Australian Group on Antimicrobial Resistance (AGAR) Australian Staphylococcus aureus Sepsis Outcome Programme (ASSOP) Annual Report 2020

被引:8
作者
Coombs, Geoffrey W. [1 ,2 ,3 ]
Daley, Denise A. [2 ,3 ]
Yee, Nicholas W. T. [1 ]
Shoby, Princy [1 ]
Mowlaboccus, Shakeel [1 ,2 ]
机构
[1] Murdoch Univ, Antimicrobial Resistance & Infect Dis AMRID Res L, Murdoch, WA, Australia
[2] Fiona Stanley Hosp, Dept Microbiol, PathWest Lab Med WA, Murdoch, WA, Australia
[3] Fiona Stanley Hosp, Australian Grp Antimicrobial Resistance, Murdoch, WA, Australia
来源
COMMUNICABLE DISEASES INTELLIGENCE | 2022年 / 46卷
关键词
Australian Group on Antimicrobial Resistance (AGAR); antimicrobial resistance surveillance; Staphylococcus aureus; methicillin-susceptible Staphylococcus aureus (MSSA); methicillinresistant Staphylococcus aureus (MRSA); bacteraemia; BLOOD-STREAM INFECTION; MRSA BACTEREMIA; EPIDEMIOLOGY; SURVEILLANCE; MORTALITY;
D O I
10.33321/cdi.2022.46.18
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
From 1 January to 31 December 2020, forty-nine institutions around Australia participated in the Australian Staphylococcus aureus Sepsis Outcome Programme (ASSOP). The aims of ASSOP 2020 were to determine the proportion of Staphylococcus aureus bacteraemia (SAB) isolates in Australia that were antimicrobial resistant, with particular emphasis on susceptibility to methicillin; and to characterise the molecular epidemiology of the methicillin-resistant isolates. A total of 2,734 SAB episodes were reported, of which 79.7% were community-onset. Of S. aureus isolates, 17.6% were methicillin resistant. The 30-day all-cause mortality associated with methicillin-resistant SAB was 14.2%, which was not significantly different from the 13.3% mortality associated with methicillin-susceptible SAB (p = 0.6). With the exception of the beta-lactams and erythromycin, antimicrobial resistance in methicillin-susceptible S. aureus was rare. However, in addition to the beta-lactams, approximately 35% of methicillin-resistant S. aureus (MRSA) were resistant to erythromycin, 33% to ciprofloxacin, 13% to tetracycline, 13% to gentamicin and 4% to co-trimoxazole. When applying the European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoints, teicoplanin resistance was detected in four S. aureus isolates. Resistance was not detected for vancomycin and linezolid. Resistance to non-beta-lactam antimicrobials was largely attributable to two healthcare-associated MRSA (HA-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 HA-MRSA clone in Australia. However, 85% percent of methicillin-resistant SAB isolates were community-associated MRSA (CA-MRSA) clones. Although polyclonal, approximately 77% of CA-MRSA clones were characterised as: ST93-IV [2B] (Queensland CA-MRSA); STS-IV [2B]; ST45-V [5C2 & 5]; ST1-IV [2B]; ST30-IV [2B]; ST8-IV [2B]; and ST97-IV [2B]. The CA-MRSA clones, in particular ST45-V [5C2&5], have acquired multiple antimicrobial resistance determinants including ciprofloxacin, erythromycin, clindamycin, gentamicin and tetracycline. The multi-resistant ST45-V [5C2&5] clone accounted for 11.0% of CA-MRSA. As CA-MRSA is well established in the Australian community, it is important to monitor antimicrobial resistance patterns in community- and healthcare-associated SAB as this information will guide therapeutic practices in treating S. aureus sepsis.
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页数:19
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