沙特阿拉伯一家三级医院ICU患者中多重耐药革兰氏阴性菌:临床和直肠拭子样本中碳青霉烯酶基因的分布

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Amal Daher Alshammari, Alharbi Mohammed Salem, Sumayyah Mohammad Almarshedy, Ehab Rakha, Mohd Saleem
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引用次数: 0

摘要

革兰氏阴性菌的抗微生物药物耐药性是一个日益严峻的临床挑战。本研究旨在评估临床分离株的细菌分布、抗菌药物敏感性和碳青霉烯酶基因流行率。共纳入154例患者(平均年龄:57.51±18.75岁)。标本主要为痰液(42.2%)、血液(22.7%)和尿液(18.8%)。分离细菌包括肺炎克雷伯菌(43.8%)、鲍曼不动杆菌(24%)和铜绿假单胞菌(13.5%)。采用药敏试验(AST)评价耐药模式。发现耐多药,对碳青霉烯类、β-内酰胺类和氟喹诺酮类药物的耐药性惊人。鲍曼杆菌和铜绿假单胞菌对亚胺培南(IPM)、美罗培南(MRP)和厄他培南(ETP)几乎完全耐药,表明广泛耐药(XDR)。肺炎克雷伯菌对碳青霉烯类抗菌药物(IPM: 90.5%, MRP: 92.9%)和β-内酰胺类抗菌药物(>:90%)表现出异常高的耐药性。鲍曼假单胞菌、铜绿假单胞菌和肺炎克雷伯菌对环丙沙星和左氧氟沙星氟喹诺酮类药物的耐药性超过90%。氨基糖苷类,尤其是庆大霉素,表现出中等耐药性(鲍曼假单胞菌:87%,铜绿假单胞菌:69.2%)。替加环素仍然是对抗肺炎克雷伯菌的少数可行的治疗选择之一。生物膜形成显著,63.6%的分离菌产生生物膜,特别是铜绿假单胞菌(80.9%)、肺炎克雷伯菌(67.2%)和鲍曼假单胞菌(48.6%),增加了它们的致病潜力。42.9%的分离株检测到碳青霉烯酶的产生。最常见的基因是blaOXA- 48(15.6%)、blaNDM(8.4%)和blaVIM(7.1%),共表达9.7%的分离株。肺炎克雷伯菌碳青霉烯酶产生的风险最高(OR: 4.23, p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multidrug-resistant gram-negative bacteria in ICU patients of a tertiary care hospital in Saudi Arabia: distribution of carbapenemase genes in clinical and rectal swab samples.

Antimicrobial resistance among Gram-negative bacteria is a growing clinical challenge. This study aimed to assess bacterial distribution, antimicrobial susceptibility, and carbapenemase gene prevalence in clinical isolates. A total of 154 patients (mean age: 57.51 ± 18.75 years) were included. Specimens were primarily sputum (42.2%), blood (22.7%), and urine (18.8%). Bacterial isolates included K pneumoniae (43.8%), A. baumannii (24%), and P. aeruginosa (13.5%). Antimicrobial susceptibility testing (AST) was conducted to evaluate resistance patterns. MDR was detected, with alarming resistance to carbapenems, β-lactams, and fluoroquinolones. A. baumannii and P. aeruginosa exhibited near-total resistance to Imipenem (IPM), Meropenem (MRP), and Ertapenem (ETP), indicating extensive drug resistance (XDR). K. pneumoniae demonstrated exceptionally high resistance to carbapenems (IPM: 90.5%, MRP: 92.9%) and β-lactam antibacterial drugs (> 90%). Fluoroquinolone resistance exceeded 90% for Ciprofloxacin and Levofloxacin in A. baumannii, P. aeruginosa, and K. pneumoniae. Aminoglycosides, particularly Gentamicin, showed moderate resistance (A. baumannii: 87%, P. aeruginosa: 69.2%). Tigecycline remained one of the few viable treatment options against K. pneumoniae. Biofilm formation was significant, with 63.6% of isolates producing biofilm, particularly P. aeruginosa (80.9%), K. pneumoniae (67.2%), and A. baumannii (48.6%), increasing their pathogenic potential. Carbapenemase production was detected in 42.9% of isolates. The most prevalent genes were blaOXA- 48 (15.6%), blaNDM (8.4%), and blaVIM (7.1%), with co-expression in 9.7% of isolates. K. pneumoniae exhibited the highest risk for carbapenemase production (OR: 4.23, p < 0.001), whereas A. baumannii had a significantly lower risk (OR: 0.20, p = 0.005). Screening swabs showed more OXA- 48 (42.1%), while clinical isolates had more NDM and VIM. Alternative resistance mechanisms were suggested in 57.3% of clinical cases. The overwhelming prevalence of MDR and Carbapenem resistance among Gram-negative bacteria, particularly K. pneumoniae and A. baumannii, emphasizes an urgent need for strict antimicrobial stewardship, advanced infection control strategies, and novel therapeutic interventions to combat resistance spread.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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