Aspirin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform

    Lancet (London, England)
    |November 20, 2021
    PubMed

    Insights

    Aspirin did not reduce 28-day mortality in hospitalized COVID-19 patients. However, aspirin use was linked to a slight increase in patients discharged alive and a reduction in thrombotic events, alongside a rise in major bleeding.

    Area of Science:

    • Clinical Medicine
    • Infectious Diseases
    • Pharmacology

    Background:

    • Aspirin's anti-thrombotic properties suggested its potential as a COVID-19 treatment.
    • The RECOVERY trial investigated aspirin's efficacy and safety in hospitalized COVID-19 patients.

    Purpose of the Study:

    • To evaluate the efficacy and safety of aspirin in patients admitted to hospital with COVID-19.
    • To determine aspirin's impact on 28-day mortality and other clinical outcomes.

    Main Methods:

    • A randomized, controlled, open-label, platform trial involving 14,892 eligible patients across 177 UK hospitals and others internationally.
    • Patients were allocated 1:1 to receive aspirin (150 mg daily) or usual care.
    • The primary outcome was 28-day mortality, with analyses conducted by intention to treat.

    Main Results:

    • No significant difference in 28-day mortality between aspirin and usual care groups (17% vs 17%; rate ratio 0.96).
    • Aspirin group showed a shorter hospital stay and a higher rate of discharge alive within 28 days (75% vs 74%).
    • Aspirin use reduced thrombotic events but increased major bleeding events.

    Conclusions:

    • Aspirin did not reduce 28-day mortality or the risk of mechanical ventilation/death in hospitalized COVID-19 patients.
    • Aspirin was associated with a small increase in the rate of being discharged alive within 28 days.
    • The study highlights a trade-off between reduced thrombotic events and increased bleeding risk with aspirin use.
    Abstract

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