Evidence map›Paper›PMID 32698605›Full record

ArticleAnnals of internal medicine2020

The Contribution of the Age Distribution of Cases to COVID-19 Case Fatality Across Countries : A Nine-Country Demographic Study.

Nikkil Sudharsanan, Oliver Didzun, Till Bärnighausen, Pascal Geldsetzer

Abstract read
In one paragraph

Article in Annals of internal medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 2 pooled it
–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

63 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  15. Estimating the infection burden of COVID-19 in Malaysia.PLoS neglected tropical diseases · 2022
    Article
  16. How German and Italian Laypeople Reason about Distributive Shortages during COVID-19.International journal of environmental research and public health · 2022
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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Nikkil SudharsananHeidelberg Institute of Global Health, Heidelberg University, Heidelberg, Germany (N.S., T.B.).ORCID 0000-0003-1710-4634
Oliver DidzunJustus Liebig University Giessen, Giessen, Germany (O.D.).
Till BärnighausenHeidelberg Institute of Global Health, Heidelberg University, Heidelberg, Germany (N.S., T.B.).
Pascal GeldsetzerPrimary Care and Population Health, Stanford University, Stanford, California (P.G.).

Funding

Institutional Career Development Core (KL2)KL2TR003143 · NCATS · STANFORD UNIVERSITY · PI ASCH, STEVEN M. · 2019 to 2023
$8.7M
NCATS NIH HHS KL2 TR003143
6 · The paper itself

Abstract

backgroundThere is wide variation in coronavirus disease 2019 (COVID-19) case-fatality rates (CFRs) across countries, leading to uncertainty about the true lethality of the disease. A large part of this variation may be due to the ages of individuals who are tested and identified.

objectiveTo measure the contribution of distortions from the age distributions of confirmed cases to CFRs within and across populations.

designCross-sectional demographic study using aggregate data on COVID-19 cases and deaths by age.

settingPopulation-based data from China, France, Germany, Italy, the Netherlands, South Korea, Spain, Switzerland, and the United States.

participantsAll individuals with confirmed COVID-19, as reported by each country as of 19 April 2020 ( MEASUREMENTS: Age-specific COVID-19 CFRs and age-specific population shares by country.

resultsThe overall observed CFR varies widely, with the highest rates in Italy (9.3%) and the Netherlands (7.4%) and the lowest rates in South Korea (1.6%) and Germany (0.7%). Adjustment for the age distribution of cases explains 66% of the variation across countries, with a resulting age-standardized median CFR of 1.9%. Among a larger sample of 95 countries, the observed variation in COVID-19 CFRs is 13 times larger than what would be expected on the basis of just differences in the age composition of countries. LIMITATION: The age-adjusted rates assume that, conditional on age, COVID-19 mortality among diagnosed cases is the same as that among undiagnosed cases and that individuals of all ages are equally susceptible to severe acute respiratory syndrome coronavirus 2 infection.

conclusionSelective testing and identification of older cases considerably warps estimates of the lethality of COVID-19 within populations and comparisons across countries. Removing age distortions and focusing on differences in age-adjusted case fatality will be essential for accurately comparing countries' performance in caring for patients with COVID-19 and for monitoring the epidemic over time. PRIMARY FUNDING SOURCE: Alexander von Humboldt Foundation.

Indexed as

AdolescentAdultAgedAged, 80 and overAge FactorsChildChild, PreschoolChinaCoronavirus InfectionsCOVID-19Cross-Sectional StudiesFranceGermanyHumansInfantInfant, Newborn

Identifiers

PMID32698605
PMCPMC7397549

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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.