Evidence map›Paper›PMID 36137106›Full record

ArticlePloS one2022

Machine-learning-derived predictive score for early estimation of COVID-19 mortality risk in hospitalized patients.

Alba González-Cebrián, Joan Borràs-Ferrís, Juan Pablo Ordovás-Baines, Marta Hermenegildo-Caudevilla, Mónica Climente-Marti, Sonia Tarazona, Raffaele Vitale, Daniel Palací-López, Jesús Francisco Sierra-Sánchez, Javier Saez de la Fuente and 1 more

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Alba González-CebriánMultivariate Statistical Engineering Group, Department of Applied Statistics and Operational Research and Quality, Universitat Politècnica de València, València, España.ORCID 0000-0002-7519-4917
Joan Borràs-FerrísMultivariate Statistical Engineering Group, Department of Applied Statistics and Operational Research and Quality, Universitat Politècnica de València, València, España.ORCID 0000-0001-6066-8836
Juan Pablo Ordovás-BainesPharmacy Service, Hospital Universitario Dr. Peset, València, España.
Marta Hermenegildo-CaudevillaPharmacy Service, Hospital Universitario Dr. Peset, València, España.
Mónica Climente-MartiPharmacy Service, Hospital Universitario Dr. Peset, València, España.
Sonia TarazonaMultivariate Statistical Engineering Group, Department of Applied Statistics and Operational Research and Quality, Universitat Politècnica de València, València, España.ORCID 0000-0001-5346-1407
Raffaele VitaleUniv. Lille, CNRS, LASIRE - UMR 8516 - Laboratory of Advanced Spectroscopy for Interaction, Reactivity and Environmental Studies, Lille, France.ORCID 0000-0002-7497-1673
Daniel Palací-LópezMultivariate Statistical Engineering Group, Department of Applied Statistics and Operational Research and Quality, Universitat Politècnica de València, València, España.
Jesús Francisco Sierra-SánchezPharmacy Service, Hospital Universitario Jerez de la Frontera, Área de Gestión Sanitaria Jerez-Costa Noroeste y Sierra de Cádiz, Jerez de la Frontera, España.
Javier Saez de la FuentePharmacy Service, Hospital Universitario Ramón y Cajal, Madrid, España.ORCID 0000-0003-2965-3008
Alberto FerrerMultivariate Statistical Engineering Group, Department of Applied Statistics and Operational Research and Quality, Universitat Politècnica de València, València, España.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical course of COVID-19 is highly variable. It is therefore essential to predict as early and accurately as possible the severity level of the disease in a COVID-19 patient who is admitted to the hospital. This means identifying the contributing factors of mortality and developing an easy-to-use score that could enable a fast assessment of the mortality risk using only information recorded at the hospitalization. A large database of adult patients with a confirmed diagnosis of COVID-19 (n = 15,628; with 2,846 deceased) admitted to Spanish hospitals between December 2019 and July 2020 was analyzed. By means of multiple machine learning algorithms, we developed models that could accurately predict their mortality. We used the information about classifiers' performance metrics and about importance and coherence among the predictors to define a mortality score that can be easily calculated using a minimal number of mortality predictors and yielded accurate estimates of the patient severity status. The optimal predictive model encompassed five predictors (age, oxygen saturation, platelets, lactate dehydrogenase, and creatinine) and yielded a satisfactory classification of survived and deceased patients (area under the curve: 0.8454 with validation set). These five predictors were additionally used to define a mortality score for COVID-19 patients at their hospitalization. This score is not only easy to calculate but also to interpret since it ranges from zero to eight, along with a linear increase in the mortality risk from 0% to 80%. A simple risk score based on five commonly available clinical variables of adult COVID-19 patients admitted to hospital is able to accurately discriminate their mortality probability, and its interpretation is straightforward and useful.

Indexed as

COVID-19AdultCreatinineHospitalizationHospital MortalityHumansLactate DehydrogenasesMachine LearningRetrospective StudiesRisk AssessmentCreatinineLactate Dehydrogenases

Identifiers

PMID36137106
PMCPMC9499271

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.