Evidence map›Paper›PMID 38710936›Full record

ArticleCommunications medicine2024

Vaccine effectiveness against emerging COVID-19 variants using digital health data.

Tanner J Varrelman, Benjamin Rader, Christopher Remmel, Gaurav Tuli, Aimee R Han, Christina M Astley, John S Brownstein

Abstract read
In one paragraph

Article in Communications medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

7 authors.

Tanner J VarrelmanComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA. tannervarrelman@gmail.com.ORCID http://orcid.org/0000-0002-8766-0129
Benjamin RaderComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.
Christopher RemmelComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.
Gaurav TuliComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.
Aimee R HanComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0001-8927-3432
Christina M AstleyComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-5063-8470
John S BrownsteinComputational Epidemiology Lab, Boston Children's Hospital, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0001-8568-5317

Funding

Seasonal and Viral Determinants of Type 1 Diabetes Onset, Remission, and Glycemic ControlK23DK120899 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI ASTLEY, CHRISTINA M. · 2019 to 2021
$682k
NIDDK NIH HHS K23 DK120899
6 · The paper itself

Abstract

backgroundParticipatory surveillance of self-reported symptoms and vaccination status can be used to supplement traditional public health surveillance and provide insights into vaccine effectiveness and changes in the symptoms produced by an infectious disease. The University of Maryland COVID Trends and Impact Survey provides an example of participatory surveillance that leveraged Facebook's active user base to provide self-reported symptom and vaccination data in near real-time.

methodsHere, we develop a methodology for identifying changes in vaccine effectiveness and COVID-19 symptomatology using the University of Maryland COVID Trends and Impact Survey data from three middle-income countries (Guatemala, Mexico, and South Africa). We implement conditional logistic regression to develop estimates of vaccine effectiveness conditioned on the prevalence of various definitions of self-reported COVID-like illness in lieu of confirmed diagnostic test results.

resultsWe highlight a reduction in vaccine effectiveness during Omicron-dominated waves of infections when compared to periods dominated by the Delta variant (median change across COVID-like illness definitions: -0.40, IQR[-0.45, -0.35]. Further, we identify a shift in COVID-19 symptomatology towards upper respiratory type symptoms (i.e., cough and sore throat) during Omicron periods of infections. Stratifying COVID-like illness by the National Institutes of Health's (NIH) description of mild and severe COVID-19 symptoms reveals a similar level of vaccine protection across different levels of COVID-19 severity during the Omicron period.

conclusionsParticipatory surveillance data alongside methodologies described in this study are particularly useful for resource-constrained settings where diagnostic testing results may be delayed or limited.

Identifiers

PMID38710936
PMCPMC11074297

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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.