Respiratory failure & ventilation

Novel subtypes of severe COVID-19 respiratory failure based on biological heterogeneity: a secondary analysis of a randomized controlled trial

Crit CarePublished Secondary analysis of the I-SPY COVID randomised controlled trial

Authors' conclusion

We discovered evidence of two novel biological subtypes of severe COVID-19 with significantly different clinical outcomes. These subtypes differed from previously established hyper- and hypo-inflammatory non-COVID subtypes of ARDS.

Study context

Population
Adults with severe COVID-19 hypoxemic respiratory failure requiring ≥ 6 L/min supplemental O2, enrolled September 2020 to October 2021
Participants
400 adults
Comparison
Latent biological subtypes
Methodological detailslatent class analysis, multi-institutional platform trial
  • Latent class analysis
  • Multi-institutional platform trial

Primary result

As reported in the abstract

Latent subtypes and mortality
Only one person classified as hyper-inflammatory by the validated non-COVID acute respiratory distress syndrome (ARDS) model
1

Further findings

Biomarkers associated with mortality · 28 and 60 days

Inflammation (IL-6, IL-8, IL-10, sTNFR-1, TREM-1), epithelial injury (sRAGE) and endothelial injury (Ang-1, thrombomodulin) biomarkers associated with 28- and 60-day mortality

Overall 28-day mortality (all participants)

28-day mortality
25%

Original publication

Novel subtypes of severe COVID-19 respiratory failure based on biological heterogeneity: a secondary analysis of a randomized controlled trial. Crit Care. Published 21 February 2024. doi:10.1186/s13054-024-04819-0

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