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在患有发热性尿路感染的儿科人群中,克拉维酸与美西林、头孢克肟或头孢泊肟组合用于对抗产超广谱β-内酰胺酶(ESBL)的肠杆菌科细菌,这些细菌常与blaOXA-1相关。

Clavulanate combinations with mecillinam, cefixime or cefpodoxime against ESBL-producing Enterobacterales frequently associated with blaOXA-1 in a paediatric population with febrile urinary tract infections.

作者信息

Birgy André, Madhi Fouad, Jung Camille, Levy Corinne, Cointe Aurélie, Bidet Philippe, Hobson Claire Amaris, Bechet Stéphane, Sobral Elsa, Vuthien Hoang, Ferroni Agnès, Aberrane Saïd, Cuzon Gaëlle, Beraud Laetitia, Gajdos Vincent, Launay Elise, Pinquier Didier, Haas Hervé, Desmarest Marie, Dommergues Marie-Aliette, Cohen Robert, Bonacorsi Stéphane

机构信息

Université de Paris, IAME, INSERM, F-75018 Paris, France.

AP-HP, Hôpital Robert Debré, Service de Microbiologie, F-75019 Paris, France.

出版信息

J Antimicrob Chemother. 2021 Oct 11;76(11):2839-2846. doi: 10.1093/jac/dkab289.

Abstract

OBJECTIVES

Oral treatment of febrile urinary tract infections (FUTIs) can be impaired by MDR Enterobacterales often combining ESBL and inhibitor-resistant genes. We studied the impact of β-lactamases and Enterobacterales' genotypes on the cefixime, cefpodoxime and mecillinam ± amoxicillin/clavulanate MICs.

MATERIALS AND METHODS

In this multicentric study, we included 251 previously whole-genome-sequenced ESBL-producing Enterobacterales, isolated in French children with FUTIs. The MICs of cefixime, cefpodoxime, mecillinam alone and combined with amoxicillin/clavulanate were determined and analysed with respect to genomic data. We focused especially on the isolates' ST and their type of β-lactamases. Clinical outcomes of patients who received cefixime + amoxicillin/clavulanate were also analysed.

RESULTS

All isolates were cefixime and cefpodoxime resistant. Disparities depending on blaCTX-M variants were observed for cefixime. The addition of amoxicillin/clavulanate restored susceptibility for cefixime and cefpodoxime in 97.2% (MIC50/90 of 0.38/0.75 mg/L) and 55.4% (MIC50/90 of 1/2 mg/L) of isolates, respectively, whatever the ST, the blaCTX-M variants or the association with inhibitor-resistant β-lactamases (34.2%). All isolates were susceptible to mecillinam + amoxicillin/clavulanate with MIC50/90 of 0.19/0.25 mg/L, respectively. Neither therapeutic failure nor any subsequent positive control urine culture were reported for patients who received cefixime + amoxicillin/clavulanate as an oral relay therapy (n = 54).

CONCLUSIONS

Despite the frequent association of ESBL genes with inhibitor-resistant β-lactamases, the cefixime + amoxicillin/clavulanate MICs remain low. The in vivo efficacy of this combination was satisfying even when first-line treatment was ineffective. Considering the MIC distributions and pharmacokinetic parameters, mecillinam + amoxicillin/clavulanate should also be an alternative to consider when treating FUTIs in children.

摘要

目的

产超广谱β-内酰胺酶(ESBL)且常携带抑制剂耐药基因的多重耐药肠杆菌科细菌,可能会影响发热性尿路感染(FUTIs)的口服治疗效果。我们研究了β-内酰胺酶和肠杆菌科细菌基因型对头孢克肟、头孢泊肟和美西林±阿莫西林/克拉维酸最低抑菌浓度(MIC)的影响。

材料与方法

在这项多中心研究中,我们纳入了251株先前已进行全基因组测序的产ESBL肠杆菌科细菌,这些细菌分离自法国患有FUTIs的儿童。测定了头孢克肟、头孢泊肟、单独使用的美西林以及与阿莫西林/克拉维酸联合使用时的MIC,并根据基因组数据进行分析。我们特别关注分离株的序列型(ST)及其β-内酰胺酶类型。还分析了接受头孢克肟+阿莫西林/克拉维酸治疗的患者的临床结局。

结果

所有分离株均对头孢克肟和头孢泊肟耐药。观察到头孢克肟的MIC因blaCTX-M变体不同而存在差异。无论ST、blaCTX-M变体或与抑制剂耐药β-内酰胺酶的关联情况(34.2%)如何,添加阿莫西林/克拉维酸后,分别有97.2%(MIC50/90为0.38/0.75mg/L)和55.4%(MIC50/90为1/2mg/L)的分离株对头孢克肟和头孢泊肟恢复了敏感性。所有分离株对美西林+阿莫西林/克拉维酸均敏感,MIC50/90分别为0.19/0.25mg/L。接受头孢克肟+阿莫西林/克拉维酸作为口服序贯治疗的患者(n = 54),未报告治疗失败情况,也未出现后续尿培养阳性对照结果。

结论

尽管ESBL基因常与抑制剂耐药β-内酰胺酶相关联,但头孢克肟+阿莫西林/克拉维酸的MIC仍然较低。即使一线治疗无效,该联合用药的体内疗效也令人满意。考虑到MIC分布和药代动力学参数,美西林+阿莫西林/克拉维酸也应作为治疗儿童FUTIs时可供考虑的替代方案。

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