Evidence map›Paper›PMID 35605128›Full record

ArticleJMIR public health and surveillance2022

Causal Modeling to Mitigate Selection Bias and Unmeasured Confounding in Internet-Based Epidemiology of COVID-19: Model Development and Validation.

Nathaniel Stockham, Peter Washington, Brianna Chrisman, Kelley Paskov, Jae-Yoon Jung, Dennis Paul Wall

Abstract read
In one paragraph

Article in JMIR public health and surveillance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

6 authors.

Nathaniel StockhamNeurosciences Interdepartmental Program, Stanford University, Palo Alto, CA, United States.ORCID 0000-0002-0752-6801
Peter WashingtonDepartment of Bioengineering, Stanford University, Stanford, CA, United States.ORCID 0000-0003-3276-4411
Brianna ChrismanDepartment of Bioengineering, Stanford University, Stanford, CA, United States.ORCID 0000-0002-7157-607X
Kelley PaskovBiomedical Informatics Program, Stanford University, Stanford, CA, United States.ORCID 0000-0002-5252-1401
Jae-Yoon JungDepartment of Biomedical Data Science, Stanford University, Stanford, CA, United States.ORCID 0000-0001-7948-9803
Dennis Paul WallDepartment of Biomedical Data Science, Stanford University, Stanford, CA, United States.ORCID 0000-0002-7889-9146

Funding

Training Program in Basic NeuroscienceT32MH020016 · NIMH · STANFORD UNIVERSITY · PI Justin L Gardner, Merritt C Maduke · 1997 to 2026
$16.2M
A Mobile Game for Domain Adaptation and Deep Learning in Autism HealthcareR01LM013364 · NLM · STANFORD UNIVERSITY · PI WALL, DENNIS PAUL · 2021 to 2025
$3.2M
Creating an artificial intelligence therapy-to-data feedback loop for child developmental healthcareR01LM013083 · NLM · STANFORD UNIVERSITY · PI WALL, DENNIS PAUL · 2019 to 2022
$2.6M
QuBBD: Wearable artificial intelligence for bid data-driven healthcare in child development R01EB025025 · NIBIB · STANFORD UNIVERSITY · PI WALL, DENNIS PAUL · 2017 to 2019
$1.1M
Evaluation of machine learning to mobilize detection and therapy of developmental delay in childrenR21HD091500 · NICHD · STANFORD UNIVERSITY · PI WALL, DENNIS PAUL · 2017 to 2018
$432k
NIBIB NIH HHS R01 EB025025NICHD NIH HHS R21 HD091500NIMH NIH HHS T32 MH020016NLM NIH HHS R01 LM013083NLM NIH HHS R01 LM013364
6 · The paper itself

Abstract

backgroundSelection bias and unmeasured confounding are fundamental problems in epidemiology that threaten study internal and external validity. These phenomena are particularly dangerous in internet-based public health surveillance, where traditional mitigation and adjustment methods are inapplicable, unavailable, or out of date. Recent theoretical advances in causal modeling can mitigate these threats, but these innovations have not been widely deployed in the epidemiological community.

objectiveThe purpose of our paper is to demonstrate the practical utility of causal modeling to both detect unmeasured confounding and selection bias and guide model selection to minimize bias. We implemented this approach in an applied epidemiological study of the COVID-19 cumulative infection rate in the New York City (NYC) spring 2020 epidemic.

methodsWe collected primary data from Qualtrics surveys of Amazon Mechanical Turk (MTurk) crowd workers residing in New Jersey and New York State across 2 sampling periods: April 11-14 and May 8-11, 2020. The surveys queried the subjects on household health status and demographic characteristics. We constructed a set of possible causal models of household infection and survey selection mechanisms and ranked them by compatibility with the collected survey data. The most compatible causal model was then used to estimate the cumulative infection rate in each survey period.

resultsThere were 527 and 513 responses collected for the 2 periods, respectively. Response demographics were highly skewed toward a younger age in both survey periods. Despite the extremely strong relationship between age and COVID-19 symptoms, we recovered minimally biased estimates of the cumulative infection rate using only primary data and the most compatible causal model, with a relative bias of +3.8% and -1.9% from the reported cumulative infection rate for the first and second survey periods, respectively.

conclusionsWe successfully recovered accurate estimates of the cumulative infection rate from an internet-based crowdsourced sample despite considerable selection bias and unmeasured confounding in the primary data. This implementation demonstrates how simple applications of structural causal modeling can be effectively used to determine falsifiable model conditions, detect selection bias and confounding factors, and minimize estimate bias through model selection in a novel epidemiological context. As the disease and social dynamics of COVID-19 continue to evolve, public health surveillance protocols must continue to adapt; the emergence of Omicron variants and shift to at-home testing as recent challenges. Rigorous and transparent methods to develop, deploy, and diagnosis adapted surveillance protocols will be critical to their success.

Indexed as

COVID-19Confounding Factors, EpidemiologicHumansInternetNew York CitySARS-CoV-2Selection BiasbiascausalityCOVID-19designdevelopmentepidemiologic research designepidemiologyimplementationmethodmodelpublic healthresearchselection biassensitivitysensitivity analysissurveillanceutilityvalidation

Identifiers

PMID35605128
PMCPMC9307267

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.