新西兰奥特亚罗瓦州奥克兰市 Tāmaki Makaurau 五岁以下儿童因血清型 19A 而患上严重侵袭性肺炎球菌疾病。

Cameron Burton,Rachel Webb,Andrew Anglemyer,Alexander Humphrey,Amelie Tuato'o,Emma Best
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背景据报道,随着 COVID-19 大流行缓解措施的放松,一些国家的儿童侵袭性肺炎球菌疾病(IPD)有所增加。在新西兰奥特亚罗瓦(AoNZ),随着肺炎球菌疫苗的变化和免疫覆盖率的下降,幼儿侵袭性肺炎球菌疾病的发病率也在激增。我们试图研究 COVID-19 后 3 年间新西兰奥特亚罗瓦一个大城市地区 5 岁以下儿童中 IPD 的流行病学和临床特征。方法我们整理了 2021 年 1 月 1 日至 2023 年 12 月 31 日期间在新西兰奥克兰市塔玛基-马考劳区(Tāmaki Makaurau Auckland)正常无菌场所发现的 5 岁以下肺炎链球菌患儿的人口统计学、临床和实验室数据。在 68 例病例中确定了血清型,其中 46 例(68%)为血清型 19A。太平洋裔儿童的发病率高于非毛利、非太平洋裔儿童(发病率比:2.3;95% 置信区间:1.4-3.7)。65例(70%)发生了菌血症,47例(51%)发生了肺水肿,11例(12%)发生了脑膜炎,7例(7.5%)发生了溶血性尿毒症。所有溶血性尿毒症和肺水肿病例都只发生在血清型为 19A 的儿童中。结论使用效价较低的肺炎球菌结合疫苗和放宽 COVID-19 封闭措施可能是导致澳新地区 IPD 增加的原因之一。血清型 19A 与肺水肿有关,会导致幼儿患上严重疾病。亟需努力提高 PCV13 在澳新地区的覆盖率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe Invasive Pneumococcal Disease Caused by Serotype 19A in Children Under Five Years in Tāmaki Makaurau Auckland, Aotearoa New Zealand.
BACKGROUND Increases in childhood invasive pneumococcal disease (IPD) have been reported in several countries following the easing of COVID-19 pandemic mitigations. In Aotearoa New Zealand (AoNZ), a surge in IPD is occurring in young children concurrent with changes in pneumococcal vaccines and declining immunization coverage. We sought to examine epidemiologic and clinical features of IPD among children under 5 years in a large urban region of AoNZ in the 3 years post-COVID-19. METHODS Demographic, clinical and laboratory data were collated from children under 5 years with Streptococcus pneumoniae identified from normally sterile sites between January 1, 2021, and December 31, 2023, in Tāmaki Makaurau Auckland, AoNZ. RESULTS We identified 93 episodes of IPD (annual incidence of 18-40 cases per 100,000 population per year). Serotype was identified in 68 episodes and 46 (68%) were serotype 19A. Incidence was higher in Pacific children compared with non-Māori, non-Pacific children (incidence rate ratio: 2.3; 95% confidence interval: 1.4-3.7). Bacteremia occurred in 65 (70%) episodes, empyema in 47 (51%), meningitis in 11 (12%) and hemolytic uremic syndrome in 7 (7.5%). All cases of hemolytic uremic syndrome and empyema were only among children with serotype 19A. Two children died, both had serotype 19A, and 13/91 survivors (14%) experienced serious sequelae. CONCLUSIONS The use of the pneumococcal conjugate vaccine with lower valency and easing of COVID-19 containment measures each may have contributed to an increase in IPD in AoNZ. Serotype 19A is associated with empyema and causes severe disease in young children. Urgent efforts are required to improve PCV13 coverage in AoNZ.
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