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碳青霉烯类药物管理与厄他培南和抗菌药物耐药性:范围综述。

Carbapenem stewardship with ertapenem and antimicrobial resistance-a scoping review.

机构信息

Pontifícia Universidade Católica do Paraná, Faculdade de Medicina, Laboratório de Doenças Infecciosas Emergentes, Curitiba, PR, Brasil.

A.C.Camargo Cancer Center, São Paulo, SP, Brasil.

出版信息

Rev Soc Bras Med Trop. 2020 Nov 6;53:e20200413. doi: 10.1590/0037-8682-0413-2020. eCollection 2020.

DOI:10.1590/0037-8682-0413-2020
PMID:33174959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7670755/
Abstract

Consumption of carbapenem has increased due to extended-spectrum beta-lactamase-producing bacteria spreading. Ertapenem has been suggested as a not carbapenem-resistance inducer. We performed a scoping review of carbapenem-sparing stewardship with ertapenem and its impact on the antibiotic resistance of Gram-negative bacilli. We searched PubMed for studies that used ertapenem as a strategy to reduce resistance to carbapenems and included epidemiologic studies with this strategy to evaluate susceptibility patterns to cephalosporins, quinolones, and carbapenems in Gram-negative-bacilli. The search period included only studies in English, up to February 2018. From 1294 articles, 12 studies were included, mostly from the Americas. Enterobacteriaceae resistance to quinolones and cephalosporins was evaluated in 6 studies and carbapenem resistance in 4 studies. Group 2 carbapenem (imipenem/meropenem/doripenem) resistance on A. baumannii was evaluated in 6 studies. All studies evaluated P. aeruginosa resistance to Group 2 carbapenem. Resistance profiles of Enterobacteriaceae and P. aeruginosa to Group 2 carbapenems were not associated with ertapenem consumption. The resistance rate of A. baumannii to Group 2 carbapenems after ertapenem introduction was not clear due to a lack of studies without bias. In summary, ertapenem as a strategy to spare use of Group 2 carbapenems may be an option to stewardship programs without increasing resistance of Enterobacteriaceae and P. aeruginosa. More studies are needed to evaluate the influence of ertapenem on A. baumannii.

摘要

由于产超广谱β-内酰胺酶的细菌的传播,碳青霉烯类药物的消耗增加。厄他培南被认为是一种不会诱导碳青霉烯类耐药的药物。我们对使用厄他培南作为节约碳青霉烯类药物的管理策略进行了范围界定综述,并评估了其对革兰氏阴性杆菌抗生素耐药性的影响。我们在 PubMed 上搜索了使用厄他培南作为降低碳青霉烯类药物耐药性策略的研究,并纳入了这项策略的流行病学研究,以评估革兰氏阴性杆菌对头孢菌素、喹诺酮类和碳青霉烯类药物的敏感性模式。搜索期仅包括截至 2018 年 2 月的英文研究。从 1294 篇文章中,纳入了 12 项研究,主要来自美洲。有 6 项研究评估了肠杆菌科对喹诺酮类和头孢菌素的耐药性,4 项研究评估了碳青霉烯类耐药性。有 6 项研究评估了鲍曼不动杆菌对第 2 代碳青霉烯(亚胺培南/美罗培南/多利培南)的耐药性。所有研究均评估了铜绿假单胞菌对第 2 代碳青霉烯类药物的耐药性。肠杆菌科和铜绿假单胞菌对第 2 代碳青霉烯类药物的耐药谱与厄他培南的消耗无关。由于缺乏无偏倚的研究,厄他培南引入后鲍曼不动杆菌对第 2 代碳青霉烯类药物的耐药率尚不清楚。总之,作为节约第 2 代碳青霉烯类药物使用策略的厄他培南可能是管理方案的一个选择,而不会增加肠杆菌科和铜绿假单胞菌的耐药性。需要更多的研究来评估厄他培南对鲍曼不动杆菌的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6d/7670755/12c1d6d47349/1678-9849-rsbmt-53-e20200413-gf2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6d/7670755/334a76b13cc2/1678-9849-rsbmt-53-e20200413-gf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6d/7670755/12c1d6d47349/1678-9849-rsbmt-53-e20200413-gf2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6d/7670755/334a76b13cc2/1678-9849-rsbmt-53-e20200413-gf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b6d/7670755/12c1d6d47349/1678-9849-rsbmt-53-e20200413-gf2.jpg

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