Effectiveness of Paxlovid in Reducing Severe Coronavirus Disease 2019 and Mortality in High-Risk Patients

  • Ronza Najjar-Debbiny
    Infection Control and Prevention Unit, Lady Davis Carmel Medical Center , Haifa , Israel
  • Naomi Gronich
    Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology , Haifa , Israel
  • Gabriel Weber
    Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology , Haifa , Israel
  • Johad Khoury
    Pulmonology Division, Lady Davis Carmel Medical Center , Haifa , Israel
  • Maisam Amar
    Infectious Diseases Unit, Lady Davis Carmel Medical Center , Haifa , Israel
  • Nili Stein
    Department of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center , Haifa , Israel
  • Lee Hilary Goldstein
    Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology , Haifa , Israel
  • Walid Saliba
    Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology , Haifa , Israel

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<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Paxlovid was granted an Emergency Use Authorization for the treatment of mild to moderate coronavirus disease 2019 (COVID-19), based on the interim analysis of the Evaluation of Protease Inhibition for COVID-19 in High-Risk Patients (EPIC-HR) trial. Paxlovid effectiveness needs to be assessed in a noncontrolled setting. In this study we used population-based real-world data to evaluate the effectiveness of Paxlovid.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>The database of the largest healthcare provider in Israel was used to identify all adults aged 18 years or older with first-ever positive test for severe acute respiratory syndrome coronavirus 2 between January and February 2022, who were at high risk for severe COVID-19 and had no contraindications for Paxlovid use. Patients were included irrespective of their COVID-19 vaccination status. Cox hazard regression was used to estimate the 28-day hazard ratio (HR) for severe COVID-19 or mortality with Paxlovid examined as time-dependent variable.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Overall, 180 351 eligible patients were included; of these, only 4737 (2.6%) were treated with Paxlovid, and 135 482 (75.1%) had adequate COVID-19 vaccination status. Both Paxlovid and adequate COVID-19 vaccination status were associated with significant decrease in the rate of severe COVID-19 or mortality with adjusted HRs of 0.54 (95% confidence interval [CI], .39–.75) and 0.20 (95% CI, .17–.22), respectively. Paxlovid appears to be more effective in older patients, immunosuppressed patients, and patients with underlying neurological or cardiovascular disease (interaction P &lt; .05 for all). No significant interaction was detected between Paxlovid treatment and COVID-19 vaccination status.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>This study suggests that in the era of Omicron and in real-life settings, Paxlovid is highly effective in reducing the risk of severe COVID-19 or mortality.</jats:p></jats:sec>

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