Svenja Ravioli, Annemarie Edenhofner, Christoph Schwarz, Susanne Oswald, Gregor Lindner
>This publication, published in 2026, compares sodium and potassium measurements performed in the emergency department using point-of-care testing (POCT) and those obtained from the central laboratory. It is a retrospective single-center study conducted over a one-year period.
The authors emphasize that only a limited number of studies have evaluated discrepancies in electrolyte measurements, particularly sodium and potassium, despite the fact that these parameters are easily accessible on blood gas analyzers used for point-of-care testing. Nevertheless, these differences are already known.
The study compared 6,404 sodium measurements and 5,622 potassium measurements performed:
on the one hand, on whole blood samples in the emergency department using a Radiometer ABL90 blood gas analyzer;
on the other hand, in the central laboratory on plasma samples using a Roche analyzer.
Samples for point-of-care testing and laboratory analysis were collected less than one minute apart. Laboratory analyses were performed within two hours after the POCT measurement.
The main finding demonstrated a systematic difference between values obtained by point-of-care testing and those obtained in the central laboratory, with POCT values being generally higher than laboratory values. However, across more than 5,500 measurements, this discrepancy did not result in any major overall clinical impact on patient management.
The authors observed that sodium measurements showed only moderate agreement with laboratory results, whereas potassium measurements demonstrated better concordance.
For sodium, the difference between the two methods exceeded 4 mmol/L in 8.5% of cases and exceeded 8 mmol/L in 0.5% of cases. They also observed that the discrepancy between methods tended to increase at higher sodium concentrations.
For potassium, the difference exceeded 0.5 mmol/L in 4.5% of cases and exceeded 1 mmol/L in 1% of cases.
These discrepancies may nevertheless have important consequences for certain clinical situations, which constitutes one of the central points of the discussion.
In particular, in severe hyponatremia, management relies on the administration of hypertonic saline with repeated biological reassessments. Additional treatment is indicated if sodium levels fail to increase sufficiently, generally by approximately 5 mmol/L. The accuracy of sodium measurement is therefore essential in order to avoid undercorrection or overcorrection. Similar concerns apply to the management of hyperkalemia.
The authors therefore strongly recommend maintaining the same analytical method for electrolyte monitoring throughout the patient’s management.
Regarding the study limitations, the authors point out that this retrospective analysis does not allow precise identification of the causes of the observed discrepancies. Several hypotheses are discussed, including:
differences related to the electrodes used by the different analytical techniques;
the fact that point-of-care testing is performed on whole blood whereas laboratory measurements are performed on plasma;
potential biases related to hematocrit, protein concentration, lipemia, or hemolysis, which were not specifically collected in this study.
The authors also highlight the limited number of patients presenting with severe electrolyte disturbances, particularly severe hypernatremia.