Epidemiological Trends of Carbapenemase-Producing Pseudomonas aeruginosa in a Tertiary Care Hospital in Athens, Greece, During 2020-2023.

IF 4.6 2区 医学 Q1 INFECTIOUS DISEASES
Vasiliki Koumaki, Eleni Voudanta, Aikaterini Michelaki, Maria Orfanidou, Eleni Vagiakou, Georgia Vrioni, Athanasios Tsakris
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引用次数: 0

Abstract

Background: Infections caused by carbapenemase-producing Pseudomonas aeruginosa (CPPA) isolates have become a worldwide clinical challenge for clinicians due to the limited treatment options. This study provides epidemiological data on CPPA clinical isolates recovered from one of the largest tertiary care hospitals in Athens, Greece, serving a diverse patient population during and after the COVID-19 pandemic. Materials and Methods: The study included all consecutive single-patient CPPA clinical isolates identified from January 2020 to December 2023 in the clinical laboratory. Identification and antimicrobial susceptibility testing were performed using the VITEK-2 automated system. A lateral flow immunoassay and the FilmArray system for blood cultures only were used for the detection of the five most prevalent carbapenemases. Their epidemiological and antimicrobial susceptibility trends were retrospectively analyzed. Results: During the study period, a total of 628 single-patient CPPA were identified among 902 carbapenem-resistant P. aeruginosa clinical isolates. An increasing number of CPPA was revealed during the survey, especially in the post-COVID period (rising from n = 102 in 2020, n = 105 in 2021, and n = 123 in 2022 to n = 298 in 2023; p < 0.05). Regarding the type of carbapenemase, VIM metallo-beta-lactamase was the only carbapenemase identified during the first two years of the study (2020 to 2021). In 2022, VIM- and NDM-producing isolates split almost evenly at proportions of 57% and 43%, respectively. In 2023, NDM-producing isolates seem to have surpassed VIM producers with rates of 54.4% and 45.6%, respectively. As far as antimicrobial resistance profiles, high rates of resistance were observed for most of the antipseudomonal drugs, exceeding 90% across all study years, with little significant variation. However, aztreonam exhibited moderate activity and colistin exhibited excellent activity, remaining the most viable drugs in this setting. Conclusions: Following the COVID-19 pandemic, an increase in CPPA pathogens was identified, while an epidemiological shift was also observed, with the carbapenemase NDM dominating over VIM since 2023. Continuous surveillance is required to track resistance patterns and guide empirical therapy. In this context, new antimicrobials and antimicrobial combinations are also urgently needed.

Abstract Image

2020-2023年希腊雅典某三级医院产碳青霉烯酶铜绿假单胞菌流行病学趋势
背景:由产碳青霉烯酶铜绿假单胞菌(CPPA)引起的感染,由于治疗方案有限,已成为全球临床医生面临的一个临床挑战。本研究提供了从希腊雅典最大的三级医院之一恢复的CPPA临床分离株的流行病学数据,该医院在COVID-19大流行期间和之后为不同的患者群体提供服务。材料和方法:该研究纳入了2020年1月至2023年12月在临床实验室连续鉴定的所有单例CPPA临床分离株。使用VITEK-2自动化系统进行鉴定和药敏试验。横向流动免疫分析法和仅用于血液培养的FilmArray系统用于检测五种最常见的碳青霉烯酶。回顾性分析其流行病学及药敏趋势。结果:研究期间,在902株耐碳青霉烯类P. aeruginosa临床分离株中共检出单例CPPA 628株。在调查期间,CPPA数量不断增加,特别是在covid后时期(从2020年的n = 102, 2021年的n = 105, 2022年的n = 123上升到2023年的n = 298, p < 0.05)。关于碳青霉烯酶的类型,VIM金属β -内酰胺酶是研究前两年(2020年至2021年)唯一确定的碳青霉烯酶。到2022年,产生VIM和ndm的分离株几乎平均分布,比例分别为57%和43%。到2023年,产生ndm的分离株的比例将分别达到54.4%和45.6%,超过产生VIM的分离株。就抗菌素耐药情况而言,大多数抗假单胞菌药物的耐药率很高,在所有研究年份中均超过90%,且差异不大。然而,aztreonam表现出中等活性,粘菌素表现出优异的活性,在这种情况下仍然是最可行的药物。结论:在2019冠状病毒病大流行之后,CPPA病原体数量增加,同时流行病学也发生了变化,碳青霉烯酶NDM自2023年以来主导了VIM。需要持续监测以跟踪耐药性模式并指导经验性治疗。在这种情况下,还迫切需要新的抗菌素和抗菌素组合。
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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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