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Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding
BACKGROUND: This series on whole blood viscosity issues has been trying to elucidate the sensitivity, specificity and usefulness of the laboratory parameter in clinical practice. The postulation has been that since antiplatelet is used in the management of stasis, of which blood viscosity is an inde...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339107/ https://www.ncbi.nlm.nih.gov/pubmed/22558547 http://dx.doi.org/10.4297/najms.2010.2457 |
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author | Nwose, Ezekiel Uba Cann, Nathan |
author_facet | Nwose, Ezekiel Uba Cann, Nathan |
author_sort | Nwose, Ezekiel Uba |
collection | PubMed |
description | BACKGROUND: This series on whole blood viscosity issues has been trying to elucidate the sensitivity, specificity and usefulness of the laboratory parameter in clinical practice. The postulation has been that since antiplatelet is used in the management of stasis, of which blood viscosity is an index, the latter would be useful laboratory indication and/or contraindication. AIM: The aim of this study was to observe whether blood level of acetylsalicylic acid differs with the level of whole blood viscosity. PATIENTS AND METHODS: Out of the ten years database, 538 cases that were concomitantly tested for haematocrit, total proteins and blood level of salicylate were selected for this study. A separate nine cases of positive faecal occult blood tests were audited for blood viscosity and reviewed. RESULTS: A statistically significant difference is observed with lower blood viscosity being associated with higher salicylate level in comparison of the former between the highest vs. lowest quartiles (p < 0.002). This observation demonstrates the effect of aspirin in lowering blood stasis. Reviewing the positive faecal occult blood cases indicate that gastrointestinal bleeding is characterized by relative hypoviscosity and that hyperviscosity is not present during bleeding complications. CONCLUSION: The findings affirm that whole blood viscosity is a valid clinical laboratory parameter for evidence-based contraindication, indication and monitoring of antiplatelet medication. It calls for better appreciation and clinical utility of whole blood viscosity, which (in the absence of viscometer) can now be extrapolated from haematocrit and total proteins. |
format | Online Article Text |
id | pubmed-3339107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33391072012-05-03 Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding Nwose, Ezekiel Uba Cann, Nathan N Am J Med Sci Original Article BACKGROUND: This series on whole blood viscosity issues has been trying to elucidate the sensitivity, specificity and usefulness of the laboratory parameter in clinical practice. The postulation has been that since antiplatelet is used in the management of stasis, of which blood viscosity is an index, the latter would be useful laboratory indication and/or contraindication. AIM: The aim of this study was to observe whether blood level of acetylsalicylic acid differs with the level of whole blood viscosity. PATIENTS AND METHODS: Out of the ten years database, 538 cases that were concomitantly tested for haematocrit, total proteins and blood level of salicylate were selected for this study. A separate nine cases of positive faecal occult blood tests were audited for blood viscosity and reviewed. RESULTS: A statistically significant difference is observed with lower blood viscosity being associated with higher salicylate level in comparison of the former between the highest vs. lowest quartiles (p < 0.002). This observation demonstrates the effect of aspirin in lowering blood stasis. Reviewing the positive faecal occult blood cases indicate that gastrointestinal bleeding is characterized by relative hypoviscosity and that hyperviscosity is not present during bleeding complications. CONCLUSION: The findings affirm that whole blood viscosity is a valid clinical laboratory parameter for evidence-based contraindication, indication and monitoring of antiplatelet medication. It calls for better appreciation and clinical utility of whole blood viscosity, which (in the absence of viscometer) can now be extrapolated from haematocrit and total proteins. Medknow Publications & Media Pvt Ltd 2010-10 /pmc/articles/PMC3339107/ /pubmed/22558547 http://dx.doi.org/10.4297/najms.2010.2457 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 Cann, Nathan Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title | Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title_full | Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title_fullStr | Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title_full_unstemmed | Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title_short | Whole blood viscosity issues VI: Association with blood salicylate level and gastrointestinal bleeding |
title_sort | whole blood viscosity issues vi: association with blood salicylate level and gastrointestinal bleeding |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3339107/ https://www.ncbi.nlm.nih.gov/pubmed/22558547 http://dx.doi.org/10.4297/najms.2010.2457 |
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