y Microbiología, Departamento de Medicina, Instituto de Biomedicina de Sevilla (IBiS)/CSIC, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Seville, Spain.
Pedro María Martínez Pérez-CrespoUnidad de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen de Valme, Seville, Spain.
María Teresa Pérez-RodríguezUnidad de Enfermedades Infecciosas, Departamento de Medicina Interna, Complexo Hospitalario Universitario de Vigo/Galicia Sur Health Research Institute, Vigo, Spain.
Adrian SousaUnidad de Enfermedades Infecciosas, Departamento de Medicina Interna, Complexo Hospitalario Universitario de Vigo/Galicia Sur Health Research Institute, Vigo, Spain.
Antonio PlataServicio de Enfermedades Infecciosas, Hospital Regional Universitario de Málaga, IBIMA Málaga, Málaga, Spain.
Jose María Reguera-IglesiasServicio de Enfermedades Infecciosas, Hospital Regional Universitario de Málaga, IBIMA Málaga, Málaga, Spain.
Lucía Boix-PalopServicio de Enfermedades Infecciosas, Hospital Universitari Mútua de Terrassa, Barcelona, Spain.
Beatriz DietlServicio de Enfermedades Infecciosas, Hospital Universitari Mútua de Terrassa, Barcelona, Spain.
Juan Sevilla BlancoUnidad de Enfermedades Infecciosas y Microbiologia Clinica, Hospital Universitario Jerez De La Frontera, Jerez De La Frontera, Cádiz, Spain.
Carlos Armiñanzas CastilloCIBERINFEC, Instituto de Salud Carlos III, Madrid, Spain.
Fátima Galán-SánchezUnidad de Gestión Clínica de Microbiología, Hospital Universitario Puerta del Mar, Cádiz, Spain.
Clara Natera KindelánUnidad de Enfermedades Infecciosas, Hospital Universitario Reina Sofia, Cordoba, Spain.
Alfredo Jover-SaenzUnidad de Infección Nosocomial, Hospital Universitario Arnau de Vilanova, Lleida, Spain.
Josune Goikoetxea AguirreUnidad de Enfermedades Infecciosas, Hospital Universitario de Cruces, Barakaldo, Spain.
Ana Alemán AlemánUnidad de Gestión Clínica de Enfermedades Infecciosas, Hospital Universitario de Burgos, Burgos, Spain.
Teresa Marrodán CiordiaDepartamento de Microbiología Clínica, Complejo Asistencial Universitario de León (CAULE), León, Spain.
Alfonso Del Arco JiménezGrupo Enfermedades Infecciosas, Servicio de Medicina Interna, Hospital Costa del Sol, Marbella, Spain.
Jonathan Fernandez-SuarezUnidad de Microbiología, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Hospital Universitario Central de Asturias, Oviedo, Spain.
Luis Eduardo Lopez-Cortes *Unidad Clínica de Enfermedades Infecciosas y Microbiología, Departamento de Medicina, Instituto de Biomedicina de Sevilla (IBiS)/CSIC, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Seville, Spain.
Jesús Rodríguez-Baño *Unidad Clínica de Enfermedades Infecciosas y Microbiología, Departamento de Medicina, Instituto de Biomedicina de Sevilla (IBiS)/CSIC, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Seville, Spain.
PROBAC/GEIRAS-SEIMC/SAMICEI group

Funding

Plan Nacional de I + D + i 2013-2016, Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministerio de Ciencia, Innovación y Universidades PI16/01432Spanish Network for Research in Infectious Diseases (REIPI) RD16/0016/0001Spanish Network for Research in Infectious Diseases (REIPI) RD16/0016/0008
6 · The paper itself

Abstract

backgroundKlebsiella aerogenes has been reclassified from Enterobacter to Klebsiella genus due to its phenotypic and genotypic similarities with Klebsiella pneumoniae. It is unclear if clinical outcomes are also more similar. This study aims to assess clinical outcomes of bloodstreams infections (BSI) caused by K. aerogenes, K. pneumoniae and Enterobacter cloacae, through secondary data analysis, nested in PRO-BAC cohort study.

methodsHospitalized patients between October 2016 and March 2017 with monomicrobial BSI due to K. aerogenes, K. pneumoniae or E. cloacae were included. Primary outcome was a composite clinical outcome including all-cause mortality or recurrence until 30 days follow-up. Secondary outcomes were fever ≥ 72 h, persistent bacteraemia, and secondary device infection. Multilevel mixed-effect Poisson regression was used to estimate the association between microorganisms and outcome.

resultsOverall, 29 K. aerogenes, 77 E. cloacae and 337 K. pneumoniae BSI episodes were included. Mortality or recurrence was less frequent in K. aerogenes (6.9%) than in E. cloacae (20.8%) or K. pneumoniae (19.0%), but statistical difference was not observed (rate ratio (RR) 0.35, 95% CI 0.08 to 1.55; RR 0.42, 95% CI 0.10 to 1.71, respectively). Fever ≥ 72 h and device infection were more common in K. aerogenes group. In the multivariate analysis, adjusted for confounders (age, sex, BSI source, hospital ward, Charlson score and active antibiotic therapy), the estimates and direction of effect were similar to crude results.

conclusionsResults suggest that BSI caused by K. aerogenes may have a better prognosis than E. cloacae or K. pneumoniae BSI.

Indexed as

BacteremiaEnterobacter aerogenesEnterobacter cloacaeEnterobacteriaceae InfectionsKlebsiella InfectionsKlebsiella pneumoniaeAgedAged, 80 and overAnti-Bacterial AgentsCohort StudiesFemaleHumansMaleMiddle AgedRecurrenceTreatment OutcomeAnti-Bacterial AgentsBloodstream infectionEnterobacter cloacaeKlebsiella aerogenesKlebsiella pneumoniaeMortalityRecurrence

Identifiers

PMID38711045
PMCPMC11071190

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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.