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新西兰儿童无菌性脑膜炎的流行病学:1991 年至 2020 年。

The epidemiology of aseptic meningitis in New Zealand children from 1991 to 2020.

机构信息

Department of Paediatrics, University of Otago Christchurch, Christchurch, New Zealand.

Department of Population Health, University of Otago Christchurch, Christchurch, New Zealand.

出版信息

J Paediatr Child Health. 2022 Nov;58(11):1980-1989. doi: 10.1111/jpc.16131. Epub 2022 Jul 21.

DOI:10.1111/jpc.16131
PMID:35861029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9796418/
Abstract

AIM

Aseptic meningitis, including culture negative and viral meningitis, contributes a significant health-care burden, including unnecessary antibiotic use and hospitalisation to treat possible bacterial meningitis. This study analysed aseptic meningitis hospitalisations in New Zealand (NZ) children over 29 years.

METHODS

In this population-based study, aseptic meningitis hospitalisations in NZ children <15 years old were analysed from 1991 to 2020. Incident rate ratios were calculated using Poisson regression models. Variations in hospitalisations by age, year, sex, ethnicity, geographical region and socio-economic deprivation were analysed.

RESULTS

There were 5142 paediatric aseptic meningitis hospitalisations from 1991 to 2020. Most were unspecified viral meningitis (64%), followed by enterovirus (29%). Hospitalisation rates varied annually with a median of 18.4/100 000 children including a peak in 2001 of 56.4/100 000 (51.7-61.6). From 2002 to 2019, rates increased by 8.4%/year (7.2-9.5%) in infants <90 days old but decreased in all other age groups. In 2020, a reduction in hospitalisations to 9.6/100 000 (7.9-11.8) occurred, and in infants <90 days old were 0.37 times expected. Hospitalisations were 1.50 times (1.49-1.68) higher in males than females; higher in children of Māori (P < 0.001) and Pacific (P < 0.001) versus European ethnicity; and higher for children living in the most (2.44 times, (2.16-2.75)) versus least deprived households; and in northern versus southern NZ.

CONCLUSIONS

Aseptic meningitis hospitalisations increased in young infants during 29 years of surveillance, apart from 2020 when admissions reduced during the COVID-19 pandemic. In contrast, hospitalisations decreased in children aged >1 year. Further investigation into reasons for higher admissions by ethnic group, geographical location and increased deprivation are required.

摘要

目的

无菌性脑膜炎,包括培养阴性和病毒性脑膜炎,对医疗保健造成了重大负担,包括不必要的抗生素使用和住院治疗可能的细菌性脑膜炎。本研究分析了新西兰(NZ)29 年来儿童无菌性脑膜炎住院情况。

方法

在这项基于人群的研究中,分析了 1991 年至 2020 年期间新西兰<15 岁儿童的无菌性脑膜炎住院情况。使用泊松回归模型计算发病率比值。分析了年龄、年份、性别、种族、地理位置和社会经济贫困程度对住院情况的影响。

结果

1991 年至 2020 年期间,共有 5142 例儿科无菌性脑膜炎住院。大多数为未明确病毒性脑膜炎(64%),其次是肠道病毒(29%)。住院率每年变化,中位数为 18.4/100000 名儿童,2001 年达到峰值 56.4/100000(51.7-61.6)。2002 年至 2019 年,<90 天的婴儿的发病率每年增加 8.4%(7.2-9.5%),但所有其他年龄组的发病率均下降。2020 年,住院率降至 9.6/100000(7.9-11.8),<90 天的婴儿的住院率预计为 0.37 倍。与女性相比,男性的住院率高 1.50 倍(1.49-1.68);毛利人(P<0.001)和太平洋岛民(P<0.001)高于欧洲裔;生活在最贫困(2.44 倍,(2.16-2.75))和最贫困(2.44 倍,(2.16-2.75))的家庭中的儿童的住院率较高;以及新西兰北部与南部。

结论

在 29 年的监测期间,除了 2020 年 COVID-19 大流行期间住院人数减少外,<90 天的婴儿无菌性脑膜炎住院人数增加。相比之下,1 岁以上儿童的住院人数减少。需要进一步调查为什么某些族裔、地理位置和更高的贫困程度导致住院率较高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/2ef340629df3/JPC-58-1980-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/84c6cb139065/JPC-58-1980-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/229c254cdcfc/JPC-58-1980-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/114a52496a71/JPC-58-1980-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/a0972feb36ce/JPC-58-1980-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/06623a3b7b74/JPC-58-1980-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/2ef340629df3/JPC-58-1980-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/84c6cb139065/JPC-58-1980-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/229c254cdcfc/JPC-58-1980-g015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/114a52496a71/JPC-58-1980-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/a0972feb36ce/JPC-58-1980-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/06623a3b7b74/JPC-58-1980-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e360/9796418/2ef340629df3/JPC-58-1980-g009.jpg

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