Multi-body-site colonization screening cultures for predicting multi-drug resistant Gram-negative and Gram-positive bacteremia in hematological patients.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
21 Feb 2022
Historique:
received: 19 09 2021
accepted: 12 02 2022
entrez: 22 2 2022
pubmed: 23 2 2022
medline: 24 2 2022
Statut: epublish

Résumé

To investigate the multi-drug resistant bacteria (MDRB) colonization rate in hematological patients hospitalized for any cause using a multi-body-site surveillance approach, and determine the extent to which this screening strategy helped anticipate MDRB bloodstream infections (BSI). Single-center retrospective observational study including 361 admissions documented in 250 adult patients. Surveillance cultures of nasal, pharyngeal, axillary and rectal specimens (the latter two combined) were performed at admission and subsequently on a weekly basis. Blood culture samples were incubated in an automated continuous monitoring blood culturing instrument (BACTEC FX). In total, 3463 surveillance cultures were performed (pharyngeal, n = 1201; axillary-rectal, n = 1200; nasal, n = 1062). MDRB colonization was documented in 122 out of 361 (33.7%) admissions corresponding to 86 patients (34.4%). A total of 149 MDRB were isolated from one or more body sites, of which most were Gram-negative bacteria, most frequently non-fermenting (n = 83) followed by Enterobacterales (n = 51). BSI were documented in 102 admissions (28%) involving 87 patients. Overall, the rate of BSI caused by MDRB was significantly higher (p = 0.04) in the presence of colonizing MDRB (16 out of 47 admissions in 14 patients) than in its absence (9 out of 55 admissions in 9 patients). Colonization by any MDRB was independently associated with increased risk of MDRB-BSI (HR, 3.70; 95% CI, 1.38-9.90; p = 0.009). MDRB colonization is a frequent event in hematological patients hospitalized for any reason and is associated with an increased risk of MDRB BSI. The data lend support to the use of MDRB colonization surveillance cultures for predicting the occurrence of MDRB BSI in this cohort.

Sections du résumé

BACKGROUND BACKGROUND
To investigate the multi-drug resistant bacteria (MDRB) colonization rate in hematological patients hospitalized for any cause using a multi-body-site surveillance approach, and determine the extent to which this screening strategy helped anticipate MDRB bloodstream infections (BSI).
METHODS METHODS
Single-center retrospective observational study including 361 admissions documented in 250 adult patients. Surveillance cultures of nasal, pharyngeal, axillary and rectal specimens (the latter two combined) were performed at admission and subsequently on a weekly basis. Blood culture samples were incubated in an automated continuous monitoring blood culturing instrument (BACTEC FX).
RESULTS RESULTS
In total, 3463 surveillance cultures were performed (pharyngeal, n = 1201; axillary-rectal, n = 1200; nasal, n = 1062). MDRB colonization was documented in 122 out of 361 (33.7%) admissions corresponding to 86 patients (34.4%). A total of 149 MDRB were isolated from one or more body sites, of which most were Gram-negative bacteria, most frequently non-fermenting (n = 83) followed by Enterobacterales (n = 51). BSI were documented in 102 admissions (28%) involving 87 patients. Overall, the rate of BSI caused by MDRB was significantly higher (p = 0.04) in the presence of colonizing MDRB (16 out of 47 admissions in 14 patients) than in its absence (9 out of 55 admissions in 9 patients). Colonization by any MDRB was independently associated with increased risk of MDRB-BSI (HR, 3.70; 95% CI, 1.38-9.90; p = 0.009).
CONCLUSION CONCLUSIONS
MDRB colonization is a frequent event in hematological patients hospitalized for any reason and is associated with an increased risk of MDRB BSI. The data lend support to the use of MDRB colonization surveillance cultures for predicting the occurrence of MDRB BSI in this cohort.

Identifiants

pubmed: 35189833
doi: 10.1186/s12879-022-07154-3
pii: 10.1186/s12879-022-07154-3
pmc: PMC8862203
doi:

Substances chimiques

Anti-Bacterial Agents 0
Pharmaceutical Preparations 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

172

Informations de copyright

© 2022. The Author(s).

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Auteurs

Ignacio Torres (I)

Microbiology Service, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Dixie Huntley (D)

Microbiology Service, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Mar Tormo (M)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Marisa Calabuig (M)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Juan Carlos Hernández-Boluda (JC)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

María José Terol (MJ)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Carlos Carretero (C)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Paula de Michelena (P)

Microbiology Service, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Ariadna Pérez (A)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

José Luis Piñana (JL)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Javier Colomina (J)

Microbiology Service, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.

Carlos Solano (C)

Hematology Department, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain.
Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.

David Navarro (D)

Microbiology Service, Clinic University Hospital, INCLIVA Health Research Institute, Valencia, Spain. david.navarro@uv.es.
Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain. david.navarro@uv.es.
Department of Microbiology, School of Medicine, University of Valencia, Av. Blasco Ibáñez 17, 46010, Valencia, Spain. david.navarro@uv.es.

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Classifications MeSH