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Real World Evidence of Neutralizing Monoclonal Antibodies for Preventing Hospitalization and Mortality in COVID-19 Outpatients
Matthew K Wynia; Laurel E Beaty; Tellen D Bennett; Nichole E Carlson; Christopher B Davis; Bethany M Kwan; David A Mayer; Toan C Ong; Seth Russell; Jeffrey Steele; Heather R Stocker; Adane F Wogu; Richard D Zane; Ronald J Sokol; Adit A Ginde.
Afiliação
  • Matthew K Wynia; University of Colorado School of Medicine
  • Laurel E Beaty; Colorado School of Public Health
  • Tellen D Bennett; University of Colorado School of Medicine
  • Nichole E Carlson; Colorado School of Public Health
  • Christopher B Davis; University of Colorado School of Medicine
  • Bethany M Kwan; University of Colorado School of Medicine
  • David A Mayer; Colorado School of Public Health
  • Toan C Ong; University of Colorado School of Medicine
  • Seth Russell; University of Colorado Anschutz Medical Campus
  • Jeffrey Steele; Children's Hospital Colorado
  • Heather R Stocker; University of Colorado School of Medicine
  • Adane F Wogu; Colorado School of Public Health
  • Richard D Zane; University of Colorado School of Medicine
  • Ronald J Sokol; University of Colorado School of Medicine
  • Adit A Ginde; University of Colorado School of Medicine
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22268963
ABSTRACT
BackgroundNeutralizing monoclonal antibodies (mAbs) are authorized for early symptomatic COVID-19 patients. Whether mAbs are effective against the SARS-CoV-2 Delta variant, among vaccinated patients, or for prevention of mortality remains unknown. ObjectiveTo evaluate the effectiveness of mAb treatment in preventing progression to severe disease during the Delta phase of the pandemic and based on key baseline risk factors. Design, Setting, and PatientsObservational cohort study of non-hospitalized adult patients with SARS-CoV-2 infection from November 2020-October 2021, using electronic health records from a statewide health system plus state-level vaccine and mortality data. Using propensity matching, we selected approximately 2.5 patients not receiving mAbs for each patient who received mAbs. ExposureNeutralizing mAb treatment under emergency use authorization Main OutcomesThe primary outcome was 28-day hospitalization; secondary outcomes included mortality and severity of hospitalization. ResultsOf 36,077 patients with SARS-CoV-2 infection, 2,675 receiving mAbs were matched to 6,677 not receiving mAbs. Compared to mAb-untreated patients, mAb-treated patients had lower all-cause hospitalization (4.0% vs 7.7%; adjusted OR 0.48, 95%CI 0.38-0.60) and all-cause mortality (0.1% vs. 0.9%; adjusted OR 0.11, 95%CI 0.03-0.29) to day 28; differences persisted to day 90. Among hospitalized patients, mAb-treated patients had shorter hospital length of stay (5.8 vs. 8.5 days) and lower risk of mechanical ventilation (4.6% vs. 16.6%). Relative effectiveness was similar in preventing hospitalizations during the Delta variant phase (adjusted OR 0.35, 95%CI 0.25-0.50) and across subgroups. Lower number-needed-to-treat (NNT) to prevent hospitalization were observed for subgroups with higher baseline risk of hospitalization (e.g., multiple comorbidities (NNT=17) and not fully vaccinated (NNT=24) vs. no comorbidities (NNT=88) and fully vaccinated (NNT=81). ConclusionReal-world evidence demonstrated mAb effectiveness in reducing hospitalization among COVID-19 outpatients, including during the Delta variant phase, and conferred an overall 89% reduction in 28-day mortality. Early outpatient treatment with mAbs should be prioritized, especially for individuals with highest risk for hospitalization.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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