Evidence map›Paper›PMID 39948196›Full record

ArticleScientific reports2025

Improving case fatality ratio estimates in ongoing pandemics through case-to-death time distribution analysis.

Zia Farooq, Henrik Sjödin, Joacim Rocklöv, Åke Brännström

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Zia FarooqDepartment of Epidemiology and Global Health, Umeå University, Umeå, 901 87, Sweden. zia.farooq@umu.se.
Henrik SjödinDepartment of Epidemiology and Global Health, Umeå University, Umeå, 901 87, Sweden.
Joacim RocklövDepartment of Epidemiology and Global Health, Umeå University, Umeå, 901 87, Sweden.
Åke BrännströmDepartment of Mathematics and Mathematical Statistics, Umeå University, Umeå, 901 87, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The case fatality ratio (CFR) is a vital metric for assessing the disease severity of novel pathogens. The widely used direct method of CFR estimation-the ratio of total confirmed deaths to total confirmed cases-is inherently simplistic, as it fails to account for the essential time lag between case confirmation to death, and reporting delays. These limitations often lead to biased CFR estimates, particularly in the early stages of outbreaks. This study introduces a novel approach-the distributed-delay method that, like the direct method, utilizes publicly available aggregate time-series data on cases and deaths. It estimates CFR by flexibly incorporating a case-to-death time distribution without requiring a priori assumptions on distribution parameters. Using a fitting approach to forecast case fatalities based on known or assumed case-to-death time distributions, the method consistently recovers true CFR much earlier than the direct method under various simulation settings. These settings reflect variability in disease severity, uncertainties in case-to-death time parameters, and limited knowledge of case-to-death time distributions. It outperforms other methods such as Baud's, which assumes a non-zero constant case-to-death time, and the Generalized Baud's method, which allows for a direct comparison with our new approach. While evaluations based on empirical data are challenging, our conclusions are supported by CFR estimates obtained using empirical COVID-19 data from 34 countries. As an added value, this analysis also demonstrates a significant negative association between eventual CFR and the expected case-to-death time within the context of COVID-19 data. Our study highlights the complexities of inferring real-time CFR from aggregate time-series case and death data, highlighting that refining this method can lead to accurate real-time CFR estimations for actual outbreaks.

Indexed as

COVID-19PandemicsHumansModels, StatisticalSARS-CoV-2Time FactorsCase fatality ratioCase-to-death timesCFRCOVID-19Distributed-delay methodParticle-swarm optimization

Identifiers

PMID39948196
PMCPMC11825655

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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.