V. Rege et al., COMPARISON OF KODAK AMERLITE FT4 AND TSH-30 WITH T-4 AND TSH AS FIRST-LINE THYROID-FUNCTION TESTS, Clinical biochemistry, 29(1), 1996, pp. 1-4
Objectives: To evaluate the effect of test automation and a change in
strategy for thyroid function tests (TFT) on personnel needs and turn-
around time. The first-line TFT were changed from T-4 and TSH to FT4 a
nd TSH-30. Design and Methods: Samples received for TFT from 357 rando
mly selected patients were analyzed by RIA for T-4, and by IRMA for TS
H as first-line tests. FT3 and TBG were requested as back-up tests whe
n indicated. Patients were classified on the basis of these results an
d the clinical information received. All the samples were reanalyzed f
or FT4 and TSH on the Amerlite Processing Center, which is a batch, se
miautomated immunoassay system. The thyroid status of the patients was
compared using the two protocols and available clinical data. Results
: There was good correlation between TSH-IRMA and TSH-30 in the 160 pa
tients classified as euthyroid (r = 0.956; p < 0.001) and no euthyroid
patient was reclassified with the new strategy. In 21 patients with b
orderline raised TSH-IRMA, FT4 was found to be low in only 2. All If p
atients classified as hypothyroid had TSH results greater than 10 mU/L
and all except 2 patients had FT4 less than 11 nmol/L. The status of
21 hyperthyroid as well as 40 patients on carbimazole could be determi
ned biochemically on the basis of agreement between both the FT4 and T
SH-30 results. FT3 was only required if the FT4 and TSH-30 results wer
e not in agreement. In 42 patients on T-4 therapy, adequacy of replace
ment was assessed better using FT4 and TSH-30. No patient required bac
kup testing with TBG to determine thyroid status using the new testing
protocol. The change in TFT protocol reduced the 95% turn-around time
from 3 days to 1 day. Conclusion: The introduction of FT4 and TSH-30
as first-line TFT improved the turn-around time for TFT, resulted in 2
5% reduction in personnel requirements, 60% reduction in FT3 assays, a
nd discontinuation of TBG assay.