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全球范围内 B 群链球菌疾病后儿童的神经发育障碍:系统评价和荟萃分析。

Neurodevelopmental Impairment in Children After Group B Streptococcal Disease Worldwide: Systematic Review and Meta-analyses.

机构信息

Maternal, Adolescent, Reproductive and Child Health Centre, London School of Hygiene & Tropical Medicine, United Kingdom.

Centre for Child and Adolescent Health, School of Social and Community Medicine, University of Bristol, United Kingdom.

出版信息

Clin Infect Dis. 2017 Nov 6;65(suppl_2):S190-S199. doi: 10.1093/cid/cix663.

Abstract

BACKGROUND

Survivors of infant group B streptococcal (GBS) disease are at risk of neurodevelopmental impairment (NDI), a burden not previously systematically quantified. This is the 10th of 11 articles estimating the burden of GBS disease. Here we aimed to estimate NDI in survivors of infant GBS disease.

METHODS

We conducted systematic literature reviews (PubMed/Medline, Embase, Latin American and Caribbean Health Sciences Literature [LILACS], World Health Organization Library Information System [WHOLIS], and Scopus) and sought unpublished data on the risk of NDI after invasive GBS disease in infants <90 days of age. We did meta-analyses to derive pooled estimates of the percentage of infants with NDI following GBS meningitis.

RESULTS

We identified 6127 studies, of which 18 met eligibility criteria, all from middle- or high-income contexts. All 18 studies followed up survivors of GBS meningitis; only 5 of these studies also followed up survivors of GBS sepsis and were too few to pool in a meta-analysis. Of meningitis survivors, 32% (95% CI, 25%-38%) had NDI at 18 months of follow-up, including 18% (95% CI, 13%-22%) with moderate to severe NDI.

CONCLUSIONS

GBS meningitis is an important risk factor for moderate to severe NDI, affecting around 1 in 5 survivors. However, data are limited, and we were unable to estimate NDI after GBS sepsis. Comparability of studies is difficult due to methodological differences including variability in timing of clinical reviews and assessment tools. Follow-up of clinical cases and standardization of methods are essential to fully quantify the total burden of NDI associated with GBS disease, and inform program priorities.

摘要

背景

婴儿 B 群链球菌(GBS)疾病幸存者存在神经发育损伤(NDI)风险,这一负担此前尚未被系统量化。本文是评估 GBS 疾病负担的 11 篇系列文章中的第 10 篇,旨在评估婴儿 GBS 疾病幸存者的 NDI 情况。

方法

我们进行了系统文献回顾(PubMed/Medline、Embase、拉丁美洲和加勒比健康科学文献 [LILACS]、世界卫生组织图书馆信息系统 [WHOLIS] 和 Scopus),并寻找了婴儿 <90 天侵袭性 GBS 疾病后 NDI 风险的未发表数据。我们进行了荟萃分析,以得出 GBS 脑膜炎后婴儿发生 NDI 的百分比的汇总估计值。

结果

我们确定了 6127 项研究,其中 18 项符合纳入标准,均来自中高收入环境。所有 18 项研究均随访了 GBS 脑膜炎幸存者;仅有 5 项研究还随访了 GBS 败血症幸存者,但数量太少,无法进行荟萃分析。脑膜炎幸存者中,18 个月随访时 32%(95%CI,25%-38%)存在 NDI,其中 18%(95%CI,13%-22%)存在中重度 NDI。

结论

GBS 脑膜炎是中重度 NDI 的重要危险因素,影响约 1/5 的幸存者。然而,数据有限,我们无法估计 GBS 败血症后 NDI 的情况。由于方法学差异,包括临床评估和评估工具的时间差异,研究之间的可比性存在困难。对临床病例的随访和方法的标准化对于充分量化与 GBS 疾病相关的 NDI 总负担以及确定项目重点至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d45/5848372/7e8e3f4e793d/cix66301.jpg

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