Simulation-based inference of the time-dependent reproduction number from temporally aggregated and under-reported disease incidence time series data.

IF 4.3 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Isaac Ogi-Gittins, Nicholas Steyn, Jonathan Polonsky, William S Hart, Mory Keita, Steve Ahuka-Mundeke, Edward M Hill, Robin N Thompson
{"title":"Simulation-based inference of the time-dependent reproduction number from temporally aggregated and under-reported disease incidence time series data.","authors":"Isaac Ogi-Gittins, Nicholas Steyn, Jonathan Polonsky, William S Hart, Mory Keita, Steve Ahuka-Mundeke, Edward M Hill, Robin N Thompson","doi":"10.1098/rsta.2024.0412","DOIUrl":null,"url":null,"abstract":"<p><p>During infectious disease outbreaks, the time-dependent reproduction number ([Formula: see text]) can be estimated to monitor pathogen transmission. In previous work, we developed a simulation-based method for estimating [Formula: see text] from temporally aggregated disease incidence data (e.g. weekly case reports). While that approach is straightforward to use, it assumes implicitly that all cases are reported and the computation can be slow when applied to large datasets. In this article, we extend our previous approach and develop a computationally efficient simulation-based method for estimating [Formula: see text] in real-time accounting for both temporal aggregation of incidence data and under-reporting (with a fixed reporting probability per case). Using simulated data, we show that failing to consider stochastic under-reporting can lead to inappropriately precise estimates, including scenarios in which the true [Formula: see text] value lies outside inferred credible intervals more often than expected. We then apply our approach to data from the 2018 to 2020 Ebola outbreak in the Democratic Republic of the Congo (DRC), again exploring the effects of case under-reporting. Finally, we show how our method can be extended to account for temporal variations in reporting. Given information about the level of case reporting, our framework can be used to estimate [Formula: see text] during future outbreaks with under-reported and temporally aggregated case data.This article is part of the theme issue 'Uncertainty quantification for healthcare and biological systems (Part 2)'.</p>","PeriodicalId":19879,"journal":{"name":"Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences","volume":"383 2293","pages":"20240412"},"PeriodicalIF":4.3000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1098/rsta.2024.0412","RegionNum":3,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

During infectious disease outbreaks, the time-dependent reproduction number ([Formula: see text]) can be estimated to monitor pathogen transmission. In previous work, we developed a simulation-based method for estimating [Formula: see text] from temporally aggregated disease incidence data (e.g. weekly case reports). While that approach is straightforward to use, it assumes implicitly that all cases are reported and the computation can be slow when applied to large datasets. In this article, we extend our previous approach and develop a computationally efficient simulation-based method for estimating [Formula: see text] in real-time accounting for both temporal aggregation of incidence data and under-reporting (with a fixed reporting probability per case). Using simulated data, we show that failing to consider stochastic under-reporting can lead to inappropriately precise estimates, including scenarios in which the true [Formula: see text] value lies outside inferred credible intervals more often than expected. We then apply our approach to data from the 2018 to 2020 Ebola outbreak in the Democratic Republic of the Congo (DRC), again exploring the effects of case under-reporting. Finally, we show how our method can be extended to account for temporal variations in reporting. Given information about the level of case reporting, our framework can be used to estimate [Formula: see text] during future outbreaks with under-reported and temporally aggregated case data.This article is part of the theme issue 'Uncertainty quantification for healthcare and biological systems (Part 2)'.

基于模拟的从时间聚合和低报的疾病发病率时间序列数据中推断时间相关的复制数。
在传染病暴发期间,可以估计随时间变化的繁殖数([公式:见文本]),以监测病原体的传播。在之前的工作中,我们开发了一种基于模拟的方法,用于从暂时汇总的疾病发病率数据(例如每周病例报告)中估计[公式:见文本]。虽然这种方法使用起来很简单,但它隐含地假设所有情况都被报告,并且在应用于大型数据集时计算可能很慢。在本文中,我们扩展了之前的方法,并开发了一种基于计算效率的模拟方法,用于估算[公式:见文本],用于实时计算发生率数据的时间聚合和漏报(每个病例的固定报告概率)。使用模拟数据,我们表明,不考虑随机低报可能导致不适当的精确估计,包括真实值超出推断可信区间的情况。然后,我们将我们的方法应用于2018年至2020年刚果民主共和国(DRC)埃博拉疫情的数据,再次探索病例少报的影响。最后,我们展示了如何扩展我们的方法来解释报告中的时间变化。鉴于有关病例报告水平的信息,我们的框架可用于估计未来疫情期间报告不足和临时汇总病例数据的[公式:见文本]。本文是主题问题“医疗保健和生物系统的不确定性量化(第2部分)”的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.30
自引率
2.00%
发文量
367
审稿时长
3 months
期刊介绍: Continuing its long history of influential scientific publishing, Philosophical Transactions A publishes high-quality theme issues on topics of current importance and general interest within the physical, mathematical and engineering sciences, guest-edited by leading authorities and comprising new research, reviews and opinions from prominent researchers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信