医院获得性感染耐碳青霉烯类肠杆菌科细菌的耐药性及感染者的临床结局

邓勇, 毛平, 何艳红, 张梅, 翁鉴

武警医学 ›› 2024, Vol. 35 ›› Issue (7) : 621-626.

PDF(973 KB)
PDF(973 KB)
武警医学 ›› 2024, Vol. 35 ›› Issue (7) : 621-626.
论著

医院获得性感染耐碳青霉烯类肠杆菌科细菌的耐药性及感染者的临床结局

  • 邓勇, 毛平, 何艳红, 张梅, 翁鉴
作者信息 +

Drug resistance of CRE in hospital-acquired infections and clinical outcomes of infected patients

  • DENG Yong, MAO Ping, HE Yanhong, ZHANG Mei, WENG Jian
Author information +
文章历史 +

摘要

目的 探讨医院获得性感染耐碳青霉烯类肠杆菌科细菌(CRE)的耐药性及感染者的临床结局。方法 选择2017-01至2023-06在武警四川总队医院住院的成年CRE感染患者341例作为病例组,336例碳青霉烯类敏感肠杆菌科细菌(CSE)感染患者作为敏感组,354例非肠杆菌科细菌感染的同时期住院患者作为对照组。使用药敏板条、肉汤稀释法检测临床常用抗菌药物对CRE的最低抑菌浓度,另外采用单变量和多变量分析医院获得性感染CRE患者的临床结局。结果 分离CRE最常见的标本类型依次是痰液、尿液和血液,CRE中占比前三依次为耐碳青霉烯类肺炎克雷伯菌(CR-Kpn)、耐碳青霉烯类大肠埃希菌(CR-Eco)、耐碳青霉烯类阴沟肠杆菌(CR-Ecl)。替加环素和黏菌素为CR-Kpn和CR-Eco体外敏感率最高的前两位药物,四环素对CR-Kpn的敏感率为71.86%,而对CR-Eco敏感率较低,呋喃妥因及氨基糖苷类抗生素对CR-Eco的敏感率显著高于CR-Kpn。CRE组的院内死亡率与其他两组相比,差异无统计学意义(P>0.05),不过CRE组预后不良率为19.35%,高于CSE组(11.31%)和控制组(12.15%),差异有统计学意义(P<0.05)。CRE感染患者中,肾功能不全和使用免疫抑制剂是导致预后不良的独立预测因素,而经验性使用抗生素为预后不良的保护因素。结论 与其他常用抗菌药物相比,黏菌素和替加环素对CRE具有更高的体外抗菌活性,呋喃妥因及氨基糖苷类抗生素适用于CR-Eco导致的感染。医院获得性感染CRE容易导致患者预后不良,而经验性使用抗生素可以有效减少感染CRE导致的不良临床结局。

Abstract

Objective To investigate the drug resistance of carbapenem-resistant enterobacteriaceae (CRE) in hospital-acquired infections and the clinical outcomes of infected patients. Methods A total of 341 adult patients with CRE infection hospitalized in Sichuan Provincial Corps Hospital of Chinese People’s Armed Police Force from January 2017 to June 2023 were selected as the case group, 336 patients with carbapenem sensitive enterobacteriidae (CSE) infection were selected as the sensitive group, and 354 hospitalized patients with non-enterobacteriidae infection during the same period were selected as the control group. The minimum inhibitory concentration of commonly used antibiotics to CRE were detected by drug sensitive strip and broth dilution method, and univariate and multivariate methods were used to analyze the clinical outcomes of hospital-acquired CRE patients. Results The most common types of CRE were sputum, urine and blood, and the top three types of CRE were carbapenem-resistant Klebsiella pneumoniae(CR-Kp), carbapenem-resistant Escherichia coli (CR-Eco) and carbapenem-resistant Enterobacter cloacae (CR-Ecl). Tigecycline and colistin were the top two sensitive drugs of CR-Kpn and CR-Eco in vitro. The sensitivity rate of tetracycline to CR-Kpn was 71.86%, while the sensitivity rate of tetracycline to CR-Eco was low. The sensitivity rate of nitrofuranins and aminoglycosides to CR-Eco was significantly higher than that of CR-Kpn. There was no significant difference in in-hospital mortality between CRE group and the other two groups (P>0.05), but the poor prognosis rate of CRE group (19.35%) was higher than that of CSE group (11.31%) and control group (12.15%), with statistical significance (P<0.05). In patients with CRE infection, renal insufficiency and the use of immunosuppressive agents were independent predictors of poor prognosis, while the empirical use of antibiotics was a protective factor. Conclusions Colistin and tigecycline have higher antibacterial activity against CRE than other commonly used antibiotics. Nitrofurantoin and aminoglycoside antibiotics are suitable for infection caused by CR-Eco. Hospital-acquired CRE infection is prone to lead to poor prognosis in patients, but the empirical use of antibiotics can effectively reduce the adverse clinical outcomes caused by CRE infection.

关键词

耐碳青霉烯类肠杆菌科细菌 / 耐药性 / 临床结局

Key words

carbapenem-resistant enterobacteriaceae / drug resistance / clinical outcome

引用本文

导出引用
邓勇, 毛平, 何艳红, 张梅, 翁鉴. 医院获得性感染耐碳青霉烯类肠杆菌科细菌的耐药性及感染者的临床结局[J]. 武警医学. 2024, 35(7): 621-626
DENG Yong, MAO Ping, HE Yanhong, ZHANG Mei, WENG Jian. Drug resistance of CRE in hospital-acquired infections and clinical outcomes of infected patients[J]. Medical Journal of the Chinese People Armed Police Forces. 2024, 35(7): 621-626
中图分类号: R378   

参考文献

[1] Yigit H, Queenan A M, Anderson G J, et al. Novel carbapenem-hydrolyzing beta-lactamase, kpc-1, from a carbapenem-resistant strain of klebsiella pneumoniae[J]. Antimicrob Agents Chemother, 2001, 45(4): 1151-1161.
[2] Wangchinda W, Thamlikitkul V, Watcharasuwanseree S, et al. Active surveillance for carbapenem-resistant enterobacterales (CRE) colonization and clinical course of cre colonization among cospitalized patients at a university hospital in Thailand[J]. Antibiotics (Basel), 2022, 11(10):1401.
[3] Sharma K, Tak V, Nag V L, et al. An observational study on carbapenem-resistant enterobacterales (CRE) colonisation and subsequent risk of infection in an adult intensive care unit (ICU) at a tertiary care hospital in India[J]. Infect Prev Pract, 2023, 5(4): 100312.
[4] Castanheira M, Deshpande L M, Mendes R E, et al. Prevalence of carbapenemase genes among carbapenem-nonsusceptibleenterobacterales collected in US hospitals in a five-year period and activity of ceftazidime/avibactam and comparator agents[J]. JAC Antimicrob Resist, 2022, 4(5): 98.
[5] Brown A L, van Kamp I. WHO environmental noise guidelines for the european region: asystematic review of transport noise interventions and their impacts on health[J]. Int J Environ Res Public Health, 2017, 14(8):873.
[6] Saito S, Hayakawa K, Tsuzuki S, et al. A matched case-case-control study of the impact of clinical outcomes and risk factors of patients with imp-type carbapenemase-producing carbapenem-resistant enterobacteriaceae in Japan[J]. Antimicrob Agents Chemother, 2021, 65(3):e01483-20.
[7] Madney Y, Aboubakr S, Khedr R, et al. Carbapenem-resistant enterobacteriaceae (CRE) among children with cancer: predictors of mortality and treatment outcome[J]. Antibiotics (Basel), 2023, 12(2):405.
[8] Chen Y, Wang W L, Zhang W, et al. Risk factors and outcomes of carbapenem-resistant enterobacteriaceae infection after liver transplantation: a retrospective study in a Chinese population[J]. Infect Drug Resist, 2020, 13: 4039-4045.
[9] Horan T C M, Andrus M R B C, Dudeck M A M. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting[J]. AJIC, 2008, 36(5): 309-332.
[10] 全国细菌耐药监测网.2014-2019年耐碳青霉烯类肺炎克雷伯菌流行病学变迁[J]. 中国感染控制杂志, 2021, 20(2): 175-179.
[11] Tamma P D, Aitken S L, Bonomo R A, et al. Infectious diseases society of America guidance on the treatment of extended-spectrum beta-lactamase producing enterobacterales (ESBL-e), carbapenem-resistant enterobacterales (CRE), and pseudomonas aeruginosa with difficult-to-treat resistance (dtr-p. aeruginosa)[J]. Clin Infect Dis, 2021, 72(7): e169-e183.
[12] Zhang Y, Wang Q, Yin Y, et al. Epidemiology of carbapenem-resistant enterobacteriaceae infections: report from the China crenetwork[J]. Antimicrob Agents Chemother, 2018, 62(2) : e01882-17.
[13] 张 梅,谢祥红,魏文波,等. 武警某部医院碳青霉烯耐药肺炎克雷伯菌的耐药基因分析[J]. 武警医学, 2021, 32(1): 38-41.
[14] Cassini A, Hogberg L D, Plachouras D, et al. Attributable deaths and disability-adjusted life-years caused by infections with antibiotic-resistant bacteria in the EU and the European Economic Area in 2015: a population-level modelling analysis[J]. Lancet Infect Dis, 2019, 19(1): 56-66.
[15] Wang M, Earley M, Chen L, et al. Clinical outcomes and bacterial characteristics of carbapenem-resistant klebsiella pneumoniae complex among patients from different global regions (crackle-2): a prospective, multicentre, cohort study[J]. Lancet Infect Dis, 2022, 22(3): 401-412.
[16] Bernas A A, Aveiga V D, Etxeberria Z L, et al. Acute pancreatitis in ICU secondary to treatment with tigecycline[J]. Rev Esp Anestesiol Reanim, 2017, 64(1): 46-49.
[17] Humphries R, Bobenchik A M, Hindler J A, et al. Overview of changes to the clinical and laboratory standards institute performance standards for antimicrobial susceptibility testing, m100, 31st edition[J]. J Clin Microbiol, 2021, 59(12): e21321.
[18] Aleidan F, Alkhelaifi H, Alsenaid A, et al. Incidence and risk factors of carbapenem-resistant enterobacteriaceae infection in intensive care units: a matched case-control study[J]. Expert Rev Anti Infect Ther, 2021, 19(3): 393-398.
[19] Ruvinsky S, Voto C, Roel M, et al. Carbapenem-resistant enterobacteriaceae bloodstream infections: a case-control study from a pediatric referral hospital in Argentina[J]. Front Public Health, 2022, 10: 983174.
[20] Saito S, Hayakawa K, Tsuzuki S, et al. A matched case-case-control study of the impact of clinical outcomes and risk factors of patients with imp-type carbapenemase-producing carbapenem-resistant enterobacteriaceae in Japan[J]. Antimicrob Agents Chemother, 2021, 65(3): e01483-20.
[21] Tian X, Sun S, Jia X, et al. Epidemiology of and risk factors for infection with extended-spectrum beta-lactamase-producing carbapenem-resistant enterobacteriaceae: results of a double case-control study[J]. Infect Drug Resist, 2018, 11: 1339-1346.
[22] Li C, Li Y, Zhao Z, et al. Treatment options and clinical outcomes for carbapenem-resistantenterobacteriaceae bloodstream infection in a Chinese university hospital[J]. J Infect Public Health, 2019, 12(1): 26-31.
[23] Seo H, Lee S C, Chung H, et al. Clinical and microbiological analysis of risk factors for mortality in patients with carbapenem-resistant enterobacteriaceae bacteremia[J]. Int J Antimicrob Agents, 2020, 56(4): 106126.

PDF(973 KB)

Accesses

Citation

Detail

段落导航
相关文章

/