Clinical presentation and antimicrobial resistance of invasive Escherichia coli disease in hospitalized older adults: a prospective multinational observational study.

Antimicrobial resistance Bacteremia Bloodstream infection Elderly Extraintestinal pathogenic E. coli Invasive E. coli disease Sepsis

Journal

Infection
ISSN: 1439-0973
Titre abrégé: Infection
Pays: Germany
ID NLM: 0365307

Informations de publication

Date de publication:
25 Jan 2024
Historique:
received: 16 08 2023
accepted: 18 12 2023
medline: 25 1 2024
pubmed: 25 1 2024
entrez: 24 1 2024
Statut: aheadofprint

Résumé

Clinical data characterizing invasive Escherichia coli disease (IED) are limited. We assessed the clinical presentation of IED and antimicrobial resistance (AMR) patterns of causative E. coli isolates in older adults. EXPECT-2 (NCT04117113) was a prospective, observational, multinational, hospital-based study conducted in patients with IED aged ≥ 60 years. IED was determined by the microbiological confirmation of E. coli from blood; or by the microbiological confirmation of E. coli from urine or an otherwise sterile body site in the presence of requisite criteria of systemic inflammatory response syndrome (SIRS), Sequential Organ Failure Assessment (SOFA), or quick SOFA (qSOFA). The primary outcomes were the clinical presentation of IED and AMR rates of E. coli isolates to clinically relevant antibiotics. Complications and in-hospital mortality were assessed through 28 days following IED diagnosis. Of 240 enrolled patients, 80.4% had bacteremic and 19.6% had non-bacteremic IED. One-half of infections (50.4%) were community-acquired. The most common source of infection was the urinary tract (62.9%). Of 240 patients, 65.8% fulfilled ≥ 2 SIRS criteria, and 60.4% had a total SOFA score of ≥ 2. Investigator-diagnosed sepsis and septic shock were reported in 72.1% and 10.0% of patients, respectively. The most common complication was kidney dysfunction (12.9%). The overall in-hospital mortality was 4.6%. Of 299 E. coli isolates tested, the resistance rates were: 30.4% for trimethoprim-sulfamethoxazole, 24.1% for ciprofloxacin, 22.1% for levofloxacin, 16.4% for ceftriaxone, 5.7% for cefepime, and 4.3% for ceftazidime. The clinical profile of identified IED cases was characterized by high rates of sepsis. IED was associated with high rates of AMR to clinically relevant antibiotics. The identification of IED can be optimized by using a combination of clinical criteria (SIRS, SOFA, or qSOFA) and culture results.

Sections du résumé

BACKGROUND BACKGROUND
Clinical data characterizing invasive Escherichia coli disease (IED) are limited. We assessed the clinical presentation of IED and antimicrobial resistance (AMR) patterns of causative E. coli isolates in older adults.
METHODS METHODS
EXPECT-2 (NCT04117113) was a prospective, observational, multinational, hospital-based study conducted in patients with IED aged ≥ 60 years. IED was determined by the microbiological confirmation of E. coli from blood; or by the microbiological confirmation of E. coli from urine or an otherwise sterile body site in the presence of requisite criteria of systemic inflammatory response syndrome (SIRS), Sequential Organ Failure Assessment (SOFA), or quick SOFA (qSOFA). The primary outcomes were the clinical presentation of IED and AMR rates of E. coli isolates to clinically relevant antibiotics. Complications and in-hospital mortality were assessed through 28 days following IED diagnosis.
RESULTS RESULTS
Of 240 enrolled patients, 80.4% had bacteremic and 19.6% had non-bacteremic IED. One-half of infections (50.4%) were community-acquired. The most common source of infection was the urinary tract (62.9%). Of 240 patients, 65.8% fulfilled ≥ 2 SIRS criteria, and 60.4% had a total SOFA score of ≥ 2. Investigator-diagnosed sepsis and septic shock were reported in 72.1% and 10.0% of patients, respectively. The most common complication was kidney dysfunction (12.9%). The overall in-hospital mortality was 4.6%. Of 299 E. coli isolates tested, the resistance rates were: 30.4% for trimethoprim-sulfamethoxazole, 24.1% for ciprofloxacin, 22.1% for levofloxacin, 16.4% for ceftriaxone, 5.7% for cefepime, and 4.3% for ceftazidime.
CONCLUSIONS CONCLUSIONS
The clinical profile of identified IED cases was characterized by high rates of sepsis. IED was associated with high rates of AMR to clinically relevant antibiotics. The identification of IED can be optimized by using a combination of clinical criteria (SIRS, SOFA, or qSOFA) and culture results.

Identifiants

pubmed: 38267801
doi: 10.1007/s15010-023-02163-z
pii: 10.1007/s15010-023-02163-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523
Organisme : Innovative Medicines Initiative Joint Undertaking
ID : 115523

Investigateurs

Madison Violette (M)
Sonal Munshi (S)
Moussa Aitabi (M)
Christine Lammens (C)
Sofie Van Mieghem (S)
Sandra Van Puyvelde (S)
Basil Britto Xavier (BB)
Anna Maria Azzini (AM)
Elda Righi (E)
Nicola Duccio Salerno (ND)
Giuliana Lo (G)
Cascio Eleonora Cremonini (CE)
Álvaro Pascual (Á)
Reinaldo Espíndola (R)
Virginia Palomo (V)
Sarah Walker (S)
Felicia Ruffin (F)
Michael Dagher (M)
Andreja Varjačić (A)

Informations de copyright

© 2024. The Author(s).

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Auteurs

Joachim Doua (J)

Janssen Research and Development, Infectious Diseases and Vaccines, Janssen Pharmaceutica, Beerse, Belgium.
European and Developing Countries Clinical Trials Partnership (EDCTP), Brussels, Belgium.

Jesús Rodríguez-Baño (J)

Unidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena, Seville, Spain.
Department of Medicine, University of Sevilla and Biomedicine Institute of Sevilla/CSIC, Seville, Spain.
CIBERINFEC, Instituto de Salud Carlos III, Madrid, Spain.

Rachel Froget (R)

Inserm Clinical Investigation Center 1435, Dupuytren University Hospital, Limoges, France.

Padma Puranam (P)

Health Sciences North Research Institute, Sudbury, ON, Canada.

Oscar Go (O)

Janssen Research and Development, Raritan, NJ, USA.

Jeroen Geurtsen (J)

Bacterial Vaccines Discovery and Early Development, Janssen Vaccines & Prevention B.V., Leiden, The Netherlands.

Sanne van Rooij (S)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.

Tuba Vilken (T)

Laboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.

Inage Minoru (I)

Department of Respiratory Medicine, Okitama Public General Hospital, 2000, Nishi-Otsuka, Kawanishi, Yamagata, Japan.

Izumi Yasumori (I)

Department of General Internal Medicine, National Hospital Organization Nagasaki Medical Center, Nagasaki, Japan.

Bart Spiessens (B)

Janssen Research and Development, Infectious Diseases and Vaccines, Janssen Pharmaceutica, Beerse, Belgium.

Evelina Tacconelli (E)

Division of Infectious Diseases, Department of Diagnostic and Public Health, University of Verona, Verona, Italy.

Lena M Biehl (LM)

Department I of Internal Medicine, Faculty of Medicine and University Hospital of Cologne, University of Cologne, 50924, Cologne, Germany.
German Centre for Infection Research, Partner Site Bonn-Cologne, Cologne, Germany.

Joshua T Thaden (JT)

Department of Medicine, Division of Infectious Diseases, Duke University School of Medicine, Durham, NC, USA.

Michal Sarnecki (M)

Janssen Vaccines, Branch of Cilag GmbH International, Bern, Switzerland. sarnecki.michal@gmail.com.

Herman Goossens (H)

Laboratory of Medical Microbiology, Vaccine and Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.

Jan Poolman (J)

Bacterial Vaccines Discovery and Early Development, Janssen Vaccines & Prevention B.V., Leiden, The Netherlands.

Marc Bonten (M)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.

Miquel Ekkelenkamp (M)

Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Classifications MeSH