Evidence map›Paper›PMID 34312227›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Estimating SARS-CoV-2 infections from deaths, confirmed cases, tests, and random surveys.

Nicholas J Irons, Adrian E Raftery

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

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  19. Inferring COVID-19 testing and vaccination behavior from New Jersey testing data.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. Article

1 more citing papers are in PubMed but not listed here.

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

2 authors.

Nicholas J IronsDepartment of Statistics, University of Washington, Seattle, WA 98195.ORCID 0000-0002-9720-8259
Adrian E RafteryDepartment of Statistics, University of Washington, Seattle, WA 98195; raftery@uw.edu.ORCID 0000-0002-6589-301X

Funding

Scientific/Technical CoreP2CHD042828 · NICHD · UNIVERSITY OF WASHINGTON · PI SARA R. CURRAN · 2017 to 2026
$6.3M
Statistical Methods for Population ProjectionsR01HD070936 · NICHD · UNIVERSITY OF WASHINGTON · PI RAFTERY, ADRIAN E · 2012 to 2021
$3.3M
T32 Data Science and Demography Training BSSRT32HD101442 · NICHD · UNIVERSITY OF WASHINGTON · PI Zack W Almquist, SARA R. CURRAN · 2020 to 2026
$2.0M
NICHD NIH HHS P2C HD042828NICHD NIH HHS R01 HD070936NICHD NIH HHS T32 HD101442
6 · The paper itself

Abstract

There are multiple sources of data giving information about the number of SARS-CoV-2 infections in the population, but all have major drawbacks, including biases and delayed reporting. For example, the number of confirmed cases largely underestimates the number of infections, and deaths lag infections substantially, while test positivity rates tend to greatly overestimate prevalence. Representative random prevalence surveys, the only putatively unbiased source, are sparse in time and space, and the results can come with big delays. Reliable estimates of population prevalence are necessary for understanding the spread of the virus and the effectiveness of mitigation strategies. We develop a simple Bayesian framework to estimate viral prevalence by combining several of the main available data sources. It is based on a discrete-time Susceptible-Infected-Removed (SIR) model with time-varying reproductive parameter. Our model includes likelihood components that incorporate data on deaths due to the virus, confirmed cases, and the number of tests administered on each day. We anchor our inference with data from random-sample testing surveys in Indiana and Ohio. We use the results from these two states to calibrate the model on positive test counts and proceed to estimate the infection fatality rate and the number of new infections on each day in each state in the United States. We estimate the extent to which reported COVID cases have underestimated true infection counts, which was large, especially in the first months of the pandemic. We explore the implications of our results for progress toward herd immunity.

Indexed as

Basic Reproduction NumberBayes TheoremCOVID-19Health SurveysHumansImmunity, HerdIncidenceModels, StatisticalMortalityPrevalenceSARS-CoV-2United StatesBayesian estimationcoronavirus infectionsSARS-CoV-2 incidenceUnited States COVID data

Identifiers

PMID34312227
PMCPMC8346866

What OpenQuestion holds

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LicenceCC BY
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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.