Evidence map›Paper›PMID 34685377›Full record

ArticleLife (Basel, Switzerland)2021

Platelet-Based Biomarkers for Diagnosis and Prognosis in COVID-19 Patients.

Ricardo Wesley Alberca, Rosa Liliana Solis-Castro, Maria Edith Solis-Castro, Fernanda Cardoso, Alberto Jose da Silva Duarte, Luana de Mendonça Oliveira, Nátalli Zanete Pereira, Sarah Cristina Gozzi-Silva, Emily Araujo de Oliveira, Valeria Aoki and 4 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

14 authors at 2 institutions in 2 countries.

Ricardo Wesley AlbercaLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0002-3602-3306
Rosa Liliana Solis-CastroDepartamento Académico de Biología y Bioquímica, Facultad de Ciencias de la Salud, Universidad Nacional de Tumbes, Av. Universitaria s/n, Tumbes 24000, Peru.ORCID 0000-0002-1813-8644
Maria Edith Solis-CastroDepartamento Académico de Medicina Humana, Facultad de Ciencias de la Salud, Universidad Nacional de Tumbes, Av. Universitaria s/n, Tumbes 24000, Peru.ORCID 0000-0001-5514-849X
Fernanda CardosoLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Alberto Jose da Silva DuarteLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Luana de Mendonça OliveiraLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0002-5546-1977
Nátalli Zanete PereiraLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Sarah Cristina Gozzi-SilvaLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Emily Araujo de OliveiraLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Valeria AokiLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Raquel Leao OrfaliLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0002-2807-1404
Danielle Rosa BeserraLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.
Milena Mary de Souza AndradeLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0003-0226-3413
Maria Notomi SatoLaboratory of Dermatology and Immunodeficiencies, LIM-56, Department of Dermatology, School of Medicine and Institute of Tropical Medicine of São Paulo, University of São Paulo, São Paulo 01246-903, Brazil.ORCID 0000-0002-7911-1824
Universidade de São Paulo · BRUniversidad Nacional de Tumbes · PE

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 88887.503842/2020-00Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/18199-9Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/02679-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2019/22448-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2020/13148-0
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) caused millions of deaths worldwide. COVID-19's clinical manifestations range from no symptoms to a severe acute respiratory syndrome, which can result in multiple organ failure, sepsis, and death. Severe COVID-19 patients develop pulmonary and extrapulmonary infections, with a hypercoagulable state. Several inflammatory or coagulatory biomarkers are currently used with predictive values for COVID-19 severity and prognosis. In this manuscript, we investigate if a combination of coagulatory and inflammatory biomarkers could provide a better biomarker with predictive value for COVID-19 patients, being able to distinguish between patients that would develop a moderate or severe COVID-19 and predict the disease outcome. We investigated 306 patients with COVID-19, confirmed by severe acute respiratory syndrome coronavirus 2 RNA detected in the nasopharyngeal swab, and retrospectively analyzed the laboratory data from the first day of hospitalization. In our cohort, biomarkers such as neutrophil count and neutrophil-to-lymphocyte ratio from the day of hospitalization could predict if the patient would need to be transferred to the intensive care unit but failed to identify the patients´ outcomes. The ratio between platelets and inflammatory markers such as creatinine, C-reactive protein, and urea levels is associated with patient outcomes. Finally, the platelet/neutrophil-to-lymphocyte ratio on the first day of hospitalization can be used with predictive value as a novel severity and lethality biomarker in COVID-19. These new biomarkers with predictive value could be used routinely to stratify the risk in COVID-19 patients since the first day of hospitalization.

Indexed as

biomarkercoagulationCOVID-19inflammationplateletprognosisSARS-CoV-2thrombocytopenia

Identifiers

PMID34685377
PMCPMC8538377
OpenAlexW3202766159

What OpenQuestion holds

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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.