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Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction

BACKGROUND: Although both leukocytosis and leukopenia have been considered Systemic Inflammatory Response Syndrome criteria, leukopenia is not generally considered a normal response to infection. We sought to evaluate the prognostic validity of leukopenia as a sign of sepsis-defining hematological o...

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Autores principales: Belok, Samuel H., Bosch, Nicholas A., Klings, Elizabeth S., Walkey, Allan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224900/
https://www.ncbi.nlm.nih.gov/pubmed/34166406
http://dx.doi.org/10.1371/journal.pone.0252206
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author Belok, Samuel H.
Bosch, Nicholas A.
Klings, Elizabeth S.
Walkey, Allan J.
author_facet Belok, Samuel H.
Bosch, Nicholas A.
Klings, Elizabeth S.
Walkey, Allan J.
author_sort Belok, Samuel H.
collection PubMed
description BACKGROUND: Although both leukocytosis and leukopenia have been considered Systemic Inflammatory Response Syndrome criteria, leukopenia is not generally considered a normal response to infection. We sought to evaluate the prognostic validity of leukopenia as a sign of sepsis-defining hematological organ dysfunction within the Sepsis-3 framework. We hypothesized that leukopenia is associated with higher risk of mortality than leukocytosis among patients with suspected infection. METHODS: We performed a retrospective cohort study using the Medical Information Mart v1.4 in Intensive Care-III database. Multivariable regression models were used to evaluate the association between leukopenia and mortality in patients with suspected infection defined by Sepsis-3. RESULTS: We identified 5,909 ICU patients with suspected infection; 250 (4.2%) had leukopenia. Leukopenia was associated with increased in-hospital mortality compared with leukocytosis (OR, 1.5; 95% CI 1.1–1.9). After adjusting for demographics and comorbidities in the Sepsis-3 consensus model, leukopenia remained associated with increased risk of mortality compared with leukocytosis (OR 1.6, 95% CI 1.2–2.2). Further adjustment for the platelet component of the SOFA attenuated the association between leukopenia and mortality (OR decreased from 1.5 to 1.1). However, 83 (1.4%) of patients had leukopenia without thrombocytopenia and 14 had leukopenia prior to thrombocytopenia. CONCLUSIONS: Among ICU patients with suspected infection, leukopenia was associated with increased risk of death compared with leukocytosis. Due to correlation with thrombocytopenia, leukopenia did not independently improve the prognostic validity of SOFA; however, leukopenia may present as a sign of sepsis prior to thrombocytopenia in a small subset of patients.
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spelling pubmed-82249002021-07-19 Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction Belok, Samuel H. Bosch, Nicholas A. Klings, Elizabeth S. Walkey, Allan J. PLoS One Research Article BACKGROUND: Although both leukocytosis and leukopenia have been considered Systemic Inflammatory Response Syndrome criteria, leukopenia is not generally considered a normal response to infection. We sought to evaluate the prognostic validity of leukopenia as a sign of sepsis-defining hematological organ dysfunction within the Sepsis-3 framework. We hypothesized that leukopenia is associated with higher risk of mortality than leukocytosis among patients with suspected infection. METHODS: We performed a retrospective cohort study using the Medical Information Mart v1.4 in Intensive Care-III database. Multivariable regression models were used to evaluate the association between leukopenia and mortality in patients with suspected infection defined by Sepsis-3. RESULTS: We identified 5,909 ICU patients with suspected infection; 250 (4.2%) had leukopenia. Leukopenia was associated with increased in-hospital mortality compared with leukocytosis (OR, 1.5; 95% CI 1.1–1.9). After adjusting for demographics and comorbidities in the Sepsis-3 consensus model, leukopenia remained associated with increased risk of mortality compared with leukocytosis (OR 1.6, 95% CI 1.2–2.2). Further adjustment for the platelet component of the SOFA attenuated the association between leukopenia and mortality (OR decreased from 1.5 to 1.1). However, 83 (1.4%) of patients had leukopenia without thrombocytopenia and 14 had leukopenia prior to thrombocytopenia. CONCLUSIONS: Among ICU patients with suspected infection, leukopenia was associated with increased risk of death compared with leukocytosis. Due to correlation with thrombocytopenia, leukopenia did not independently improve the prognostic validity of SOFA; however, leukopenia may present as a sign of sepsis prior to thrombocytopenia in a small subset of patients. Public Library of Science 2021-06-24 /pmc/articles/PMC8224900/ /pubmed/34166406 http://dx.doi.org/10.1371/journal.pone.0252206 Text en © 2021 Belok et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Belok, Samuel H.
Bosch, Nicholas A.
Klings, Elizabeth S.
Walkey, Allan J.
Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title_full Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title_fullStr Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title_full_unstemmed Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title_short Evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
title_sort evaluation of leukopenia during sepsis as a marker of sepsis-defining organ dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224900/
https://www.ncbi.nlm.nih.gov/pubmed/34166406
http://dx.doi.org/10.1371/journal.pone.0252206
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