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成功治疗产碳青霉烯酶肠杆菌科腹膜炎:“旧疗法应对新问题”。

Successful treatment of carbapenemase producing Enterobacteriaceae peritonitis: 'Old therapy for a new bug'.

机构信息

Renal Services, North Shore Hospital, Waitematā District Health Board, Auckland, New Zealand.

Infectious Diseases, North Shore Hospital, Waitematā District Health Board, Auckland, New Zealand.

出版信息

Perit Dial Int. 2020 Jan;40(1):100-102. doi: 10.1177/0896860819879879.

DOI:10.1177/0896860819879879
PMID:32063148
Abstract

Multidrug-resistant organisms cause significant morbidity and mortality. Infections due to resistant gram-negative bacilli are increasingly being reported. For years, carbapenem antibiotics have been successfully used to treat infections due to resistant Enterobacteriaceae, such as and , including those producing extended spectrum β-lactamases, a subset of β-lactamase enzymes that confer broad resistance to penicillins and cephalosporins. More recently, carbapenem-resistant Enterobacteriaceae have emerged as pathogenic organisms, which confer broad resistance to most β-lactam antibiotics including 'last-line' carbapenems. However, different types of carbapenemases confer diverse spectra of antibiotic resistance. Here, we describe the case of an 84-year-old lady on peritoneal dialysis (PD) for 3 years who, on developing carbapenem-resistant PD peritonitis, was successfully treated with colistin, an antimicrobial agent first used in the 1950s.

摘要

耐多药生物体可导致严重的发病率和死亡率。越来越多的报道称,耐药革兰氏阴性杆菌引起的感染。多年来,碳青霉烯类抗生素已成功用于治疗耐药肠杆菌科细菌引起的感染,包括产生超广谱β-内酰胺酶的细菌,这些酶可广泛抵抗青霉素和头孢菌素类抗生素。最近,碳青霉烯类耐药肠杆菌科细菌已成为致病生物体,对包括“最后一线”碳青霉烯类在内的大多数β-内酰胺类抗生素具有广泛的耐药性。然而,不同类型的碳青霉烯酶可导致不同类型的抗生素耐药性。在这里,我们描述了一位 84 岁的女性腹膜透析(PD)患者的病例,她患有 3 年的腹膜透析相关腹膜炎,对碳青霉烯类耐药。她成功地使用了多粘菌素,这是一种在 20 世纪 50 年代首次使用的抗菌药物。

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引用本文的文献

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BMC Infect Dis. 2024 Jun 5;24(1):561. doi: 10.1186/s12879-024-09459-x.
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Peritoneal Dialysis-Related Peritonitis With Carbapenem-Resistant and Vancomycin-Resistant .伴有碳青霉烯类耐药和万古霉素耐药的腹膜透析相关性腹膜炎
Open Forum Infect Dis. 2021 Jan 18;8(1):ofaa525. doi: 10.1093/ofid/ofaa525. eCollection 2021 Jan.
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Phosphonopeptides Revisited, in an Era of Increasing Antimicrobial Resistance.
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