Evidence map›Paper›PMID 38662648›Full record

ArticlePLOS digital health2024

COVID-19 cluster surveillance using exposure data collected from routine contact tracing: The genomic validation of a novel informatics-based approach to outbreak detection in England.

Simon Packer, Piotr Patrzylas, Iona Smith, Cong Chen, Adrian Wensley, Olisaeloka Nsonwu, Kyle Dack, Charlie Turner, Charlotte Anderson, Rachel Kwiatkowska and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLOS digital health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 93% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Simon PackerUnited Kingdom Health Security Agency, London, United Kingdom.ORCID https://orcid.org/0000-0002-9157-3650
Piotr PatrzylasUnited Kingdom Health Security Agency, London, United Kingdom.
Iona SmithUnited Kingdom Health Security Agency, London, United Kingdom.
Cong ChenUnited Kingdom Health Security Agency, London, United Kingdom.ORCID https://orcid.org/0000-0003-0355-3930
Adrian WensleyUnited Kingdom Health Security Agency, London, United Kingdom.
Olisaeloka NsonwuUnited Kingdom Health Security Agency, London, United Kingdom.
Kyle DackUnited Kingdom Health Security Agency, London, United Kingdom.
Charlie TurnerUnited Kingdom Health Security Agency, London, United Kingdom.
Charlotte AndersonUnited Kingdom Health Security Agency, London, United Kingdom.
Rachel KwiatkowskaUnited Kingdom Health Security Agency, London, United Kingdom.ORCID https://orcid.org/0000-0001-9100-2623
Isabel OliverUnited Kingdom Health Security Agency, London, United Kingdom.
Obaghe EdeghereUnited Kingdom Health Security Agency, London, United Kingdom.
Graham FraserUnited Kingdom Health Security Agency, London, United Kingdom.
Gareth HughesUnited Kingdom Health Security Agency, London, United Kingdom.ORCID https://orcid.org/0000-0002-3781-0117

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contact tracing was used globally to prevent onwards transmission of COVID-19. Tracing contacts alone is unlikely to be sufficient in controlling community transmission, due to the pre-symptomatic, overdispersed and airborne nature of COVID-19 transmission. We describe and demonstrate the validity of a national enhanced contact tracing programme for COVID-19 cluster surveillance in England. Data on cases occurring between October 2020 and September 2021 were extracted from the national contact tracing system. Exposure clusters were identified algorithmically by matching ≥2 cases attending the same event, identified by matching postcode and event category within a 7-day rolling window. Genetic validity was defined as exposure clusters with ≥2 cases from different households with identical viral sequences. Exposure clusters were fuzzy matched to the national incident management system (HPZone) by postcode and setting description. Multivariable logistic regression modelling was used to determine cluster characteristics associated with genetic validity. Over a quarter of a million (269,470) exposure clusters were identified. Of the eligible clusters, 25% (3,306/13,008) were genetically valid. 81% (2684/3306) of these were not recorded on HPZone and were identified on average of one day earlier than incidents recorded on HPZone. Multivariable analysis demonstrated that exposure clusters occurring in workplaces (aOR = 5·10, 95% CI 4·23-6·17) and education (aOR = 3·72, 95% CI 3·08-4·49) settings were those most strongly associated with genetic validity. Cluster surveillance using enhanced contact tracing in England was a timely, comprehensive and systematic approach to the detection of transmission events occurring in community settings. Cluster surveillance can provide intelligence to stakeholders to support the assessment and management of clusters of COVID-19 at a local, regional, and national level. Future systems should include predictive modelling and network analysis to support risk assessment of exposure clusters to improve the effectiveness of enhanced contract tracing for outbreak detection.

Identifiers

PMID38662648
PMCPMC11045073
OpenAlexW4395481007

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.