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囊性纤维化患者中铜绿假单胞菌的抗生素耐药性演变(2010 - 2013年)

Antibiotic resistance evolution of Pseudomonas aeruginosa in cystic fibrosis patients (2010-2013).

作者信息

Lucca Francesca, Guarnieri Margherita, Ros Mirco, Muffato Giovanna, Rigoli Roberto, Da Dalt Liviana

机构信息

Department of Woman's and Child's Health, University of Padova, Padova, Italy.

Cystic Fibrosis Unit, Pediatric Department, Treviso Hospital, Treviso, Italy.

出版信息

Clin Respir J. 2018 Jul;12(7):2189-2196. doi: 10.1111/crj.12787. Epub 2018 Apr 1.

DOI:10.1111/crj.12787
PMID:29498795
Abstract

INTRODUCTION

Pseudomonas aeruginosa is the predominant pathogen responsible of chronic colonization of the airways in cystic fibrosis (CF) patients. There are few European data about antibiotic susceptibility evolution of P aeruginosa in CF patients.

OBJECTIVES

The aim of this study is to evaluate the evolution of antibiotic resistance in the period 2010-2013 in CF patients chronically colonized by P aeruginosa and to highlight the characteristics of this evolution in patients younger than 20 years.

METHODS

Clinical and microbiological data were extracted from two electronic databases and analyzed. Antibiotic resistance was defined according to European Committee of Antimicrobial Susceptibility Testing for levofloxacin, ciprofloxacin, meropenem, amikacin and ceftazidime. The between-group comparison was drawn with the Chi-square test for proportions, with the T-test for unpaired samples for normally distributed data and with Mann-Whitney test for non-normally distributed data. Significancy was defined by P < .05.

RESULTS

Fifty-seven CF patients, including thirteen subjects aged less than 20 years, were enrolled. P.. aeruginosa antibiotic sensitivity decreased significantly for fluoroquinolones, mainly in patients aged <20 years, while it increased for amikacin and colistin. The analysis of minimum inhibitory concentration confirmed these trends. In pediatric patients treated with more than three antibiotic cycles per year, greater resistance was found, except for amikacin and colistin.

CONCLUSION

An evolution in P aeruginosa antibiotic resistances is observed in the 4-year period studied. Responsible and informed use of antibiotics is mandatory in CF.

摘要

引言

铜绿假单胞菌是囊性纤维化(CF)患者气道慢性定植的主要病原体。关于CF患者中铜绿假单胞菌抗生素敏感性演变的欧洲数据较少。

目的

本研究旨在评估2010 - 2013年期间长期被铜绿假单胞菌定植的CF患者的抗生素耐药性演变,并突出20岁以下患者这一演变的特征。

方法

从两个电子数据库中提取并分析临床和微生物学数据。根据欧洲抗菌药物敏感性测试委员会的标准定义左氧氟沙星、环丙沙星、美罗培南、阿米卡星和头孢他啶的抗生素耐药性。组间比较采用比例的卡方检验、正态分布数据的非配对样本t检验以及非正态分布数据的曼 - 惠特尼检验。显著性定义为P < 0.05。

结果

纳入了57例CF患者,其中包括13例年龄小于20岁的受试者。铜绿假单胞菌对氟喹诺酮类药物的抗生素敏感性显著下降,主要发生在年龄<20岁的患者中,而对阿米卡星和黏菌素的敏感性增加。最低抑菌浓度分析证实了这些趋势。在每年接受超过三个抗生素疗程治疗的儿科患者中,除阿米卡星和黏菌素外,发现耐药性更高。

结论

在所研究的4年期间观察到铜绿假单胞菌抗生素耐药性的演变。在CF中必须合理且明智地使用抗生素。

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