Department of Pediatrics and Child Health, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Department of Neurology, Amsterdam Neuroscience, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands; Department of Pediatrics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.
Clin Microbiol Infect. 2024 Jan;30(1):28-37. doi: 10.1016/j.cmi.2023.04.017. Epub 2023 Apr 19.
Neonatal bacterial infections have long been recognized as an important cause of acute morbidity and mortality, but long-term neurodevelopmental consequences have not been comprehensively described and discussed.
We aimed to summarize evidence on the pathogenesis, diagnosis, and epidemiology of long-term sequelae after neonatal bacterial sepsis and meningitis. We also discuss approaches for future studies to quantify the public health impact of neonatal infection-associated neurodevelopmental impairment.
We identified studies, both research articles and reviews, which provide mechanistic information on the long-term disease, as well as epidemiological studies that describe the frequency of neurodevelopmental impairment in children with and, for comparison, without a history of neonatal bacterial infection. Tools currently used in clinical practice and research settings to assess neurodevelopmental impairment were also reviewed.
We first enumerate potential direct and indirect mechanisms that can lead to brain injury following neonatal infections. We then discuss summary data, either frequencies or measures of association, from epidemiological studies. Risk factors that predict long-term outcomes are also described. Finally, we describe clinical approaches for identifying children with neurodevelopmental impairment and provide an overview of common diagnostic tools.
The limited number of studies that describe the long-term consequences of neonatal infections, often undertaken in high-income settings and using variable designs and diagnostic tools, are not sufficient to inform clinical practice and policy prioritization. Multi-country studies with follow-up into adolescence, standardized diagnostic approaches, and local comparator groups are needed, especially in low and middle-income countries where the incidence of neonatal sepsis is high.
新生儿细菌感染长期以来一直被认为是导致急性发病率和死亡率的重要原因,但长期神经发育后果尚未得到全面描述和讨论。
我们旨在总结关于新生儿细菌性败血症和脑膜炎后长期后遗症的发病机制、诊断和流行病学的证据。我们还讨论了未来研究的方法,以量化与新生儿感染相关的神经发育障碍对公共卫生的影响。
我们确定了研究论文和综述,这些研究提供了有关长期疾病的机制信息,以及描述有和没有新生儿细菌感染史的儿童神经发育障碍发生率的流行病学研究。还回顾了目前用于临床实践和研究环境评估神经发育障碍的工具。
我们首先列举了可能导致新生儿感染后脑损伤的直接和间接机制。然后,我们讨论了来自流行病学研究的汇总数据,无论是频率还是关联度量。还描述了预测长期结局的风险因素。最后,我们描述了识别神经发育障碍儿童的临床方法,并提供了常见诊断工具的概述。
描述新生儿感染长期后果的研究数量有限,这些研究通常在高收入环境中进行,采用不同的设计和诊断工具,不足以为临床实践和政策优先事项提供信息。需要在多国开展研究,包括青少年随访、标准化诊断方法和当地对照组,特别是在新生儿败血症发病率较高的低收入和中等收入国家。