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. 2016 Apr;7(2):90-5.
doi: 10.1016/j.phrp.2015.11.003. Epub 2015 Nov 25.

Inorganic Phosphorus and Potassium Are Putative Indicators of Delayed Separation of Whole Blood

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Inorganic Phosphorus and Potassium Are Putative Indicators of Delayed Separation of Whole Blood

Jae-Eun Lee et al. Osong Public Health Res Perspect. 2016 Apr.

Abstract

Objectives: The delayed separation of whole blood can influence the concentrations of circulating blood components, including metabolites and cytokines. The aim of this study was to determine whether clinical-biochemistry analytes can be used to assess the delayed separation of whole blood.

Methods: We investigated the plasma and serum concentrations of five clinical-biochemistry analytes and free hemoglobin when the centrifugation of whole blood stored at 4°C or room temperature was delayed for 4 hours, 6 hours, 24 hours, or 48 hours, and compared the values with those of matched samples that had been centrifuged within 2 hours after whole-blood collection.

Results: The inorganic phosphorus (IP) levels in the plasma and serum samples were elevated ≥ 1.5-fold when whole-blood centrifugation was delayed at room temperature for 48 hours. Furthermore, the IP levels in the plasma samples showed excellent assessment accuracy [area under the receiver-operating-characteristic curve (AUC) > 0.9] after a 48-hour delay in whole-blood separation, and high sensitivity (100%) and specificity (95%) at an optimal cutoff point. The IP levels in the serum samples also exhibited good assessment accuracy (AUC > 0.8), and high sensitivity (81%) and specificity (100%). The potassium (K(+)) levels were elevated 1.4-fold in the serum samples following a 48-hour delay in whole-blood separation. The K(+) levels showed excellent assessment accuracy (AUC > 0.9) following a 48-hour delay in whole-blood separation, and high sensitivity (95%) and specificity (91%) at an optimal cutoff point.

Conclusion: Our study showed that the IP and K(+) levels in the plasma or serum samples could be considered as putative indicators to determine whether whole-blood separation had been delayed for extended periods.

Keywords: clinical biochemistry; plasma; preanalytical variation; serum; stability.

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Figures

Figure 1
Figure 1
Concentration changes of five clinical-biochemistry analytes in (A) plasma and (B) serum samples when whole-blood separation was delayed at room temperature for 48 hours as compared to separation within 2 hours of whole-blood collection. * Indicates p < 0.05, calculated using a paired two-tailed t test. ALT = alanine aminotransferase; AST = aspartate aminotransferase; IP = inorganic phosphorous; K+ = potassium; LDH = lactate dehydrogenase.

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