Abstract
Whole blood apparent viscosity was measured at a shear rate of 135s−1 and 37°C, using a conicylindrical rotational viscometer. Multiparameter models were produced by multiple regression analysis of the relationship between measured viscosity and packed cell volume (PCV), plasma fibrinogen concentration and plasma viscosity. The best fit models included PCV and plasma viscosity but not fibrinogen concentration. The 95% confidence limits for the prediction of whole blood viscosity was c ± 21% for data having a wide range of PCV, (22%–77%), and was c ± 10% for data with a smaller PCV range (36% to 48.5%).
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