Importance of blood-collection tubes in plasma lidocaine determinations.
Author(s): Stargel WW, Roe CR, Routledge PA, Shand DG
Publication: Clin Chem, 1979, Vol. 25, Page 617-9
PubMed ID: 380842 PubMed Review Paper? No
Purpose of Paper
Conclusion of Paper
Studies
-
Study Purpose
The purpose of this study was to determine the effects of blood or plasma contact with collection tube stoppers on lidocaine concentration. Clinical specimens and lidocaine spiked specimens from a normal volunteer were collected in plastic syringes and whole blood or plasma was then distributed to the various tubes.
Summary of Findings:
In 25 clinical specimens, contact of whole blood with the red stoppers on Vacutainer tubes resulted in a decrease in mean lidocaine concentration in serum from 6.5 ug/mL to 4.9 ug/mL (p<0.001). Similarly, there was a significant decrease in measured lidocaine when whole blood, but not plasma, was added to red or green Vacutainer or red Monoject tubes containing exogenous lidocaine. The effect of using plastic Vacutainer tubes versus an all glass system decreased as lidocaine concentrations increased. However, in plastic Vacutainer tubes or an all glass system, increasing lidocaine concentration decreased the ratio of lidocaine in blood to lidocaine in plasma. Finally, when blood was collected in Vacutainer tubes, lidocaine binding of plasma was 28%, versus 56% when blood was collected in glass.
Biospecimens
Preservative Types
- None (Fresh)
Diagnoses:
- Not specified
- Normal
Platform:
Analyte Technology Platform Small molecule Immunoassay Pre-analytical Factors:
Classification Pre-analytical Factor Value(s) Storage Type of storage container Green Vacutainer
Red Vacutainer
Red Monoject
All glass system
Storage Storage conditions Without stopper
In contact with stopper or with inversion
Biospecimen Aliquots and Components Blood and blood products Plasma
Serum
Whole blood
Preaquisition Biomarker level 2 ug/mL lidocaine
4 ug/mL lidocaine
6 ug/mL lidocaine
8 ug/mL lidocaine
10 ug/mL lidocaine
12 ug/mL lidocaine
