Vis enkel innførsel

dc.contributor.authorBrynildsrud, Ola Brønstad
dc.date.accessioned2020-11-11T10:47:43Z
dc.date.available2020-11-11T10:47:43Z
dc.date.created2020-10-16T11:51:44Z
dc.date.issued2020
dc.identifier.citationBMC Medical Research Methodology. 2020, 20en_US
dc.identifier.issn1471-2288
dc.identifier.urihttps://hdl.handle.net/11250/2687339
dc.description.abstractBackground The number of confirmed COVID-19 cases divided by population size is used as a coarse measurement for the burden of disease in a population. However, this fraction depends heavily on the sampling intensity and the various test criteria used in different jurisdictions, and many sources indicate that a large fraction of cases tend to go undetected. Methods Estimates of the true prevalence of COVID-19 in a population can be made by random sampling and pooling of RT-PCR tests. Here I use simulations to explore how experiment sample size and degrees of sample pooling impact precision of prevalence estimates and potential for minimizing the total number of tests required to get individual-level diagnostic results. Results Sample pooling can greatly reduce the total number of tests required for prevalence estimation. In low-prevalence populations, it is theoretically possible to pool hundreds of samples with only marginal loss of precision. Even when the true prevalence is as high as 10% it can be appropriate to pool up to 15 samples. Sample pooling can be particularly beneficial when the test has imperfect specificity by providing more accurate estimates of the prevalence than an equal number of individual-level tests.en_US
dc.language.isoengen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleCOVID-19 prevalence estimation by random sampling in population - Optimal sample pooling under varying assumptions about true prevalenceen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume20en_US
dc.source.journalBMC Medical Research Methodologyen_US
dc.identifier.doi10.1186/s12874-020-01081-0
dc.identifier.cristin1840117
dc.source.articlenumber196en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal