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碳青霉烯类耐药肠杆菌科血流感染的死亡因素和抗生素选择:具有同时存在的 NDM-1 和 OXA-48 的高流行地区的相关见解。

Mortality factors and antibiotic options in carbapenem-resistant Enterobacterales bloodstream infections: Insights from a high-prevalence setting with co-occurring NDM-1 and OXA-48.

机构信息

Division of Clinical Pharmacy, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.

Department of Pharmacy Practice, College of Pharmacy, Rangsit University, Pathum Thani, Thailand.

出版信息

Clin Transl Sci. 2024 Jun;17(6):e13855. doi: 10.1111/cts.13855.


DOI:10.1111/cts.13855
PMID:38853376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11163016/
Abstract

Bloodstream infections (BSI) caused by carbapenem-resistant Enterobacterales (CRE) are associated with a high mortality rate. This study aimed to investigate factors associated with 14-day mortality and identify a potential treatment option. A retrospective cohort study was conducted on patients with CRE-BSI in Thailand from 2015 to 2020. The multivariate Cox proportional-hazards model was employed to identify factors influencing 14-day mortality. Out of 134 diagnosed cases of CRE-BSI, the all-cause 14-day mortality rate was 35.1%. The most prevalent organism isolated was Klebsiella pneumoniae (85.8%), followed by Escherichia coli (11.9%). Among the 60 isolates tested for carbapenemase genes, the majority exhibited co-occurring bla and bla (51.7%), followed by bla (31.7%) and bla (15.0%). In the multivariate analysis, neutropenia (adjusted hazard ratio [aHR] 2.55; 95% confidence interval [95%CI] 1.28-5.06; p = 0.008), sepsis/septic shock (aHR 3.02; 95%CI 1.33-6.86; p = 0.008), and previous metronidazole exposures (aHR 3.58; 95%CI 1.89-6.71; p < 0.001) were identified as independent factors for 14-day mortality. The fosfomycin-based regimen was found to be protective (aHR 0.37; 95%CI 0.15-0.92; p = 0.032). In patients with CRE-BSI, particularly in regions with a high occurrence of co-occurring bla and bla, neutropenia, sepsis/septic shock, and previous metronidazole exposures emerged as independent risk factors for mortality. Moreover, the fosfomycin-based regimen showed an improvement in the survival rate.

摘要

血流感染(BSI)由碳青霉烯类耐药肠杆菌科(CRE)引起,死亡率高。本研究旨在探讨与 14 天死亡率相关的因素,并确定潜在的治疗选择。对 2015 年至 2020 年泰国 CRE-BSI 患者进行了回顾性队列研究。采用多变量 Cox 比例风险模型确定影响 14 天死亡率的因素。在确诊的 134 例 CRE-BSI 患者中,全因 14 天死亡率为 35.1%。最常见的分离菌为肺炎克雷伯菌(85.8%),其次是大肠埃希菌(11.9%)。在对 60 株碳青霉烯酶基因进行检测的菌株中,大多数同时存在 bla 和 bla(51.7%),其次是 bla(31.7%)和 bla(15.0%)。多变量分析显示,中性粒细胞减少症(调整后的危险比[aHR] 2.55;95%置信区间[95%CI] 1.28-5.06;p=0.008)、败血症/感染性休克(aHR 3.02;95%CI 1.33-6.86;p=0.008)和先前甲硝唑暴露(aHR 3.58;95%CI 1.89-6.71;p<0.001)是 14 天死亡率的独立因素。磷霉素方案被发现具有保护作用(aHR 0.37;95%CI 0.15-0.92;p=0.032)。在 CRE-BSI 患者中,特别是在同时存在 bla 和 bla 的高发地区,中性粒细胞减少症、败血症/感染性休克和先前甲硝唑暴露是死亡率的独立危险因素。此外,基于磷霉素的方案显示出生存率的提高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d4/11163016/1ffe7ec0928a/CTS-17-e13855-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d4/11163016/1ffe7ec0928a/CTS-17-e13855-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54d4/11163016/1ffe7ec0928a/CTS-17-e13855-g001.jpg

相似文献

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Mortality factors and antibiotic options in carbapenem-resistant Enterobacterales bloodstream infections: Insights from a high-prevalence setting with co-occurring NDM-1 and OXA-48.

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引用本文的文献

[1]
Clinical outcomes in patients with cancer and Gram-negative bloodstream infection: impact of carbapenem resistance.

Support Care Cancer. 2025-7-16

[2]
Carbapenem-resistant Enterobacterales bloodstream infections related to death in two Brazilian tertiary hospitals.

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[3]
Real-World Use, Effectiveness, and Safety of Intravenous Fosfomycin: The FORTRESS Study.

Infect Dis Ther. 2025-4

本文引用的文献

[1]
Infectious Diseases Society of America 2023 Guidance on the Treatment of Antimicrobial Resistant Gram-Negative Infections.

Clin Infect Dis. 2023-7-18

[2]
Clinical Characteristics and Associated Factors for Mortality in Patients with Carbapenem-Resistant Bloodstream Infection.

Microorganisms. 2023-4-25

[3]
Comparison of in vitro fosfomycin susceptibility testing methods with agar dilution for carbapenem resistant Klebsiella pneumoniae and Escherichiacoli.

Indian J Med Microbiol. 2023

[4]
Changing Epidemiology of Carbapenemases Among Carbapenem-Resistant Enterobacterales From United States Hospitals and the Activity of Aztreonam-Avibactam Against Contemporary Enterobacterales (2019-2021).

Open Forum Infect Dis. 2023-1-31

[5]
Prescription Pattern of Intravenous Fosfomycin in a Provincial Hospital in Thailand.

Infect Chemother. 2022-12

[6]
The burden of carbapenem-resistant infection in a large Thai tertiary care hospital.

Front Pharmacol. 2022-9-2

[7]
Antimicrobial Activity Profiles and Potential Antimicrobial Regimens against Carbapenem-Resistant Enterobacterales Isolated from Multi-Centers in Western Thailand.

Antibiotics (Basel). 2022-3-7

[8]
A retrospective observational cohort study of the clinical epidemiology of bloodstream infections due to carbapenem-resistant Klebsiella pneumoniae in an OXA-48 endemic setting.

Int J Antimicrob Agents. 2022-4

[9]
European Society of Clinical Microbiology and Infectious Diseases (ESCMID) guidelines for the treatment of infections caused by multidrug-resistant Gram-negative bacilli (endorsed by European society of intensive care medicine).

Clin Microbiol Infect. 2022-4

[10]
The Potential Use of Ceftazidime-Avibactam Against Carbapenem Resistant Clinical Isolates Harboring Different Carbapenemase Types in a Thai University Hospital.

Drug Des Devel Ther. 2021

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