Evidence map›Paper›PMID 39699047›Full record

ArticleInternational journal of immunopathology and pharmacology

Use of CRP/lymphocyte ratio as a predictor of treatment selection and mortality in COVID-19 patients in the intensive care unit.

Efraim Guzel, Burak Mete, Oya Baydar Toprak, Nazire Ates Ayhan, Ahmet Firat, Yurdaer Bulut, Sinem Bayrakci, Aysun Ozel Yesilyurt, Ezgi Ozyilmaz

Abstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

9 authors.

Efraim GuzelDepartment of Chest Diseases, Cukurova University, Adana, Turkey.ORCID 0000-0001-6677-9254
Burak MeteDepartment of Public Health, Cukurova University, Adana, Turkey.ORCID 0000-0002-0780-6176
Oya Baydar ToprakDepartment of Chest Diseases, Cukurova University, Adana, Turkey.
Nazire Ates AyhanDepartment of Intensive Care Unit, Sanliurfa Training and Research Hospital, Sanliurfa, Turkey.
Ahmet FiratDepartment of Intensive Care Unit, Aksaray Training and Research Hospital, Aksaray, Turkey.
Yurdaer BulutDepartment of Intensive Care Unit, Adana Baskent University Seyhan Application and Research Hospital, Adana, Turkey.
Sinem BayrakciDepartment of Intensive Care Unit, Dr. Ersin Arslan Training and Research Hospital, Gaziantep, Turkey.
Aysun Ozel YesilyurtDepartment of Intensive Care Unit, Cukurova University, Adana, Turkey.
Ezgi OzyilmazDepartment of Intensive Care Unit, Cukurova University, Adana, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study primarily aimed to examine the significance of the C-reactive protein to lymphocyte ratio (CLR), a key marker of inflammation, in relation to the disease progression and management of COVID-19 patients admitted to the intensive care unit (ICU). A total of 464 patients aged 18 years or older, diagnosed with COVID-19 and admitted to the ICU between April 1, 2021, and February 1, 2022, were included in the study. Sociodemographic, laboratory, radiological, and clinical data were collected for each patient. The cohort was then divided into two groups-those who survived and those who did not-and analyzed accordingly. Among the patients included in the study, 58.2% were male, and the mean age was 62.39 ± 15.65 years. The mortality rate was 42%. The analysis revealed that the need for high-flow oxygen and mechanical ventilation increased the risk of death by 9.64 times. Furthermore, for each 1-point increase in the SOFA Score, Charlson Comorbidity Index, and Nutric Score, the risk of death increased by 1.27, 1.18, and 1.40 times, respectively. Intravenous immunoglobulin, administered to a select group of patients, reduced the risk of death by 23.8 times. The optimal threshold value for CLR was identified as 103.05, with values above this increasing the risk of death by 1.84 times. Critically ill patients with CLR values exceeding the identified threshold should receive more intensive monitoring and timely adjustments in treatment. Given that CLR is a simple, accessible, and cost-effective marker, it holds particular value in managing aggressive diseases like COVID-19.

Indexed as

COVID-19C-Reactive ProteinIntensive Care UnitsAdultAgedBiomarkersFemaleHumansImmunoglobulins, IntravenousLymphocyte CountLymphocytesMaleMiddle AgedRespiration, ArtificialSARS-CoV-2BiomarkersC-Reactive ProteinImmunoglobulins, IntravenousCOVID-19c-reactive proteinintensive care unitlymphocytemortality

Identifiers

PMID39699047
PMCPMC11660357

What Socratic holds

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LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.