Evidence map›Paper›PMID 36882240›Full record

ArticleBMJ open2023

Geographically skewed recruitment and COVID-19 seroprevalence estimates: a cross-sectional serosurveillance study and mathematical modelling analysis.

Tyler Brown, Pablo Martinez de Salazar Munoz, Abhishek Bhatia, Bridget Bunda, Ellen K Williams, David Bor, James S Miller, Amir Mohareb, Julia Thierauf, Wenxin Yang and 13 more

Abstract read
In one paragraph

Article in BMJ open, 2023. 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

23 authors.

Tyler BrownInfectious Diseases Division, Massachusetts General Hospital, Boston, Massachusetts, USA tsbrown@mgh.harvard.edu.ORCID 0000-0003-2559-2789
Pablo Martinez de Salazar MunozCenter for Communicable Disease Dynamics, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA.
Abhishek BhatiaFrançois-Xavier Bagnoud Center for Health and Human Rights, Harvard University, Boston, Massachusetts, USA.
Bridget BundaInfectious Diseases Division, Massachusetts General Hospital, Boston, Massachusetts, USA.
Ellen K WilliamsMassachusetts General Hospital, Boston, MA, USA.
David BorHarvard Medical School, Boston, Massachusetts, USA.
James S MillerGlobal Medicine Program, Massachusetts General Hospital, Boston, Massachusetts, USA.
Amir MoharebInfectious Diseases Division, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-3761-6154
Julia ThieraufHarvard Medical School, Boston, Massachusetts, USA.
Wenxin YangDepartment of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Julian VillalbaInfectious Diseases Division, Massachusetts General Hospital, Boston, Massachusetts, USA.
Vivek NaranbaiHarvard Medical School, Boston, Massachusetts, USA.
Wilfredo Garcia BeltranHarvard Medical School, Boston, Massachusetts, USA.
Tyler E MillerHarvard Medical School, Boston, Massachusetts, USA.
Doug KressCity of Somerville, Somerville, Massachusetts, USA.
Kristen StelljesCity of Somerville, Somerville, Massachusetts, USA.
Keith JohnsonCity of Somerville, Somerville, Massachusetts, USA.
Dan LarremoreBioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado, USA.
Jochen LennerzHarvard Medical School, Boston, Massachusetts, USA.
A John IafrateHarvard Medical School, Boston, Massachusetts, USA.
Satchit BalsariHarvard Medical School, Boston, Massachusetts, USA.
Caroline BuckeeCenter for Communicable Disease Dynamics, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA.
Yonatan GradCenter for Communicable Disease Dynamics, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA.ORCID 0000-0001-5646-1314

Funding

INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
PROGRAM FOR AIDS CLINICAL RESEARCH TRAINING (PACRT)T32AI007433 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MARK J SIEDNER · 1992 to 2026
$11.4M
Casual, Statistical and Mathematical Modeling with Serologic DataU01CA261277 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANAGE, WILLIAM, LIPSITCH, MARC · 2020 to 2023
$2.8M
6 · The paper itself

Abstract

objectivesConvenience sampling is an imperfect but important tool for seroprevalence studies. For COVID-19, local geographic variation in cases or vaccination can confound studies that rely on the geographically skewed recruitment inherent to convenience sampling. The objectives of this study were: (1) quantifying how geographically skewed recruitment influences SARS-CoV-2 seroprevalence estimates obtained via convenience sampling and (2) developing new methods that employ Global Positioning System (GPS)-derived foot traffic data to measure and minimise bias and uncertainty due to geographically skewed recruitment.

designWe used data from a local convenience-sampled seroprevalence study to map the geographic distribution of study participants' reported home locations and compared this to the geographic distribution of reported COVID-19 cases across the study catchment area. Using a numerical simulation, we quantified bias and uncertainty in SARS-CoV-2 seroprevalence estimates obtained using different geographically skewed recruitment scenarios. We employed GPS-derived foot traffic data to estimate the geographic distribution of participants for different recruitment locations and used this data to identify recruitment locations that minimise bias and uncertainty in resulting seroprevalence estimates.

resultsThe geographic distribution of participants in convenience-sampled seroprevalence surveys can be strongly skewed towards individuals living near the study recruitment location. Uncertainty in seroprevalence estimates increased when neighbourhoods with higher disease burden or larger populations were undersampled. Failure to account for undersampling or oversampling across neighbourhoods also resulted in biased seroprevalence estimates. GPS-derived foot traffic data correlated with the geographic distribution of serosurveillance study participants.

conclusionsLocal geographic variation in seropositivity is an important concern in SARS-CoV-2 serosurveillance studies that rely on geographically skewed recruitment strategies. Using GPS-derived foot traffic data to select recruitment sites and recording participants' home locations can improve study design and interpretation.

Indexed as

COVID-19Computer SimulationCross-Sectional StudiesHumansSARS-CoV-2Seroepidemiologic StudiesCOVID-19epidemiologyinformation technologypublic healthstatistics & research methods

Identifiers

PMID36882240
PMCPMC10008195

What OpenQuestion holds

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LicenceCC BY-NC
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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.