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巴西塞尔希培州产碳青霉烯酶肺炎克雷伯菌和产新德里金属β-内酰胺酶肺炎克雷伯菌的流行情况,以及联合治疗作为一种潜在的治疗选择。

Prevalence of Klebsiella pneumoniae carbapenemase - and New Delhi metallo-beta-lactamase-positive K. pneumoniae in Sergipe, Brazil, and combination therapy as a potential treatment option.

机构信息

Programa de Pós-Graduação em Biologia Parasitária, Universidade Federal de Sergipe, São Cristóvão, SE, Brasil.

出版信息

Rev Soc Bras Med Trop. 2020;53:e20200064. doi: 10.1590/0037-8682-0064-2020. Epub 2020 May 11.

Abstract

INTRODUCTION

Carbapenem-resistant Klebsiella pneumoniae infection lacks treatment options and is associated with prolonged hospital stays and high mortality rates. The production of carbapenemases is one of the most important factors responsible for this multi-resistance phenomenon.

METHODS

In the present study, we analyzed the presence of genes encoding carbapenemases in K. pneumoniae isolates circulating in one of the public hospitals in the city of Aracaju, Sergipe, Brazil. We also determined the best combination of drugs that display in vitro antimicrobial synergy. First, 147 carbapenem-resistant K. pneumoniae isolates were validated for the presence of blaKPC, bla GES, bla NDM, bla SPM, bla IMP, bla VIM, and bla OXA-48 genes using multiplex polymerase chain reaction. Thereafter, using two isolates (97 and 102), the role of double and triple combinational drug therapy as a treatment option was analyzed.

RESULTS

Seventy-four (50.3%) isolates were positive for bla NDM, eight (5.4%) for bla KPC, and one (1.2%) for both bla NDM and bla KPC. In the synergy tests, double combinations were better than triple combinations. Polymyxin B and amikacin for isolate 97 and polymyxin B coupled with meropenem for isolate 102 showed the best response.

CONCLUSIONS

Clinicians in normal practice use multiple drugs to treat infections caused by multi-resistant microorganism; however, in most cases, the benefit of the combinations is unknown. In vitro synergistic tests, such as those described herein, are important as they might help select an appropriate multi-drug antibiotic therapy and a correct dosage, ultimately reducing toxicities and the development of antibiotic resistance.

摘要

简介

耐碳青霉烯类肺炎克雷伯菌感染缺乏治疗选择,与住院时间延长和高死亡率相关。碳青霉烯酶的产生是导致这种多药耐药现象的最重要因素之一。

方法

本研究分析了巴西塞阿腊州阿雷格里港的一家公立医院中流行的肺炎克雷伯菌分离株中编码碳青霉烯酶的基因的存在情况。我们还确定了显示体外抗菌协同作用的最佳药物组合。首先,使用多重聚合酶链反应验证了 147 株耐碳青霉烯类肺炎克雷伯菌分离株中 blaKPC、blaGES、blaNDM、blaSPM、blaIMP、blaVIM 和 blaOXA-48 基因的存在。然后,使用两个分离株(97 和 102),分析了双组合和三组合药物治疗作为治疗选择的作用。

结果

74 株(50.3%)分离株blaNDM 阳性,8 株(5.4%)blaKPC 阳性,1 株(1.2%)同时blaNDM 和 blaKPC 阳性。协同试验中,双组合优于三组合。对于分离株 97,多黏菌素 B 和阿米卡星,对于分离株 102,多黏菌素 B 与美罗培南联合使用显示出最佳反应。

结论

临床医生在常规实践中使用多种药物治疗多药耐药微生物引起的感染;然而,在大多数情况下,组合的益处是未知的。如本文所述的体外协同试验非常重要,因为它们可以帮助选择适当的多药抗生素治疗和正确的剂量,最终减少毒性和抗生素耐药性的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af8/7269519/c5eacd898fdf/1678-9849-rsbmt-53-e20200064-gf1.jpg

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