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Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation
BACKGROUND: Hyperviscosity syndrome has been suggested as not simply an acute reaction. Yet, erythrocyte sedimentation rate is associated with whole blood viscosity and it is an indirect acute phase inflammation marker. AIMS: This work investigates the prevalence of hyperviscosity in acute phase inf...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339058/ https://www.ncbi.nlm.nih.gov/pubmed/22737672 http://dx.doi.org/10.4297/najms.2010.2353 |
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author | Nwose, Ezekiel Uba |
author_facet | Nwose, Ezekiel Uba |
author_sort | Nwose, Ezekiel Uba |
collection | PubMed |
description | BACKGROUND: Hyperviscosity syndrome has been suggested as not simply an acute reaction. Yet, erythrocyte sedimentation rate is associated with whole blood viscosity and it is an indirect acute phase inflammation marker. AIMS: This work investigates the prevalence of hyperviscosity in acute phase inflammation. MATERIALS AND METHODS: Archived clinical pathology data for the period of 1999 to 2008 were utilized. 40,632-cases tested for C-reactive protein and/or erythrocyte sedimentation rate from five alternate years, which were concomitantly tested for haematocrit and total proteins, were extracted. The prevalence of abnormal viscosity associated with positive results of C-reactive protein and erythrocyte sedimentation rate were evaluated. RESULTS: Hyperviscosity is infrequently associated with positive C-reactive protein (2.9%) and erythrocyte sedimentation rate (2.7%) sub-populations, and are not statistically different from their respective negative sub-populations. Normoviscosity is significantly more prevalent in the positive sub-populations (p < 0.01). Further analyses indicate that prevalence of acute phase inflammation is statistically significantly less in hyperviscosity compared to normoviscosity sub-population (p < 0.00001). Actual blood viscosity level increases with level of inflammation though. CONCLUSION: The study demonstrates that although blood viscosity level may increase with inflammation, hyperviscosity is not frequent in, or sensitive to acute phase inflammation. It portends that whole blood viscosity is not unspecific as acute phase inflammation markers. It calls for clinicians to consider utilizing whole blood viscosity in disease conditions where stasis is implicated, in which it is specific and valuable. It would also benefit to establish whether hyperviscosity is a chronic phase inflammation marker. |
format | Online Article Text |
id | pubmed-3339058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33390582012-06-25 Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation Nwose, Ezekiel Uba N Am J Med Sci Original Article BACKGROUND: Hyperviscosity syndrome has been suggested as not simply an acute reaction. Yet, erythrocyte sedimentation rate is associated with whole blood viscosity and it is an indirect acute phase inflammation marker. AIMS: This work investigates the prevalence of hyperviscosity in acute phase inflammation. MATERIALS AND METHODS: Archived clinical pathology data for the period of 1999 to 2008 were utilized. 40,632-cases tested for C-reactive protein and/or erythrocyte sedimentation rate from five alternate years, which were concomitantly tested for haematocrit and total proteins, were extracted. The prevalence of abnormal viscosity associated with positive results of C-reactive protein and erythrocyte sedimentation rate were evaluated. RESULTS: Hyperviscosity is infrequently associated with positive C-reactive protein (2.9%) and erythrocyte sedimentation rate (2.7%) sub-populations, and are not statistically different from their respective negative sub-populations. Normoviscosity is significantly more prevalent in the positive sub-populations (p < 0.01). Further analyses indicate that prevalence of acute phase inflammation is statistically significantly less in hyperviscosity compared to normoviscosity sub-population (p < 0.00001). Actual blood viscosity level increases with level of inflammation though. CONCLUSION: The study demonstrates that although blood viscosity level may increase with inflammation, hyperviscosity is not frequent in, or sensitive to acute phase inflammation. It portends that whole blood viscosity is not unspecific as acute phase inflammation markers. It calls for clinicians to consider utilizing whole blood viscosity in disease conditions where stasis is implicated, in which it is specific and valuable. It would also benefit to establish whether hyperviscosity is a chronic phase inflammation marker. Medknow Publications & Media Pvt Ltd 2010-08 /pmc/articles/PMC3339058/ /pubmed/22737672 http://dx.doi.org/10.4297/najms.2010.2353 Text en Copyright: © North American Journal of Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nwose, Ezekiel Uba Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title | Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title_full | Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title_fullStr | Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title_full_unstemmed | Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title_short | Whole blood viscosity assessment issues IV: Prevalence in acute phase inflammation |
title_sort | whole blood viscosity assessment issues iv: prevalence in acute phase inflammation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339058/ https://www.ncbi.nlm.nih.gov/pubmed/22737672 http://dx.doi.org/10.4297/najms.2010.2353 |
work_keys_str_mv | AT nwoseezekieluba wholebloodviscosityassessmentissuesivprevalenceinacutephaseinflammation |