2021
DOI: 10.1016/s2213-2600(21)00365-9
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Longitudinal respiratory subphenotypes in patients with COVID-19-related acute respiratory distress syndrome: results from three observational cohorts

Abstract: Introduction Patients with COVID-19-related acute respiratory distress syndrome (ARDS) have been postulated to present with distinct respiratory subphenotypes. However, most phenotyping schema have been limited by sample size, disregard for temporal dynamics, and insufficient validation. We aimed to identify respiratory subphenotypes of COVID-19-related ARDS using unbiased data-driven approaches. Methods PRoVENT–COVID was an investigator-initiated, national, multicentre… Show more

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Cited by 86 publications
(75 citation statements)
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“…Our results support the concept of the role of endothelial dysfunction as one of the mechanisms contributing to organ damage in COVID-19 patients and the higher incidence of thromboembolic events in this population [46][47][48]. syndrome have already been identified [50].…”
Section: Discussionsupporting
confidence: 88%
“…Our results support the concept of the role of endothelial dysfunction as one of the mechanisms contributing to organ damage in COVID-19 patients and the higher incidence of thromboembolic events in this population [46][47][48]. syndrome have already been identified [50].…”
Section: Discussionsupporting
confidence: 88%
“…For example, this paper and another large study using serial biomarker systemic measurements consistently show angiopoietin 2, a marker of endothelial dysfunction, is found in higher concentrations in the plasma of patients requiring ICU treatment and that the temporal change in this biomarker is prognostic in this population ( 9 ). Ventilatory ratio trajectories have also been identified in this patient group ( 10 ), and dynamic changes in this surrogate of dead space ventilation are confirmed in the study by Leisman and colleagues. However, no relation with endothelial dysfunction markers and ventilatory ratio change was found, which may suggest that these two phenomena do not share the same pathophysiology as microvascular thrombosis.…”
supporting
confidence: 61%
“…Opposed to a syndromic approach, clustering within a specific disease such as COVID-19 using routine clinical data has yielded conflicting results. Whereas direct translation of the inflammatory/reactive framework to a single-center cohort has identified equivalent groups 11 , other multicenter studies failed to identify COVID-19 subgroups at ICU admission 12 .…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have tried to identify severe COVID-19 phenotypes using clinical data, yielding sometimes conflicting results. Although translation of the previously identified ARDS phenotypes to COVID-19 showed two groups of patients with different responses to steroid therapy 11 , other studies failed to identify clear groups of patients using clinical data at admission 12 .…”
Section: Introductionmentioning
confidence: 99%