Clustering based on renal and inflammatory admission parameters in critically ill patients admitted to the ICU.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 19 04 2024
accepted: 15 07 2024
medline: 2 11 2024
pubmed: 2 11 2024
entrez: 1 11 2024
Statut: epublish

Résumé

The COVID-19 pandemic has been associated with significant variability in acute kidney injury (AKI) incidence, leading to concerns regarding patient heterogeneity. The study's primary objective was a cluster analysis, to identify homogeneous subgroups of patients (clusters) using baseline characteristics, including inflammatory biomarkers. The secondary objectives were the comparisons of MAKE-90 and mortality between the different clusters at three months. This retrospective single-center study was conducted in the Medical Intensive Care Unit of the University Hospital of Clermont-Ferrand, France. Baseline data, clinical and biological characteristics on ICU admission, and outcomes at day 90 were recorded. The primary outcome was the risk of major adverse kidney events at 90 days (MAKE-90). Clusters were determined using hierarchical clustering on principal components approach based on admission characteristics, biomarkers and serum values of immune dysfunction and kidney function. It included consecutive adult patients admitted between March 20, 2020 and February 28, 2021 for severe COVID-19. A total of 149 patients were included in the study. Three clusters were identified of which two were fully described (cluster 3 comprising 2 patients). Cluster 1 comprised 122 patients with fewer organ dysfunctions, moderate immune dysfunction, and was associated with reduced mortality and a lower incidence of MAKE-90. Cluster 2 comprised 25 patients with greater disease severity, immune dysfunction, higher levels of suPAR and L-FABP/U Creat, and greater organ support requirement, incidence of AKI, day-90 mortality and MAKE-90. This study identified two clusters of severe COVID-19 patients with distinct biological characteristics and renal event risks. Such clusters may help facilitate the identification of targeted populations for future clinical trials. Also, it may help to understand the significant variability in AKI incidence observed in COVID-19 patients.

Identifiants

pubmed: 39485788
doi: 10.1371/journal.pone.0307938
pii: PONE-D-24-14131
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0307938

Informations de copyright

Copyright: © 2024 Mascle et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Olivier Mascle (O)

CHU de Clermont-Ferrand, Service de Médecine Intensive et Réanimation, Clermont-Ferrand, France.

Claire Dupuis (C)

CHU de Clermont-Ferrand, Service de Médecine Intensive et Réanimation, Clermont-Ferrand, France.
Unité de Nutrition Humaine, INRAe, CRNH Auvergne, Université Clermont Auvergne, Clermont Ferrand, France.

Marina Brailova (M)

CHU de Clermont-Ferrand, Service de Biochimie Médicale, Clermont-Ferrand, France.

Benjamin Bonnet (B)

CHU de Clermont-Ferrand, Service d'Immunologie, Clermont-Ferrand, France.
Laboratoire d'Immunologie, ECREIN, UMR1019 UNH, UFR Médecine de Clermont-Ferrand, Université Clermont Auvergne, Clermont-Ferrand, France.

Audrey Mirand (A)

CHU de Clermont-Ferrand, 3IHP, Service de Virologie, Clermont-Ferrand, France.
UMR CNRS 6023 LMGE, Université Clermont Auvergne, Clermont-Ferrand, France.

Romain Chauvot De Beauchene (RC)

CHU de Clermont-Ferrand, Service de Radiologie, Clermont-Ferrand, France.

Carole Philipponnet (C)

CHU de Clermont-Ferrand, Service de Néphrologie, Clermont-Ferrand, France.

Mireille Adda (M)

CHU de Clermont-Ferrand, Service de Médecine Intensive et Réanimation, Clermont-Ferrand, France.

Laure Calvet (L)

CHU de Clermont-Ferrand, Service de Médecine Intensive et Réanimation, Clermont-Ferrand, France.

Lucie Cassagnes (L)

CHU de Clermont-Ferrand, Service de Radiologie, Clermont-Ferrand, France.

Cécile Henquell (C)

CHU de Clermont-Ferrand, 3IHP, Service de Virologie, Clermont-Ferrand, France.
UMR CNRS 6023 LMGE, Université Clermont Auvergne, Clermont-Ferrand, France.

Vincent Sapin (V)

CHU de Clermont-Ferrand, Service de Biochimie Médicale, Clermont-Ferrand, France.

Bertrand Evrard (B)

CHU de Clermont-Ferrand, Service d'Immunologie, Clermont-Ferrand, France.
Laboratoire d'Immunologie, ECREIN, UMR1019 UNH, UFR Médecine de Clermont-Ferrand, Université Clermont Auvergne, Clermont-Ferrand, France.

Bertrand Souweine (B)

CHU de Clermont-Ferrand, Service de Médecine Intensive et Réanimation, Clermont-Ferrand, France.
UMR CNRS 6023 LMGE, Université Clermont Auvergne, Clermont-Ferrand, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH