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澳大利亚抗菌药物耐药性小组(AGAR)澳大利亚金黄色葡萄球菌败血症结局项目(ASSOP)2018年年度报告。

Australian Group on Antimicrobial Resistance (AGAR) Australian Staphylococcus aureus Sepsis Outcome Programme (ASSOP) Annual Report 2018.

作者信息

Coombs Geoffrey W, Daley Denise A, Mowlaboccus Shakeel, Lee Yung Thin, Pang Stanley

机构信息

Antimicrobial Resistance and Infectious Disease (AMRID) Research Laboratory, Murdoch University, Murdoch, Western Australia, Australia; Department of Microbiology, PathWest Laboratory Medicine-WA, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Department of Microbiology, PathWest Laboratory Medicine-WA, Fiona Stanley Hospital, Murdoch, Western Australia, Australia; Australian Group on Antimicrobial Resistance, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

出版信息

Commun Dis Intell (2018). 2020 Mar 16;44. doi: 10.33321/cdi.2020.44.18.

Abstract

From 1 January to 31 December 2018, thirty-six institutions around Australia participated in the Australian Sepsis Outcome Programme (ASSOP). The aim of ASSOP 2018 was to determine the proportion of bacteraemia (SAB) isolates in Australia that are antimicrobial resistant, with particular emphasis on susceptibility to methicillin, and to characterise the molecular epidemiology of the methicillin-resistant isolates. A total of 2,673 bacteraemia episodes were reported, of which 78.9% were community-onset. A total of 17.4% of isolates were methicillin resistant. The 30-day all-cause mortality associated with methicillin-resistant SAB was 17.1% which was not significantly higher than the 13.6% mortality associated with methicillin-susceptible SAB (p = 0.1). With the exception of the β-lactams and erythromycin, antimicrobial resistance in methicillin-susceptible was rare. However in addition to the β-lactams approximately 42% of methicillin-resistant (MRSA) were resistant to erythromycin, 36% to ciprofloxacin and approximately 13% resistant to co-trimoxazole, tetracycline and gentamicin. When applying the EUCAST breakpoints teicoplanin resistance was detected in two isolates. Resistance was not detected for vancomycin and linezolid. Resistance to non-beta-lactam antimicrobials was largely attributable to two healthcare-associated MRSA clones: ST22-IV [2B] (EMRSA-15) and ST239-III [3A] (Aus-2/3 EMRSA). The ST22-IV [2B] (EMRSA-15) clone is the predominant healthcare-associated clone in Australia. Seventy-eight percent of methicillin-resistant SAB episodes in 2018 were due to community-associated clones. Although polyclonal, approximately 76.3% of community-associated clones were characterised as ST93-IV [2B] (Queensland CA-MRSA), ST5-IV [2B], ST45-VT [5C2&5], ST1-IV [2B], ST30-IV [2B], ST78-IV [2B] and ST97-IV [2B]. Community-associated MRSA, in particular the ST45-VT [5C2&5] clone, has acquired multiple antimicrobial resistance determinants including ciprofloxacin, erythromycin, clindamycin, gentamicin and tetracycline. The ST45-VT [5C2&5] clone accounted for 11.7% of CA-MRSA. As CA-MRSA is well established in the Australian community, it is important that antimicrobial resistance patterns in community- and healthcare-associated SAB are monitored, as this information will guide therapeutic practices in treating sepsis.

摘要

2018年1月1日至12月31日,澳大利亚各地的36家机构参与了澳大利亚脓毒症结果项目(ASSOP)。2018年ASSOP的目的是确定澳大利亚血液感染(SAB)分离株中耐抗菌药物的比例,特别关注对甲氧西林的敏感性,并描述耐甲氧西林分离株的分子流行病学特征。共报告了2673例血液感染病例,其中78.9%为社区发病。共有17.4%的分离株耐甲氧西林。耐甲氧西林SAB相关的30天全因死亡率为17.1%,并不显著高于耐甲氧西林敏感SAB相关的13.6%的死亡率(p = 0.1)。除β-内酰胺类和红霉素外,耐甲氧西林敏感菌的抗菌药物耐药性很少见。然而,除β-内酰胺类外,约42%的耐甲氧西林(MRSA)对红霉素耐药,36%对环丙沙星耐药,约13%对复方新诺明、四环素和庆大霉素耐药。应用欧盟CAST标准检测到两株替考拉宁耐药菌。未检测到对万古霉素和利奈唑胺的耐药性。对非β-内酰胺类抗菌药物的耐药性主要归因于两个与医疗保健相关的MRSA克隆:ST22-IV [2B](EMRSA-15)和ST239-III [3A](Aus-2/3 EMRSA)。ST22-IV [2B](EMRSA-15)克隆是澳大利亚主要的与医疗保健相关的克隆。2018年78%的耐甲氧西林SAB病例归因于社区相关克隆。虽然是多克隆的,但约76.3%的社区相关克隆被鉴定为ST93-IV [2B](昆士兰社区获得性MRSA)、ST5-IV [2B]、ST45-VT [5C2&5]、ST1-IV [2B]、ST30-IV [2B]、ST78-IV [2B]和ST97-IV [2B]。社区获得性MRSA,特别是ST45-VT [5C2&5]克隆,获得了多种抗菌药物耐药决定因素,包括环丙沙星、红霉素、克林霉素、庆大霉素和四环素。ST45-VT [5C2&5]克隆占社区获得性MRSA的11.7%。由于社区获得性MRSA在澳大利亚社区已广泛存在,监测社区和医疗保健相关SAB中的抗菌药物耐药模式很重要,因为这些信息将指导脓毒症治疗的实践。

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