社区医院中产碳青霉烯酶肠杆菌科菌血症的流行病学和治疗

Q3 Medicine JAMMI Pub Date : 2018-08-20 DOI:10.3138/JAMMI.2017-0010
Sheena Pang, Ehsan Haghshenas, David Richardson, M. Baqi
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引用次数: 0

摘要

背景:产碳青霉烯酶的肠杆菌科(CPE)感染是一种迅速演变的全球威胁。菌血症死亡率超过40%,关于最佳抗菌治疗的共识有限。目的:描述本机构CPE菌血症人群的特征,并描述用于治疗的抗菌方案。方法:对2010年1月1日至2017年4月30日期间入院的成人CPE菌血症患者进行双中心回顾性分析。基线人口统计数据包括国外住院、病原体和易感性。治疗细节包括抗菌剂、给药方案以及单药治疗或联合治疗的使用。临床结果包括30天全因死亡率和30天再次入院率。结果:对13例CPE菌血症进行回顾性分析。9名患者此前曾在印度次大陆住院治疗。12个分离株产生了新德里金属-β-乳糖酶-1(NDM-1)。所有分离株均对替加环素敏感(n=8)或为中间体(n=5)。同样数量的病例接受了单药治疗(n=6)和联合治疗(n=6)。最常见的处方抗菌药物是粘菌素(n=7)和替加环素(n=8)。总的30天死亡率和再次入院率分别为54%(7/13)和50%(3/6),尽管没有考虑潜在混杂因素的影响,如致病性CPE、单菌或多菌感染或治疗延迟。结论:本研究强调了迄今为止加拿大最大的CPE菌血症队列。CPE菌血症最常见于印度次大陆既往住院的患者。根据我们的抗菌药物敏感性测试结果,替加环素可能在我们机构的经验性治疗中发挥作用。
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Epidemiology and treatment of carbapenemase-producing Enterobacteriaceae bacteremia in a community hospital setting
Background: Carbapenemase-producing Enterobacteriaceae (CPE) infections are a rapidly evolving global threat. With bacteremia mortality rates exceeding 40%, limited consensus exists regarding optimal antimicrobial treatment. Objectives: To characterize our institution’s CPE bacteremia population and describe the antimicrobial regimens used for treatment. Methods: A dual-centre retrospective chart review was conducted of adult CPE bacteremia patients admitted between January 1, 2010 and April 30, 2017. Baseline demographics included out-of-country hospitalization, causative organism, and susceptibilities. Treatment details included antimicrobial agent, dosing regimen, and use of monotherapy or combination therapy. Clinical outcomes included 30-day all-cause mortality and 30-day re-admission rates. Results: Thirteen cases of CPE bacteremia were reviewed. Nine patients had previously been hospitalized in the Indian subcontinent. Twelve isolates produced the New Delhi metallo-beta-lactamase-1 (NDM-1). All isolates were sensitive (n = 8) or intermediate (n = 5) to tigecycline. An equal number of cases were treated with monotherapy (n = 6) and combination therapy (n = 6). The most commonly prescribed antimicrobials were colistin (n = 7) and tigecycline (n = 8). The overall 30-day mortality and re-admission rates were 54% (7/13) and 50% (3/6), respectively, although the effect of potential confounders such as causative CPE, monomicrobial or polymicrobial infection, or delay in therapy were not considered. Conclusions: This study highlights the largest Canadian CPE bacteremia cohort to date. CPE bacteremia most commonly occurred in patients with prior hospitalization in the Indian subcontinent. Based on our antimicrobial susceptibility testing results, tigecycline may have a role as part of empiric therapy at our institution.
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来源期刊
JAMMI
JAMMI Medicine-Infectious Diseases
CiteScore
3.80
自引率
0.00%
发文量
48
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