Background Inadvertent submission of ethylenediaminetetraacetic acid (EDTA) based plasma in place of heparinized plasma or contamination of serum or heparinized plasma with EDTA can alter select laboratory measurements. While factitious hypocalcaemia and abnormally low alkaline phosphatase (ALP) are recognized indicators of EDTA contamination, the impact of EDTA on Mg2+ and Fe2+ remains controversial.
Method Herein, we derived the EDTA concentration required to cause a 50% decline (EC50[EDTA]) for Ca2+, ALP, Mg2+, and Fe2+ across two methodologies (Roche Cobas c303 and Abbott Alinity c) by varying EDTA concentration across plasma and serum pools. The concentration of EDTA required to exceed the allowable performance limit (APL[EDTA]) was also evaluated across methods.
Results Mg2+ measured by an isocitrate dehydrogenase enzymatic method was resilient against EDTA, while Mg2+ measured by xylidyl blue had an EC50[EDTA] and APL[EDTA] of 0.78 – 1.18 mmol/L and 0.16 – 0.34 mmol/L, respectively. Fe2+ measured with a ferene method was resilient to EDTA, whereas ferrrozine method indicated EC50[EDTA] and APL[EDTA] of 5.6 – 8.86 mmol/L and 4.68 – 5.46 mmol/L, respectively. Ca2+ and ALP exhibited larger EC50[EDTA] on the Abbott Alinity c.
Conclusion Hypomagnesemia and hypoferremia are not definitive markers of potential EDTA contamination, as Mg2+ and Fe2+ measurements show method-dependent susceptibilities.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding.
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Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
We used aggregated/summary data obtained from de-identified and pooled blood samples. In other words, residual blood samples were pooled together to make the samples used in the study for analysis . No individual-level data had been used in this study. This work has been reviewed by the division head, who confirms that this works is regulated as per Laboratory Medicine Program (LMP) and UHN policies, Accreditation Canada Diagnostics, and health regulations as per the Province of Ontario and Health Canada. As such, there is no need for further review by the UHN Quality Improvement Review Committee(QIRC) or the UHN Research Ethics Boards.
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Yes
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Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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