产多碳青霉烯酶肠杆菌的携带和感染。

IF 1.8 4区 医学 Q3 INFECTIOUS DISEASES
Matteo Boattini, Paulo Bastos, Cristina Costa, Gabriele Bianco
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引用次数: 0

摘要

多碳青霉烯酶产生肠杆菌(MCP-EB)代表了一个新的公共卫生挑战,由于它们能够显示复杂的耐药表型。方法:纳入从2020-2024年意大利某中心收治的患者中鉴定出的MCP-EB分离株。收集临床特征。结果:3117株产碳青霉烯酶肠杆菌临床菌株中,31株(1%)为MCP-EB,检出于28例患者;最常见的MCP-EB种是肺炎克雷伯菌(78.6%);N = 22)。观察到两种不同碳青霉烯酶的6种组合:KPC+VIM (75%;n = 21), KPC+NDM (10.7%;n=3), VIM+NDM (10.7%;n = 3), KPC+ oxa -48 like (3.6%;n = 1), VIM+ oxa -48 like (7.1%;n = 2), NDM+ oxa -48 like (3.6%;N = 1)。MCP-EB患者的中位年龄为67岁[IQR 59-73],以男性为主(57.1%;n = 16), Charlson共病指数中位数为5 [IQR 4-6]。合并症主要为心血管疾病(53.6%);15例),慢性呼吸道疾病(39.3%;N = 11),慢性肾病(32.1%;N = 9)。50% (n = 14)的患者在过去180天内住院,75% (n = 21)的患者在过去30天内接触过抗生素。从入院到采集MCP-EB标本的中位时间为16天[IQR 10-24], 28.6% (n = 8)的患者在两个以上的身体区域显示携带MCP-EB。14天、30天和住院死亡率分别为10.7%、25%和32.1%。MCP-EB对除氨曲南/阿维巴坦外的所有抗生素均表现出较高的耐药率。MCP-EB感染患者占35.7%;10例患者采用阿曲南联合头孢他啶/阿维巴坦或头孢地罗为主的治疗方案。2例(20%)患者复发MCP-EB感染,4例(40%)患者未能在住院期间存活。结论:MCP-EB患者的临床特征在医院慢性疾病患者中很常见,无论是感染患者还是单纯携带者,其死亡率都很高。阿曲南/阿维巴坦和头孢地罗可能是治疗MCP-EB感染的有希望的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carriage and infections by multi-carbapenemases producing Enterobacterales.

Introduction: Multi-carbapenemases producing Enterobacterales (MCP-EB) represents a new public health challenge due to their ability to display complex resistance phenotypes.

Methods: MCP-EB isolates identified from patients admitted to an Italian Center in the period 2020-2024 were included. Clinical features were collected.

Results: Among 3,117 carbapenemase-producing Enterobacterales clinical strains, 31 (1 %) were MCP-EB and were detected from 28 patients. The most common MCP-EB species was Klebsiella pneumoniae (78.6 %; n = 22). Six combinations of two different carbapenemases were observed: KPC+VIM (75 %; n = 21), KPC+NDM (10.7 %; n=3), VIM+NDM (10.7 %; n = 3), KPC+OXA-48-like (3.6 %; n = 1), VIM+OXA-48-like (7.1 %; n = 2), and NDM+OXA-48-like (3.6 %; n = 1). Patients with MCP-EB had a median age of 67 years [IQR 59-73], were predominantly men (57.1 %; n = 16), and a median Charlson Comorbidity Index of 5 [IQR 4-6]. The comorbidities mainly observed were cardiovascular disease (53.6 %; n = 15), chronic respiratory disease (39.3 %; n = 11), and chronic kidney disease (32.1 %; n = 9). Fifty per cent (n = 14) of patients had been hospitalized in the previous 180 days and 75 % (n = 21) had been exposed to antibiotics in the previous 30 days. Median time from admission to MCP-EB specimen collection was 16 days [IQR 10-24] and 28.6 % (n = 8) of patients showed to carry MCP-EB in more than two body districts. Fourteen-day, 30-day, and in-hospital mortality were 10.7 %, 25 %, and 32.1 %, respectively. MCP-EB showed high rates of resistance to all antibiotics tested except aztreonam/avibactam. Patients with MCP-EB infection (35.7 %; n = 10) were treated with combination regimens, mainly including aztreonam plus ceftazidime/avibactam or cefiderocol. Two patients (20 %) had a recurrence of MCP-EB infection and four (40 %) patients did not survive hospitalisation.

Conclusion: Clinical features of patients with MCP-EB are common in the hospital population with chronic diseases and showed high mortality rates both in infected and carriers-only patients. Aztreonam/avibactam and cefiderocol could be promising treatment options against MCP-EB infections.

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来源期刊
CiteScore
5.30
自引率
3.40%
发文量
149
审稿时长
56 days
期刊介绍: Diagnostic Microbiology and Infectious Disease keeps you informed of the latest developments in clinical microbiology and the diagnosis and treatment of infectious diseases. Packed with rigorously peer-reviewed articles and studies in bacteriology, immunology, immunoserology, infectious diseases, mycology, parasitology, and virology, the journal examines new procedures, unusual cases, controversial issues, and important new literature. Diagnostic Microbiology and Infectious Disease distinguished independent editorial board, consisting of experts from many medical specialties, ensures you extensive and authoritative coverage.
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