Abstract
A positive-pressure, washed-erythrocyte method for the measurement of red cell filterability has been compared with a negative-pressure, whole-blood technique. Using 5 µm pore-size polycarbonate filters, both methods detected a sub-population of 4–5 × 107/l glutaraldehyde-hardened erythrocytes and both showed a decrease in erythrocyte filterability in proportion to increasing concentrations of added fibrinogen. The washed-erythrocyte method gave better reproducibility with less variation between filter batches and is recommended for the study of patients in whom plasma hyperproteinaemia may adversely affect erythrocyte filtration.
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