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Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks
To complement labour-intensive conventional contact tracing, digital proximity tracing was implemented widely during the COVID-19 pandemic. However, the privacy-centred design of the dominant Google-Apple exposure notification framework has hindered assessment of its effectiveness. Between October 2...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593825/ https://www.ncbi.nlm.nih.gov/pubmed/37872213 http://dx.doi.org/10.1038/s41467-023-42518-6 |
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author | Geenen, Caspar Raymenants, Joren Gorissen, Sarah Thibaut, Jonathan McVernon, Jodie Lorent, Natalie André, Emmanuel |
author_facet | Geenen, Caspar Raymenants, Joren Gorissen, Sarah Thibaut, Jonathan McVernon, Jodie Lorent, Natalie André, Emmanuel |
author_sort | Geenen, Caspar |
collection | PubMed |
description | To complement labour-intensive conventional contact tracing, digital proximity tracing was implemented widely during the COVID-19 pandemic. However, the privacy-centred design of the dominant Google-Apple exposure notification framework has hindered assessment of its effectiveness. Between October 2021 and January 2022, we systematically collected app use and notification receipt data within a test and trace programme targeting around 50,000 university students in Leuven, Belgium. Due to low success rates in each studied step of the digital notification cascade, only 4.3% of exposed contacts (CI: 2.8-6.1%) received such notifications, resulting in 10 times more cases detected through conventional contact tracing. Moreover, the infection risk of digitally traced contacts (5.0%; CI: 3.0–7.7%) was lower than that of conventionally traced non-app users (9.8%; CI: 8.8-10.7%; p = 0.002). Contrary to common perception as near instantaneous, there was a 1.2-day delay (CI: 0.6–2.2) between case PCR result and digital contact notification. These results highlight major limitations of a digital proximity tracing system based on the dominant framework. |
format | Online Article Text |
id | pubmed-10593825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105938252023-10-25 Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks Geenen, Caspar Raymenants, Joren Gorissen, Sarah Thibaut, Jonathan McVernon, Jodie Lorent, Natalie André, Emmanuel Nat Commun Article To complement labour-intensive conventional contact tracing, digital proximity tracing was implemented widely during the COVID-19 pandemic. However, the privacy-centred design of the dominant Google-Apple exposure notification framework has hindered assessment of its effectiveness. Between October 2021 and January 2022, we systematically collected app use and notification receipt data within a test and trace programme targeting around 50,000 university students in Leuven, Belgium. Due to low success rates in each studied step of the digital notification cascade, only 4.3% of exposed contacts (CI: 2.8-6.1%) received such notifications, resulting in 10 times more cases detected through conventional contact tracing. Moreover, the infection risk of digitally traced contacts (5.0%; CI: 3.0–7.7%) was lower than that of conventionally traced non-app users (9.8%; CI: 8.8-10.7%; p = 0.002). Contrary to common perception as near instantaneous, there was a 1.2-day delay (CI: 0.6–2.2) between case PCR result and digital contact notification. These results highlight major limitations of a digital proximity tracing system based on the dominant framework. Nature Publishing Group UK 2023-10-23 /pmc/articles/PMC10593825/ /pubmed/37872213 http://dx.doi.org/10.1038/s41467-023-42518-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Geenen, Caspar Raymenants, Joren Gorissen, Sarah Thibaut, Jonathan McVernon, Jodie Lorent, Natalie André, Emmanuel Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title | Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title_full | Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title_fullStr | Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title_full_unstemmed | Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title_short | Individual level analysis of digital proximity tracing for COVID-19 in Belgium highlights major bottlenecks |
title_sort | individual level analysis of digital proximity tracing for covid-19 in belgium highlights major bottlenecks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593825/ https://www.ncbi.nlm.nih.gov/pubmed/37872213 http://dx.doi.org/10.1038/s41467-023-42518-6 |
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