Navigating an evolving microbial landscape: emerging antimicrobial resistance trends and precision stewardship in Tianjin tertiary hospitals (2021-2023).

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-09-08 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1629038
Yong-Li Wan, Tao Han, Qiang Sun, Donghao Wang, Jun Li, Li-Jie Wang, Min Peng, Yin Li, Qing-Guo Feng, Chun-Guang Liu, Jie Xu, Bin Bao, Mei Su, Zhi-Yong Fei, Xu-Liang Wang, Xiao-Bo Liu
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引用次数: 0

Abstract

Objective: To evaluate microbial distribution and antimicrobial resistance (AMR) patterns in clinical isolates from 13 tertiary hospitals and one secondary hospital in Tianjin (2021-2023) to inform precision-driven antimicrobial stewardship and infection control interventions.

Methods: In this retrospective, multicenter study, we collected routine diagnostic specimens-including sputum, fecal samples, secretions, blood, and drainage fluids. Data were processed per standardized protocols (CARSS, CHINET) and interpreted using current CLSI-M100 breakpoints. Statistical analyses were performed with SPSS 20.0 (significance set at two-tailed P < 0.05).

Results: Sputum specimens increased from 39.1% to 43.0%, while urine samples and secretions declined. Klebsiella pneumoniae prevalence rose from 18.3% to 20.3%, whereas Escherichia coli remained stable. E. coli maintained excellent susceptibility to carbapenems and amikacin (≤2% resistance); notably, ceftazidime/avibactam resistance declined from 7.2% to 3.4% (P = 0.005) amid a significant increase in cefepime resistance (24.4% to 29.6%, P < 0.001). K. pneumoniae exhibited parallel trends, with escalating resistance to β-lactam/β-lactamase inhibitor agents. In Pseudomonas aeruginosa, aminoglycoside, and carbapenem profiles remained stable, while ceftazidime/avibactam sensitivity markedly improved, suggesting shifts in underlying resistance mechanisms. Acinetobacter baumannii showed enhanced susceptibility to aminoglycosides, β-lactam inhibitors, and fluoroquinolones; however, carbapenem-resistant isolates continued to exhibit near-universal resistance. Among gram-positive pathogens, methicillin-resistant Staphylococcus aureus sustained near-universal β-lactam resistance with improved rifampicin sensitivity, while glycopeptides and linezolid remained fully active. Enterococcus faecalis demonstrated reduced ampicillin resistance, contrasting with E. faecium's near-pan-resistance to β-lactams and fluoroquinolones.

Conclusion: Evolving, species-specific AMR patterns in Tianjin hospitals highlight the urgent need for real-time, regionally stratified surveillance and molecularly informed stewardship strategies to guide targeted antimicrobial interventions and improve clinical outcomes.

导航不断变化的微生物景观:天津三级医院新出现的抗菌素耐药性趋势和精确管理(2021-2023)
目的:评价天津市13所三级医院和1所二级医院临床分离菌2021-2023年的微生物分布及耐药性(AMR)模式,为精准抗菌药物管理和感染控制干预提供依据。方法:在这项回顾性的多中心研究中,我们收集了常规诊断标本,包括痰、粪便、分泌物、血液和引流液。数据按照标准化协议(CARSS, CHINET)进行处理,并使用当前的CLSI-M100断点进行解释。采用SPSS 20.0软件进行统计学分析(双尾P显著性设置)。结果痰标本从39.1%上升到43.0%,尿标本和分泌物标本下降。肺炎克雷伯菌的流行率从18.3%上升到20.3%,而大肠杆菌保持稳定。大肠杆菌对碳青霉烯类和阿米卡星保持良好的敏感性(耐药≤2%);值得注意的是,头孢他啶/阿维巴坦耐药性从7.2%下降到3.4% (P = 0.005),头孢吡肟耐药性显著增加(24.4%至29.6%,P = 0.005)。肺炎表现出类似的趋势,对β-内酰胺/β-内酰胺酶抑制剂的耐药性不断上升。在铜绿假单胞菌中,氨基糖苷和碳青霉烯谱保持稳定,而头孢他啶/阿维巴坦的敏感性明显改善,表明潜在的耐药机制发生了变化。鲍曼不动杆菌对氨基糖苷类、β-内酰胺抑制剂和氟喹诺酮类药物的敏感性增强;然而,碳青霉烯耐药菌株继续表现出几乎普遍的耐药性。在革兰氏阳性病原体中,耐甲氧西林金黄色葡萄球菌维持了几乎普遍的β-内酰胺耐药性,并改善了利福平的敏感性,而糖肽类和利奈唑胺仍保持完全活性。粪肠球菌对氨苄西林的耐药性降低,而粪肠球菌对β-内酰胺类药物和氟喹诺酮类药物几乎全耐药。结论:天津市医院不断演变的物种特异性抗菌素耐药性模式凸显了实时、区域分层监测和分子知情管理策略的迫切需要,以指导有针对性的抗菌素干预和改善临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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