Panagiotis Dimitrios Katsoulos; Labrini Vasileiou Athanasiou; Anna Dedousi; Zoe Polizopoulou
Volume 13, Issue 4 , December 2022, , Pages 475-480
Abstract
Despite being important, there are no equations for prediction of ionized calcium (iCa) in sheep and cattle. The objectives of this study were i) to create equations for the calculation of serum iCa concentration based on the serum concentrations of total calcium (tCa), albumin (Alb) and total proteins ...
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Despite being important, there are no equations for prediction of ionized calcium (iCa) in sheep and cattle. The objectives of this study were i) to create equations for the calculation of serum iCa concentration based on the serum concentrations of total calcium (tCa), albumin (Alb) and total proteins (TP) and ii) to investigate whether predicted serum iCa values are beneficial in clinical practice. Serum samples from 30 sheep and 30 dairy cattle were used. Serum tCa was determined colorimetrically, while serum iCa was determined with an ion selective electrode method. Serum Alb and TP concentration were determined using bromo-cresol green and biuret methods, respectively. Ionized calcium was also calculated based on serum tCa, using regression analysis, and with two equations based on Alb and TP concentration. Bland–Altman plots were plotted to evaluate the agreement between measured and predicted iCa; Passing and Bablok (P - B) regression analysis was used to assess their agreement. The initial equations were corrected using the P - B generated equation and Bland – Altman plots were run to evaluate the level of agreement between measured and predicted iCa using the final equations. Six equations were finally created for cattle and 6 for sheep. The total bias exceeded 10.00% in all of them indicating that they are clinically unacceptable for iCa prediction especially when the predicted result is very close to the cut-off point of < 1.00 mmol L-1. So, it could be suggested that, when necessary, iCa concentration should be directly determined.
Clinical Pathology
Labrini Vasileiou Athanasiou; Zoe Polizopoulou; Maria Rafaela Kalafati; George Ntararas; Vasileios Kontos
Volume 7, Issue 4 , December 2016, , Pages 281-285
Abstract
To assess the effects of pre-analytical handling (storage time and temperature) on selected hematological parameters, whole blood samples were collected in EDTA coated tubes from each of 30 clinically normal male adult beagle dogs. Each sample was separated in 2 aliquots, of which one was stored in ambient ...
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To assess the effects of pre-analytical handling (storage time and temperature) on selected hematological parameters, whole blood samples were collected in EDTA coated tubes from each of 30 clinically normal male adult beagle dogs. Each sample was separated in 2 aliquots, of which one was stored in ambient temperature (25 ˚C) and the other one was refrigerated (2 to 4 ˚C). Complete blood counts were performed in 1, 2.5, 5, 12, 24, 36 and 60 hr post-sampling for each aliquot of every sample using a flow cytometer. Packed cell volume values remained stable in the samples kept in room temperature (RT), whereas a significant increase was noted in the refrigerated ones 24 hr post-sampling. Statistically significant increases in red blood cell counts were noted after 24hr in the samples stored in 2 to 4 ˚C and after 12 hr in those kept in RT. No significant changes were observed in haemoglobin concentration. A significant decrease was evident only 60 hr post-sampling for the white blood cells kept in RT, but not for those kept in 2 to 4 ˚C. Platelet counts significantly decreased after 24 hr in the refrigerated aliquots and after 5 hr in those kept in RT. The results of this study indicate that storage of blood samples for up to 24 hr in 2 to 4 ˚C is associated with the least artifactual changes.