A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies

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A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies. / Vehreschild, Maria J G T; Hamprecht, Axel; Peterson, Lisa; Schubert, Sören; Häntschel, Maik; Peter, Silke; Schafhausen, Philippe; Rohde, Holger; Lilienfeld-Toal, Marie V; Bekeredjian-Ding, Isabelle; Libam, Johannes; Hellmich, Martin; Vehreschild, Jörg J; Cornely, Oliver A; Seifert, Harald.

in: J ANTIMICROB CHEMOTH, Jahrgang 69, Nr. 12, 01.12.2014, S. 3387-92.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Vehreschild, MJGT, Hamprecht, A, Peterson, L, Schubert, S, Häntschel, M, Peter, S, Schafhausen, P, Rohde, H, Lilienfeld-Toal, MV, Bekeredjian-Ding, I, Libam, J, Hellmich, M, Vehreschild, JJ, Cornely, OA & Seifert, H 2014, 'A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies', J ANTIMICROB CHEMOTH, Jg. 69, Nr. 12, S. 3387-92. https://doi.org/10.1093/jac/dku305

APA

Vehreschild, M. J. G. T., Hamprecht, A., Peterson, L., Schubert, S., Häntschel, M., Peter, S., Schafhausen, P., Rohde, H., Lilienfeld-Toal, M. V., Bekeredjian-Ding, I., Libam, J., Hellmich, M., Vehreschild, J. J., Cornely, O. A., & Seifert, H. (2014). A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies. J ANTIMICROB CHEMOTH, 69(12), 3387-92. https://doi.org/10.1093/jac/dku305

Vancouver

Bibtex

@article{9276712edcf7421da66542d78cdede8b,
title = "A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies",
abstract = "BACKGROUND: Bloodstream infections (BSIs) caused by enterobacteria remain a leading cause of mortality in patients with chemotherapy-induced neutropenia. The rate and type of colonization and infection with ESBL-producing Enterobacteriaceae (ESBL-E) and their mode of transmission in German cancer centres is largely unknown.METHODS: We performed a prospective, observational study at five German university-based haematology departments. Participating sites screened for intestinal ESBL-E colonization within 72 h of admission, every 10 ± 2 days thereafter and before discharge. Three of the five centres performed contact isolation for patients colonized or infected with ESBL-E. Molecular characterization of resistance mechanisms and epidemiological typing of isolates by repetitive extragenic palindromic PCR (rep-PCR) and PFGE was performed to assess strain transmission between patients.RESULTS: Between October 2011 and December 2012, 719 hospitalizations of 497 haematological high-risk patients comprising 20,143 patient-days were analysed. Mean duration of in-hospital stay was 36.6 days (range: 2-159 days). ESBL-E were identified from screening samples (82.8% Escherichia coli and 14.6% Klebsiella pneumoniae) in 55/497 patients (11.1%; range by centre: 5.8%-23.1%). PFGE and rep-PCR revealed only a single case of potential cross-transmission among two patients colonized with K. pneumoniae. Six episodes of BSI with ESBL-E were observed. Multivariate analysis revealed previous colonization with ESBL-E as the most important risk factor for BSI with ESBL-E (OR 52.00; 95% CI 5.71-473.89).CONCLUSIONS: Even though BSI with ESBL-E is still rare in this high-risk population, colonization rates are substantial and vary considerably between centres. In-hospital transmission of ESBL-E as assessed by molecular typing was the exception.",
author = "Vehreschild, {Maria J G T} and Axel Hamprecht and Lisa Peterson and S{\"o}ren Schubert and Maik H{\"a}ntschel and Silke Peter and Philippe Schafhausen and Holger Rohde and Lilienfeld-Toal, {Marie V} and Isabelle Bekeredjian-Ding and Johannes Libam and Martin Hellmich and Vehreschild, {J{\"o}rg J} and Cornely, {Oliver A} and Harald Seifert",
note = "{\textcopyright} The Author 2014. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.",
year = "2014",
month = dec,
day = "1",
doi = "10.1093/jac/dku305",
language = "English",
volume = "69",
pages = "3387--92",
journal = "J ANTIMICROB CHEMOTH",
issn = "0305-7453",
publisher = "Oxford University Press",
number = "12",

}

RIS

TY - JOUR

T1 - A multicentre cohort study on colonization and infection with ESBL-producing Enterobacteriaceae in high-risk patients with haematological malignancies

AU - Vehreschild, Maria J G T

AU - Hamprecht, Axel

AU - Peterson, Lisa

AU - Schubert, Sören

AU - Häntschel, Maik

AU - Peter, Silke

AU - Schafhausen, Philippe

AU - Rohde, Holger

AU - Lilienfeld-Toal, Marie V

AU - Bekeredjian-Ding, Isabelle

AU - Libam, Johannes

AU - Hellmich, Martin

AU - Vehreschild, Jörg J

AU - Cornely, Oliver A

AU - Seifert, Harald

N1 - © The Author 2014. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

PY - 2014/12/1

Y1 - 2014/12/1

N2 - BACKGROUND: Bloodstream infections (BSIs) caused by enterobacteria remain a leading cause of mortality in patients with chemotherapy-induced neutropenia. The rate and type of colonization and infection with ESBL-producing Enterobacteriaceae (ESBL-E) and their mode of transmission in German cancer centres is largely unknown.METHODS: We performed a prospective, observational study at five German university-based haematology departments. Participating sites screened for intestinal ESBL-E colonization within 72 h of admission, every 10 ± 2 days thereafter and before discharge. Three of the five centres performed contact isolation for patients colonized or infected with ESBL-E. Molecular characterization of resistance mechanisms and epidemiological typing of isolates by repetitive extragenic palindromic PCR (rep-PCR) and PFGE was performed to assess strain transmission between patients.RESULTS: Between October 2011 and December 2012, 719 hospitalizations of 497 haematological high-risk patients comprising 20,143 patient-days were analysed. Mean duration of in-hospital stay was 36.6 days (range: 2-159 days). ESBL-E were identified from screening samples (82.8% Escherichia coli and 14.6% Klebsiella pneumoniae) in 55/497 patients (11.1%; range by centre: 5.8%-23.1%). PFGE and rep-PCR revealed only a single case of potential cross-transmission among two patients colonized with K. pneumoniae. Six episodes of BSI with ESBL-E were observed. Multivariate analysis revealed previous colonization with ESBL-E as the most important risk factor for BSI with ESBL-E (OR 52.00; 95% CI 5.71-473.89).CONCLUSIONS: Even though BSI with ESBL-E is still rare in this high-risk population, colonization rates are substantial and vary considerably between centres. In-hospital transmission of ESBL-E as assessed by molecular typing was the exception.

AB - BACKGROUND: Bloodstream infections (BSIs) caused by enterobacteria remain a leading cause of mortality in patients with chemotherapy-induced neutropenia. The rate and type of colonization and infection with ESBL-producing Enterobacteriaceae (ESBL-E) and their mode of transmission in German cancer centres is largely unknown.METHODS: We performed a prospective, observational study at five German university-based haematology departments. Participating sites screened for intestinal ESBL-E colonization within 72 h of admission, every 10 ± 2 days thereafter and before discharge. Three of the five centres performed contact isolation for patients colonized or infected with ESBL-E. Molecular characterization of resistance mechanisms and epidemiological typing of isolates by repetitive extragenic palindromic PCR (rep-PCR) and PFGE was performed to assess strain transmission between patients.RESULTS: Between October 2011 and December 2012, 719 hospitalizations of 497 haematological high-risk patients comprising 20,143 patient-days were analysed. Mean duration of in-hospital stay was 36.6 days (range: 2-159 days). ESBL-E were identified from screening samples (82.8% Escherichia coli and 14.6% Klebsiella pneumoniae) in 55/497 patients (11.1%; range by centre: 5.8%-23.1%). PFGE and rep-PCR revealed only a single case of potential cross-transmission among two patients colonized with K. pneumoniae. Six episodes of BSI with ESBL-E were observed. Multivariate analysis revealed previous colonization with ESBL-E as the most important risk factor for BSI with ESBL-E (OR 52.00; 95% CI 5.71-473.89).CONCLUSIONS: Even though BSI with ESBL-E is still rare in this high-risk population, colonization rates are substantial and vary considerably between centres. In-hospital transmission of ESBL-E as assessed by molecular typing was the exception.

U2 - 10.1093/jac/dku305

DO - 10.1093/jac/dku305

M3 - SCORING: Journal article

C2 - 25103492

VL - 69

SP - 3387

EP - 3392

JO - J ANTIMICROB CHEMOTH

JF - J ANTIMICROB CHEMOTH

SN - 0305-7453

IS - 12

ER -