A. Kallner, PREANALYTICAL PROCEDURES IN THE MEASUREMENT OF IONIZED CALCIUM IN SERUM AND PLASMA, European journal of clinical chemistry and clinical biochemistry, 34(1), 1996, pp. 53-58
To investigate the effects of sampling routines, ionized calcium (corr
ected for pH) was measured after sampling in different types of tubes
and under fasting and postprandial conditions. The results are discuss
ed with respect to analytical goals. Serum samples, collected in vacuu
m tubes and spun after coagulation, could be safely measured during 24
h. This time window was expanded to 48 hours by using gel-containing
tubes. Properly prepared specimens withstand mail transportation. Diff
erent brands of gel-containing tubes gave different results, and these
differences were clinically significant. An ''American-type'' breakfa
st causes an average decrease of corrected ionized calcium ion concent
ration of 0.04 mmol/l and an increased interindividual variation of re
sults. Characterisation of reference intervals should include the ''nu
tritional status'' and the brand of vacuum tube used.