» Articles » PMID: 35916537

Hyperviscosity Syndromes; Hemorheology for Physicians and the Use of Microfluidic Devices

Overview
Specialty Hematology
Date 2022 Aug 2
PMID 35916537
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: Hyperviscosity syndromes can lead to significant morbidity and mortality. Existing methods to measure microcirculatory rheology are not readily available and limited in relevance and accuracy at this level. In this review, we review selected hyperviscosity syndromes and the advancement of their knowledge using microfluidic platforms.

Recent Findings: Viscosity changes drastically at the microvascular level as the physical properties of the cells themselves become the major determinants of resistance to blood flow. Current, outdated viscosity measurements only quantify whole blood or serum. Changes in blood composition, cell number, or the physical properties themselves lead to increased blood viscosity. Given the significant morbidity and mortality from hyperviscosity syndromes, new biophysical tools are needed and being developed to study microvascular biophysical and hemodynamic conditions at this microvascular level to help predict those at risk and guide therapeutic treatment.

Summary: The use of 'lab-on-a-chip' technology continues to rise to relevance with point of care, personalized testing and medicine as customizable microfluidic platforms enable independent control of many in vivo factors and are a powerful tool to study microcirculatory hemorheology.

Citing Articles

Microbiome-metabolome analysis insight into the effects of high-salt diet on hemorheological functions in SD rats.

Qi L, Li Y, Chen Z, Wei C, Wen X, Hu S Front Nutr. 2024; 11:1408778.

PMID: 39381352 PMC: 11460366. DOI: 10.3389/fnut.2024.1408778.

References
1.
Fay M, Myers D, Kumar A, Turbyfield C, Byler R, Crawford K . Cellular softening mediates leukocyte demargination and trafficking, thereby increasing clinical blood counts. Proc Natl Acad Sci U S A. 2016; 113(8):1987-92. PMC: 4776450. DOI: 10.1073/pnas.1508920113. View

2.
Karel M, Tullemans B, DItalia G, Lemmens T, Claushuis T, Kuijpers M . The effect of Bruton's tyrosine kinase inhibitor ibrutinib on atherothrombus formation under stenotic flow conditions. Thromb Res. 2022; 212:72-80. DOI: 10.1016/j.thromres.2022.02.020. View

3.
Schmalzer E, Lee J, Brown A, Usami S, Chien S . Viscosity of mixtures of sickle and normal red cells at varying hematocrit levels. Implications for transfusion. Transfusion. 1987; 27(3):228-33. DOI: 10.1046/j.1537-2995.1987.27387235626.x. View

4.
Oishee M, Ali T, Jahan N, Khandker S, Haq M, Khondoker M . COVID-19 Pandemic: Review of Contemporary and Forthcoming Detection Tools. Infect Drug Resist. 2021; 14:1049-1082. PMC: 7982560. DOI: 10.2147/IDR.S289629. View

5.
Alapan Y, Little J, Gurkan U . Heterogeneous red blood cell adhesion and deformability in sickle cell disease. Sci Rep. 2014; 4:7173. PMC: 4241514. DOI: 10.1038/srep07173. View