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产碳青霉烯酶的耐碳青霉烯菌携带者中,出现另一种基因型临床分离株时死亡率增加。

Increased Mortality Among Carbapenemase-Producing Carbapenem-Resistant Carriers Who Developed Clinical Isolates of Another Genotype.

作者信息

Chen Wen Kai, Yang Yong, Tan Ban Hock

机构信息

Department of Epidemiology, Singapore General Hospital, Singapore.

Department of Infectious Diseases, Singapore General Hospital, Singapore.

出版信息

Open Forum Infect Dis. 2019 Feb 1;6(2):ofz006. doi: 10.1093/ofid/ofz006. eCollection 2019 Feb.

Abstract

BACKGROUND

Carbapenemase production by carbapenemase-producing carbapenem-resistant (CP-CRE) is encoded by a variety of genes on mobile genetic elements. Patients colonized by 1 genotype of CP-CRE may be subsequently infected by another genotype of CP-CRE. We sought to determine whether CP-CRE carriers who developed infection with another genotype had a higher mortality risk.

METHODS

A retrospective cohort study was conducted using collected data from January 2012 to December 2016. Clinical isolates of CP-CRE were analyzed among the CP-CRE carriers who had developed an infection during their stay in the hospital. Comparison was made between CP-CRE carriers who developed clinical isolates of another genotype and those whose clinical isolates were of the same CP-CRE genotype that they were originally colonized with. The primary outcome analyzed was the 14-day mortality rate.

RESULTS

A total of 73 CP-CRE carriers who had developed infection were analyzed. Ten (15.4%) of the carriers who developed an infection with clinical isolates of the same CP-CRE genotype died within 14 days, whereas 5 (62.5%) of those who developed an infection with clinical isolates of a different genotype died. This represented a 6-fold increase (adjusted relative risk, 6.36; 95% confidence interval, 1.75-23.06; = .005) in the 14-day mortality rate.

CONCLUSIONS

CP-CRE carriers who developed clinical isolates of another genotype are at risk of increased mortality. This is a novel finding that is of interest to health care organizations worldwide, with profound implications for infection control measures, such as patient and staff cohorting.

摘要

背景

产碳青霉烯酶的耐碳青霉烯肠杆菌科细菌(CP-CRE)产生的碳青霉烯酶由移动遗传元件上的多种基因编码。被一种基因型的CP-CRE定植的患者随后可能会被另一种基因型的CP-CRE感染。我们试图确定感染另一种基因型的CP-CRE携带者是否有更高的死亡风险。

方法

利用2012年1月至2016年12月收集的数据进行回顾性队列研究。对住院期间发生感染的CP-CRE携带者的临床分离株进行分析。比较出现另一种基因型临床分离株的CP-CRE携带者和临床分离株与最初定植的CP-CRE基因型相同的携带者。分析的主要结局是14天死亡率。

结果

共分析了73例发生感染的CP-CRE携带者。感染相同CP-CRE基因型临床分离株的携带者中有10例(15.4%)在14天内死亡,而感染不同基因型临床分离株的携带者中有5例(62.5%)死亡。这表明14天死亡率增加了6倍(调整后的相对风险为6.36;95%置信区间为1.75 - 23.06;P = 0.005)。

结论

出现另一种基因型临床分离株的CP-CRE携带者有死亡风险增加的情况。这是一项新发现,引起了全球医疗机构的关注,对感染控制措施(如患者和工作人员分组)具有深远影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ed7/6364863/5970929a2d20/ofz006f0001.jpg

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