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Clinical Chemistry 46: 1020-1022, 2000;
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(Clinical Chemistry. 2000;46:1020-1022.)
© 2000 American Association for Clinical Chemistry, Inc.


Letters

Serum and Plasma Samples for ACS:Systems Cardiac Markers

Franca Pagani1, Graziella Bonetti1, Francesca Stefini1, Claudio Cuccia2 and Mauro Panteghini1,a

1 Laboratorio Analisi Chimico Cliniche 1, and,
2 Cattedra e Divisione di Cardiologia, Azienda Ospedaliera ‘Spedali Civili’, and Universita’, 25125 Brescia, Italy
a Author for correspondence. Fax 39-0303995369; e-mail panteghi@osp.unibs.it.


To The Editor:

The ACS:180® immunoassay system (Bayer Diagnostics) is an automated random analyzer that uses acridinium ester-based chemiluminescence detection. The architecture of the cardiac marker assays is a heterologous sandwich format, using monoclonal anti-marker antibody immobilized onto paramagnetic particles (capture) and polyclonal goat anti-human myoglobin, creatine kinase MB isoenzyme (CK-MB), or cardiac troponin I (cTnI) antibody labeled with acridinium ester (detector). Its processing time (~20 min if the analyzer is in standby mode) and precision (overall CV <5%) make the system suitable for emergency use (1). However, optimal performance of an assay system for cardiac markers depends not only on the instrument’s analysis time, but also on factors that affect the overall turnaround time, including the preanalytical steps necessary to prepare the sample (2). The use of plasma samples eliminates the extra time needed for clotting, thereby reducing the overall preanalytical time, but there can be significant differences between serum and plasma concentrations of cardiac markers (3). The aim of this study was to validate the possible use of two different anticoagulants (lithium heparinate and EDTA, tripotassium salt) for cardiac marker determinations on the ACS:180 immunoassay system.

Twenty-five patients with acute myocardial infarction were studied. All gave informed consent. We collected three separate tubes (Sarstedt) to prepare serum, heparin plasma, and EDTA plasma in random order during one phlebotomy. ACS myoglobin, . . . [Full Text of this Article]


Acknowledgments


References

Barry Bluestein3,a, Brian Markham3 and David Waskiewicz3

3 Cardiovascular Disease R&D, Lab Testing Segment, Bayer Corporation, 511 Benedict Ave., Tarrytown, NY 10591-5097
a Author for correspondence.


To the Editor:


References




The following articles in journals at HighWire Press have cited this article:


Home page
Clin. Chem.Home page
M. Panteghini and F. Pagani
On the Comparison of Serum and Plasma Samples in Troponin Assays
Clin. Chem., May 1, 2003; 49(5): 835 - 836.
[Full Text]


Home page
Clin. Chem.Home page
M. Panteghini
Performance of Today's Cardiac Troponin Assays and Tomorrow's
Clin. Chem., June 1, 2002; 48(6): 809 - 810.
[Full Text] [PDF]




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