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Original article

Vol. 153 No. 8 (2023)

Treatment effect of remdesivir on the mortality of hospitalised COVID-19 patients in Switzerland across different patient groups: a tree-based model analysis

  • Janne Estill
  • Plamenna Venkova-Marchevska
  • Huldrych F. Günthard
  • Sara Botero-Mesa
  • Amaury Thiabaud
  • Maroussia Roelens
  • Laure Vancauwenberghe
  • Lauro Damonti
  • Ulrich Heininger
  • Anne Iten
  • Peter W. Schreiber
  • Rami Sommerstein
  • Sarah Tschudin-Sutter
  • Nicolas Troillet
  • Danielle Vuichard-Gysin
  • Andreas Widmer
  • Torsten Hothorn
  • Olivia Keiser
DOI
https://doi.org/10.57187/smw.2023.40095
Cite this as:
Swiss Med Wkly. 2023;153:40095
Published
28.08.2023

Summary

AIMS OF THE STUDY: Remdesivir has shown benefits against COVID-19. However, it remains unclear whether, to what extent, and among whom remdesivir can reduce COVID-19-related mortality. We explored whether the treatment response to remdesivir differed by patient characteristics.

METHODS: We analysed data collected from a hospital surveillance study conducted in 21 referral hospitals in Switzerland between 2020 and 2022. We applied model-based recursive partitioning to group patients by the association between treatment levels and mortality. We included either treatment (levels: none, remdesivir within 7 days of symptom onset, remdesivir after 7 days, or another treatment), age and sex, or treatment only as regression variables. Candidate partitioning variables included a range of risk factors and comorbidities (and age and sex unless included in regression). We repeated the analyses using local centring to correct the results for the propensity to receive treatment.

RESULTS: Overall (n = 21,790 patients), remdesivir within 7 days was associated with increased mortality (adjusted hazard ratios 1.28–1.54 versus no treatment). The CURB-65 score caused the most instability in the regression parameters of the model. When adjusted for age and sex, patients receiving remdesivir within 7 days of onset had higher mortality than those not treated in all identified eight patient groups. When age and sex were included as partitioning variables instead, the number of groups increased to 19–20; in five to six of those branches, mortality was lower among patients who received early remdesivir. Factors determining the groups where remdesivir was potentially beneficial included the presence of oncological comorbidities, male sex, and high age.

CONCLUSIONS: Some subgroups of patients, such as individuals with oncological comorbidities or elderly males, may benefit from remdesivir.

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