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A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification
Sepsis, a potentially life-threatening complication of an infection, has the highest burden of death and medical expenses in hospitals worldwide. Leukocyte count and CD64 expression on neutrophils (nCD64) are known to correlate strongly with improved sensitivity and specificity of sepsis diagnosis a...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500847/ https://www.ncbi.nlm.nih.gov/pubmed/28671185 http://dx.doi.org/10.1038/ncomms15949 |
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author | Hassan, U. Ghonge, T. Reddy Jr., B. Patel, M. Rappleye, M. Taneja, I. Tanna, A. Healey, R. Manusry, N. Price, Z. Jensen, T. Berger, J. Hasnain, A. Flaugher, E. Liu, S. Davis, B. Kumar, J. White, K. Bashir, R. |
author_facet | Hassan, U. Ghonge, T. Reddy Jr., B. Patel, M. Rappleye, M. Taneja, I. Tanna, A. Healey, R. Manusry, N. Price, Z. Jensen, T. Berger, J. Hasnain, A. Flaugher, E. Liu, S. Davis, B. Kumar, J. White, K. Bashir, R. |
author_sort | Hassan, U. |
collection | PubMed |
description | Sepsis, a potentially life-threatening complication of an infection, has the highest burden of death and medical expenses in hospitals worldwide. Leukocyte count and CD64 expression on neutrophils (nCD64) are known to correlate strongly with improved sensitivity and specificity of sepsis diagnosis at its onset. A major challenge is the lack of a rapid and accurate point-of-care (PoC) device that can perform these measurements from a minute blood sample. Here, we report a PoC microfluidic biochip to enumerate leukocytes and quantify nCD64 levels from 10 μl of whole blood without any manual processing. Biochip measurements have shown excellent correlation with the results from flow cytometer. In clinical studies, we have used PoC biochip to monitor leukocyte counts and nCD64 levels from patients’ blood at different times of their stay in the hospital. Furthermore, we have shown the biochip’s utility for improved sepsis diagnosis by combining these measurements with electronic medical record (EMR). |
format | Online Article Text |
id | pubmed-5500847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55008472017-07-11 A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification Hassan, U. Ghonge, T. Reddy Jr., B. Patel, M. Rappleye, M. Taneja, I. Tanna, A. Healey, R. Manusry, N. Price, Z. Jensen, T. Berger, J. Hasnain, A. Flaugher, E. Liu, S. Davis, B. Kumar, J. White, K. Bashir, R. Nat Commun Article Sepsis, a potentially life-threatening complication of an infection, has the highest burden of death and medical expenses in hospitals worldwide. Leukocyte count and CD64 expression on neutrophils (nCD64) are known to correlate strongly with improved sensitivity and specificity of sepsis diagnosis at its onset. A major challenge is the lack of a rapid and accurate point-of-care (PoC) device that can perform these measurements from a minute blood sample. Here, we report a PoC microfluidic biochip to enumerate leukocytes and quantify nCD64 levels from 10 μl of whole blood without any manual processing. Biochip measurements have shown excellent correlation with the results from flow cytometer. In clinical studies, we have used PoC biochip to monitor leukocyte counts and nCD64 levels from patients’ blood at different times of their stay in the hospital. Furthermore, we have shown the biochip’s utility for improved sepsis diagnosis by combining these measurements with electronic medical record (EMR). Nature Publishing Group 2017-07-03 /pmc/articles/PMC5500847/ /pubmed/28671185 http://dx.doi.org/10.1038/ncomms15949 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hassan, U. Ghonge, T. Reddy Jr., B. Patel, M. Rappleye, M. Taneja, I. Tanna, A. Healey, R. Manusry, N. Price, Z. Jensen, T. Berger, J. Hasnain, A. Flaugher, E. Liu, S. Davis, B. Kumar, J. White, K. Bashir, R. A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title | A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title_full | A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title_fullStr | A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title_full_unstemmed | A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title_short | A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification |
title_sort | point-of-care microfluidic biochip for quantification of cd64 expression from whole blood for sepsis stratification |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500847/ https://www.ncbi.nlm.nih.gov/pubmed/28671185 http://dx.doi.org/10.1038/ncomms15949 |
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