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重症监护患者肠道菌群中产碳青霉烯类耐药革兰阴性杆菌的出现。

Emergence of imipenem-resistant gram-negative bacilli in intestinal flora of intensive care patients.

机构信息

French National Reference Center for Bacterial Resistance in Commensal Flora, Laboratory of Bacteriology, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

出版信息

Antimicrob Agents Chemother. 2013 Mar;57(3):1488-95. doi: 10.1128/AAC.01823-12. Epub 2013 Jan 14.

Abstract

Intestinal flora contains a reservoir of Gram-negative bacilli (GNB) resistant to cephalosporins, which are potentially pathogenic for intensive care unit (ICU) patients; this has led to increasing use of carbapenems. The emergence of carbapenem resistance is a major concern for ICUs. Therefore, in this study, we aimed to assess the intestinal carriage of imipenem-resistant GNB (IR-GNB) in intensive care patients. For 6 months, 523 consecutive ICU patients were screened for rectal IR-GNB colonization upon admission and weekly thereafter. The phenotypes and genotypes of all isolates were determined, and a case control study was performed to identify risk factors for colonization. The IR-GNB colonization rate increased regularly from 5.6% after 1 week to 58.6% after 6 weeks in the ICU. In all, 56 IR-GNB strains were collected from 50 patients: 36 Pseudomonas aeruginosa strains, 12 Stenotrophomonas maltophilia strains, 6 Enterobacteriaceae strains, and 2 Acinetobacter baumannii strains. In P. aeruginosa, imipenem resistance was due to chromosomally encoded resistance (32 strains) or carbapenemase production (4 strains). In the Enterobacteriaceae strains, resistance was due to AmpC cephalosporinase and/or extended-spectrum β-lactamase production with porin loss. Genomic comparison showed that the strains were highly diverse, with 8 exceptions (4 VIM-2 carbapenemase-producing P. aeruginosa strains, 2 Klebsiella pneumoniae strains, and 2 S. maltophilia strains). The main risk factor for IR-GNB colonization was prior imipenem exposure. The odds ratio for colonization was already as high as 5.9 (95% confidence interval [95% CI], 1.5 to 25.7) after 1 to 3 days of exposure and increased to 7.8 (95% CI, 2.4 to 29.8) thereafter. In conclusion, even brief exposure to imipenem is a major risk factor for IR-GNB carriage.

摘要

肠道菌群中存在着对头孢菌素耐药的革兰氏阴性杆菌(GNB),这些细菌对重症监护病房(ICU)患者具有潜在的致病性;这导致了碳青霉烯类药物的使用越来越多。碳青霉烯类耐药的出现是 ICU 面临的主要问题之一。因此,在这项研究中,我们旨在评估 ICU 患者肠道携带耐亚胺培南的 GNB(IR-GNB)的情况。在 6 个月的时间里,连续筛查了 523 例 ICU 患者的直肠 IR-GNB 定植情况,入院时和此后每周进行一次。所有分离株的表型和基因型均已确定,并进行了病例对照研究,以确定定植的危险因素。IR-GNB 的定植率从入院后第 1 周的 5.6%逐渐上升,第 6 周达到 58.6%。总共从 50 例患者中收集了 56 株 IR-GNB 菌株:36 株铜绿假单胞菌菌株、12 株嗜麦芽寡养单胞菌菌株、6 株肠杆菌科菌株和 2 株鲍曼不动杆菌菌株。在铜绿假单胞菌中,亚胺培南耐药是由于染色体编码的耐药(32 株)或碳青霉烯酶的产生(4 株)所致。在肠杆菌科菌株中,耐药是由于 AmpC 头孢菌素酶和/或广泛的β-内酰胺酶的产生以及孔蛋白的缺失所致。基因组比较表明,这些菌株具有高度的多样性,有 8 个例外(4 株产 VIM-2 碳青霉烯酶的铜绿假单胞菌菌株、2 株肺炎克雷伯菌菌株和 2 株嗜麦芽寡养单胞菌菌株)。IR-GNB 定植的主要危险因素是先前使用亚胺培南。在接触 1 至 3 天后,定植的优势比已经高达 5.9(95%置信区间[95%CI],1.5 至 25.7),此后增加到 7.8(95%CI,2.4 至 29.8)。总之,即使短暂接触亚胺培南也是 IR-GNB 定植的一个主要危险因素。

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