Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study
Summary Background International travel contributes to the dissemination of antimicrobial resistance. We investigated the acquisition of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) during international travel, with a focus on predictive factors for acquisition, duration of co...
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Veröffentlicht in: | The Lancet infectious diseases 2017, Vol.17 (1), p.78-85 |
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creator | Arcilla, Maris S, MD van Hattem, Jarne M, MD Haverkate, Manon R, PhD Bootsma, Martin C J, PhD van Genderen, Perry J J, PhD Goorhuis, Abraham, PhD Grobusch, Martin P, Prof Lashof, Astrid M Oude, PhD Molhoek, Nicky, MSc Schultsz, Constance, PhD Stobberingh, Ellen E, PhD Verbrugh, Henri A, Prof de Jong, Menno D, Prof Melles, Damian C, PhD Penders, John, Dr |
description | Summary Background International travel contributes to the dissemination of antimicrobial resistance. We investigated the acquisition of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) during international travel, with a focus on predictive factors for acquisition, duration of colonisation, and probability of onward transmission. Methods Within the prospective, multicentre COMBAT study, 2001 Dutch travellers and 215 non-travelling household members were enrolled. Faecal samples and questionnaires on demographics, illnesses, and behaviour were collected before travel and immediately and 1, 3, 6, and 12 months after return. Samples were screened for the presence of ESBL-E. In post-travel samples, ESBL genes were sequenced and PCR with specific primers for plasmid-encoded β-lactamase enzymes TEM, SHV, and CTX-M group 1, 2, 8, 9, and 25 was used to confirm the presence of ESBL genes in follow-up samples. Multivariable regression analyses and mathematical modelling were used to identify predictors for acquisition and sustained carriage, and to determine household transmission rates. This study is registered with ClinicalTrials.gov , number NCT01676974. Findings 633 (34·3%) of 1847 travellers who were ESBL negative before travel and had available samples after return had acquired ESBL-E during international travel (95% CI 32·1–36·5), with the highest number of acquisitions being among those who travelled to southern Asia in 136 of 181 (75·1%, 95% CI 68·4–80·9). Important predictors for acquisition of ESBL-E were antibiotic use during travel (adjusted odds ratio 2·69, 95% CI 1·79–4·05), traveller's diarrhoea that persisted after return (2·31, 1·42–3·76), and pre-existing chronic bowel disease (2·10, 1·13–3·90). The median duration of colonisation after travel was 30 days (95% CI 29–33). 65 (11·3%) of 577 remained colonised at 12 months. CTX-M enzyme group 9 ESBLs were associated with a significantly increased risk of sustained carriage (median duration 75 days, 95% CI 48–102, p=0·0001). Onward transmission was found in 13 (7·7%) of 168 household members. The probability of transmitting ESBL-E to another household member was 12% (95% CI 5–18). Interpretation Acquisition and spread of ESBL-E during and after international travel was substantial and worrisome. Travellers to areas with a high risk of ESBL-E acquisition should be viewed as potential carriers of ESBL-E for up to 12 months after return. Funding Netherlands Organisation for Health Res |
doi_str_mv | 10.1016/S1473-3099(16)30319-X |
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We investigated the acquisition of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) during international travel, with a focus on predictive factors for acquisition, duration of colonisation, and probability of onward transmission. Methods Within the prospective, multicentre COMBAT study, 2001 Dutch travellers and 215 non-travelling household members were enrolled. Faecal samples and questionnaires on demographics, illnesses, and behaviour were collected before travel and immediately and 1, 3, 6, and 12 months after return. Samples were screened for the presence of ESBL-E. In post-travel samples, ESBL genes were sequenced and PCR with specific primers for plasmid-encoded β-lactamase enzymes TEM, SHV, and CTX-M group 1, 2, 8, 9, and 25 was used to confirm the presence of ESBL genes in follow-up samples. Multivariable regression analyses and mathematical modelling were used to identify predictors for acquisition and sustained carriage, and to determine household transmission rates. This study is registered with ClinicalTrials.gov , number NCT01676974. Findings 633 (34·3%) of 1847 travellers who were ESBL negative before travel and had available samples after return had acquired ESBL-E during international travel (95% CI 32·1–36·5), with the highest number of acquisitions being among those who travelled to southern Asia in 136 of 181 (75·1%, 95% CI 68·4–80·9). Important predictors for acquisition of ESBL-E were antibiotic use during travel (adjusted odds ratio 2·69, 95% CI 1·79–4·05), traveller's diarrhoea that persisted after return (2·31, 1·42–3·76), and pre-existing chronic bowel disease (2·10, 1·13–3·90). The median duration of colonisation after travel was 30 days (95% CI 29–33). 65 (11·3%) of 577 remained colonised at 12 months. CTX-M enzyme group 9 ESBLs were associated with a significantly increased risk of sustained carriage (median duration 75 days, 95% CI 48–102, p=0·0001). Onward transmission was found in 13 (7·7%) of 168 household members. The probability of transmitting ESBL-E to another household member was 12% (95% CI 5–18). Interpretation Acquisition and spread of ESBL-E during and after international travel was substantial and worrisome. Travellers to areas with a high risk of ESBL-E acquisition should be viewed as potential carriers of ESBL-E for up to 12 months after return. Funding Netherlands Organisation for Health Research and Development (ZonMw).</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(16)30319-X</identifier><identifier>PMID: 27751772</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Anti-Bacterial Agents - therapeutic use ; beta-Lactamases ; Diarrhea - etiology ; Enterobacteriaceae ; Enterobacteriaceae - enzymology ; Enterobacteriaceae Infections - epidemiology ; Enterobacteriaceae Infections - transmission ; Feces - microbiology ; Female ; Humans ; Infectious Disease ; Male ; Middle Aged ; Prospective Studies ; Risk Factors ; Surveys and Questionnaires ; Time Factors ; Travel</subject><ispartof>The Lancet infectious diseases, 2017, Vol.17 (1), p.78-85</ispartof><rights>Elsevier Ltd</rights><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-7187cdf0255e274984f031782ee28376fed63873d23a3bfe746610c341b8aafd3</citedby><cites>FETCH-LOGICAL-c552t-7187cdf0255e274984f031782ee28376fed63873d23a3bfe746610c341b8aafd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S147330991630319X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27751772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arcilla, Maris S, MD</creatorcontrib><creatorcontrib>van Hattem, Jarne M, MD</creatorcontrib><creatorcontrib>Haverkate, Manon R, PhD</creatorcontrib><creatorcontrib>Bootsma, Martin C J, PhD</creatorcontrib><creatorcontrib>van Genderen, Perry J J, PhD</creatorcontrib><creatorcontrib>Goorhuis, Abraham, PhD</creatorcontrib><creatorcontrib>Grobusch, Martin P, Prof</creatorcontrib><creatorcontrib>Lashof, Astrid M Oude, PhD</creatorcontrib><creatorcontrib>Molhoek, Nicky, MSc</creatorcontrib><creatorcontrib>Schultsz, Constance, PhD</creatorcontrib><creatorcontrib>Stobberingh, Ellen E, PhD</creatorcontrib><creatorcontrib>Verbrugh, Henri A, Prof</creatorcontrib><creatorcontrib>de Jong, Menno D, Prof</creatorcontrib><creatorcontrib>Melles, Damian C, PhD</creatorcontrib><creatorcontrib>Penders, John, Dr</creatorcontrib><title>Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>Summary Background International travel contributes to the dissemination of antimicrobial resistance. We investigated the acquisition of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) during international travel, with a focus on predictive factors for acquisition, duration of colonisation, and probability of onward transmission. Methods Within the prospective, multicentre COMBAT study, 2001 Dutch travellers and 215 non-travelling household members were enrolled. Faecal samples and questionnaires on demographics, illnesses, and behaviour were collected before travel and immediately and 1, 3, 6, and 12 months after return. Samples were screened for the presence of ESBL-E. In post-travel samples, ESBL genes were sequenced and PCR with specific primers for plasmid-encoded β-lactamase enzymes TEM, SHV, and CTX-M group 1, 2, 8, 9, and 25 was used to confirm the presence of ESBL genes in follow-up samples. Multivariable regression analyses and mathematical modelling were used to identify predictors for acquisition and sustained carriage, and to determine household transmission rates. This study is registered with ClinicalTrials.gov , number NCT01676974. Findings 633 (34·3%) of 1847 travellers who were ESBL negative before travel and had available samples after return had acquired ESBL-E during international travel (95% CI 32·1–36·5), with the highest number of acquisitions being among those who travelled to southern Asia in 136 of 181 (75·1%, 95% CI 68·4–80·9). Important predictors for acquisition of ESBL-E were antibiotic use during travel (adjusted odds ratio 2·69, 95% CI 1·79–4·05), traveller's diarrhoea that persisted after return (2·31, 1·42–3·76), and pre-existing chronic bowel disease (2·10, 1·13–3·90). The median duration of colonisation after travel was 30 days (95% CI 29–33). 65 (11·3%) of 577 remained colonised at 12 months. CTX-M enzyme group 9 ESBLs were associated with a significantly increased risk of sustained carriage (median duration 75 days, 95% CI 48–102, p=0·0001). Onward transmission was found in 13 (7·7%) of 168 household members. The probability of transmitting ESBL-E to another household member was 12% (95% CI 5–18). Interpretation Acquisition and spread of ESBL-E during and after international travel was substantial and worrisome. Travellers to areas with a high risk of ESBL-E acquisition should be viewed as potential carriers of ESBL-E for up to 12 months after return. Funding Netherlands Organisation for Health Research and Development (ZonMw).</description><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>beta-Lactamases</subject><subject>Diarrhea - etiology</subject><subject>Enterobacteriaceae</subject><subject>Enterobacteriaceae - enzymology</subject><subject>Enterobacteriaceae Infections - epidemiology</subject><subject>Enterobacteriaceae Infections - transmission</subject><subject>Feces - microbiology</subject><subject>Female</subject><subject>Humans</subject><subject>Infectious Disease</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Surveys and Questionnaires</subject><subject>Time Factors</subject><subject>Travel</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctu1TAQhiMEoqXwCCAvTyUCvsYJC1A5KlCpqAuKdHaWY0_AJTds54jzPjwBD8Iz4SSFBRuQF7bH3_wznj_LHhP8jGBSPP9AuGQ5w1W1IcUpw4xU-e5OdpzCPOdcyLvLeUWOsgch3GBMJMH8fnZEpRRESnqcfb_oxsFHpHuLwuhBWzQ0CL5F6C3YPIxgop869PNH3moTdacD5KMf7GRc_wmd9xH8UKcX8E4b0IDqA3JztNfRDb1uUfR6D20LPqDN9ur967NrFOJkD6cvkEZJaqnh9vAUdVMbnYE-ekBm-Dz3tZAPs3uNbgM8ut1Pso9vzq-37_LLq7cX27PL3AhBYy5JKY1tMBUCqORVyZs0FllSAFoyWTRgC1ZKZinTrG5A8qIg2DBO6lLrxrKTbLPqpq6-ThCi6lwwqXfdwzAFRUpR8Qqn9R8oE1xQQVhCxYqa9NfgoVGjd532B0Wwmr1Ui5dqNkql2-Kl2qW8J7clproD-yfrt3kJeLUCkGayd-BVMA56A9b5NFJlB_fPEi__UjCt653R7Rc4QLgZpmRjm36jAlV4FZk1SLEo7Ngvs0zHAQ</recordid><startdate>2017</startdate><enddate>2017</enddate><creator>Arcilla, Maris S, MD</creator><creator>van Hattem, Jarne M, MD</creator><creator>Haverkate, Manon R, PhD</creator><creator>Bootsma, Martin C J, PhD</creator><creator>van Genderen, Perry J J, PhD</creator><creator>Goorhuis, Abraham, PhD</creator><creator>Grobusch, Martin P, Prof</creator><creator>Lashof, Astrid M Oude, PhD</creator><creator>Molhoek, Nicky, MSc</creator><creator>Schultsz, Constance, PhD</creator><creator>Stobberingh, Ellen E, PhD</creator><creator>Verbrugh, Henri A, Prof</creator><creator>de Jong, Menno D, Prof</creator><creator>Melles, Damian C, PhD</creator><creator>Penders, John, Dr</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QL</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>2017</creationdate><title>Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study</title><author>Arcilla, Maris S, MD ; van Hattem, Jarne M, MD ; Haverkate, Manon R, PhD ; Bootsma, Martin C J, PhD ; van Genderen, Perry J J, PhD ; Goorhuis, Abraham, PhD ; Grobusch, Martin P, Prof ; Lashof, Astrid M Oude, PhD ; Molhoek, Nicky, MSc ; Schultsz, Constance, PhD ; Stobberingh, Ellen E, PhD ; Verbrugh, Henri A, Prof ; de Jong, Menno D, Prof ; Melles, Damian C, PhD ; Penders, John, Dr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c552t-7187cdf0255e274984f031782ee28376fed63873d23a3bfe746610c341b8aafd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>beta-Lactamases</topic><topic>Diarrhea - etiology</topic><topic>Enterobacteriaceae</topic><topic>Enterobacteriaceae - enzymology</topic><topic>Enterobacteriaceae Infections - epidemiology</topic><topic>Enterobacteriaceae Infections - transmission</topic><topic>Feces - microbiology</topic><topic>Female</topic><topic>Humans</topic><topic>Infectious Disease</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Surveys and Questionnaires</topic><topic>Time Factors</topic><topic>Travel</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arcilla, Maris S, MD</creatorcontrib><creatorcontrib>van Hattem, Jarne M, MD</creatorcontrib><creatorcontrib>Haverkate, Manon R, PhD</creatorcontrib><creatorcontrib>Bootsma, Martin C J, PhD</creatorcontrib><creatorcontrib>van Genderen, Perry J J, PhD</creatorcontrib><creatorcontrib>Goorhuis, Abraham, PhD</creatorcontrib><creatorcontrib>Grobusch, Martin P, Prof</creatorcontrib><creatorcontrib>Lashof, Astrid M Oude, PhD</creatorcontrib><creatorcontrib>Molhoek, Nicky, MSc</creatorcontrib><creatorcontrib>Schultsz, Constance, PhD</creatorcontrib><creatorcontrib>Stobberingh, Ellen E, PhD</creatorcontrib><creatorcontrib>Verbrugh, Henri A, Prof</creatorcontrib><creatorcontrib>de Jong, Menno D, Prof</creatorcontrib><creatorcontrib>Melles, Damian C, PhD</creatorcontrib><creatorcontrib>Penders, John, Dr</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arcilla, Maris S, MD</au><au>van Hattem, Jarne M, MD</au><au>Haverkate, Manon R, PhD</au><au>Bootsma, Martin C J, PhD</au><au>van Genderen, Perry J J, PhD</au><au>Goorhuis, Abraham, PhD</au><au>Grobusch, Martin P, Prof</au><au>Lashof, Astrid M Oude, PhD</au><au>Molhoek, Nicky, MSc</au><au>Schultsz, Constance, PhD</au><au>Stobberingh, Ellen E, PhD</au><au>Verbrugh, Henri A, Prof</au><au>de Jong, Menno D, Prof</au><au>Melles, Damian C, PhD</au><au>Penders, John, Dr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2017</date><risdate>2017</risdate><volume>17</volume><issue>1</issue><spage>78</spage><epage>85</epage><pages>78-85</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><abstract>Summary Background International travel contributes to the dissemination of antimicrobial resistance. We investigated the acquisition of extended-spectrum β-lactamase-producing Enterobacteriaceae (ESBL-E) during international travel, with a focus on predictive factors for acquisition, duration of colonisation, and probability of onward transmission. Methods Within the prospective, multicentre COMBAT study, 2001 Dutch travellers and 215 non-travelling household members were enrolled. Faecal samples and questionnaires on demographics, illnesses, and behaviour were collected before travel and immediately and 1, 3, 6, and 12 months after return. Samples were screened for the presence of ESBL-E. In post-travel samples, ESBL genes were sequenced and PCR with specific primers for plasmid-encoded β-lactamase enzymes TEM, SHV, and CTX-M group 1, 2, 8, 9, and 25 was used to confirm the presence of ESBL genes in follow-up samples. Multivariable regression analyses and mathematical modelling were used to identify predictors for acquisition and sustained carriage, and to determine household transmission rates. This study is registered with ClinicalTrials.gov , number NCT01676974. Findings 633 (34·3%) of 1847 travellers who were ESBL negative before travel and had available samples after return had acquired ESBL-E during international travel (95% CI 32·1–36·5), with the highest number of acquisitions being among those who travelled to southern Asia in 136 of 181 (75·1%, 95% CI 68·4–80·9). Important predictors for acquisition of ESBL-E were antibiotic use during travel (adjusted odds ratio 2·69, 95% CI 1·79–4·05), traveller's diarrhoea that persisted after return (2·31, 1·42–3·76), and pre-existing chronic bowel disease (2·10, 1·13–3·90). The median duration of colonisation after travel was 30 days (95% CI 29–33). 65 (11·3%) of 577 remained colonised at 12 months. CTX-M enzyme group 9 ESBLs were associated with a significantly increased risk of sustained carriage (median duration 75 days, 95% CI 48–102, p=0·0001). Onward transmission was found in 13 (7·7%) of 168 household members. The probability of transmitting ESBL-E to another household member was 12% (95% CI 5–18). Interpretation Acquisition and spread of ESBL-E during and after international travel was substantial and worrisome. Travellers to areas with a high risk of ESBL-E acquisition should be viewed as potential carriers of ESBL-E for up to 12 months after return. Funding Netherlands Organisation for Health Research and Development (ZonMw).</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>27751772</pmid><doi>10.1016/S1473-3099(16)30319-X</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents - therapeutic use beta-Lactamases Diarrhea - etiology Enterobacteriaceae Enterobacteriaceae - enzymology Enterobacteriaceae Infections - epidemiology Enterobacteriaceae Infections - transmission Feces - microbiology Female Humans Infectious Disease Male Middle Aged Prospective Studies Risk Factors Surveys and Questionnaires Time Factors Travel |
title | Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study |
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