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国际旅行者携带和传播产超广谱β-内酰胺酶肠杆菌科细菌(COMBAT 研究):一项前瞻性、多中心队列研究。

Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study.

机构信息

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Centre, Rotterdam, Netherlands.

Department of Medical Microbiology, Academic Medical Centre, Amsterdam, Netherlands.

出版信息

Lancet Infect Dis. 2017 Jan;17(1):78-85. doi: 10.1016/S1473-3099(16)30319-X. Epub 2016 Oct 14.

Abstract

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).

摘要

背景

国际旅行促进了抗生素耐药性的传播。我们研究了国际旅行期间产超广谱β-内酰胺酶肠杆菌科(ESBL-E)的获得情况,重点是获得的预测因素、定植时间以及传播的可能性。

方法

在前瞻性、多中心 COMBAT 研究中,招募了 2001 名荷兰旅行者和 215 名非旅行者的家庭成员。在旅行前、旅行后立即以及 1、3、6 和 12 个月采集粪便样本和关于人口统计学、疾病和行为的问卷。对 ESBL-E 的存在进行了筛查。在旅行后的样本中,对 ESBL 基因进行了测序,并使用针对质粒编码的β-内酰胺酶 TEM、SHV 和 CTX-M 组 1、2、8、9 和 25 的特定引物进行 PCR,以确认后续样本中存在 ESBL 基因。使用多变量回归分析和数学模型来确定获得和持续携带的预测因素,并确定家庭传播率。这项研究在 ClinicalTrials.gov 注册,编号为 NCT01676974。

结果

在旅行前 ESBL 阴性且有旅行后样本的 1847 名旅行者中,有 633 名(34.3%,95%CI 32.1-36.5)在国际旅行期间获得了 ESBL-E,其中获得数量最多的是 181 名前往南亚的旅行者中的 136 名(75.1%,95%CI 68.4-80.9)。获得 ESBL-E 的重要预测因素是旅行期间使用抗生素(调整后的优势比 2.69,95%CI 1.79-4.05)、旅行后持续存在的旅行者腹泻(2.31,1.42-3.76)和预先存在的慢性肠道疾病(2.10,1.13-3.90)。旅行后的定植中位时间为 30 天(95%CI 29-33)。577 名中有 65 名(11.3%)在 12 个月时仍定植。CTX-M 酶组 9 ESBL 与持续携带的风险显著增加相关(中位时间 75 天,95%CI 48-102,p=0.0001)。在 168 名家庭成员中发现了 13 名(7.7%)的传播。将 ESBL-E 传播给另一个家庭成员的概率为 12%(95%CI 5-18)。

解释

在国际旅行期间和之后,ESBL-E 的获得和传播相当多且令人担忧。旅行者到 ESBL-E 获得风险高的地区旅行,在返回后长达 12 个月内应被视为潜在的 ESBL-E 携带者。

资金

荷兰健康研究与发展组织(ZonMw)。

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