Objectives: To evaluate the analytical performance of the Bio-Rad Variant I
I HbA(IC) analyzer (a completely automated system for the quantification of
glycohemoglobin [HbA(IC)] in blood).
Design and Methods: The analytical parameters of precision, linearity and a
nalytical range were assessed and HbA(IC) results from the Variant II were
compared to HbA(IC) results from the Bio-Rad Variant (a method certified by
the National Glycohemoglobin Standardization Program). The effect of a var
iety of hemoglobin variants on HbA(IC) obtained on the system was investiga
ted.
Results: Total imprecision was less than 5% and the results compared well w
ith those from an established method. The method has a wide analytical rang
e with no carryover between specimens.
Conclusion: The HbA(IC) method on the Variant II gives acceptable analytica
l performance. (C) 2001 The Canadian Society of Clinical Chemists. All righ
ts reserved.