Clinical phenotypes from fatal cases of acute respiratory distress syndrome caused by pneumonia.
APACHE
Aged
Aged, 80 and over
Female
Follow-Up Studies
Humans
Infections
/ physiopathology
Intensive Care Units
Male
Phenotype
Pneumonia
/ complications
Prognosis
Prospective Studies
ROC Curve
Respiratory Distress Syndrome
/ diagnostic imaging
Retrospective Studies
Survival Rate
Tomography, X-Ray Computed
/ methods
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
08 10 2021
08 10 2021
Historique:
received:
31
03
2021
accepted:
27
09
2021
entrez:
9
10
2021
pubmed:
10
10
2021
medline:
27
1
2022
Statut:
epublish
Résumé
There have been no report of objective clinical characteristics or prognostic factors that predict fatal outcome of acute respiratory distress syndrome (ARDS) since the Berlin definition was published. The aim of this study is to identify clinically available predictors that distinguish between two phenotypes of fatal ARDS due to pneumonia. In total, 104 cases of Japanese patients with pneumonia-induced ARDS were extracted from our prospectively collected database. Fatal cases were divided into early (< 7 days after diagnosis) and late (≥ 7 days) death groups, and clinical variables and prognostic factors were statistically evaluated. Of the 50 patients who died within 180 days, 18 (36%) and 32 (64%) were in the early (median 2 days, IQR [1, 5]) and late (median 16 days, IQR [13, 29]) death groups, respectively. According to multivariate regression analyses, the APACHE II score (HR 1.25, 95%CI 1.12-1.39, p < 0.001) and the disseminated intravascular coagulation score (HR 1.54, 95%CI 1.15-2.04, p = 0.003) were independent prognostic factors for early death. In contrast, late death was associated with high-resolution computed tomography (HRCT) score indicating early fibroproliferation (HR 1.28, 95%CI 1.13-1.42, p < 0.001) as well as the disseminated intravascular coagulation score (HR 1.24, 95%CI 1.01-1.52, p = 0.039). The extent of fibroproliferation on HRCT, and the APACHE II scores along with coagulation abnormalities, should be considered for use in predictive enrichment and personalized medicine for patients with ARDS due to pneumonia.
Identifiants
pubmed: 34625618
doi: 10.1038/s41598-021-99540-1
pii: 10.1038/s41598-021-99540-1
pmc: PMC8501115
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
20051Informations de copyright
© 2021. The Author(s).
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