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Articles |
1
Istituto Scientifico H S Raffaele, Laboratorio Analisi, Via Olgettina 60, 20132 Milano, Italy.
2
IRCCS Centro Auxologico Italiano, Laboratorio
Analisi, Milano, Italy.
3
Università di Milano Istituto Scienze Biomediche,
Ospedale L.Sacco, Milano, Italy.
4
Dipartimento di Chimica e Biochimica Medica, Via
Saldini 50, Università di Milano, Italy.
a Author for correspondence. Fax +39-2-2643-2640; e-mail ceriotf{at}hsr.it
The results of an external quality-assessment experiment for serum
creatinine measurement are described. Fifty-one laboratories performed
quintuplicate analyses during three different analytical runs on six
lyophilized sera and two frozen human serum pools. Isotope dilution gas
chromatographymass spectrometry (ID GC-MS) target values were
assigned to all the materials. Intralaboratory within- and between-run
imprecision results were very similar for all the materials tested (CV
2.20% and
4.70%, respectively). The overall imprecision obtained
was high (CV 6.520.0%) because of increased
interlaboratoryintermethod variability. A significant positive bias
(+9.2+43.7%) was found for all the materials at lower creatinine
concentration. By using two human sera at different concentrations, we
could calculate the constant and the proportional calibration bias
displayed by each peer group. The majority of the lyophilized materials
showed a behavior divergent from the frozen pools, indicating
matrix-related problems. We propose a new algorithm for calculating
matrix bias correction factor instrumentreagent specific for each
material.
Key Words: indexing terms: quality control reference method control materials
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