澳大利亚脑膜炎球菌监测计划年度报告,2023年。

Q3 Medicine
Monica M Lahra, C R Robert George, Sebastiaan van Hal, Tiffany R Hogan
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引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Australian Meningococcal Surveillance Programme Annual Report, 2023.

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.

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