The Role of Neutrophil-lymphocyte Ratio in the Diagnosis and Prognosis Evaluation of Sepsis: a Single-center, Retrospective Study

Sponsor
Wuhan Union Hospital, China (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05636202
Collaborator
(none)
500
10

Study Details

Study Description

Brief Summary

Neutrophil-lymphocyte ratio (NLR), as an inflammatory index, is cheap and easy to obtain, and could be widely used in hospitals at all levels. NLR is a valuable biomarker that is significantly correlated with the status of immune and inflammatory responses. In the past few years, NLR has been continuously and extensively explored in various diseases, and the research progress is considerable. In cardiovascular disease, NLR can predict arrhythmia and short - and long-term mortality in patients with acute coronary syndrome. NLR may be associated with heart failure and valvular heart disease. Moreover, NLR has been shown to be associated with respiratory diseases (such as chronic obstructive pulmonary disease), immune diseases (rheumatoid arthritis and systemic lupus erythematosus), and digestive diseases (acute appendicitis, hepatocellular carcinoma, liver fibrosis, and cirrhosis).

Importantly, the study of NLR in sepsis has received much attention in recent years. A 2019 meta-analysis concluded that peripheral white blood cell ratios, including NLR, lymphocyte-to-monocyte ratio (LMR), and platelet-to-lymphocyte ratio (PLR), are associated with clinical outcomes in sepsis and are useful biomarkers of infection. They recommended that NLR be evaluated in future hierarchical models, To clarify its relationship with NLR and clinical outcome and the prognostic value of NLR, it is worth mentioning that NLR has also been found to have the ability to predict the outcome of sepsis. In 2019, Martins et al. and Westerdijk et al. came to a similar conclusion by analyzing two retrospective studies that NLR, together with other inflammatory parameters, might be a marker for early detection of sepsis in the intensive care unit. However, a large body of evidence demonstrating the association between NLR and adverse clinical outcomes in sepsis remains controversial. Another study concluded that "no association was found between NLR and 28-day in-hospital mortality in patients with sepsis". In addition, the reliability of NLR on admission in predicting the prognosis of critical illness was also lower than that of traditional markers (including CRP, PCT, serum lactic acid and APACHEⅡ score).

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
The Role of Neutrophil-lymphocyte Ratio in the Diagnosis and Prognosis Evaluation of Sepsis: a Single-center, Retrospective Study
Anticipated Study Start Date :
Dec 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Survival group

Patients who survived sepsis

Other: No intervention
There was no intervention in the retrospective study

Death group

Patients who died of sepsis

Other: No intervention
There was no intervention in the retrospective study

Outcome Measures

Primary Outcome Measures

  1. NLR [day 1, day2, day 3, and day 7 after admission.]

    NLR values were collected on day 1, day 2, day 3, and day 7 after admission.

Secondary Outcome Measures

  1. NE% [on day 1, day 2, day 3, and day 7 after admission.]

    NE% were collected on day 1, day 2, day 3, and day 7 after admission.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 1.Patients with sepsis

  • 2.ICU stay time ≥3 days;

Exclusion Criteria:
    1. History of solid organ or bone marrow transplantation;
    1. Diseases that may affect immune-related indicators, such as autoimmune diseases such as rheumatoid arthritis and SLE, or hematological malignancies such as leukemia and lymphoma;
    1. Have received radiotherapy or chemotherapy within the past 30 days, or have received immunosuppressive drugs (tripterygium, mycophenolate, cyclophosphamide, FK506, etc.), or have received continuous treatment with more than 10mg of prednisolone/day (or the same dose of other hormones);
    1. Pregnancy or lactation;c

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Wuhan Union Hospital, China

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wuhan Union Hospital, China
ClinicalTrials.gov Identifier:
NCT05636202
Other Study ID Numbers:
  • NLR01
First Posted:
Dec 5, 2022
Last Update Posted:
Dec 5, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2022