Carriage of multidrug-resistant Gram-negative bacilli: duration and risk factors.


Journal

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
ISSN: 1435-4373
Titre abrégé: Eur J Clin Microbiol Infect Dis
Pays: Germany
ID NLM: 8804297

Informations de publication

Date de publication:
May 2023
Historique:
received: 24 11 2022
accepted: 24 02 2023
medline: 18 4 2023
pubmed: 26 3 2023
entrez: 25 3 2023
Statut: ppublish

Résumé

Identification of risk factors influencing the duration of carriage of multidrug-resistant Gram-negative bacilli (MDR-GNB) may be useful for infection control. The aim of this study is to estimate the impact of several factors collected for routine hospital surveillance on the duration of carriage of selected MDR-GNB. From January 2015 to July 2021, patients with at least two clinical/surveillance samples positive for MDR-GNB different from ESBL-producing E. coli or AmpC - exclusively producing Enterobacterales were assessed. Microorganisms, age, number of admissions, clinical or rectal sample, sex, and admission service were evaluated as risk factors. Multivariate analysis was performed by a Cox proportional hazard model. A total of 1981 episodes of colonization were included. Involved microorganisms were ESBL-Klebsiella pneumoniae (KP) in 1057 cases (53.4%), other ESBL-non-E. coli Enterobacterales in 91 (4.6%), OXA-48-KP in 263 (13.3%), KPC-KP in 90 (4.5%), VIM-KP in 29 (1.5%), carbapenemase-producing non-KP Enterobacterales (CP-non-KP) in 124 (6.3%), and MDR Pseudomonas aeruginosa (MDR-PAER) in 327 (16.5%). No differences in duration of colonization were observed among ESBL-KP (median colonization time 320 days), ESBL-non-E. coli Enterobacterales (226 days), OXA48-KP (305 days), and MDR-PAER (321 days). For each group, duration of colonization was significantly longer than that of KPC-KP (median colonization time 60 days), VIM-KP (138 days), and CP-non-KP (71 days). Male sex (HR = 0.88; 95% CI 0.78-0.99), detection in Hepatology-Gastroenterology (HR = 0.71; 95% CI 0.54-0.93), clinical sample (HR = 0.61; 95% CI 0.53-0.69), and > 2 admissions after first detection (HR = 0.47; 95% CI 0.42-0.52) were independent predictors of longer carriage, whereas VIM-KP (HR = 1.61; 95% CI 1.04-2.48), KPC-KP (HR = 1.85; 95% CI 1.49-2.3), and CP-non-KP (HR = 1.92; 95% CI 1.49-2.47) were associated with shorter colonization time. Duration of colonization was significantly longer for ESBL-KP, other ESBL-non-E. coli Enterobacterales, OXA-48-KP, and MDR-PAER. For these microorganisms, prolonging surveillance up to 2.5-3 years should be considered. Male sex, clinical sample, multiple readmissions, admission service, and type of microorganism are independent predictors of the duration of carriage.

Identifiants

pubmed: 36964885
doi: 10.1007/s10096-023-04581-1
pii: 10.1007/s10096-023-04581-1
doi:

Substances chimiques

beta-Lactamases EC 3.5.2.6
Anti-Bacterial Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

631-638

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

S Herrera (S)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

B Torralbo (B)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

S Herranz (S)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

J Bernal-Maurandi (J)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

E Rubio (E)

Department of Microbiology, Hospital Clinic, University of Barcelona, ISGLOBAL, Barcelona, Spain.

C Pitart (C)

Department of Microbiology, Hospital Clinic, University of Barcelona, ISGLOBAL, Barcelona, Spain.

I Fortes (I)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

S Valls (S)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

L Rodríguez (L)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

G Santana (G)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

M Bodro (M)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

C Garcia-Vidal (C)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

M Hernández-Meneses (M)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

P Puerta (P)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

L Morata (L)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

A Villella (A)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

M J Bertran (MJ)

Preventive Medicine, Hospital Clinic of Barcelona-IDIBAPS, Barcelona, Spain.

M Brey (M)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

A Soriano (A)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

A Del Río (A)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain.

J A Martinez (JA)

Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, C. de Villarroel, 170, 08036, Barcelona, Spain. jamarti@clinic.cat.

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