Evidence map›Paper›PMID 32505172›Full record

ArticleBMC medical research methodology2020

Towards reduction in bias in epidemic curves due to outcome misclassification through Bayesian analysis of time-series of laboratory test results: case study of COVID-19 in Alberta, Canada and Philadelphia, USA.

Igor Burstyn, Neal D Goldstein, Paul Gustafson

Open access · goldAbstract read
In one paragraph

Article in BMC medical research methodology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

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  14. It can be dangerous to take epidemic curves of COVID-19 at face value.Canadian journal of public health = Revue canadienne de sante publique · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Igor BurstynDepartment of Environmental and Occupational Health, Drexel University Dornsife School of Public Health, 3215 Market St, Philadelphia, PA, 19104, USA. ib68@drexel.edu.ORCID 0000-0002-7153-4478
Neal D GoldsteinDepartment of Epidemiology & Biostatistics, Drexel University Dornsife School of Public Health, Philadelphia, PA, USA.
Paul GustafsonDepartment of Statistics, University of British Columbia, Vancouver, BC, Canada.
Drexel University · USUniversity of British Columbia · CA

Funding

Towards prevention of HIV among vulnerable and stigmatized populations using geospatial dataK01AI143356 · NIAID · DREXEL UNIVERSITY · PI GOLDSTEIN, NEAL D · 2019 to 2023
$607k
National Institute of Allergy and Infectious Diseases K01AI143356NIAID NIH HHS K01 AI143356
6 · The paper itself

Abstract

backgroundDespite widespread use, the accuracy of the diagnostic test for SARS-CoV-2 infection is poorly understood. The aim of our work was to better quantify misclassification errors in identification of true cases of COVID-19 and to study the impact of these errors in epidemic curves using publicly available surveillance data from Alberta, Canada and Philadelphia, USA.

methodsWe examined time-series data of laboratory tests for SARS-CoV-2 viral infection, the causal agent for COVID-19, to try to explore, using a Bayesian approach, the sensitivity and specificity of the diagnostic test.

resultsOur analysis revealed that the data were compatible with near-perfect specificity, but it was challenging to gain information about sensitivity. We applied these insights to uncertainty/bias analysis of epidemic curves under the assumptions of both improving and degrading sensitivity. If the sensitivity improved from 60 to 95%, the adjusted epidemic curves likely falls within the 95% confidence intervals of the observed counts. However, bias in the shape and peak of the epidemic curves can be pronounced, if sensitivity either degrades or remains poor in the 60-70% range. In the extreme scenario, hundreds of undiagnosed cases, even among the tested, are possible, potentially leading to further unchecked contagion should these cases not self-isolate.

conclusionThe best way to better understand bias in the epidemic curves of COVID-19 due to errors in testing is to empirically evaluate misclassification of diagnosis in clinical settings and apply this knowledge to adjustment of epidemic curves.

Indexed as

Bayes TheoremPandemicsPneumonia, ViralAlbertaBetacoronavirusBiasClinical Laboratory TechniquesCoronavirus InfectionsCOVID-19COVID-19 TestingHumansPhiladelphiaSARS-CoV-2Sensitivity and SpecificityUncertaintyBias analysisEpidemicSensitivitySimulationSpecificityUncertaintyUnder-diagnosis

Identifiers

PMID32505172
PMCPMC7275354
OpenAlexW3033836482

What OpenQuestion holds

Textmetadata
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.