澳大利亚脑膜炎球菌监测规划年度报告,2016年。

IF 1.6 Q4 INFECTIOUS DISEASES Communicable Diseases Intelligence Pub Date : 2017-12-01
Monica M Lahra, Rodney Enriquez
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引用次数: 0

摘要

2016年,澳大利亚国家奈瑟菌网络分析了243例实验室确诊的侵袭性脑膜炎球菌病病例。这一数字是自2008年以来实验室确诊病例的最高数字。在澳大利亚,可能的和实验室确认的侵袭性脑膜炎球菌病(IMD)是必须报告的,2016年向国家法定疾病监测系统通报了252例IMD病例,是自2010年以来报告的最高数字。98%(237/243)的实验室确诊IMD病例能够确定脑膜炎球菌血清分型。血清B组感染占87例(37%),这是自1997年澳大利亚脑膜炎球菌监测方案(AMSP)开始以来报告的最低数量和比例。相比之下,2016年血清W组感染的数量和比例(44%,107例)是自AMSP开始以来最高的。此外,Y型血清感染的人数和比例(16%,40例)也是AMSP记录的最高水平。243例IMD中有225例获得分子分型结果。在能够进行基因分型的血清W型IMD菌株中,92%(97/105)具有PorA抗原编码基因P1.5,2,其中72%(70/97)为序列11型,与自2009年以来在英国和南美洲流行的高毒血清W型菌株相同。原发性IMD发病高峰出现在45岁及以上的成年人,继发性发病高峰出现在5岁以下和15-19岁的青少年。血清B组感染主要发生在1岁以下和20-24岁年龄组,而血清W组感染主要发生在45岁或以上年龄组。对于所有其他年龄组,血清B组和血清W组感染的分布大致相等。在对IMD进行药物敏感性测试的分离株中,6%(11/189)对青霉素耐药,另外90%(170/189)分离株对青霉素敏感性降低。一株Men W菌株对头孢曲松的最低抑制浓度(MIC)升高(0.125mg/L),为澳大利亚报道的最高。所有分离株均对利福平和环丙沙星敏感。
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Australian Meningococcal Surveillance Programme annual report, 2016.

In 2016, there were 243 laboratory-confirmed cases of invasive meningococcal disease analysed by the Australian National Neisseria Network. This number was the highest number of laboratory confirmed cases since 2008. Probable and laboratory confirmed invasive meningococcal disease (IMD) are notifiable in Australia, and there were 252 IMD cases notified to the National Notifiable Diseases Surveillance System in 2016, the highest number reported since 2010. Meningococcal serogrouping was able to be determined for 98% (237/243) of laboratory confirmed IMD cases. Serogroup B infections accounted for 87 cases (37%), the lowest number and proportion reported since inception of the Australian Meningococcal Surveillance Programme (AMSP) in 1997. In contrast, the number and proportion of serogroup W infections (44%, 107 cases) in 2016 was the highest since the AMSP began. In addition, the number and proportion of serogroup Y infections (16%, 40 cases) was also the highest recorded by the AMSP. Molecular typing results were available for 225 of the 243 IMD cases. Of the serogroup W IMD strains that were able to be genotyped, 92% (97/105) have the PorA antigen encoding gene type P1.5,2 and of these, 72% (70/97) were sequence type 11, the same type as the hypervirulent serogroup W strain that has been circulating in the UK and South America since 2009. The primary IMD age peak was observed in adults aged 45 years or more, whilst secondary disease peaks were observed in those aged less than 5 years, and in adolescents aged 15-19 years. Serogroup B infections predominated in the age groups less than 1 year and 20-24 years, whereas serogroup W infections predominated in those aged 45 years or more. For all other age groups, distribution of serogroup B and W infections was roughly equal. Of the IMD isolates tested for antimicrobial susceptibility, 6% (11/189) were resistant to penicillin, and decreased susceptibility to penicillin was observed in a further 90% (170/189) of isolates. One Men W isolate demonstrated an elevated minimum inhibitory concentration (MIC) to ceftriaxone (0.125mg/L), the highest reported in Australia. All isolates tested were susceptible to rifampicin and ciprofloxacin.

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Communicable Diseases Intelligence
Communicable Diseases Intelligence INFECTIOUS DISEASES-
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Professor Mary-Louise McLaws (17 March 1953 – 12 August 2023) Summary of National Surveillance Data on Vaccine Preventable Diseases in Australia, 2016-2018 Final Report - Erratum to Commun Dis Intell (2018) 2022;46. (https://doi.org/10.33321/cdi.2022.46.28) COVID-19 Australia: Epidemiology Report 73 Reporting period ending 9 April 2023 Australian Rotavirus Surveillance Program: Annual Report, 2017 Invasive Pneumococcal Disease Surveillance, 1 January to 31 March 2017.
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