The association between early country‐level COVID‐19 testing capacity and later COVID‐19 mortality outcomes

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Abstract

Background

The COVID‐19 pandemic has overrun hospital systems while exacerbating economic hardship and food insecurity on a global scale. In an effort to understand how early action to find and control the virus is associated with cumulative outcomes, we explored how country‐level testing capacity affects later COVID‐19 mortality.

Methods

We used the Our World in Data database to explore testing and mortality records in 27 countries from December 31, 2019, to September 30, 2020; we applied Cox proportional hazards regression to determine the relationship between early COVID‐19 testing capacity (cumulative tests per case) and later COVID‐19 mortality (time to specified mortality thresholds), adjusting for country‐level confounders, including median age, GDP, hospital bed capacity, population density, and nonpharmaceutical interventions.

Results

Higher early testing implementation, as indicated by more cumulative tests per case when mortality was still low, was associated with a lower risk for higher per capita deaths. A sample finding indicated that a higher cumulative number of tests administered per case at the time of six deaths per million persons was associated with a lower risk of reaching 15 deaths per million persons, after adjustment for all confounders (HR = 0.909; P  = 0.0001).

Conclusions

Countries that developed stronger COVID‐19 testing capacity at early timepoints, as measured by tests administered per case identified, experienced a slower increase of deaths per capita. Thus, this study operationalizes the value of testing and provides empirical evidence that stronger testing capacity at early timepoints is associated with reduced mortality and improved pandemic control.

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  1. SciScore for 10.1101/2021.01.18.21249998: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    Institutional Review Board Statementnot detected.
    RandomizationBootstrap analysis: To approximate the variance of the model effect estimates, we conducted 1000 bootstraps on the model coefficients, randomly selecting all 27 countries in the sample, with replacement (Figure Suppl 1A-1E).
    Blindingnot detected.
    Power Analysisnot detected.
    Sex as a biological variablenot detected.

    Table 2: Resources

    No key resources detected.


    Results from OddPub: Thank you for sharing your code and data.


    Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:
    There were certain limitations in our study design approach. We did not identify the type of diagnostic test used in each country. Countries may have had differential access to rapid antigen tests (RAT), or reverse transcription polymerase chain reaction (RT-PCR) tests. These differences are important given that RT-PCR yields higher sensitivity and specificity than RAT, although RAT is relatively quick to administer. We additionally did not account for the type of healthcare system implemented in a country: healthcare access may influence an individual’s access to COVID-19 testing. We also coarsely categorized the NPI variable, which quantified the number of NPIs in place; this variable did not include information regarding the stringency of a specific NPI measure or public compliance. Lastly, the study may have yielded limited generalizability, as findings may only correspond to the countries used in this analysis, during this specific period. Future directions for research may address using a longer time span to determine if this association between early testing capacity and later mortality outcomes continues to hold at longer time intervals. It may also be helpful to explore whether hospitalization rates per capita play a mediating role between country-level testing capacity and mortality rates per capita in order to assess if higher positivity rates may overrun the capacity of the healthcare system, which may increase COVID-19 mortality rates. Future analyses may also co...

    Results from TrialIdentifier: No clinical trial numbers were referenced.


    Results from Barzooka: We did not find any issues relating to the usage of bar graphs.


    Results from JetFighter: We did not find any issues relating to colormaps.


    Results from rtransparent:
    • Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
    • No protocol registration statement was detected.

    About SciScore

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