Longwise Cluster Analysis for the Prediction of COVID-19 Severity within 72 h of Admission: COVID-DATA-SAVE-LIFES Cohort.

COVID-19 Charlson Comorbidities Index cluster analysis individualized management longitudinal cluster

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
10 Jun 2022
Historique:
received: 05 04 2022
revised: 02 06 2022
accepted: 07 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

The use of routine laboratory biomarkers plays a key role in decision making in the clinical practice of COVID-19, allowing the development of clinical screening tools for personalized treatments. This study performed a short-term longitudinal cluster from patients with COVID-19 based on biochemical measurements for the first 72 h after hospitalization. Clinical and biochemical variables from 1039 confirmed COVID-19 patients framed on the “COVID Data Save Lives” were grouped in 24-h blocks to perform a longitudinal k-means clustering algorithm to the trajectories. The final solution of the three clusters showed a strong association with different clinical severity outcomes (OR for death: Cluster A reference, Cluster B 12.83 CI: 6.11−30.54, and Cluster C 14.29 CI: 6.66−34.43; OR for ventilation: Cluster-B 2.22 CI: 1.64−3.01, and Cluster-C 1.71 CI: 1.08−2.76), improving the AUC of the models in terms of age, sex, oxygen concentration, and the Charlson Comorbidities Index (0.810 vs. 0.871 with p < 0.001 and 0.749 vs. 0.807 with p < 0.001, respectively). Patient diagnoses and prognoses remarkably diverged between the three clusters obtained, evidencing that data-driven technologies devised for the screening, analysis, prediction, and tracking of patients play a key role in the application of individualized management of the COVID-19 pandemics.

Identifiants

pubmed: 35743398
pii: jcm11123327
doi: 10.3390/jcm11123327
pmc: PMC9224935
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Community of Madrid and the European Union, through the European Regional Development Fund (ERDF) - REACT-EU resources of the Madrid Operational Program 2014-2020, in the action line of R+D+i projects in response to COVID 19
ID : FACINGLCOVID-CM
Organisme : Synergic R&amp;D Projects in New and Emerging Scientific Areas on the Frontier Of Science And In-terdisciplinary Nature Of The Community Of Madrid
ID : METAINFLAMATION - Y2020/BIO-6600

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Auteurs

Rodrigo San-Cristobal (R)

Precision Nutrition and Cardiometabolic Health Researh Program, Institute on Food and Health Sciences (Institute IMDEA Food), 28049 Madrid, Spain.

Roberto Martín-Hernández (R)

Biostatistics & Bioinformatics Unit, Madrid Institute for Advanced Studies (IMDEA) Food, CEI UAM + CSIS, 28049 Madrid, Spain.

Omar Ramos-Lopez (O)

Medicine and Psychology School, Autonomous University of Baja California, Tijuana 22390, Baja California, Mexico.

Diego Martinez-Urbistondo (D)

Internal Medicine Department, Hospital Universitario HM Sanchinarro, 28050 Madrid, Spain.

Víctor Micó (V)

Precision Nutrition and Cardiometabolic Health Researh Program, Institute on Food and Health Sciences (Institute IMDEA Food), 28049 Madrid, Spain.

Gonzalo Colmenarejo (G)

Biostatistics & Bioinformatics Unit, Madrid Institute for Advanced Studies (IMDEA) Food, CEI UAM + CSIS, 28049 Madrid, Spain.

Paula Villares Fernandez (P)

Internal Medicine Department, Hospital Universitario HM Sanchinarro, 28050 Madrid, Spain.

Lidia Daimiel (L)

Nutritional Control of the Epigenome Group, IMDEA Food Institute, CEI UAM + CSIC, 28049 Madrid, Spain.

Jose Alfredo Martínez (JA)

Precision Nutrition and Cardiometabolic Health Researh Program, Institute on Food and Health Sciences (Institute IMDEA Food), 28049 Madrid, Spain.
CIBERobn Physiopathology of Obesity and Nutrition, Institute of Health Carlos III (ISCIII), 28029 Madrid, Spain.

Classifications MeSH