• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非碳青霉烯类药物用于治疗产超广谱β-内酰胺酶细菌引起的尿路感染

Noncarbapenems for the Treatment of Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Bacteria.

作者信息

White C Whitney, Kyle Jeffrey A, Deas Crystal M, Campbell Jacob

机构信息

From the University of Mississippi School of Pharmacy, Jackson, the Samford University McWhorter School of Pharmacy, Birmingham, Alabama, and Madison Hospital, Madison, Alabama.

出版信息

South Med J. 2019 Aug;112(8):438-443. doi: 10.14423/SMJ.0000000000001002.

DOI:10.14423/SMJ.0000000000001002
PMID:31375841
Abstract

OBJECTIVES

Urinary tract infections (UTIs) caused by extended-spectrum β-lactamase (ESBL)-producing are resistant to many conventional therapies, including third-generation cephalosporins. Carbapenems are considered first-line agents for ESBL infections, but their use is associated with increased multidrug resistance and should be reserved when absolutely necessary. Because of the increased rates of UTIs caused by ESBL-producing organisms and incidence of carbapenem resistance, safe and effective alternatives to carbapenems are needed. This study was conducted to evaluate the outcomes associated with the treatment of ESBL UTIs with noncarbapenem antibiotics.

METHODS

A retrospective cohort study of adults with ESBL UTIs was conducted at a community hospital. Patients were categorized as those receiving definitive carbapenem therapy and those receiving definitive noncarbapenem therapy. Calculated measurements included infection-related mortality, length of hospital stay, and duration of definitive antibiotic therapy. Microbiological failure was assessed as a secondary outcome. Data on the safety of antibiotic therapy were not collected. < 0.05 was considered significant.

RESULTS

Fifty patients met inclusion criteria for the study, divided evenly between the two cohorts. No statistical differences were observed for length of hospital stay ( = 0.601), duration of therapy ( = 0.398), or rate of microbiological failure between the groups ( = 0.115).

CONCLUSIONS

Noncarbapenems did not demonstrate significant differences compared with carbapenems in the treatment of adults with ESBL UTIs. In certain patient populations, noncarbapenems that demonstrate in vitro activity may be appropriate for UTIs caused by ESBL-producing organisms.

摘要

目的

由产超广谱β-内酰胺酶(ESBL)的细菌引起的尿路感染(UTIs)对包括第三代头孢菌素在内的许多传统疗法均具有耐药性。碳青霉烯类药物被视为治疗ESBL感染的一线药物,但其使用会增加多重耐药性,因此应仅在绝对必要时使用。由于产ESBL细菌引起的UTIs发病率上升以及碳青霉烯类耐药的发生率增加,需要有安全有效的碳青霉烯类替代药物。本研究旨在评估使用非碳青霉烯类抗生素治疗ESBL UTIs的疗效。

方法

在一家社区医院对患有ESBL UTIs的成人进行了一项回顾性队列研究。患者被分为接受确定性碳青霉烯类治疗的患者和接受确定性非碳青霉烯类治疗的患者。计算的指标包括感染相关死亡率、住院时间和确定性抗生素治疗的持续时间。微生物学治疗失败作为次要结局进行评估。未收集抗生素治疗安全性的数据。P < 0.05被认为具有统计学意义。

结果

50名患者符合该研究的纳入标准,两组各占一半。两组之间在住院时间(P = 0.601)、治疗持续时间(P = 0.398)或微生物学治疗失败率(P = 0.115)方面未观察到统计学差异。

结论

在治疗患有ESBL UTIs的成人患者时,非碳青霉烯类药物与碳青霉烯类药物相比未显示出显著差异。在某些患者群体中,具有体外活性的非碳青霉烯类药物可能适用于由产ESBL细菌引起的UTIs。

相似文献

1
Noncarbapenems for the Treatment of Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Bacteria.非碳青霉烯类药物用于治疗产超广谱β-内酰胺酶细菌引起的尿路感染
South Med J. 2019 Aug;112(8):438-443. doi: 10.14423/SMJ.0000000000001002.
2
An update on the management of urinary tract infections in the era of antimicrobial resistance.抗菌药物耐药时代泌尿道感染管理的最新进展
Postgrad Med. 2017 Mar;129(2):242-258. doi: 10.1080/00325481.2017.1246055. Epub 2016 Oct 21.
3
Cefepime versus carbapenems for the treatment of urinary tract infections caused by extended-spectrum β-lactamase-producing enterobacteriaceae.头孢吡肟与碳青霉烯类药物治疗产超广谱β-内酰胺酶肠杆菌科引起的尿路感染。
Int J Antimicrob Agents. 2018 Jan;51(1):155-158. doi: 10.1016/j.ijantimicag.2017.09.013. Epub 2017 Sep 21.
4
Aminoglycoside therapy for childhood urinary tract infection due to extended-spectrum β-lactamase-producing Escherichia coli or Klebsiella pneumoniae.氨基糖苷类药物治疗由产超广谱β-内酰胺酶的大肠埃希菌或肺炎克雷伯菌引起的儿童尿路感染。
BMC Infect Dis. 2015 Oct 13;15:414. doi: 10.1186/s12879-015-1153-z.
5
Emergency Department Urinary Tract Infections Caused by Extended-Spectrum β-Lactamase-Producing Enterobacteriaceae: Many Patients Have No Identifiable Risk Factor and Discordant Empiric Therapy Is Common.产超广谱β-内酰胺酶肠杆菌科导致的急诊科尿路感染:许多患者无明确的危险因素,且经验性治疗不一致的情况很常见。
Ann Emerg Med. 2018 Oct;72(4):449-456. doi: 10.1016/j.annemergmed.2018.05.006. Epub 2018 Jul 3.
6
Efficacy of empirical therapy with non-carbapenems for urinary tract infections with extended-spectrum beta-lactamase-producing Enterobacteriaceae.非碳青霉烯类经验性治疗产超广谱β-内酰胺酶肠杆菌科细菌所致尿路感染的疗效
Int J Infect Dis. 2014 Dec;29:91-5. doi: 10.1016/j.ijid.2014.08.018. Epub 2014 Oct 24.
7
The efficacy of cefmetazole against pyelonephritis caused by extended-spectrum beta-lactamase-producing Enterobacteriaceae.头孢美唑治疗产超广谱β-内酰胺酶肠杆菌科引起的肾盂肾炎的疗效。
Int J Infect Dis. 2013 Mar;17(3):e159-63. doi: 10.1016/j.ijid.2012.09.010. Epub 2012 Nov 8.
8
Carbapenem-resistant Klebsiella pneumoniae urinary tract infection following solid organ transplantation.实体器官移植后耐碳青霉烯类肺炎克雷伯菌尿路感染
Antimicrob Agents Chemother. 2015 Jan;59(1):553-7. doi: 10.1128/AAC.04284-14. Epub 2014 Nov 10.
9
Oral treatment options for patients with urinary tract infections caused by extended spectrum βeta-lactamase (ESBL) producing Enterobacteriaceae.产超广谱β内酰胺酶(ESBL)肠杆菌科导致的尿路感染患者的口服治疗选择。
J Infect Public Health. 2019 Nov-Dec;12(6):843-846. doi: 10.1016/j.jiph.2019.05.012. Epub 2019 Jun 6.
10
Extended spectrum beta lactamase producing organisms causing urinary tract infections in Sri Lanka and their antibiotic susceptibility pattern -A hospital based cross sectional study.在斯里兰卡引起尿路感染的产超广谱β-内酰胺酶生物体及其抗生素敏感性模式——一项基于医院的横断面研究。
BMC Infect Dis. 2017 Feb 10;17(1):138. doi: 10.1186/s12879-017-2250-y.