Evidence map›Paper›PMID 33125396›Full record

ArticlePloS one2020

Effect of blood analysis and immune function on the prognosis of patients with COVID-19.

Yue-Qiang Fu, Yue-Lin Sun, Si-Wei Lu, Yang Yang, Yi Wang, Feng Xu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 3 pooled it
0.4field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 3 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  12. Hypoxia may be a determinative factor in COVID-19 progression.Current research in pharmacology and drug discovery · 2021
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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

6 authors at 2 institutions in 1 country.

Yue-Qiang FuDepartment of Critical Care Medicine, Children's Hospital, Chongqing Medical University, Chongqing, P.R. China.ORCID 0000-0003-1222-8099
Yue-Lin SunDepartment of Critical Care Medicine, Children's Hospital, Chongqing Medical University, Chongqing, P.R. China.
Si-Wei LuDepartment of Critical Care Medicine, Children's Hospital, Chongqing Medical University, Chongqing, P.R. China.
Yang YangDepartment of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, P.R. China.
Yi WangDepartment of Critical Care Medicine, Children's Hospital, Chongqing Medical University, Chongqing, P.R. China.
Feng XuDepartment of Critical Care Medicine, Children's Hospital, Chongqing Medical University, Chongqing, P.R. China.
Children's Hospital of Chongqing Medical University · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis retrospective study investigated the implications of changes in blood parameters and cellular immune function in patients with Coronavirus Disease 2019 (COVID-19).

methodsRecords were reviewed of 85 patients admitted with COVID-19 between February 4 and 16, 2020. The primary outcome was in-hospital death.

resultsFourteen patients died. The baseline leukocyte count, neutrophil count and hemoglobin was significantly higher in non-survivors compared with survivors, while the reverse was true of lymphocyte count, platelet, PaO2/FiO2, CD3+ count and CD4+ count. The percentage of neutrophil count > 6.3×109/L in death group was significantly higher than that in survival group, and multivariate logistic regression showed neutrophil count > 6.3×109/L was independently associated with mortality. However, there were not significant difference in IgG, IgM, IgA, C3, C4 and the percentage of IgE > 100 IU/ml between the death group and survival group. Areas under the receiver operating characteristic curves of the following at baseline could significantly predict mortality: leukocyte, neutrophil, lymphocyte, CD3+ and CD4+ counts.

conclusionsFor hospitalized patients with COVID-19, lymphocyte, CD3+ and CD4+ counts that marked decrease suggest a poor outcome. Admission neutrophil count > 6.3 ×109/L is independently associated with mortality. At admission, leukocyte, neutrophil, lymphocyte, CD3+ and CD4+ counts should receive added attention.

Indexed as

AgedCD4-Positive T-LymphocytesChinaCOVID-19FemaleHospital MortalityHumansLeukocyte CountLymphocyte CountMaleMiddle AgedNeutrophilsPrognosisRetrospective StudiesSARS-CoV-2

Identifiers

PMID33125396
PMCPMC7598452
OpenAlexW3096568172

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.