Association of microbiological factors with mortality in Escherichia coli bacteraemia presenting with sepsis/septic shock: A prospective cohort study

感染性休克 败血症 前瞻性队列研究 医学 菌血症 队列研究 休克(循环) 大肠杆菌 队列 重症监护医学 微生物学 内科学 生物 抗生素 遗传学 基因
作者
Natália Maldonado,Inmaculada López-Hernández,Luis Eduardo López‐Cortés,Pedro María Martínez Pérez-Crespo,Pilar Retamar-Gentil,Andrea García-Montaner,Sabino Riestra,Adrián Sousa-Domínguez,Josune Goikoetxea,Ángeles Pulido-Navazo,María del Valle Ortíz,Clara Natera-Kindelán,Alfredo Jóver-Saenz,Alfonso del Arco-Jiménez,Carlos Armiñanzas-Castillo,Ana Isabel Aller-García,Jonathan Fernández-Suarez,Teresa Marrodán-Ciordia,Lucía Boix-Palop,Alejandro Smithson-Amat,José Ma Reguera-Iglesias,Fátima Galán-Sanchez,Alberto Bahamonde,Juan Manuel Sánchez-Calvo,Isabel Gea-Lázaro,Inés Pérez‐Camacho,Armando Reyes-Bertos,Berta Becerril-Carral,Álvaro Pascual,Jesús Rodríguez-Baño
出处
期刊:Clinical Microbiology and Infection [Elsevier]
标识
DOI:10.1016/j.cmi.2024.04.001
摘要

Abstract

Objectives

This study aimed to determine the association of E. coli microbiological factors with 30-day mortality in BSI patients presenting with a dysregulated response to infection (i.e., sepsis or septic shock).

Methods

Whole genome sequencing was performed on 224 E. coli isolates of patients with sepsis/septic shock, from 22 Spanish hospitals. Phylogroup, sequence type, virulence, antibiotic resistance and pathogenicity islands were assessed. A multivariable model for 30-day mortality including clinical and epidemiological variables was built, to which microbiological variables were hierarchically added. The predictive capacity of the models was estimated by the area under the receiver operating characteristic curve (AUROC) with 95% confidence intervals (CI).

Results

Mortality at day 30 was 31% (69 patients). The clinical model for mortality included (adjusted OR; 95% CI) age (1.04; 1.02-1.07), Charlson index ≥3 (1.78; 0.95-3.32), urinary BSI source (0.30; 0.16-0.57) and active empirical treatment (0.36; 0.11-1.14) with an AUROC of 0.73 (95% CI, 0.67-0.80). Addition of microbiological factors selected clone ST95 (3.64; 0.94-14.04), eilA gene (2.62; 1.14-6.02) and astA gene (2.39; 0.87-6.59) as associated with mortality, with an AUROC of 0.76 (0.69-0.82).

Conclusions

Despite having a modest overall contribution, some microbiological factors were associated with increased odds of death and would deserve being studied as potential therapeutic or preventive targets.
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