Critical Care (Jun 2022)

One-year patient outcomes based on lung morphology in acute respiratory distress syndrome: secondary analysis of LIVE trial

  • Florian Blanchard,
  • Thomas Godet,
  • Stephanie Pons,
  • Natacha Kapandji,
  • Matthieu Jabaudon,
  • Vincent Degos,
  • Lucile Borao,
  • Adrien Bougle,
  • Antoine Monsel,
  • Emmanuel Futier,
  • Jean-Michel Constantin,
  • Arthur James

DOI
https://doi.org/10.1186/s13054-022-04036-7
Journal volume & issue
Vol. 26, no. 1
pp. 1 – 10

Abstract

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Abstract Background Acute respiratory distress syndrome (ARDS) has different phenotypes and distinct short-term outcomes. Patients with non-focal ARDS have a higher short-term mortality than focal ones. The aim of this study was to assess the impact of the morphological phenotypes of ARDS on long-term outcomes. Methods This was a secondary analysis of the LIVE study, a prospective, randomised control trial, assessing the usefulness of a personalised ventilator setting according to lung morphology in moderate-to-severe ARDS. ARDS was classified as focal (consolidations only in the infero-posterior part of the lungs) or non-focal. Outcomes were assessed using mortality and functional scores for quality of life at the 1-year follow-up. Results A total of 124 focal ARDS and 236 non-focal ARDS cases were included. The 1-year mortality was higher for non-focal ARDS than for focal ARDS (37% vs. 24%, p = 0.012). Non-focal ARDS (hazard ratio, 3.44; 95% confidence interval, 1.80–6.59; p < 0.001), age, McCabe score, haematological cancers, SAPS II, and renal replacement therapy were independently associated with 1-year mortality. This difference was driven by mortality during the first 90 days (28 vs. 16%, p = 0.010) but not between 90 days and 1 year (7 vs. 6%, p = 0.591), at which point only the McCabe score was independently associated with mortality. Morphological phenotypes had no impact on patient-reported outcomes. Conclusion Lung morphologies reflect the acute phase of ARDS and its short-term impact but not long-term outcomes, which seem only influenced by comorbidities. Trial registration: NCT 02149589; May 29, 2014.

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