首页 > 最新文献

Communicable diseases intelligence (2018)最新文献

英文 中文
Act Now-A Global Call to Confront Antimicrobial Resistance. 立即行动——应对抗菌素耐药性的全球呼吁。
IF 1.6 Q3 Medicine Pub Date : 2025-11-18 DOI: 10.33321/cdi.2025.49.065
Christina Bareja

An editorial by Christina Bareja, CDI's Editor and the Director of the Antimicrobial Resistance Policy and Surveillance Section, marking the start of World AMR Awareness Week 2025. The editorial highlights the several surveillance reports of the Australian Group on Antimicrobial Resistance, and of the National Neisseria Network, Australia, which accompany the editorial in a special CDI 'issue' on AMR.

CDI编辑兼抗菌素耐药性政策和监测科科长Christina Bareja在2025年世界抗菌素耐药性宣传周开始之际发表的社论。这篇社论强调了澳大利亚抗微生物药物耐药性小组和澳大利亚国家奈瑟菌网络的几份监测报告,这些报告与CDI关于抗菌素耐药性的特刊一起发表。
{"title":"Act Now-A Global Call to Confront Antimicrobial Resistance.","authors":"Christina Bareja","doi":"10.33321/cdi.2025.49.065","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.065","url":null,"abstract":"<p><p>An editorial by Christina Bareja, CDI's Editor and the Director of the Antimicrobial Resistance Policy and Surveillance Section, marking the start of World AMR Awareness Week 2025. The editorial highlights the several surveillance reports of the Australian Group on Antimicrobial Resistance, and of the National Neisseria Network, Australia, which accompany the editorial in a special CDI 'issue' on AMR.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145542542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2024. 澳大利亚克雅氏病监测:更新至2024年12月31日
IF 1.6 Q3 Medicine Pub Date : 2025-10-22 DOI: 10.33321/cdi.2025.49.050
Christiane Stehmann, Matteo Senesi, Shannon Sarros, Amelia McGlade, Victoria Lewis, Priscilla Agustina, Daniel Barber, Genevieve Klug, Sarah Holper, Catriona McLean, Colin Masters, Steven Collins

Nationwide surveillance of Creutzfeldt-Jakob disease (CJD) and other human prion diseases is performed by the Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR). National surveillance encompasses the period since 1 January 1970, with prospective surveillance occurring from 1 October 1993. Over this prospective surveillance period, considerable improvements have been developed in pre-mortem diagnostics; in the delineation of new disease subtypes; and in heightened awareness of prion diseases in healthcare settings. Surveillance practices of the ANCJDR have evolved and adapted accordingly. This report summarises the activities of the ANCJDR during 2024. Since the ANCJDR began offering diagnostic cerebrospinal fluid (CSF) 14-3-3 protein testing in Australia in September 1997, the annual number of referrals has steadily increased. In 2024, a total of 760 domestic CSF specimens were referred for diagnostic testing and 88 persons with suspected human prion disease were formally added to the national register. As of 31 December 2024, approximately half (42) of the 83 initial case notifications for 2024 remain classified as 'incomplete'; 21 cases were classified as 'definite' and 17 as 'probable' prion disease; three cases were excluded through neuropathological examination. For 2024, seventy-two percent of all suspected human-prion-disease-related deaths in Australia underwent neuropathological examination. No cases of variant or iatrogenic CJD were identified in Australia during 2024.

克雅氏病(CJD)和其他人类朊病毒疾病的全国监测由澳大利亚国家克雅氏病登记处(ANCJDR)进行。国家监测包括自1970年1月1日以来的时期,预期监测从1993年10月1日开始。在这一预期监测期间,在死前诊断方面取得了相当大的进步;在新的疾病亚型的描述;提高卫生保健机构对朊病毒疾病的认识。ANCJDR的监测做法也随之发展和调整。本报告总结了联合国人权与发展委员会在2024年期间的活动。自1997年9月ANCJDR开始在澳大利亚提供脑脊液14-3-3蛋白诊断测试以来,每年的转诊数量稳步增加。2024年,共有760份国内脑脊液标本转诊检测,88名疑似人类朊病毒疾病患者正式加入国家登记。截至2024年12月31日,2024年83例初步病例通报中约有一半(42例)仍被列为“不完整”;21例为“明确”,17例为“可能”朊病毒病;经神经病理检查排除3例。2024年,澳大利亚72%的疑似人类朊病毒相关死亡病例接受了神经病理学检查。澳大利亚在2024年期间未发现变异型或医源性CJD病例。
{"title":"Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2024.","authors":"Christiane Stehmann, Matteo Senesi, Shannon Sarros, Amelia McGlade, Victoria Lewis, Priscilla Agustina, Daniel Barber, Genevieve Klug, Sarah Holper, Catriona McLean, Colin Masters, Steven Collins","doi":"10.33321/cdi.2025.49.050","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.050","url":null,"abstract":"<p><p>Nationwide surveillance of Creutzfeldt-Jakob disease (CJD) and other human prion diseases is performed by the Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR). National surveillance encompasses the period since 1 January 1970, with prospective surveillance occurring from 1 October 1993. Over this prospective surveillance period, considerable improvements have been developed in pre-mortem diagnostics; in the delineation of new disease subtypes; and in heightened awareness of prion diseases in healthcare settings. Surveillance practices of the ANCJDR have evolved and adapted accordingly. This report summarises the activities of the ANCJDR during 2024. Since the ANCJDR began offering diagnostic cerebrospinal fluid (CSF) 14-3-3 protein testing in Australia in September 1997, the annual number of referrals has steadily increased. In 2024, a total of 760 domestic CSF specimens were referred for diagnostic testing and 88 persons with suspected human prion disease were formally added to the national register. As of 31 December 2024, approximately half (42) of the 83 initial case notifications for 2024 remain classified as 'incomplete'; 21 cases were classified as 'definite' and 17 as 'probable' prion disease; three cases were excluded through neuropathological examination. For 2024, seventy-two percent of all suspected human-prion-disease-related deaths in Australia underwent neuropathological examination. No cases of variant or iatrogenic CJD were identified in Australia during 2024.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348971","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Invasive pneumococcal disease in Australia: 2013 and 2014. 侵袭性肺炎球菌疾病在澳大利亚:2013年和2014年。
IF 1.6 Q3 Medicine Pub Date : 2025-10-22 DOI: 10.33321/cdi.2025.49.038
Kate Pennington, Sanjay Jayasinghe, Lizzie Gorrell

In Australia, there were 1,552 cases (6.7 per 100,000 population per year) of invasive pneumococcal disease (IPD) notified to the National Notifiable Diseases Surveillance System (NNDSS) in 2013, and 1,564 cases (6.7 per 100,000 population per year) in 2014. The non-age standardised rate of IPD in Indigenous Australians was six times the rate of IPD in non-Indigenous Australians in both 2013 and 2014. Following the July 2011 introduction of the 13-valent pneumococcal conjugate vaccine (13vPCV) to the National Immunisation Program (NIP), the overall rate of IPD in children aged less than 5 years decreased from 19.8 per 100,000 population per year in 2011 to 12.5 per 100,000 population per year in 2013. In 2014 there was a slight increase in the overall rate of IPD in children aged less than 5 years to 14.1 per 100,000 population per year in 2014. In both 2013 and 2014, the rate of IPD caused by serotypes included 23-valent pneumococcal polysaccharide vaccine (23vPPV) declined in Indigenous adults aged 50 years or older (40.5 per 100,000 population per year and 35.2 per 100,000 population per year, respectively) after displaying a gradual increase between 2002 and 2012. Rates of IPD in non-Indigenous adults aged 65 years or older caused by serotypes included in the 23vPPV also declined in both 2013 and 2014 (9.5 per 100,000 population per year and 8.3 per 100,000 population per year, respectively) compared to 2011 (11.8 per 100,000 population per year). There were 134 deaths attributable to IPD in 2013 (a case fatality rate of 8.6%) and 118 in 2014 (a case fatality rate of 7.5%).

在澳大利亚,2013年向国家法定疾病监测系统(NNDSS)报告了1552例(每年每10万人6.7例)侵袭性肺炎球菌病(IPD), 2014年报告了1564例(每年每10万人6.7例)。2013年和2014年,澳大利亚土著居民的非年龄标准化IPD率是非土著澳大利亚人的6倍。在2011年7月将13价肺炎球菌结合疫苗(13vPCV)引入国家免疫规划(NIP)之后,5岁以下儿童IPD的总体发病率从2011年的每年每10万人19.8人下降到2013年的每年每10万人12.5人。2014年,5岁以下儿童IPD的总体发病率略有上升,达到每年每10万人14.1例。包括23价肺炎球菌多糖疫苗(23vPPV)在内的血清型引起的IPD发病率在2002年至2012年期间呈逐渐上升趋势,但在2013年和2014年均有所下降(分别为40.5 / 10万人/年和35.2 / 10万人/年)。与2011年(11.8 / 10万人/年)相比,2013年和2014年,23vPPV中包含的血清型导致的65岁或以上非土著成年人IPD发生率也有所下降(分别为9.5 / 10万人/年和8.3 / 10万人/年)。2013年有134人死于IPD(病死率为8.6%),2014年有118人(病死率为7.5%)。
{"title":"Invasive pneumococcal disease in Australia: 2013 and 2014.","authors":"Kate Pennington, Sanjay Jayasinghe, Lizzie Gorrell","doi":"10.33321/cdi.2025.49.038","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.038","url":null,"abstract":"<p><p>In Australia, there were 1,552 cases (6.7 per 100,000 population per year) of invasive pneumococcal disease (IPD) notified to the National Notifiable Diseases Surveillance System (NNDSS) in 2013, and 1,564 cases (6.7 per 100,000 population per year) in 2014. The non-age standardised rate of IPD in Indigenous Australians was six times the rate of IPD in non-Indigenous Australians in both 2013 and 2014. Following the July 2011 introduction of the 13-valent pneumococcal conjugate vaccine (13vPCV) to the National Immunisation Program (NIP), the overall rate of IPD in children aged less than 5 years decreased from 19.8 per 100,000 population per year in 2011 to 12.5 per 100,000 population per year in 2013. In 2014 there was a slight increase in the overall rate of IPD in children aged less than 5 years to 14.1 per 100,000 population per year in 2014. In both 2013 and 2014, the rate of IPD caused by serotypes included 23-valent pneumococcal polysaccharide vaccine (23vPPV) declined in Indigenous adults aged 50 years or older (40.5 per 100,000 population per year and 35.2 per 100,000 population per year, respectively) after displaying a gradual increase between 2002 and 2012. Rates of IPD in non-Indigenous adults aged 65 years or older caused by serotypes included in the 23vPPV also declined in both 2013 and 2014 (9.5 per 100,000 population per year and 8.3 per 100,000 population per year, respectively) compared to 2011 (11.8 per 100,000 population per year). There were 134 deaths attributable to IPD in 2013 (a case fatality rate of 8.6%) and 118 in 2014 (a case fatality rate of 7.5%).</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Australian Rotavirus Surveillance Program: Annual Report, 2024. 澳大利亚轮状病毒监测计划:年度报告,2024。
IF 1.6 Q3 Medicine Pub Date : 2025-10-22 DOI: 10.33321/cdi.2025.49.048
Sarah Thomas, Nada Bogdanovic-Sakran, Daniel Pavlic, Julie Bines, Celeste Donato

This report from the Australian Rotavirus Surveillance Program describes the circulating rotavirus genotypes identified in children and adults during the period 1 January to 31 December 2024. In 2024, we saw a continuation of a high burden of rotavirus disease in the Australian population. During this period, 2,118 faecal specimens were referred to the National Rotavirus Reference Centre (NRRC), for rotavirus G- and P-genotype analysis; of these samples, 1,880 were confirmed as rotavirus positive. This is the second highest number of samples referred to the NRRC over the past 20+ years of operation. Of the 1,880 samples confirmed rotavirus positive, 1,610 (85.6%) were identified as wildtype rotavirus; 268 (14.3%) were identified as the Rotarix vaccine-like strain; and two G1P[8] samples could not be confirmed as wildtype or vaccine-like due to inadequate sequence quality. The equine-like G3P[8] variant was the dominant genotype nationally (n = 1,297/1,610; 80.6%). Other genotypes were identified at low frequencies including G1P[8] (n = 9/1,610; 0.6%); G2P[4] (n = 34/1,610; 2.1%); G3P[8] (n = 77/1,610; 4.8%); G8P[8] (n = 46/1,610; 2.9%); G9P[4] (n = 9/1,610; 0.6%); G9P[8] (n = 6/1,610; 0.4%); and G12P[8] (n = 8/1,610; 0.5%). Genotype distribution was consistent nationally, with equine-like G3P[8] the dominant genotype in all jurisdictions. Consistent with observations in recent years, a small number of samples with unusual genotypes were identified (n = 70/1,610; 4.3%). Of these unusual genotypes, the most frequently detected was G2P[8], which accounted for 52.9% of unusual samples (n = 37/70) and 2.3% of all positive wildtype samples (n = 37/1,610). The high number of rotavirus positive samples received by the program reflected the notifications for rotavirus disease reported to the National Notifiable Disease Surveillance Service (NNDSS). Across Australia, there were 10,108 notifications recorded, the highest reported in any year since establishment of the national rotavirus notification. The ability to monitor the genotypes of rotavirus strains causing disease across ages and across jurisdictions provides important data to aid in assessing the performance of the national rotavirus vaccination program and to inform public health interventions during outbreaks. The Australian Rotavirus Surveillance Program also provides important data to monitor annual variations in genotypes circulating in the population. Understanding the diversity of genotypes in circulation, and the emergence of variants, provides important context for any changes observed in disease epidemiology in the community. The Australian Rotavirus Surveillance Program provides diagnostic laboratories with valuable feedback on laboratory data quality, by reporting incidences of wildtype, vaccine-like, and/or false positive rotavirus results.

澳大利亚轮状病毒监测规划的这份报告描述了2024年1月1日至12月31日期间在儿童和成人中发现的循环轮状病毒基因型。在2024年,我们看到澳大利亚人口中轮状病毒疾病的高负担继续存在。在此期间,向国家轮状病毒参考中心(NRRC)提交了2 118份粪便标本,用于轮状病毒G和p基因型分析;在这些样本中,1880个被确认为轮状病毒阳性。这是过去20多年来提交给NRRC的样本数量第二高的一次。1880份轮状病毒阳性样本中,1610份(85.6%)为野生型轮状病毒;经鉴定为轮虫疫苗样菌株268株(14.3%);两份G1P[8]样本由于序列质量不足而无法确认为野生型或疫苗样。马样G3P[8]变异为全国优势基因型(n = 1,297/1,610; 80.6%)。其他低频率基因型包括G1P[8] (n = 9/1,610; 0.6%);G2P[4] (n = 34/1,610; 2.1%);G3P[8] (n = 77/1,610; 4.8%);G8P[8] (n = 46/1,610; 2.9%);G9P[4] (n = 9/1,610; 0.6%);G9P[8] (n = 6/1,610; 0.4%);G12P[8] (n = 8/1,610; 0.5%)。基因型分布在全国范围内是一致的,所有辖区的优势基因型均为马类G3P[8]。与近年来的观察结果一致,发现了少数基因型异常的样本(n = 70/1,610; 4.3%)。在这些异常基因型中,最常见的是G2P[8],占异常样本的52.9% (n = 37/70),占所有阳性野生型样本的2.3% (n = 37/ 1610)。该方案收到的大量轮状病毒阳性样本反映了向国家法定疾病监测局报告的轮状病毒疾病通报。在整个澳大利亚,有10108例报告,这是自建立国家轮状病毒通报以来报告的最高年份。监测不同年龄和不同辖区引起疾病的轮状病毒毒株基因型的能力提供了重要数据,有助于评估国家轮状病毒疫苗接种规划的效果,并为疫情爆发期间的公共卫生干预提供信息。澳大利亚轮状病毒监测计划也为监测人群中传播的基因型的年度变化提供了重要数据。了解流行基因型的多样性和变异的出现,为社区疾病流行病学观察到的任何变化提供了重要的背景。澳大利亚轮状病毒监测规划通过报告野生型、疫苗样和/或假阳性轮状病毒结果的发生率,为诊断实验室提供有关实验室数据质量的宝贵反馈。
{"title":"Australian Rotavirus Surveillance Program: Annual Report, 2024.","authors":"Sarah Thomas, Nada Bogdanovic-Sakran, Daniel Pavlic, Julie Bines, Celeste Donato","doi":"10.33321/cdi.2025.49.048","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.048","url":null,"abstract":"<p><p>This report from the Australian Rotavirus Surveillance Program describes the circulating rotavirus genotypes identified in children and adults during the period 1 January to 31 December 2024. In 2024, we saw a continuation of a high burden of rotavirus disease in the Australian population. During this period, 2,118 faecal specimens were referred to the National Rotavirus Reference Centre (NRRC), for rotavirus G- and P-genotype analysis; of these samples, 1,880 were confirmed as rotavirus positive. This is the second highest number of samples referred to the NRRC over the past 20+ years of operation. Of the 1,880 samples confirmed rotavirus positive, 1,610 (85.6%) were identified as wildtype rotavirus; 268 (14.3%) were identified as the Rotarix vaccine-like strain; and two G1P[8] samples could not be confirmed as wildtype or vaccine-like due to inadequate sequence quality. The equine-like G3P[8] variant was the dominant genotype nationally (n = 1,297/1,610; 80.6%). Other genotypes were identified at low frequencies including G1P[8] (n = 9/1,610; 0.6%); G2P[4] (n = 34/1,610; 2.1%); G3P[8] (n = 77/1,610; 4.8%); G8P[8] (n = 46/1,610; 2.9%); G9P[4] (n = 9/1,610; 0.6%); G9P[8] (n = 6/1,610; 0.4%); and G12P[8] (n = 8/1,610; 0.5%). Genotype distribution was consistent nationally, with equine-like G3P[8] the dominant genotype in all jurisdictions. Consistent with observations in recent years, a small number of samples with unusual genotypes were identified (n = 70/1,610; 4.3%). Of these unusual genotypes, the most frequently detected was G2P[8], which accounted for 52.9% of unusual samples (n = 37/70) and 2.3% of all positive wildtype samples (n = 37/1,610). The high number of rotavirus positive samples received by the program reflected the notifications for rotavirus disease reported to the National Notifiable Disease Surveillance Service (NNDSS). Across Australia, there were 10,108 notifications recorded, the highest reported in any year since establishment of the national rotavirus notification. The ability to monitor the genotypes of rotavirus strains causing disease across ages and across jurisdictions provides important data to aid in assessing the performance of the national rotavirus vaccination program and to inform public health interventions during outbreaks. The Australian Rotavirus Surveillance Program also provides important data to monitor annual variations in genotypes circulating in the population. Understanding the diversity of genotypes in circulation, and the emergence of variants, provides important context for any changes observed in disease epidemiology in the community. The Australian Rotavirus Surveillance Program provides diagnostic laboratories with valuable feedback on laboratory data quality, by reporting incidences of wildtype, vaccine-like, and/or false positive rotavirus results.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348984","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Describing Australian listeriosis outbreaks, 2012 to 2022. 描述2012年至2022年澳大利亚李斯特菌病暴发。
IF 1.6 Q3 Medicine Pub Date : 2025-10-22 DOI: 10.33321/cdi.2025.49.061
Sarah Alland, Russell Stafford, Emily Fearnley, Stacey Kane, Tony Merritt, Jane McAllister, Michelle Harlock, Anthony Draper, Craig Shadbolt, Kirsty Hope

Foodborne listeriosis outbreaks occur occasionally in Australia and can lead to severe outcomes for at-risk populations. Outbreaks also have the potential to cause illness in a large number of people in a short period. We identified invasive listeriosis outbreaks investigated in Australia from 2012 to 2022. We summarised the key features of these outbreaks and assessed the implications for food safety and future outbreak investigations. Outbreak data were extracted from the national OzFoodNet Outbreak Register and described by year reported; size; severity; type of evidence; food implicated; setting in which the food was prepared and eaten; and likely cause of contamination. Twelve listeriosis outbreaks were identified. These outbreaks involved a total of 94 cases, with 20 deaths reported (an overall case fatality rate of 21.3%). The median number of cases per outbreak was three (range: 2-34) and the median number of deaths was one (range: 0-7). Except for one outbreak with a median age of 32 years, the median age per outbreak ranged within 62-92 years. The most common food type implicated was pre-prepared composite foods (25%), including frozen meals and sandwiches. Ten outbreak investigations (83.3%) identified microbiological evidence of the same aetiological agent in the cases and the suspected food vehicle, including using whole genome sequencing as an emerging laboratory method. Most outbreaks (ten outbreaks, 83.3%) were caused by contamination of the product in the production environment, with one outbreak associated with extreme weather events. Use of novel microbiologic techniques has increased listeriosis outbreak detection and has also improved the ability to identify causes of outbreaks. It is important that public health communication emphasises the risks of consuming high-risk ingredients in composite foods, not just as standalone products. Food safety protocols should undergo ongoing review to ensure they are responsive to a changing climate.

食源性李斯特菌病暴发在澳大利亚偶尔发生,可对高危人群造成严重后果。疫情也有可能在短时间内导致大量人群患病。我们确定了2012年至2022年在澳大利亚调查的侵袭性李斯特菌病暴发。我们总结了这些暴发的主要特征,并评估了对食品安全和未来暴发调查的影响。暴发数据从国家OzFoodNet暴发登记册中提取,并按报告年份描述;大小;严重程度;证据类型;食物牵连;餐具:准备和食用食物的餐具;可能是污染的原因。确定了12次李斯特菌病暴发。这些暴发共涉及94例病例,报告了20例死亡(总病死率为21.3%)。每次暴发的病例中位数为3例(范围:2-34),死亡中位数为1例(范围:0-7)。除一次爆发的中位年龄为32岁外,每次爆发的中位年龄在62-92岁之间。最常见的食物类型是预先准备好的复合食品(25%),包括冷冻食品和三明治。10次暴发调查(83.3%)确定了病例和可疑食品运输工具中相同病原的微生物证据,包括使用全基因组测序作为一种新兴的实验室方法。大多数暴发(10次暴发,占83.3%)是由生产环境中的产品污染引起的,其中一次暴发与极端天气事件有关。使用新的微生物学技术增加了李斯特菌病爆发的检测,也提高了确定爆发原因的能力。重要的是,公共卫生宣传应强调食用复合食品中高风险成分的风险,而不仅仅是作为单独的产品。食品安全规程应接受持续审查,以确保它们对不断变化的气候作出反应。
{"title":"Describing Australian listeriosis outbreaks, 2012 to 2022.","authors":"Sarah Alland, Russell Stafford, Emily Fearnley, Stacey Kane, Tony Merritt, Jane McAllister, Michelle Harlock, Anthony Draper, Craig Shadbolt, Kirsty Hope","doi":"10.33321/cdi.2025.49.061","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.061","url":null,"abstract":"<p><p>Foodborne listeriosis outbreaks occur occasionally in Australia and can lead to severe outcomes for at-risk populations. Outbreaks also have the potential to cause illness in a large number of people in a short period. We identified invasive listeriosis outbreaks investigated in Australia from 2012 to 2022. We summarised the key features of these outbreaks and assessed the implications for food safety and future outbreak investigations. Outbreak data were extracted from the national OzFoodNet Outbreak Register and described by year reported; size; severity; type of evidence; food implicated; setting in which the food was prepared and eaten; and likely cause of contamination. Twelve listeriosis outbreaks were identified. These outbreaks involved a total of 94 cases, with 20 deaths reported (an overall case fatality rate of 21.3%). The median number of cases per outbreak was three (range: 2-34) and the median number of deaths was one (range: 0-7). Except for one outbreak with a median age of 32 years, the median age per outbreak ranged within 62-92 years. The most common food type implicated was pre-prepared composite foods (25%), including frozen meals and sandwiches. Ten outbreak investigations (83.3%) identified microbiological evidence of the same aetiological agent in the cases and the suspected food vehicle, including using whole genome sequencing as an emerging laboratory method. Most outbreaks (ten outbreaks, 83.3%) were caused by contamination of the product in the production environment, with one outbreak associated with extreme weather events. Use of novel microbiologic techniques has increased listeriosis outbreak detection and has also improved the ability to identify causes of outbreaks. It is important that public health communication emphasises the risks of consuming high-risk ingredients in composite foods, not just as standalone products. Food safety protocols should undergo ongoing review to ensure they are responsive to a changing climate.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348985","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The epidemiology of amoebiasis in the Northern Territory of Australia over 20 years (2005 - 2024). 澳大利亚北部地区20多年(2005 - 2024年)阿米巴病流行病学研究。
IF 1.6 Q3 Medicine Pub Date : 2025-10-22 DOI: 10.33321/cdi.2025.49.058
Bhavya Balasubramanya, Hayley Dyke, Sarah Lynar, Kelly Lomas, Kimberley McMahon, Vicki Krause, Anthony Draper

Amoebiasis is an important parasitic cause of morbidity and mortality worldwide and is known to be endemic in Northern Australia. The Northern Territory is the only jurisdiction in Australia where amoebiasis is notifiable. The epidemiology of amoebiasis across Australia is not well described. We undertook this retrospective study to describe the epidemiology of amoebiasis in the Northern Territory from 1 January 2005 to 30 June 2024. Data were obtained from the Northern Territory Notifiable Disease System. Of the 26 cases identified, most were men (81%), non-Indigenous (88%) and with infection overseas acquired (69%). Most had extra-intestinal manifestations (65%), and most required hospitalisation (54%). There was one death related to amoebic splenic abscess. Of the seven locally acquired cases, all resided in the Top End and Katherine regions, and two were children. The highest annual incidence occurred in 2024, all of whom were returned travellers. This study highlights that amoebiasis in the Northern Territory is both endemic and overseas acquired, and that clinicians should consider this differential diagnosis in people presenting with gastrointestinal symptoms and initiate timely testing and appropriate treatment.

阿米巴病是世界范围内发病率和死亡率的重要寄生原因,已知在澳大利亚北部流行。北领地是澳大利亚唯一需要通报阿米巴病的管辖区。阿米巴病在澳大利亚的流行病学还没有得到很好的描述。我们进行了这项回顾性研究,以描述2005年1月1日至2024年6月30日北领地阿米巴病的流行病学。数据来自北领地法定疾病系统。在确定的26例病例中,大多数为男性(81%),非土著(88%)和海外获得性感染(69%)。大多数有肠道外表现(65%),大多数需要住院治疗(54%)。有一例死亡与阿米巴性脾脓肿有关。在7例本地感染病例中,所有病例都居住在高端和凯瑟琳地区,其中2例为儿童。年发病率最高的年份是2024年,所有病例均为回国旅行者。这项研究强调,阿米巴病在北领地既是地方性的,也是海外获得的,临床医生应该在出现胃肠道症状的人群中考虑这种鉴别诊断,并开始及时检测和适当治疗。
{"title":"The epidemiology of amoebiasis in the Northern Territory of Australia over 20 years (2005 - 2024).","authors":"Bhavya Balasubramanya, Hayley Dyke, Sarah Lynar, Kelly Lomas, Kimberley McMahon, Vicki Krause, Anthony Draper","doi":"10.33321/cdi.2025.49.058","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.058","url":null,"abstract":"<p><p>Amoebiasis is an important parasitic cause of morbidity and mortality worldwide and is known to be endemic in Northern Australia. The Northern Territory is the only jurisdiction in Australia where amoebiasis is notifiable. The epidemiology of amoebiasis across Australia is not well described. We undertook this retrospective study to describe the epidemiology of amoebiasis in the Northern Territory from 1 January 2005 to 30 June 2024. Data were obtained from the Northern Territory Notifiable Disease System. Of the 26 cases identified, most were men (81%), non-Indigenous (88%) and with infection overseas acquired (69%). Most had extra-intestinal manifestations (65%), and most required hospitalisation (54%). There was one death related to amoebic splenic abscess. Of the seven locally acquired cases, all resided in the Top End and Katherine regions, and two were children. The highest annual incidence occurred in 2024, all of whom were returned travellers. This study highlights that amoebiasis in the Northern Territory is both endemic and overseas acquired, and that clinicians should consider this differential diagnosis in people presenting with gastrointestinal symptoms and initiate timely testing and appropriate treatment.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145348986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
FluTracking: Weekly online community-based surveillance of respiratory illness in Australia, 2023 Report. FluTracking:澳大利亚呼吸系统疾病每周在线社区监测,2023年报告。
IF 1.6 Q3 Medicine Pub Date : 2025-10-01 DOI: 10.33321/cdi.2025.49.037
Alexandra Kerr, Sandra Kerr, Stuart Adams, Tom McKenzie, David Boettiger, Craig Dalton

FluTracking Australia, an online respiratory illness surveillance system, monitors self-reported symptoms, care-seeking, absence from normal duties, and testing and vaccination for influenza and coronavirus disease 2019 (COVID-19). From 2022 to 2023, the number of participants who completed at least one survey decreased by 16.8%, possibly due to participation fatigue and additional survey questions. In 2023, FluTracking identified a 22% reduction in the peak weekly incidence of fever and cough (FC) compared to the 2022 season. The 2023 FC peak was similar in timing to the 2022 FC influenza peak but smaller in magnitude compared to most previous years documented by FluTracking. From 2022 to 2023, FluTracking observed: • A 36% decrease in influenza polymerase chain reaction (PCR) testing among participants reporting incident FC symptoms, largely influenced by a 57% decrease in New South Wales. • A 25% decrease in SARS-CoV-2 testing, by PCR and/or rapid antigen test (RAT), among participants reporting incident runny nose and sore throat (RNST) symptoms. • An 11% decrease in SARS-CoV-2 testing (PCR and/or RAT) among participants reporting incident FC symptoms. Reduced testing accessibility coupled with modified testing practices likely contributed to these decreases. By June 2023, SARS-CoV-2 PCR testing rates among participants with incident FC symptoms aligned with influenza PCR testing rates. Period cumulative incidence of RNST symptoms showed minimal variation across age groups in 2023. In contrast, FC period cumulative incidence inversely correlated with age, suggesting young individuals experience a higher cumulative incidence of FC symptoms.

澳大利亚FluTracking是一个在线呼吸道疾病监测系统,监测自我报告的症状、求医、缺勤以及2019年流感和冠状病毒病(COVID-19)的检测和疫苗接种。从2022年到2023年,完成至少一项调查的参与者人数减少了16.8%,可能是由于参与疲劳和额外的调查问题。FluTracking发现,与2022年相比,2023年每周发烧和咳嗽(FC)的高峰发病率降低了22%。2023年FC流感高峰在时间上与2022年FC流感高峰相似,但与FluTracking记录的大多数年份相比,其规模较小。从2022年到2023年,FluTracking观察到:•在报告FC症状的参与者中,流感聚合酶链反应(PCR)检测下降了36%,这在很大程度上受到新南威尔士州下降57%的影响。•在报告有流鼻涕和喉咙痛(RNST)症状的参与者中,通过聚合酶链反应和/或快速抗原试验(RAT)进行的SARS-CoV-2检测减少25%。•在报告FC症状的参与者中,SARS-CoV-2检测(PCR和/或RAT)减少11%。减少的测试可访问性加上修改的测试实践可能导致这些减少。到2023年6月,有FC症状的参与者的SARS-CoV-2 PCR检测率与流感PCR检测率一致。2023年RNST症状的期间累积发病率在各年龄组之间的差异很小。相反,FC期累积发病率与年龄呈负相关,表明年轻人FC症状的累积发病率更高。
{"title":"FluTracking: Weekly online community-based surveillance of respiratory illness in Australia, 2023 Report.","authors":"Alexandra Kerr, Sandra Kerr, Stuart Adams, Tom McKenzie, David Boettiger, Craig Dalton","doi":"10.33321/cdi.2025.49.037","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.037","url":null,"abstract":"<p><p>FluTracking Australia, an online respiratory illness surveillance system, monitors self-reported symptoms, care-seeking, absence from normal duties, and testing and vaccination for influenza and coronavirus disease 2019 (COVID-19). From 2022 to 2023, the number of participants who completed at least one survey decreased by 16.8%, possibly due to participation fatigue and additional survey questions. In 2023, FluTracking identified a 22% reduction in the peak weekly incidence of fever and cough (FC) compared to the 2022 season. The 2023 FC peak was similar in timing to the 2022 FC influenza peak but smaller in magnitude compared to most previous years documented by FluTracking. From 2022 to 2023, FluTracking observed: • A 36% decrease in influenza polymerase chain reaction (PCR) testing among participants reporting incident FC symptoms, largely influenced by a 57% decrease in New South Wales. • A 25% decrease in SARS-CoV-2 testing, by PCR and/or rapid antigen test (RAT), among participants reporting incident runny nose and sore throat (RNST) symptoms. • An 11% decrease in SARS-CoV-2 testing (PCR and/or RAT) among participants reporting incident FC symptoms. Reduced testing accessibility coupled with modified testing practices likely contributed to these decreases. By June 2023, SARS-CoV-2 PCR testing rates among participants with incident FC symptoms aligned with influenza PCR testing rates. Period cumulative incidence of RNST symptoms showed minimal variation across age groups in 2023. In contrast, FC period cumulative incidence inversely correlated with age, suggesting young individuals experience a higher cumulative incidence of FC symptoms.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201501","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
FluTracking: Weekly online community-based surveillance of respiratory illness in Australia, 2020-2022 Report. FluTracking:澳大利亚呼吸系统疾病每周在线社区监测,2020-2022报告。
IF 1.6 Q3 Medicine Pub Date : 2025-10-01 DOI: 10.33321/cdi.2025.49.024
Alexandra Kerr, Sandra Carlson, Zoe Baldwin, Reilly Innes, Zachary Howard, Murray Bennett, Tiffany Evans, Tom McKenzie, Craig Dalton

FluTracking, an online participatory respiratory surveillance system, revealed that the coronavirus disease 2019 (COVID-19) pandemic led to historically low levels of fever and cough (FC) in the 2020-2021 influenza seasons in Australia. In 2022, the influenza peak occurred earlier and was shorter compared to pre-pandemic seasons. Based on weekly percentages of participants reporting FC, FluTracking identified four Omicron waves (BA.1, BA.2, BA.4/BA.5 and a mixed Omicron variant wave). These waves, while consistent with laboratory-confirmed COVID-19 trends, showed higher FC incidences in the BA.4/BA.5 and mixed variant waves. During the Omicron waves in 2022, up to 60% of FluTracking participants with FC reported positive SARS-CoV-2 tests, a significant increase from the less than 10% positivity rate for most of 2020-2021. These trends mirrored the timing of rises in National Notifiable Disease Surveillance System (NNDSS) COVID-19 notifications, although peak magnitudes varied between the two systems. Before November 2021, fewer than half (49.9% weekly mean) of participants with FC, and fewer than a third (27.7% weekly mean) with runny nose and sore throat reported being tested for SARS-CoV-2. Following the introduction of rapid antigen tests (RATs) in November 2021 and the spread of the Omicron variant of SARS-CoV-2 in early 2022, testing rates increased for both symptom profiles in 2022. Additionally, the reopening of international borders and the resurgence of influenza led to expanded respiratory panel testing in drive-through clinics, marked by a 36% increase in the mean weekly percentage of participants reporting an influenza polymerase chain reaction (PCR) test. FluTracking's participation grew by 107% in 2020 compared to 2019, then declined by 17.7% in 2021, likely due to participation and pandemic fatigue. However, participation stabilised with a 0.2% increase in 2022 compared to 2021. FluTracking offers valuable insights into respiratory illness trends, changes in testing behaviours, and positivity rates for influenza and SARS-CoV-2.

在线参与式呼吸监测系统FluTracking显示,2019年冠状病毒病(COVID-19)大流行导致澳大利亚2020-2021年流感季节的发烧和咳嗽(FC)水平处于历史最低水平。与大流行前季节相比,2022年流感高峰发生得更早,时间更短。基于每周报告FC的参与者百分比,FluTracking确定了四种欧米ron波(BA.1, BA.2, BA.4/BA)。5和混合欧米克隆变体波)。这些波虽然与实验室确认的COVID-19趋势一致,但在BA.4/BA中显示出更高的FC发病率。5、混合变波。在2022年的欧米克隆波期间,高达60%的患有FC的FluTracking参与者报告了SARS-CoV-2检测阳性,与2020-2021年大部分时间不到10%的阳性率相比显着增加。这些趋势反映了国家法定疾病监测系统(NNDSS) COVID-19通报增加的时间,尽管两个系统之间的峰值幅度有所不同。在2021年11月之前,只有不到一半(每周平均49.9%)的FC参与者和不到三分之一(每周平均27.7%)的流鼻涕和喉咙痛的参与者报告接受了SARS-CoV-2检测。在2021年11月引入快速抗原检测(rat)以及2022年初SARS-CoV-2的Omicron变体传播之后,2022年两种症状的检测率都有所上升。此外,国际边界的重新开放和流感的再次爆发导致在免驾车诊所扩大呼吸道小组检测,报告进行流感聚合酶链反应(PCR)检测的参与者平均每周百分比增加了36%。与2019年相比,FluTracking的参与度在2020年增长了107%,然后在2021年下降了17.7%,这可能是由于参与和大流行疲劳。然而,与2021年相比,2022年的参与率稳定增长了0.2%。FluTracking提供了有关呼吸道疾病趋势、检测行为变化以及流感和SARS-CoV-2阳性率的宝贵见解。
{"title":"FluTracking: Weekly online community-based surveillance of respiratory illness in Australia, 2020-2022 Report.","authors":"Alexandra Kerr, Sandra Carlson, Zoe Baldwin, Reilly Innes, Zachary Howard, Murray Bennett, Tiffany Evans, Tom McKenzie, Craig Dalton","doi":"10.33321/cdi.2025.49.024","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.024","url":null,"abstract":"<p><p>FluTracking, an online participatory respiratory surveillance system, revealed that the coronavirus disease 2019 (COVID-19) pandemic led to historically low levels of fever and cough (FC) in the 2020-2021 influenza seasons in Australia. In 2022, the influenza peak occurred earlier and was shorter compared to pre-pandemic seasons. Based on weekly percentages of participants reporting FC, FluTracking identified four Omicron waves (BA.1, BA.2, BA.4/BA.5 and a mixed Omicron variant wave). These waves, while consistent with laboratory-confirmed COVID-19 trends, showed higher FC incidences in the BA.4/BA.5 and mixed variant waves. During the Omicron waves in 2022, up to 60% of FluTracking participants with FC reported positive SARS-CoV-2 tests, a significant increase from the less than 10% positivity rate for most of 2020-2021. These trends mirrored the timing of rises in National Notifiable Disease Surveillance System (NNDSS) COVID-19 notifications, although peak magnitudes varied between the two systems. Before November 2021, fewer than half (49.9% weekly mean) of participants with FC, and fewer than a third (27.7% weekly mean) with runny nose and sore throat reported being tested for SARS-CoV-2. Following the introduction of rapid antigen tests (RATs) in November 2021 and the spread of the Omicron variant of SARS-CoV-2 in early 2022, testing rates increased for both symptom profiles in 2022. Additionally, the reopening of international borders and the resurgence of influenza led to expanded respiratory panel testing in drive-through clinics, marked by a 36% increase in the mean weekly percentage of participants reporting an influenza polymerase chain reaction (PCR) test. FluTracking's participation grew by 107% in 2020 compared to 2019, then declined by 17.7% in 2021, likely due to participation and pandemic fatigue. However, participation stabilised with a 0.2% increase in 2022 compared to 2021. FluTracking offers valuable insights into respiratory illness trends, changes in testing behaviours, and positivity rates for influenza and SARS-CoV-2.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigation of a Salmonella Typhi cluster among a Pacific Islander labour community in a fruit industry: perspective from a regional public health unit. 对太平洋岛民水果产业劳工社区中伤寒沙门氏菌群的调查:来自区域公共卫生单位的观点。
IF 1.6 Q3 Medicine Pub Date : 2025-10-01 DOI: 10.33321/cdi.2025.49.032
Connie Schulz, Mohammad Rashidul Hashan, Krishna Doshi, Olivia Williams, Rikki Graham, Jacina Walker, Gulam Khandaker

Background: Australia is largely dependent on immigrant workers to bridge the employment gap in the agricultural sector and in agriculture-related food production; this poses a potential risk of the introduction and transmission of non-endemic vaccine preventable disease. We report the response to a Salmonella Typhi (S. Typhi) outbreak amongst workers from the Pacific Australia Labour Mobility (PALM) scheme in regional Queensland.

Methods: A cluster of invasive Salmonella infections was investigated in accordance with the Communicable Diseases Network Australia guidelines. Active case finding of the at-risk group was undertaken to identify potential causal links and further transmission.

Results: Three confirmed cases of S. Typhi were reported, all male, with a median age of 31 years (range: 29-33 years). All cases were hospitalised and were managed with antibiotics and supportive care, with a median illness duration of nine days. Full recovery was reported for all cases, without complications. No recent travel history or contact with a recent typhoid case were reported. We identified 310 individuals in the exposed cohort, with a median age of 31 years (range: 22-55 years), all males. Of the exposed cohort, 305/310 individuals (98·4%) provided a faecal sample for S. Typhi testing; all returned a negative result. Genomic sequencing concluded the likely source of infection in this outbreak was chronic carriage of S. Typhi.

Conclusion: Australia has had a significant increase in the number of PALM workers in regional areas, particularly within the agricultural sector, to mitigate employment gaps. A greater emphasis on culturally appropriate and linguistically sound hand hygiene education, and consideration of pre-employment health checks and vaccinations in these workers, would be beneficial in the reduction of communicable disease outbreaks.

背景:澳大利亚在很大程度上依赖移民工人来弥补农业部门和与农业有关的粮食生产方面的就业差距;这构成了非地方性疫苗可预防疾病传入和传播的潜在风险。我们报告的反应伤寒沙门氏菌(S. Typhi)爆发的工人从太平洋澳大利亚劳动力流动(棕榈)计划在昆士兰地区。方法:根据澳大利亚传染病网络指南,对一群侵袭性沙门氏菌感染进行调查。对高危人群进行了积极的病例发现,以确定潜在的因果联系和进一步传播。结果:报告3例伤寒沙门氏菌确诊病例,均为男性,中位年龄31岁(范围29-33岁)。所有病例均住院治疗,并接受抗生素治疗和支持性护理,平均病程为9天。所有病例均完全康复,无并发症。没有报告最近的旅行史或与最近伤寒病例的接触。我们在暴露队列中确定了310名个体,中位年龄为31岁(范围:22-55岁),均为男性。在暴露人群中,305/310人(98.4%)提供了伤寒沙门氏菌检测的粪便样本;都返回一个否定的结果。基因组测序得出结论,本次暴发的可能感染源是伤寒沙门氏菌的慢性携带者。结论:澳大利亚在区域地区,特别是在农业部门内,大幅增加了PALM工人的人数,以减轻就业差距。更加重视文化上适当和语言上合理的手部卫生教育,并考虑对这些工人进行就业前健康检查和接种疫苗,将有利于减少传染病的爆发。
{"title":"Investigation of a Salmonella Typhi cluster among a Pacific Islander labour community in a fruit industry: perspective from a regional public health unit.","authors":"Connie Schulz, Mohammad Rashidul Hashan, Krishna Doshi, Olivia Williams, Rikki Graham, Jacina Walker, Gulam Khandaker","doi":"10.33321/cdi.2025.49.032","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.032","url":null,"abstract":"<p><strong>Background: </strong>Australia is largely dependent on immigrant workers to bridge the employment gap in the agricultural sector and in agriculture-related food production; this poses a potential risk of the introduction and transmission of non-endemic vaccine preventable disease. We report the response to a <i>Salmonella</i> Typhi (<i>S</i>. Typhi) outbreak amongst workers from the Pacific Australia Labour Mobility (PALM) scheme in regional Queensland.</p><p><strong>Methods: </strong>A cluster of invasive <i>Salmonella</i> infections was investigated in accordance with the Communicable Diseases Network Australia guidelines. Active case finding of the at-risk group was undertaken to identify potential causal links and further transmission.</p><p><strong>Results: </strong>Three confirmed cases of <i>S</i>. Typhi were reported, all male, with a median age of 31 years (range: 29-33 years). All cases were hospitalised and were managed with antibiotics and supportive care, with a median illness duration of nine days. Full recovery was reported for all cases, without complications. No recent travel history or contact with a recent typhoid case were reported. We identified 310 individuals in the exposed cohort, with a median age of 31 years (range: 22-55 years), all males. Of the exposed cohort, 305/310 individuals (98·4%) provided a faecal sample for <i>S</i>. Typhi testing; all returned a negative result. Genomic sequencing concluded the likely source of infection in this outbreak was chronic carriage of <i>S</i>. Typhi.</p><p><strong>Conclusion: </strong>Australia has had a significant increase in the number of PALM workers in regional areas, particularly within the agricultural sector, to mitigate employment gaps. A greater emphasis on culturally appropriate and linguistically sound hand hygiene education, and consideration of pre-employment health checks and vaccinations in these workers, would be beneficial in the reduction of communicable disease outbreaks.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201630","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Australian vaccine preventable disease epidemiological review series: mumps, 2013-2021. 澳大利亚疫苗可预防疾病流行病学综述系列:腮腺炎,2013-2021年。
IF 1.6 Q3 Medicine Pub Date : 2025-10-01 DOI: 10.33321/cdi.2025.49.033
Sajani Nadeeka, Joanne Jackson, Aditi Dey, Shopna Bag, Stephen Lambert, Frank Beard

Background: Mumps is a highly contagious acute viral disease. We describe Australian mumps epidemiology, 2013-2021.

Methods: National mumps notification, hospitalisation and death data were analysed by age group, Indigenous status, state/territory and vaccination status.

Results: There were 3,643 mumps notifications between 2013-2021 (average annual rate 1.65 per 100,000 population), with highest annual rates 2015-2018 (2.71-3.32 per 100,000 population). Average annual rates per 100,000 population for 2013-2021 and 2015-2018 were highest in the Northern Territory (15.8 and 35.2), Western Australia (4.7 and 9.5) and Queensland (2.6 and 5.0). Average annual rates per 100,000 population were higher in Indigenous people than other Australians in 2013-2021 (25.65 vs 0.82) and 2015-2018 (57.53 vs 1.10). Highest age-specific average annual rates per 100,000 population were in adolescents aged 10-19 years (overall 3.66, Indigenous 48.24 for 2013-2021; 7.60 and 108.52 for 2015-2018), followed by adults aged 20-29 years. Among mumps notifications with vaccination status recorded (n = 2,295 notifications), 64.2% had received ≥ 2 doses of mumps-containing vaccine and 18.1% had received one dose, with 17.7% unvaccinated. Between 2013-2021, 719 hospitalisations had mumps recorded as principal diagnosis (average annual rate, 0.34 per 100,000 population). There were 1-5 deaths coded with mumps as underlying cause of death.

Conclusion: Mumps epidemiology was dominated by large outbreaks predominantly in fully vaccinated Indigenous adolescents/young adults. Mumps outbreaks among highly vaccinated adolescent/young adult populations have occurred overseas related to waning of vaccine-induced immunity, reduced boosting from wild-type virus circulation and high force of infection in close contact settings. A third dose of mumps-containing vaccine is not warranted routinely, but should be considered in the context of outbreaks occurring in high two-dose coverage settings.

背景:腮腺炎是一种高度传染性的急性病毒性疾病。我们描述了2013-2021年澳大利亚腮腺炎流行病学。方法:按年龄组、土著身份、州/地区和疫苗接种状况分析全国腮腺炎通报、住院和死亡数据。结果:2013-2021年共有3643例腮腺炎报告病例(年均发病率1.65 / 10万),2015-2018年最高(年均发病率2.71 ~ 3.32 / 10万)。2013-2021年和2015-2018年,北领地(15.8和35.2)、西澳大利亚(4.7和9.5)和昆士兰(2.6和5.0)的年平均犯罪率最高。2013-2021年(25.65比0.82)和2015-2018年(57.53比1.10),土著居民的年平均死亡率高于其他澳大利亚人。每10万人中,10-19岁青少年的年平均死亡率最高(总体为3.66,2013-2021年为48.24,2015-2018年为7.60和108.52),其次是20-29岁的成年人。在记录了疫苗接种情况的腮腺炎通报中(n = 2295份通报),64.2%接种了≥2剂含腮腺炎疫苗,18.1%接种了1剂,17.7%未接种疫苗。2013-2021年期间,719例住院病例的主要诊断是腮腺炎(平均年发病率为每10万人0.34例)。有1-5例死亡被编码为腮腺炎的潜在死因。结论:流行性腮腺炎流行病学以大规模暴发为主,主要发生在充分接种疫苗的土著青少年/青壮年。在海外,在高度接种疫苗的青少年/年轻成人人群中发生的腮腺炎暴发与疫苗引起的免疫力减弱、野生型病毒传播的增强作用减弱以及密切接触环境中的高感染强度有关。通常不需要接种第三剂含腮腺炎疫苗,但在两剂覆盖率高的情况下发生疫情时应予以考虑。
{"title":"Australian vaccine preventable disease epidemiological review series: mumps, 2013-2021.","authors":"Sajani Nadeeka, Joanne Jackson, Aditi Dey, Shopna Bag, Stephen Lambert, Frank Beard","doi":"10.33321/cdi.2025.49.033","DOIUrl":"https://doi.org/10.33321/cdi.2025.49.033","url":null,"abstract":"<p><strong>Background: </strong>Mumps is a highly contagious acute viral disease. We describe Australian mumps epidemiology, 2013-2021.</p><p><strong>Methods: </strong>National mumps notification, hospitalisation and death data were analysed by age group, Indigenous status, state/territory and vaccination status.</p><p><strong>Results: </strong>There were 3,643 mumps notifications between 2013-2021 (average annual rate 1.65 per 100,000 population), with highest annual rates 2015-2018 (2.71-3.32 per 100,000 population). Average annual rates per 100,000 population for 2013-2021 and 2015-2018 were highest in the Northern Territory (15.8 and 35.2), Western Australia (4.7 and 9.5) and Queensland (2.6 and 5.0). Average annual rates per 100,000 population were higher in Indigenous people than other Australians in 2013-2021 (25.65 vs 0.82) and 2015-2018 (57.53 vs 1.10). Highest age-specific average annual rates per 100,000 population were in adolescents aged 10-19 years (overall 3.66, Indigenous 48.24 for 2013-2021; 7.60 and 108.52 for 2015-2018), followed by adults aged 20-29 years. Among mumps notifications with vaccination status recorded (n = 2,295 notifications), 64.2% had received ≥ 2 doses of mumps-containing vaccine and 18.1% had received one dose, with 17.7% unvaccinated. Between 2013-2021, 719 hospitalisations had mumps recorded as principal diagnosis (average annual rate, 0.34 per 100,000 population). There were 1-5 deaths coded with mumps as underlying cause of death.</p><p><strong>Conclusion: </strong>Mumps epidemiology was dominated by large outbreaks predominantly in fully vaccinated Indigenous adolescents/young adults. Mumps outbreaks among highly vaccinated adolescent/young adult populations have occurred overseas related to waning of vaccine-induced immunity, reduced boosting from wild-type virus circulation and high force of infection in close contact settings. A third dose of mumps-containing vaccine is not warranted routinely, but should be considered in the context of outbreaks occurring in high two-dose coverage settings.</p>","PeriodicalId":36867,"journal":{"name":"Communicable diseases intelligence (2018)","volume":"49 ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145201525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Communicable diseases intelligence (2018)
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1