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Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis

BACKGROUND: We measured the expression of serum procalcitonin (PCT), quantitative C-reactive protein (QCRP), neutrophil CD64 (nCD64) and monocytic HLA-DR (mHLA-DR) sequentially in patients admitted to the intensive care unit (ICU) and correlated the expression of these biomarkers to predict developm...

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Autores principales: Pandey, Kshitij, Malviya, Deepak, Awasthi, Namrata P., Nath, Soumya S., Harjai, Mamta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158489/
https://www.ncbi.nlm.nih.gov/pubmed/35257562
http://dx.doi.org/10.5114/ait.2021.108579
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author Pandey, Kshitij
Malviya, Deepak
Awasthi, Namrata P.
Nath, Soumya S.
Harjai, Mamta
author_facet Pandey, Kshitij
Malviya, Deepak
Awasthi, Namrata P.
Nath, Soumya S.
Harjai, Mamta
author_sort Pandey, Kshitij
collection PubMed
description BACKGROUND: We measured the expression of serum procalcitonin (PCT), quantitative C-reactive protein (QCRP), neutrophil CD64 (nCD64) and monocytic HLA-DR (mHLA-DR) sequentially in patients admitted to the intensive care unit (ICU) and correlated the expression of these biomarkers to predict development of sepsis and its outcome. METHODS: Consenting adult patients of more than 18 years of age, who developed sepsis during an observation period of 20 days with a sequential organ failure assessment score (SOFA) score ≥ 2 or those who already had sepsis at admission to the ICU were included. SOFA score, serum PCT, QCRP, nCD64 and mHLA-DR assays were recorded on the first and third day of admission to the ICU. A total of 27 sepsis cases and 24 controls (all admitted to the ICU) were included in the study. RESULTS: SOFA score, serum PCT, QCRP, nCD64 were significantly higher and mHLA-DR was significantly lower in cases compared to controls, both on day 1 and day 3. There was no significant difference in any of the parameters between day 1 and day 3. PCT and nCD64, both with sensitivity of 77.8% and specificity of 70.8% (95% CI, 0.73–0.95), had the best predictive value for diagnosing sepsis. Lower mHLA-DR (< 5000/cell) was associated with higher mortality among cases. CONCLUSIONS: Serum PCT and nCD64 are the best biomarkers with similar sensitivity and specificity in detecting sepsis. mHLA-DR could have a role in prognosis as lower levels were associated with higher mortality.
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spelling pubmed-101584892023-05-17 Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis Pandey, Kshitij Malviya, Deepak Awasthi, Namrata P. Nath, Soumya S. Harjai, Mamta Anaesthesiol Intensive Ther Original and Clinical Articles BACKGROUND: We measured the expression of serum procalcitonin (PCT), quantitative C-reactive protein (QCRP), neutrophil CD64 (nCD64) and monocytic HLA-DR (mHLA-DR) sequentially in patients admitted to the intensive care unit (ICU) and correlated the expression of these biomarkers to predict development of sepsis and its outcome. METHODS: Consenting adult patients of more than 18 years of age, who developed sepsis during an observation period of 20 days with a sequential organ failure assessment score (SOFA) score ≥ 2 or those who already had sepsis at admission to the ICU were included. SOFA score, serum PCT, QCRP, nCD64 and mHLA-DR assays were recorded on the first and third day of admission to the ICU. A total of 27 sepsis cases and 24 controls (all admitted to the ICU) were included in the study. RESULTS: SOFA score, serum PCT, QCRP, nCD64 were significantly higher and mHLA-DR was significantly lower in cases compared to controls, both on day 1 and day 3. There was no significant difference in any of the parameters between day 1 and day 3. PCT and nCD64, both with sensitivity of 77.8% and specificity of 70.8% (95% CI, 0.73–0.95), had the best predictive value for diagnosing sepsis. Lower mHLA-DR (< 5000/cell) was associated with higher mortality among cases. CONCLUSIONS: Serum PCT and nCD64 are the best biomarkers with similar sensitivity and specificity in detecting sepsis. mHLA-DR could have a role in prognosis as lower levels were associated with higher mortality. Termedia Publishing House 2021-08-20 2021-10 /pmc/articles/PMC10158489/ /pubmed/35257562 http://dx.doi.org/10.5114/ait.2021.108579 Text en Copyright © Polish Society of Anaesthesiology and Intensive Therapy https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access journal, all articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) ), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original and Clinical Articles
Pandey, Kshitij
Malviya, Deepak
Awasthi, Namrata P.
Nath, Soumya S.
Harjai, Mamta
Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title_full Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title_fullStr Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title_full_unstemmed Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title_short Comparison of neutrophil CD64 and monocytic HLA-DR with existing biomarkers for the diagnosis and prognosis of sepsis
title_sort comparison of neutrophil cd64 and monocytic hla-dr with existing biomarkers for the diagnosis and prognosis of sepsis
topic Original and Clinical Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158489/
https://www.ncbi.nlm.nih.gov/pubmed/35257562
http://dx.doi.org/10.5114/ait.2021.108579
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