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Ann Burns Fire Disasters. 2024 Jun 30;37(2):106-111. eCollection 2024 Jun.
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[Not Available].[无可用内容]
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本文引用的文献

1
Risk factors for Klebsiella pneumoniae carbapenemase (KPC) gene acquisition and clinical outcomes across multiple bacterial species.多种细菌中携带碳青霉烯酶基因(KPC)的危险因素及其临床结局。
J Hosp Infect. 2020 Apr;104(4):456-468. doi: 10.1016/j.jhin.2020.01.005. Epub 2020 Jan 10.
2
[Not Available].[无可用内容]
Ann Burns Fire Disasters. 2019 Mar 31;32(1):10-16.
3
Risk factors for carbapenem-resistant Enterobacteriaceae infections: a French case-control-control study.耐碳青霉烯类肠杆菌科感染的危险因素:法国病例对照对照研究。
Eur J Clin Microbiol Infect Dis. 2019 Feb;38(2):383-393. doi: 10.1007/s10096-018-3438-9. Epub 2018 Nov 28.
4
Metallo-β-lactamases and class D carbapenemases in south-east Tunisia: Implication of mobile genetic elements in their dissemination.东南突尼斯的金属β-内酰胺酶和 D 类碳青霉烯酶:移动遗传元件在其传播中的作用。
Int J Antimicrob Agents. 2018 Dec;52(6):871-877. doi: 10.1016/j.ijantimicag.2018.06.002. Epub 2018 Jun 15.
5
Trends in carbapenemase-producing Enterobacteriaceae, France, 2012 to 2014.2012年至2014年法国产碳青霉烯酶肠杆菌科细菌的流行趋势
Euro Surveill. 2017 Feb 9;22(6). doi: 10.2807/1560-7917.ES.2017.22.6.30461.
6
Rectal Carriage of Extended-Spectrum Beta-Lactamase and Carbapenemase Producing Gram-Negative Bacilli in Intensive Care Units in Tunisia.突尼斯重症监护病房中产超广谱β-内酰胺酶和碳青霉烯酶革兰氏阴性杆菌的直肠携带情况
Microb Drug Resist. 2017 Sep;23(6):695-702. doi: 10.1089/mdr.2016.0205. Epub 2017 Jan 18.
7
Early detection of metallo-β-lactamase NDM-1- and OXA-23 carbapenemase-producing Acinetobacter baumannii in Libyan hospitals.利比亚医院中产金属β-内酰胺酶 NDM-1 和 OXA-23 碳青霉烯酶的鲍曼不动杆菌的早期检测。
Int J Antimicrob Agents. 2016 Jul;48(1):46-50. doi: 10.1016/j.ijantimicag.2016.03.007. Epub 2016 Apr 25.
8
Acquisition of carbapenem-resistant Gram-negative bacilli in intensive care unit: predictors and molecular epidemiology.重症监护病房获得碳青霉烯类耐药革兰氏阴性杆菌:预测因素和分子流行病学。
Med Mal Infect. 2015 Jan-Feb;45(1-2):34-40. doi: 10.1016/j.medmal.2014.12.003. Epub 2015 Jan 29.
9
Emergence of NDM-1 in association with OXA-48 in Klebsiella pneumoniae from Tunisia.突尼斯肺炎克雷伯菌中与OXA-48相关的NDM-1的出现。
Antimicrob Agents Chemother. 2013 Aug;57(8):4089-90. doi: 10.1128/AAC.00536-13. Epub 2013 Jun 10.
10
Genotyping using whole-genome sequencing is a realistic alternative to surveillance based on phenotypic antimicrobial susceptibility testing.全基因组测序的基因分型是基于表型抗菌药物敏感性试验的监测的一种现实替代方法。
J Antimicrob Chemother. 2013 Apr;68(4):771-7. doi: 10.1093/jac/dks496. Epub 2012 Dec 11.

[突尼斯烧伤患者中碳青霉烯酶的分布]

[DISTRIBUTION OF CARBAPENEMASES IN TUNISIAN BURN PATIENTS].

作者信息

Mokline A, Zarrouk S, Jemi I, Fraj H, Gasri B, Ben Saad M, Thabet L, Messadi A A

出版信息

Ann Burns Fire Disasters. 2024 Jun 30;37(2):106-111. eCollection 2024 Jun.

PMID:38974797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11225287/
Abstract

Resistance to carpabenems in burns is rapidly spreading in many countries. Therefore identification of carbapenemase pathogen carriers is imperative in order to establish adequate infection control precautions and stop outbreaks of these multidrug-resistant bacteria. The aim of our study was to evaluate the distribution of carbapenemase producers in burn patients admitted to a burn center in Tunisia over 9 months. PCR for carbapenemase portage was performed in all patients within 48 hours of admission. Seventeen patients carried a single carbapenemase, 11 carried two, and 25 carried three. The enzymes detected were VIM (n=41), NDM (n=41) and OXA48 (n=32). Enzyme mapping revealed two main areas of carriage in central western Tunisia: Kairouan (NDM/OXA48) and Kasserine (NDM/VIM). Predictive factors for carriage of carbapenemase were: prior antibiotic therapy (n=24); mechanical ventilation (n=30); vascular catheterization (n=31) and a previous stay in intensive care (n=11).

摘要

在许多国家,烧伤患者对碳青霉烯类药物的耐药性正在迅速蔓延。因此,识别碳青霉烯酶病原体携带者对于建立适当的感染控制预防措施并阻止这些多重耐药菌的爆发至关重要。我们研究的目的是评估突尼斯一家烧伤中心9个月内入院的烧伤患者中碳青霉烯酶产生菌的分布情况。在所有患者入院48小时内进行碳青霉烯酶携带情况的PCR检测。17例患者携带一种碳青霉烯酶,11例携带两种,25例携带三种。检测到的酶为VIM(n = 41)、NDM(n = 41)和OXA48(n = 32)。酶谱分析显示突尼斯中西部有两个主要携带区域:凯鲁万(NDM/OXA48)和凯塞林(NDM/VIM)。碳青霉烯酶携带的预测因素为:先前的抗生素治疗(n = 24);机械通气(n = 30);血管插管(n = 31)以及先前在重症监护病房住院(n = 11)。