Evidence map›Paper›PMID 40699518›Full record

ArticleInfection2025

Development and validation of a predictive mortality scoring model for bloodstream infections due to Escherichia coli in the PROBAC cohort.

Paula Olivares-Navarro, María Teresa Pérez-Rodríguez, Ane Josune Goikoetxea-Agirre, José María Reguera-Iglesias, Eva León, María Ángeles Mantecón, Ángeles Pulido-Navazo, Lucía Boix-Palop, Pilar Retamar-Gentil, Carlos Armiñanzas-Castillo and 13 more

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Infection, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Paula Olivares-NavarroUnidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Avda Dr. Fedriani, 3, 41009, Seville, Spain.
María Teresa Pérez-RodríguezComplejo Hospitalario Universitario de Vigo, Galicia Sur Health Research Institute, Vigo, Spain.
Ane Josune Goikoetxea-AgirreServicio de Enfermedades Infecciosas, Hospital Universitario de Cruces, Bilbao, Spain.
José María Reguera-IglesiasHospital Regional Universitario de Málaga, IBIMA, Málaga, Spain.
Eva LeónServicio de Enfermedades Infecciosas, Hospital Universitario Virgen de Valme, Seville, Spain.
María Ángeles MantecónServicio de Enfermedades Infecciosas, Hospital Universitario de Burgos, Burgos, Spain.
Ángeles Pulido-NavazoServicio de Enfermedades Infecciosas, Hospital General de Granollers, Granollers, Spain.
Lucía Boix-PalopServicio de Enfermedades Infecciosas, Hospital Universitario Mútua de Terrassa, Terrassa, Spain.
Pilar Retamar-GentilUnidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Avda Dr. Fedriani, 3, 41009, Seville, Spain.
Carlos Armiñanzas-CastilloCIBERINFEC, Instituto de Salud Carlos III, Madrid, Spain.
Isabel Fernández-NatalServicio de Microbiología Clínica, Complejo Asistencial Universitario de León, León, Spain.
Alfredo Jover-SáenzUnidad Territorial Infección Nosocomial y Política Antibiótica (UTIN), Hospital Universitario Arnau de Vilanova, Lleida, Spain.
Alfonso Del Arco JiménezGrupo de Enfermedades Infecciosas, Servicio de Medicina Interna, Hospital Universitario Costa del Sol, Marbella, Spain.
Jonathan Fernández-SuárezServicio de Enfermedades Infecciosas, Hospital Universitario Central de Asturias, Oviedo, Spain.
Andrés Martín-AspasFacultad de Medicina, Instituto de Investigación E Innovación en Ciencias Biomédicas de Cádiz (INiBICA), Unidad de Enfermedades Infecciosas, Servicio de Medicina InternaHospital Universitario Puerta del MarUniversidad de Cádiz, Cadiz, Spain.
Alejandro Smithson-AmatUnidad de Medicina Interna, Hospital Esperit Sant, Santa Coloma de Gramenet, Barcelona, Spain.
Alberto Bahamonde CarrascoDepartamento de Medicina Interna, Hospital de El Bierzo, Ponferrada, Spain.
Clara Natera-KindelánServicio de Enfermedades Infecciosas, Hospital Universitario Reina Sofia, Córdoba, Spain.
Pedro Martínez Pérez-CrespoServicio de Enfermedades Infecciosas, Hospital Universitario Virgen de Valme, Seville, Spain.
Inmaculada López HernándezUnidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Avda Dr. Fedriani, 3, 41009, Seville, Spain.
Luis Eduardo López-CortésUnidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Avda Dr. Fedriani, 3, 41009, Seville, Spain. llopez14@us.es.
Jesús Rodríguez-BañoUnidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Avda Dr. Fedriani, 3, 41009, Seville, Spain.
PROBAC/GEIRAS-SEIMC/SAMICEI

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 la Cultura, Innovación y Universidades PI16/01432Spanish Network for Research in Infectious Diseases RD16/0016/0001; RD16/0016/0008
6 · The paper itself

Abstract

introductionEscherichia coli is the most frequent cause of bacteraemia and has a major impact on morbidity and mortality. The aim of this study is to define and internally validate a predictive risk score of 30-day all-cause mortality.

methodsA prospective, multicentre, cohort study conducted in 26 Spanish hospitals between October 2016 and March 2017 was performed. All monomicrobial E. coli bloodstream infections (BSIs) were included. The primary outcome was 30-day all-cause mortality. Cases were randomized to a derivation cohort (DC) and a validation cohort (VC). The predictive score was calculated from a multivariable model performed by logistic regression in the DC and subsequently applied to the VC. The predictive ability of the model was estimated by calculating the area under the ROC curve (AUROC) and the goodness of fit by Hosmer-Lemeshow test and calibration plot.

resultsOverall, 1435 cases were included in the DC and 715 in the VC. The final multivariable model for mortality in DC included (adjusted OR; 95% CI) age over 55 years (2.10; 1.01-4.36), dementia (2.08; 1.24-3.50), liver disease (1.81; 0.99-3.28), healthcare-associated acquisition (2.29; 1.52-3.44), Pitt index > 3 (3.59; 2.30-5.61), SOFA ≥ 2 (1.66; 1.04-2.64), and urinary tract source (0.37; 0.24-0.56). The predictive score showed an AUROC of 0.78 (95% CI 0.74-0.83) in the DC and 0.78 (95% CI 0.73-0.84) in the VC.

conclusionWe developed and internally validated a predictive scoring model to identify patients with E. coli bacteraemia at high and low risk of crude mortality on day 30 of BSI.

Indexed as

BacteremiaEscherichia coliEscherichia coli InfectionsAdultAgedAged, 80 and overCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsROC CurveSpainBloodstream infectionEscherichia coliMortalityPredictive model

Identifiers

PMID40699518
PMCPMC12675721

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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.