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Australian Gonococcal Surveillance Program, 1 January to 31 March 2024. 澳大利亚淋球菌监测计划,2024年1月1日至3月31日。
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.001
Monica M Lahra, Sebastiaan van Hal, Sonya Natasha Hutabarat, Tiffany R Hogan

Abstract: The Australian National Neisseria Network (NNN) comprises reference laboratories in each state and territory that report data on antimicrobial susceptibility testing to an agreed group of antimicrobial agents for the Australian Gonococcal Surveillance Programme (AGSP). The AGSP data are presented quarterly in tabulated form, as well as in the AGSP annual report. This report presents national gonococcal antimicrobial resistance surveillance data from 1 January to 31 March 2024.

摘要:澳大利亚国家奈瑟菌网络(NNN)由每个州和地区的参考实验室组成,这些实验室向澳大利亚淋球菌监测计划(AGSP)商定的抗微生物药物组报告抗微生物药物敏感性测试数据。AGSP数据每季度以表格形式公布一次,也在AGSP年度报告中公布一次。本报告介绍了2024年1月1日至3月31日国家淋球菌抗微生物药物耐药性监测数据。
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引用次数: 0
Emergence of locally acquired Japanese encephalitis virus in Australia, January 2021-June 2022: a national case series. 2021年1月至2022年6月澳大利亚出现本地获得性日本脑炎病毒:全国病例系列
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.005
Amanda Reyes Veliz, Stacey Kane, Anna Glynn-Robinson

Background and methods: In March 2022, an outbreak of Japanese encephalitis virus (JEV) infection was identified in temperate south-eastern Australia, with detections in humans and animals. The unexpected emergence of JEV prompted a national public health response and a Communicable Disease Incident of National Significance was declared. JEV has previously only been identified in tropical north-eastern Australia in localised outbreaks. This article provides a descriptive analysis of the human case epidemiology of the national outbreak from 1 January 2021 to 30 June 2022.

Results: There were 42 confirmed and probable human cases of JEV identified as acquired in Australia between 1 January 2021 and 30 June 2022. Seven deaths occurred (case fatality rate: 17%). Cases were identified in five Australian jurisdictions (New South Wales, Victoria, Queensland, South Australia and the Northern Territory). The majority of cases were aged 60 years and over (55%; 23/42), with a median age of 61.5 years (range: 0-79 years; interquartile range: 45-70 years); cases were predominantly of non-Indigenous status (90%; 38/42). Sixty-seven percent (28/42) were male. Of the cases with geographical data available (n = 41), all were likely exposed to the virus in 31 unique local government areas across regional and remote Australia.

Conclusions: Cases were detected across Australia in five jurisdictions, requiring a national public health response, to detect and prevent further cases. There was widespread geographical distribution over 18 months. Given the risk of further cases and possible endemicity of JEV being established in Australia, expanded environmental and human surveillance programs are required.

背景和方法:2022年3月,在温带的澳大利亚东南部发现了一次日本脑炎病毒(JEV)感染暴发,在人类和动物中均有发现。乙脑病毒的意外出现促使国家采取公共卫生应对措施,并宣布为国家重大传染病事件。以前仅在澳大利亚热带东北部的局部暴发中发现了乙脑病毒。本文对2021年1月1日至2022年6月30日期间全国暴发的人间病例流行病学进行了描述性分析。结果:在2021年1月1日至2022年6月30日期间,澳大利亚共发现42例确诊和可能的人感染乙脑病毒病例。发生7例死亡(病死率:17%)。在澳大利亚的五个司法管辖区(新南威尔士州、维多利亚州、昆士兰州、南澳大利亚州和北领地)发现了病例。大多数病例年龄在60岁及以上(55%;23/42),中位年龄61.5岁(范围:0-79岁;四分位数范围:45-70岁);病例主要是非土著居民(90%;38/42)。67%(28/42)是男性。在可获得地理数据的病例中(n = 41),所有病例都可能在澳大利亚区域和偏远地区的31个独特的地方政府区域接触过该病毒。结论:在澳大利亚的五个司法管辖区发现了病例,需要国家公共卫生应对措施,以发现和预防进一步的病例。在18个月内有广泛的地理分布。鉴于澳大利亚存在进一步病例发生的风险和乙脑病毒可能形成的地方性流行,需要扩大环境和人类监测规划。
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引用次数: 0
Australian Gonococcal Surveillance Program, 1 April to 30 June 2024. 澳大利亚淋球菌监测计划,2024年4月1日至6月30日。
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.002
Monica M Lahra, Sebastiaan van Hal, Sonya Natasha Hutabarat, Tiffany R Hogan

Abstract: The Australian National Neisseria Network (NNN) comprises reference laboratories in each state and territory that report data on antimicrobial susceptibility testing to an agreed group of antimicrobial agents for the Australian Gonococcal Surveillance Programme (AGSP). The AGSP data are presented quarterly in tabulated form, as well as in the AGSP annual report. This report presents national gonococcal antimicrobial resistance surveillance data from 1 April to 30 June 2024.

摘要:澳大利亚国家奈瑟菌网络(NNN)由每个州和地区的参考实验室组成,这些实验室向澳大利亚淋球菌监测计划(AGSP)商定的抗微生物药物组报告抗微生物药物敏感性测试数据。AGSP数据每季度以表格形式公布一次,也在AGSP年度报告中公布一次。本报告介绍了2024年4月1日至6月30日国家淋球菌抗微生物药物耐药性监测数据。
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引用次数: 0
The detection of Japanese encephalitis virus (JEV) in the Murray region, New South Wales: a public health investigation. 新南威尔士州默里地区日本脑炎病毒(JEV)的检测:一项公共卫生调查。
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.004
Gamuchirai M Shava, Katherine Todd, Tracey Oakman, Saifur Rahman, Linda Hueston, Keira Glasgow, April Roberts-Witteveen

Abstract: The detection of Japanese encephalitis virus (JEV) in pigs, at four piggeries in the Murray region in February 2022, prompted a public health investigation (PHI) by the New South Wales Department of Health (NSW Health) to identify people at greatest risk of infection. The PHI included three components: a vaccination clinic and accompanying clinic questionnaire; a serological investigation; and a cross-sectional study for consenting Australian-born participants who completed an extended questionnaire after receiving their serological results. The goals were to vaccinate a presumably naïve population to reduce associated risk and to understand the seroprevalence among Australian-born piggery workers. A total of 322 farm workers and/or residents attended clinics organised by NSW Health; 311 received a JEV vaccine (96.6%); and 302 (94%) completed a clinic questionnaire. Of 178 people from whom serology was collected (55.3%), a total of 165 returned Defined Epitope Blocking enzyme-linked immunosorbent assay (DEB ELISA) results; 153/165 of those returning DEB ELISA results were Australian born. The study's cross-sectional component involved 129 participants, ten of whom were seropositive. The overall seropositivity for 153 Australian-born participants across the identified piggeries was 6.5% (95% confidence interval [95% CI]: 3.4-12.0%), suggesting that JEV was circulating in piggeries, and plausibly more broadly, within the Murray region prior to serology collection. Male sex and working on, or visiting, a farm other than their regular workplace were both associated with JEV seropositivity (odds ratio [OR]: 5.4; 95% CI: 0.94-137.1 and OR: 37; 95% CI: 0.92-22.08 respectively). JEV vaccination uptake was high among piggery workers in the Murray region. Further studies are needed to determine if piggery workers have an increased risk of developing JEV compared to people who do not work or live on JEV-affected piggeries. The reasons for the emergence of JEV in pigs in the Murray region remain unclear.

摘要:2022年2月,新南威尔士州Murray地区的4个猪场检测到日本脑炎病毒(JEV),促使新南威尔士州卫生部(NSW health)开展公共卫生调查(PHI),以确定感染风险最高的人群。PHI包括三个组成部分:疫苗接种诊所和随附的诊所问卷;血清学调查;另一项横断面研究是针对澳大利亚出生的参与者,他们在收到血清学结果后完成了一份扩展问卷。研究的目标是为可能的naïve人群接种疫苗,以降低相关风险,并了解澳大利亚出生的养猪场工人的血清患病率。共有322名农场工人和/或居民到新南威尔士州卫生部组织的诊所就诊;311人接种了乙脑疫苗(96.6%);302例(94%)完成临床问卷调查。在收集血清学的178人(55.3%)中,共有165人返回了定义表位阻断酶联免疫吸附测定(DEB ELISA)结果;在返回DEB ELISA结果的患者中,153/165人出生在澳大利亚。该研究的横断面部分涉及129名参与者,其中10人血清检测呈阳性。在已确定的猪场中,153名澳大利亚出生的参与者的总体血清学阳性为6.5%(95%置信区间[95% CI]: 3.4-12.0%),这表明在血清学收集之前,乙脑病毒在猪场中传播,并且可能更广泛地在默里地区传播。男性性别以及在农场工作或访问农场以外的正常工作场所均与乙脑病毒血清阳性相关(优势比[or]: 5.4;95% CI: 0.94-137.1, OR: 37;95% CI分别为0.92-22.08)。默里地区养猪场工人的乙脑疫苗接种率很高。需要进一步的研究来确定养猪场工人是否比不工作或生活在受乙脑病毒影响的养猪场的人有更高的患乙脑病毒的风险。穆雷地区猪中出现乙脑病毒的原因尚不清楚。
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引用次数: 0
Australian Trachoma Surveillance Report update: 2014-2022. 澳大利亚沙眼监测报告更新:2014-2022。
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.006
Alison Jaworski, Carleigh Cowling, Gordana C Popovic, Absar Noorul, Sergio Sandler, Susana Vaz Nery, John Kaldor

Abstract: Australia is the only high-income country where trachoma has been endemic, defined as an overall trachoma prevalence in Aboriginal and Torres Strait Islander children aged 5-9 years of 5% or more. The Australian Government funds the National Trachoma Surveillance and Reporting Unit to collate and analyse trachoma prevalence data and control strategies annually. This report presents data submitted from 2014 to 2022. In 2022, there were 87 remote communities considered at-risk of endemic trachoma, a decline of 51% since 2014 when 177 communities were considered at-risk. World Health Organization grading criteria are used to diagnose trachoma in at-risk populations. Overall prevalence, which includes estimates from all communities ever considered at-risk, fell below 5% endemicity thresholds for the first time in 2022 in Western Australia (2.9%), the Northern Territory (2.1%), New South Wales (0.5%), and in Queensland and South Australia (0.0% each). New cases of trachomatous trichiasis-a severe consequence of trachoma that causes blindness-were detected in eight out of 10,806 persons, aged 15 years and over, screened in 2022. Jurisdictional trichiasis prevalence was 0.2% in Western and South Australia and 0.0% in the Northern Territory. Australia must maintain overall trachoma and trichiasis prevalence below endemicity levels for a further two years before applying for World Health Organization validation of elimination of trachoma as a public health problem.

摘要:澳大利亚是唯一一个沙眼流行的高收入国家,定义为5-9岁原住民和托雷斯海峡岛民儿童的沙眼总体患病率为5%或以上。澳大利亚政府资助国家沙眼监测和报告股,每年对沙眼流行数据和控制战略进行整理和分析。本报告提供了2014年至2022年提交的数据。2022年,有87个偏远社区被认为存在地方性沙眼风险,与2014年的177个社区相比下降了51%。世界卫生组织分级标准用于诊断高危人群的沙眼。2022年,西澳大利亚州(2.9%)、北领地(2.1%)、新南威尔士州(0.5%)以及昆士兰州和南澳大利亚州(各0.0%)的总体流行率(包括曾经被认为有风险的所有社区的估计值)首次降至5%的流行阈值以下。2022年,在10,806名15岁及以上的筛查人群中,有8人发现了沙眼性滴漏新病例。沙眼是导致失明的沙眼的严重后果。西澳大利亚和南澳大利亚的辖区倒睫患病率为0.2%,北领地为0.0%。澳大利亚必须再将沙眼和倒睫病的总体流行率保持在低于地方病水平的两年内,然后向世界卫生组织申请确认消除沙眼作为一个公共卫生问题。
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引用次数: 0
Erratum: Meningococcal Surveillance Australia: Reporting period 1 April to 30 June 2024. 更正:澳大利亚脑膜炎球菌监测:报告期为2024年4月1日至6月30日。
Q3 Medicine Pub Date : 2025-01-22 DOI: 10.33321/cdi.2025.49.008
Monica M Lahra, Sonya Natasha Hutabarat, Sebastiaan van Hal, Tiffany R Hogan

Abstract: Erratum to Commun Dis Intell (2018) 2024;48. (doi: 10.33321/cdi.2024.48.54).

摘要:《公共情报勘误》(2018)2024;48。(doi: 10.33321 / cdi.2024.48.54)。
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引用次数: 0
Australian Group on Antimicrobial Resistance (AGAR) Australian Enterococcal Surveillance Outcome Program (AESOP) Bloodstream Infection Annual Report 2023. 澳大利亚抗微生物药物耐药性小组(琼脂)澳大利亚肠球菌监测结果计划(AESOP)血液感染年度报告2023。
Q3 Medicine Pub Date : 2024-12-18 DOI: 10.33321/cdi.2024.48.56
Geoffrey W Coombs, Denise A Daley, Princy Shoby, Auriane Form, Shakeel Mowlaboccus

Abstract: From 1 January to 31 December 2023, fifty-six institutions across Australia participated in the Australian Enterococcal Surveillance Outcome Program (AESOP). The aim of AESOP 2023 was to determine the proportion of enterococcal bacteraemia isolates in Australia that were antimicrobial resistant, and to determine the Enterococcus faecium molecular epidemiology. Of the 1,599 unique episodes of enterococcal bacteraemia investigated, 92.9% were caused by either E. faecalis (51.8%) or E. faecium (41.1%). Ampicillin and vancomycin resistance were not detected in E. faecalis but were detected in 94.2% and 50.8% of E. faecium respectively. Two linezolid-resistant E. faecalis were identified in 2023. Both isolates had linezolid minimum inhibitory concentrations (MICs) of 6.0 mg/L, were vancomycin susceptible, and harboured the optrA gene. Overall, 53.2% of E. faecium harboured either the vanA or the vanB gene; of these, 27.3% harboured vanA, 72.1% harboured vanB, and 0.6% harboured vanA and vanB. The percentage of vancomycin-resistant E. faecium bacteraemia isolates in Australia remains substantially higher than that recorded in most European countries. The E. faecium isolates consisted of 58 multi-locus sequence types (STs); 85.7% of isolates were classified into seven major STs, each containing ten or more isolates. All major STs belonged to clonal complex (CC) 17, a global hospital-adapted polyclonal E. faecium CC. The major STs (ST78, ST1424, ST17, ST80, ST796, ST1421 and ST555) were found across most regions of Australia, with ST78 identified in all regions. Overall, 58.3% of isolates belonging to the seven major STs harboured the vanA or vanB gene. AESOP 2023 has shown that enterococcal bacteraemia episodes in Australia continues to be frequently caused by polyclonal ampicillin-resistant high-level gentamicin-resistant vanA- or vanB-positive E. faecium which have limited treatment options.

摘要:从2023年1月1日至12月31日,澳大利亚56家机构参加了澳大利亚肠球菌监测结果计划(AESOP)。AESOP 2023的目的是确定澳大利亚耐药肠球菌菌血症分离株的比例,并确定屎肠球菌的分子流行病学。在调查的1599例肠球菌菌血症中,92.9%由粪肠球菌(51.8%)或粪肠球菌(41.1%)引起。未检出氨苄西林和万古霉素耐药性,但检出率分别为94.2%和50.8%。在2023年发现了2只耐利奈唑胺的粪肠球菌。两株菌株利奈唑胺最低抑菌浓度(mic)均为6.0 mg/L,对万古霉素敏感,携带optrA基因。总体而言,53.2%的粪肠杆菌携带vanA或vanB基因;其中,27.3%为维纳港,72.1%为维纳港,0.6%为维纳港和维纳港。澳大利亚耐万古霉素的粪肠杆菌菌血症分离株的百分比仍然大大高于大多数欧洲国家的记录。分离的粪肠杆菌有58个多位点序列类型(STs);85.7%的菌株被划分为7个主要STs,每个STs含有10个或更多的菌株。所有主要STs都属于克隆复合体(CC) 17,这是一种全球医院适应的多克隆粪杆菌CC,主要STs (ST78、ST1424、ST17、ST80、ST796、ST1421和ST555)在澳大利亚大部分地区都被发现,其中ST78在所有地区都被发现。总体而言,属于7个主要STs的58.3%的分离株含有vanA或vanB基因。AESOP 2023显示,澳大利亚肠球菌菌血症事件仍然经常由多克隆耐氨苄西林高水平耐庆大霉素的vanA-或vanb阳性屎肠杆菌引起,治疗选择有限。
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引用次数: 0
Australian Group on Antimicrobial Resistance (AGAR) Australian Staphylococcus aureus Surveillance Outcome Program (ASSOP) Bloodstream Infection Annual Report 2023. 澳大利亚抗菌药耐药性小组(AGAR)《澳大利亚金黄色葡萄球菌监测结果计划(ASSOP)2023 年血流感染年度报告》。
Q3 Medicine Pub Date : 2024-12-18 DOI: 10.33321/cdi.2024.48.57
Geoffrey W Coombs, Denise A Daley, Princy Shoby, Sruthi Mamoottil Sudeep, Shakeel Mowlaboccus
<p><strong>Abstract: </strong>From 1 January to 31 December 2023, fifty-seven institutions across Australia participated in the Australian <i>Staphylococcus aureus</i> Surveillance Outcome Program (ASSOP). The aim of ASSOP 2023 was to determine the proportion of <i>Staphylococcus aureus</i> bacteraemia (SAB) isolates in Australia that were antimicrobial resistant, with particular emphasis on methicillin resistance, and to characterise the methicillin-resistant <i>S. aureus</i> (MRSA) molecular epidemiology. A total of 3,422 SAB episodes were reported, of which 77.0% were community-onset. Overall, 16.1% of <i>S, aureus</i> were methicillin resistant. The 30-day all-cause mortality associated with methicillin-resistant SAB was 14.8%, which was not significantly different to the 16.5% all-cause mortality associated with methicillin-susceptible SAB (<i>p</i> = 0.44). With the exception of the β-lactams and erythromycin, antimicrobial resistance in methicillin-susceptible <i>S, aureus</i> (MSSA) was infrequent. However, in addition to the β-lactams, approximately 33% of MRSA were resistant to ciprofloxacin; 30% to erythromycin; 13% to tetracycline; 13% to gentamicin; and 3% to co-trimoxazole. Two New South Wales daptomycin-resistant MRSA, with minimum inhibitory concentrations (MICs) of 3.0 and 4.0 mg/L, were identified as ST22-IV, with a V351E <i>mprF</i> mutation, and ST45-V with a T345I <i>mprF</i> mutation respectively. Three daptomycin-resistant MSSA were identified. One from Tasmania, with a daptomycin MIC of 1.5 mg/L, identified as ST9295 with a L341I <i>mprF</i> mutation; one from New South Wales, with a daptomycin MIC of 3.0 mg/L, identified as ST97 with a L776S <i>mprF</i> mutation; and one from Western Australia, with a daptomycin MIC of 2.0 mg/L, identified as ST5. No previously reported mutations in known loci were detected in the Western Australian isolate. When applying the European Committee on Antimicrobial Susceptibility Testing breakpoints, teicoplanin resistance was detected in three MSSA isolates and one MRSA isolate. Vancomycin or linezolid resistance was not detected. Resistance to non-β-lactam antimicrobials was largely attributable to the healthcare-associated MRSA (HA-MRSA) clone ST22-IV [2B] (EMRSA-15), and the community-associated MRSA (CA-MRSA) clone ST45-V [5C2&5] which has acquired resistance to multiple antimicrobials including ciprofloxacin, clindamycin, erythromycin, gentamicin, and tetracycline. ST22-IV [2B] (EMRSA-15) was the predominant HA-MRSA clone in Australia. Overall, 85% of methicillin-resistant SAB were caused by community-associated MRSA (CA-MRSA) clones. Although polyclonal, approximately 70.3% of CA-MRSA clones were characterised as ST93-IV [2B] (Queensland clone); ST5-IV [2B]; ST1-IV [2B]; ST45-V [5C2&5]; ST30-IV [2B]; ST8-IV [2B]; ST6-IV [2B]; ST97-IV [2B]; and ST953-IV [2B]. As CA-MRSA is well established in the Australian community, it is important to monitor antimicrobial resistance patterns in commu
摘要:从2023年1月1日至12月31日,澳大利亚57家机构参加了澳大利亚金黄色葡萄球菌监测结果项目(ASSOP)。ASSOP 2023的目的是确定澳大利亚耐药金黄色葡萄球菌菌血症(SAB)分离株的比例,特别强调对甲氧西林的耐药性,并表征耐甲氧西林金黄色葡萄球菌(MRSA)的分子流行病学特征。总共报告了3422例SAB发作,其中77.0%为社区发病。总体而言,16.1%的金黄色葡萄球菌耐甲氧西林。耐甲氧西林SAB的30天全因死亡率为14.8%,与甲氧西林敏感SAB的16.5%无显著差异(p = 0.44)。除β-内酰胺类和红霉素外,甲氧西林敏感金黄色葡萄球菌(MSSA)的耐药情况罕见。然而,除了β-内酰胺外,约33%的MRSA对环丙沙星耐药;红霉素占30%;13%为四环素;庆大霉素占13%;3%的复方新诺明。鉴定出两种新南威尔士州达托霉素耐药MRSA,其最低抑制浓度(mic)分别为3.0和4.0 mg/L,分别为ST22-IV,突变为V351E mprF, ST45-V突变为T345I mprF。鉴定出3例耐达托霉素MSSA。一个来自塔斯马尼亚,达托霉素MIC为1.5 mg/L,鉴定为ST9295,携带L341I mprF突变;一株来自新南威尔士州,达托霉素MIC为3.0 mg/L,鉴定为ST97,携带L776S mprF突变;1例来自西澳大利亚,达托霉素MIC为2.0 mg/L,鉴定为ST5。在西澳大利亚分离株中未发现先前报道的已知位点突变。当应用欧洲抗微生物药物敏感性试验委员会的断点时,在3株MSSA分离株和1株MRSA分离株中检测到替柯普兰耐药。未检出万古霉素或利奈唑胺耐药。对非β-内酰胺类抗菌素的耐药性主要归因于医疗相关MRSA (HA-MRSA)克隆ST22-IV [2B] (EMRSA-15)和社区相关MRSA (CA-MRSA)克隆ST45-V [5C2&5],后者对环丙沙星、克林霉素、红霉素、庆大霉素和四环素等多种抗菌素产生耐药性。ST22-IV [2B] (EMRSA-15)是澳大利亚主要的HA-MRSA克隆。总体而言,85%的耐甲氧西林SAB是由社区相关的MRSA (CA-MRSA)克隆引起的。虽然是多克隆的,但大约70.3%的CA-MRSA克隆被鉴定为ST93-IV [2B](昆士兰克隆);ST5-IV (2 b);ST1-IV (2 b);ST45-V [5 c2&5];ST30-IV (2 b);ST8-IV (2 b);ST6-IV (2 b);ST97-IV (2 b);ST953-IV [2B]。由于CA-MRSA在澳大利亚社区已经建立,因此监测社区和医疗保健相关SAB的抗菌素耐药性模式非常重要,因为这些信息将指导治疗金黄色葡萄球菌血症的治疗实践。
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引用次数: 0
An outbreak of dengue virus type 3 on Mer Island in the Torres Strait, Australia in 2024. 2024 年澳大利亚托雷斯海峡默尔岛爆发 3 型登革热病毒。
Q3 Medicine Pub Date : 2024-12-18 DOI: 10.33321/cdi.2024.48.63
A Hempenstall, A Pyke, C Taunton, U Sabatino, S Kaigey, E Pickering, G Ehlers, M O Muzari, J Davis, C Paton, C Taylor, A van den Hurk, G Hewitson, S Schlebusch, J Hanson

Abstract: In early 2024, there were eight confirmed cases of locally acquired dengue on Mer Island in the Torres Strait. This dengue outbreak prompted an in-community public health response which included active case finding, health promotion and vector control. This was the first detected dengue outbreak in the Torres Strait since 2017. It highlights the importance of testing in primary healthcare, vector control and ongoing public health surveillance to minimise the risk of local transmission and establishment of endemic viruses which may cause significant and potentially life-threatening disease within populations in northern Australia.

摘要:2024年初,托雷斯海峡梅尔岛出现8例本地获得性登革热确诊病例。这次登革热疫情促使社区内采取了公共卫生应对措施,包括积极发现病例、促进健康和媒介控制。这是自2017年以来托雷斯海峡首次发现登革热疫情。它强调了在初级保健、病媒控制和持续的公共卫生监测中进行检测的重要性,以尽量减少地方传播和建立可能在澳大利亚北部人口中造成严重和可能危及生命的疾病的地方性病毒的风险。
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引用次数: 0
Australian Meningococcal Surveillance Programme Annual Report, 2023. 澳大利亚脑膜炎球菌监测计划年度报告,2023年。
Q3 Medicine Pub Date : 2024-12-18 DOI: 10.33321/cdi.2024.48.52
Monica M Lahra, C R Robert George, Sebastiaan van Hal, Tiffany R Hogan

Abstract: In Australia, both probable and laboratory-confirmed cases of invasive meningococcal disease (IMD) are reported to the National Notifiable Diseases Surveillance System (NNDSS). When compared to 2022, the number of IMD notifications in 2023 increased by 14% to 143. Laboratory confirmation of IMD occurred in 140/143 (98%) of these cases, with 64% (90/140) diagnosed by bacterial culture and 36% (50/140) by nucleic acid amplification testing. The serogroup was determined for 96% of laboratory-confirmed cases (134/140): serogroup B (MenB) accounted for 84% of infections (112/134); MenW for 8% (11/134); MenY for 8% (11/134). There were no infections attributed to MenC disease. Fine typing was available on 75% of the cases for which the serogroup was determined (100/134). In MenB isolates, 25 porA types were detected, the most prevalent of which were P1.7-2,4 (32%; 26/82), P1.7,16-26 (16%; 13/82) and P1.22,14 (9%; 7/82). All eight typed MenW infections identified as porA type P1.5,2, with two different multi-locus sequence types (MLST) present: ST-11 (5) and ST-1287 (3) from the clonal complex 11, the hypervirulent strain reported in outbreaks in Australia and overseas. In MenY, the predominant porA type was P1.5-1,10-1 (90%; 9/10), ST-1655 and from clonal complex 23. Peaks of IMD occurred in children aged less than 5 years and in those aged 15-24 years, accounting for 21% (30/140) and 26% (37/140) of laboratory-confirmed cases respectively. In children aged under 5 years, 93% of IMD (27/29) was MenB; in those aged 15-24 years, 97% of IMD (36/37) was MenB, with serogroup not determined for one case in each of these age groups. Of note, 14-15% of IMD occurred in each of the older age groups reported: adults 25-44 years (14%, 19/140), 45-64 years (14%, 20/140), and in those aged 65 years and older (15%, 21/140). Whilst MenB predominated in all age groups, the majority of MenY and MenW IMD cases were reported in adults aged 45 years and older. All cultured IMD isolates (n = 90) had antimicrobial susceptibility testing performed. Minimum inhibitory concentration (MIC) values were reported using Clinical Laboratory Standards Institute (CLSI) interpretative criteria: 9% (8/90) were defined as penicillin resistant (MIC value: ≥ 0.5 mg/L); 71% (64/90) had intermediate susceptibility to penicillin (MIC values: 0.125 and 0.25 mg/L) and 20% (18/90) were susceptible to penicillin (MIC values: ≤ 0.064 mg/L). All isolates tested susceptible to ceftriaxone, ciprofloxacin and rifampicin.

摘要:在澳大利亚,侵袭性脑膜炎球菌病(IMD)的可能病例和实验室确诊病例均向国家法定疾病监测系统(NNDSS)报告。与2022年相比,2023年的IMD通知数量增加了14%,达到143份。这些病例中有140/143例(98%)确诊为IMD,其中64%(90/140)通过细菌培养诊断,36%(50/140)通过核酸扩增检测诊断。96%的实验室确诊病例(134/140)确定了血清型;84%的感染病例(112/134)确定了血清B型(MenB);男性占8% (11/134);价格为8%(11/134)。没有感染归因于MenC病。在确定血清组的病例中,75%(100/134)可进行精细分型。在MenB分离株中检出25种孔a型,其中以p1.7 ~ 2,4 (32%;26/82), p1.7,16-26 (16%;13/82)和P1.22,14 (9%;7/82)。所有8型MenW感染均被鉴定为P1.5,2型porA型,存在两种不同的多位点序列型(MLST): ST-11(5)和ST-1287(3),来自克隆复合体11,澳大利亚和海外暴发的高毒菌株。在MenY,主要的porA类型为P1.5-1,10-1 (90%;9/10), ST-1655,克隆配合物23。5岁以下儿童和15-24岁儿童是IMD的发病高峰,分别占实验室确诊病例的21%(30/140)和26%(37/140)。在5岁以下儿童中,93%的IMD(27/29)是MenB;在15-24岁的人群中,97%的IMD(36/37)是MenB,每个年龄组中有1例未确定血清组。值得注意的是,14-15%的IMD发生在报告的每个较大年龄组:25-44岁的成年人(14%,19/140),45-64岁的成年人(14%,20/140)和65岁及以上的老年人(15%,21/140)。虽然MenB在所有年龄组中占主导地位,但大多数MenY和MenW型IMD病例报告发生在45岁及以上的成年人中。所有培养的IMD分离株(n = 90)均进行了抗菌药敏试验。根据临床实验室标准协会(CLSI)的解释标准报告最低抑菌浓度(MIC)值:9%(8/90)被定义为青霉素耐药(MIC值:≥0.5 mg/L);71%(64/90)对青霉素有中等敏感性(MIC值分别为0.125和0.25 mg/L), 20%(18/90)对青霉素敏感(MIC值≤0.064 mg/L)。所有分离株均对头孢曲松、环丙沙星和利福平敏感。
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Communicable diseases intelligence (2018)
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