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Objectives: Haemolysis is a major preanalytical issue that affects potassium measurements, often leading to sample rejection and delayed clinical management. This study proposes a novel corrective model for accurate unhaemolysed potassium prediction.
Methods: Blood samples from 14 healthy volunteers were used to prepare a range of haemolysates via freeze-thaw method. First, the relationship between potassium variation and haemolysis variation (ΔK/ΔHI) was studied both individually and globally to assess inter-individual variability. Then, to achieve a more personalised unhaemolysed potassium prediction, a novel corrective model was developed based on: potassium levels in paired unhaemolysed and gradually haemolysed samples, measured haemolysis index, mean corpuscular haemoglobin concentration, mean corpuscular volume and intraerythrocytic potassium level. The bias between true and model-predicted unhaemolysed potassium values was calculated and compared to the reference change value (RCV%).
Results: Global data showed a strong correlation between ΔK and ΔHI (Pearson r=0.97, p<0.0001), following a linear relationship: ΔK=0.33*ΔHI (p<0.0001). However, individual data revealed substantial inter-individual variation (min ΔK=0.23*ΔHI and max ΔK=0.39*ΔHI). The correction model achieved 100 % accuracy for the 116 prepared samples, with predicted unhaemolysed potassium values falling within a ± 10 % bias range (mean ± standard deviation of bias = -0.5 ± 2.8 %).
Conclusions: We propose a novel, reliable, and cost-effective corrective model to predict unhaemolysed potassium from haemolysed samples. Compared with previously published models, the integration of red blood cells indices allows for a more personalised, patient-centred approach with high efficiency.
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http://dx.doi.org/10.1515/cclm-2025-0330 | DOI Listing |
Clin Chem Lab Med
August 2025
Clinical Biochemistry and Toxicology Laboratory, Rennes University Hospital Centre, Rennes, France.
Objectives: Haemolysis is a major preanalytical issue that affects potassium measurements, often leading to sample rejection and delayed clinical management. This study proposes a novel corrective model for accurate unhaemolysed potassium prediction.
Methods: Blood samples from 14 healthy volunteers were used to prepare a range of haemolysates via freeze-thaw method.
Ann Clin Biochem
May 2007
Biochemistry Department, Crosshouse Hospital, Kilmarnock KA2 0BE, UK.
Background: Patient specimens can be subject to subtle interference from cross contamination by liquid-based, potassium-containing EDTA anticoagulant, leading to misinterpretation of results. A rapid method for EDTA analysis to detect such contamination is described.
Method: An in-house EDTA assay on the Roche MODULAR analyser was assessed for accuracy and precision by comparison with an adjusted calcium difference measurement (atomic absorption and o-cresolphthalein complexone colorimetry).