Predictors of blood ionized calcium concentration in sick adult cattle

Abstract Background Data on the factors affecting blood ionized calcium concentration (ciCa2+) and diagnostic performance of serum total calcium concentration (ctCa) measurements to detect abnormal blood iCa2+ status are lacking in sick adult cattle. Objective Assess the association of ciCa2+ with venous blood pH, plasma concentrations of chloride (cCl), sodium (cNa), and potassium (cK), and ctCa, and total protein, albumin, and globulin concentrations in sick adult cattle. Animals Two‐hundred and sixty‐five adult cattle (≥1‐year‐old) with different diseases. Methods Prospective study. Whole blood pH, ciCa2+, cNa, cK, and cCl were measured using a blood gas and electrolyte analyzer, whereas ctCa, and total protein, and albumin concentrations were determined using an autoanalyzer. The relationship between ciCa2+ and venous blood pH, plasma cCl, cNa, cK, and ctCa, and total protein, albumin, and globulin concentrations was investigated. Sensitivity and specificity were calculated for ctCa for diagnosis of abnormal ciCa2+. Results Sensitivity of ctCa measurements to detect abnormal ciCa2+ was 66.0% whereas specificity of ctCa measurements was 72.3%. Serum total calcium concentration measurements accounted for 42% of adjusted blood ionized calcium (iCa2+ 7.40) concentration variance. Plasma cCl, and cK had explanatory power of ciCa2+ 7.40, accounting for an additional 21% and 9% of the variance, respectively. Conclusions and Clinical Importance Serum tCa measurements failed to accurately predict blood iCa2+ status in ill adult cattle. Serum tCa concentrations and plasma cCl were the strongest predictors of ciCa2+ in sick adult cattle.

Disorders of calcium (Ca 2+ ), especially hypocalcemia, are important problems in bovine medicine. 1,22][3] Calcium exists 3 different fractions in plasma or serum: protein-bound calcium, ionized calcium (iCa 2+ ), and complexed calcium. 1,4Ionized Ca 2+ is the free and biologically active form of Ca 2+ in the blood.Although blood iCa 2+ concentrations (ciCa 2+ ) can be measured using conventional blood gas analyzers in veterinary hospitals, such measurements may be unavailable and technically challenging especially in farm conditions.Therefore, clinicians continue to rely on measurement of serum total calcium (tCa) concentration (ctCa) to assess calcium status in adult cattle.
6][7] A recent study in critically ill calves indicated that plasma iCa 2+ concentration was associated with plasma tCa, venous blood pH, plasma chloride (cCl), serum magnesium, and plasma L-lactate (R 2 = 0.69) concentrations but not plasma albumin. 4Apart from tCa, pH has the next largest effect on the iCa 2+ concentration of calf plasma 8 and cow plasma, 9 with pH-corrective equations for plasma iCa 2+ concentration being similar to those used for human plasma. 4Metabolic acidosis usually develops in ill neonatal calves, but hypochloremic metabolic alkalosis is a more common clinicopathologic finding in sick adult cattle. 3fferent clinicopathologic findings between ill calves and sick adult cattle may affect blood iCa 2+ concentration in a different manner.
Therefore, the relative effect of blood pH and plasma cCl and other electrolytes on blood iCa 2+ needs to be accurately determined in sick adult cattle.In clinical settings, we commonly observed discrepancy between serum tCa and blood iCa 2+ results.For this reason, we hypothesized that tCa concentration in sick adult cattle was not a good predictor of blood iCa 2+ concentration.Our objectives were therefore to: (a) determine the relationship between serum tCa concentrations and ciCa 2+ in adult cattle affected by various diseases, (b) investigate the association between venous blood pH, plasma cCl, sodium (cNa), potassium (cK), and ctCa, and total protein, albumin, and globulin concentrations and ciCa 2+ in sick adult cattle and (c) determine the percentage of blood iCa 2+ fraction in serum tCa in adult cattle with different diseases.

| Animals
Two-hundred and sixty-five cattle (≥1-year-old) with different diseases referred to Firat University Teaching and Training Animal Hospital between January 2018 and April 2019 were recruited in this prospective study of a convenience sample.Sample size was calculated using R pwr package.Assuming a minimal coefficient of determination of the final multivariable model of 0.1 and a maximum of 10 different predictors, a minimal sample size of 193 samples was required (90% power, 5% type 1 error).Cattle with various systemic disorders were included in the study to obtain a wide range of venous blood pH and serum electrolyte, tCa, total protein, albumin, and globulin concentrations.Cattle that received calcium solutions within 48 hours before collecting blood samples were excluded from the study.The clinical diagnosis was obtained based on clinical diagnostic evaluation.When more than 1 disease was present, the main diagnosis was retained for that specific case for descriptive purposes.This study was approved by the Firat University Ethics Committee on Animal Experimentation (Permit number: 179).

| Blood samples
Blood samples were anaerobically collected from the left or right jugular vein of cattle into blood gas syringes (Pico 50, Radiometer Medical ApS, Brønshøj, Denmark) containing 80 IU dry, electrolyte-balanced heparin and plain tubes.The volume of the blood gas syringe was 0.5-2 mL, and approximately 1.5 mL of a blood sample was aspirated into a syringe in all cases except for 2 cases in which 0.5 mL of blood sample was collected because of challenges in restraining the animal.Whole blood pH, ciCa 2+ , cNa, cK, and cCl were measured within 10 minutes of blood collection using a Radiometer ABL80 analyzer.Venous blood pH was measured using a glass pH electrode, whereas ciCa 2+ , cNa, cK, and cCl were measured using direct ion selective electrode technology.Values for venous blood pH corrected for rectal temperature were not used in this study.The strong ion difference (SID 3 ) in mEq/L was calculated from the cNa, cK, and cCl: SID 3 = cNa + cK À cCl. 10 Hematocrit measurement of venous blood samples was performed once using capillary microhematocrit tubes after centrifugation for 5 minutes.Blood collected into plain tubes was allowed to clot and centrifuged at 1500Âg for 15 minutes.Serum was harvested and stored À20 C until analyzed within 7 days of collection.Serum total protein (biuret), albumin (bromocresol green), and tCa (arsenazo dye binding) concentrations were measured using a traditional bench-top autoanalyzer (SIEMENS Advia 1800, Siemens Healthcare GmbH, Erlangen, Germany).Serum globulin concentrations were calculated as the difference between serum total protein and albumin concentrations.The following equation was used to calculate the percentage of blood iCa 2+ in tCa, iCa 2+ percentage = [iCa 2+ (mmol/L) Â 100]/tCa (mmol/L), with mg/dL of serum tCa being multiplied by 0.2495 to convert into mmol/L.The intra-assay coefficient of variation (CV) of the Radiometer ABL80 analyzer for venous blood pH and ciCa 2+ , cNa, cK, and cCl measurements was determined from 8 measurements of the same sample during 1 day.The inter-assay CV of the autoanalyzer for serum total protein, albumin, and tCa measurements was calculated from 10 stored sample aliquots from the same animal that were measured on 10 consecutive days.

| Evaluation of serum total calcium concentration diagnostic performance
The diagnostic performance of ctCa was assessed for correctly predicting blood iCa 2+ status.The reference interval for ciCa 2+ was 1.06-1.26mmol/L. 2,11,12The reference range for ctCa concentration was 2.00-2.60 mmol/L. 13Cattle were categorized as hypocalcemic, normocalcemic, or hypercalcemic on the basis of ciCa 2+ and ctCa concentrations.Sensitivity (Se), specificity (Sp), negative likelihood ratio (NLR), and positive likelihood ratios (PLR) were calculated for ctCa for diagnosis of abnormal ciCa 2+ .Positive likelihood ratios >10 indicate that a positive test is good at diagnosis of abnormal ciCa 2+ , whereas NLR <0.1 indicates that a negative test is good at ruling out a diagnosis of abnormal ciCa 2+ . 14,15Diagnostic discordance was determined by use of the following equation: diagnostic discordance = (number of samples with diagnostic disagreement between measured ciCa 2+ and ctCa/total number of samples) x 100. 16Diagnostic performance of ctCa was calculated using MedCalc (software version 20.110, MedCalc, Ostend, Belgium).

| Statistical analysis
Analyses were performed using the R open access statistical software (R Core Team [2020].R: A language and environment for statistical computing.R Foundation for Statistical Computing, Vienna, Austria).
Two different types of analyses were performed based on a previous study 4 that proposed correcting ionized calcium to a pH of 7.40 using the equation: where pH m is the venous blood pH of the cow.The same approach therefore was taken for determining the association between clinical variables and iCa 2+ or iCa 2+ 7.40 to evaluate the association between clinical variables (breed, age, milking status, disease category, sex) using univariable linear regression analysis.Then, a specific modeling approach was used for determining the relationship between iCa 2+ and selected plasma or serum variables.The distribution of the different continuous predictors was visually assessed and tested using the Shapiro-Wilk test.Small deviations were observed from normality but were not significantly improved after either log transformation or Box-Cox transformation.For this reason, continuous variables were described as median, range and interquartile range as previously reported. 4After evaluating the risk of multicollinearity using Spearman rho analysis, when a pair of potential predictors had a correlation ≥0.7 only 1 of them was kept as a potential regressor.Univariable analyses then were performed to detect variables associated with ciCa 2+ or ciCa 2+ 7.40 .Predictors with univariable P values <.10 were kept for the multivariable regression analysis.
Two different models were built using ciCa or ciCa 7.40 as the dependent variable and other biochemical predictors using the general framework: where α are the coefficients associated with the covariate vector X of the different biochemical variables and ε the model residuals.
A manual backward stepwise strategy was used after including all significant variables found in univariable analysis and removing variables with P values ≥.05.The final model was the first model with all remaining significant variables (ie, P < .05).Specific attention was paid to the assumptions of the linear regression model (ie, homoscedasticity and normally-distributed residuals).The residual distribution was observed visually and considered adequate if it appeared to be normally distributed.Outliers were defined using QQplot, and standardized residuals were specifically investigated and their impact assessed after removing them from the dataset.This impact was judged negligible and therefore no specific model adjustment was performed.The fit of the models was assessed using adjusted R-squared.The relative importance of each individual independent variable in the model was assessed determining the partial R-squared of the variable as well as global R-squared of the model and variation inflation factor (VIF). Results were considered significant when P values were <.05.There were 240 female and 25 male cattle, ranging from 1 to 12 years in age (median, 3.6 years).Ninety-three animals were <3 years old (35%), 90 were between 3 and <5 years old (34%) and 82 cows were >5 years old (31%).A total of 184 of 240 (76.7%) cows were in lactation and 26 cows were ≤3 weeks postpartum.
The inter-assay CVs for the ctCa, and total protein, and albumin concentrations were 3.4%, 4.3%, and 5.2%, respectively.1).Differences also were observed based on the type of disease and sex with males having higher ciCa 2+ than females (Table 2).
Sensitivity, Sp, NLR, and PLR for ctCa measurements for the diagnosis of abnormal ciCa 2+ are presented in Table 3.To detect blood ionized hypocalcemia, Se of ctCa measurements with reference range of 2.00-2.60 mmol/L was 72.9% (95% confidential interval, 62.9-81.5).The diagnostic discordance between ctCa and ciCa 2+ measurements was 30.2%.Diagnostic discordance of ctCa measurements in cattle with blood ionized hypocalcemia was 27.1%.F I G U R E 2 Scatterplots of serum total calcium concentrations, serum albumin concentrations, venous blood pH, and plasma chloride concentrations with blood ionized calcium concentrations.Blood ionized calcium concentration is presented on y-axis.
T A B L E 3 Sensitivity, specificity, and positive and negative likelihood ratios of serum total calcium measurements for diagnosis of abnormal blood ionized calcium concentrations.
serum total protein concentrations, plasma cCl, plasma cK, and plasma cNa are presented in Figure 3.The correlations between ciCa 2+ and ctCa, plasma cCl, and cK were positive whereas, the correlations between ciCa 2+ and blood pH and plasma SID 3 were negative.The univariable analysis and multivariable analysis results of blood variable associations with ciCa 2+ and ciCa 2+ 7.40 are presented in Tables 4 and 5, respectively.The median percentage of blood iCa 2+ fraction in total serum calcium was 53.8%, ranging from 24.3% to 68.8%.The correlation between predictors showed that sodium and chloride, as well as globulin and total protein were highly correlated (r = 0.70 and 0.91, respectively).Therefore, only chloride and globulin were kept for regression analysis.The VIF analysis did not identify problems of multicollinearity (VIF < 5).

| DISCUSSION
The ability of ctCa measurements to accurately predict abnormal ciCa 2+ was assessed in adult cattle with a variety of clinical diseases.
Our findings indicated that ctCa measurements failed to accurately predict ciCa 2+ in ill adult cattle.Serum tCa concentration measurements accounted for only 42% of ciCa 2+ 7.40 variance.Plasma cCl, and cK were also predictive of ciCa 2+ 7.40 , accounting for an additional 21% and 9% of the variance, respectively.Serum total calcium concentration measurements usually have been used to assess calcium status in bovine practice although Se, Sp, PLR, NLR, and diagnostic discordance of ctCa measurements against ciCa 2+ measurements have not been previously calculated in cattle Data regarding the reference interval of ciCa 2+ in cattle is limited.
The reference interval of ciCa 2+ used in our study was taken from another study. 11In that study, 50 healthy Swedish red and white breed cows were used to determine a reference range for serum iCa 2+ concentration using a different calcium ion analyzer from that used in our study.Additional studies are necessary to determine the reference range of ciCa 2+ in healthy cattle populations using calcium ion analyzers available today.Different reference ranges of ctCa in cattle have been used in bovine clinics.The reference interval of ctCa used in our study was taken from a textbook. 13The same reference range for ctCa has been used in the clinic where the study was performed.Moreover, subclinical hypocalcemia in periparturient dairy cows was defined as ctCa <2.00 mmol/L in some studies. 18,19milarly, the lower value of the reference interval for ctCa was 2.00 mmol/L in our study.
Blood iCa 2+ concentration measurements were performed within 10 minutes of blood collection, but serum samples were stored at À20 C for ctCa measurements until analyzed within 7 days of collection.It was shown that whole blood samples may be stored at least 14 days at 4 C in plain or lithium heparin tubes with no changes in ctCa concentrations in cattle. 20Storage of serum at À80 C had no effect on ctCa for up to 12 months in cattle. 20The results of that study indicate that storage condition and timing of serum samples did not have an effect on ctCa measurements in our study.
Blood iCa 2+ concentration in critically ill neonatal calves was mainly dependent on plasma tCa concentration, plasma cCl, and venous blood pH. 4 Total calcium, serum cCl, and albumin concentrations were the most important variables affecting ciCa 2+ in dogs and cats with different clinical disorders where the effect of blood pH on ciCa 2+ was not evaluated. 17,21The multivariable regression model in our study provided valuable information on the relationships between selected variables and ciCa 2+ .Our results indicated that ctCa, plasma cCl, and cK were positively associated with ciCa 2+ in adult cattle affected by different diseases whereas a negative association was found between serum albumin concentration and ciCa 2+ .
Apart from ctCa, plasma cCl had the strongest association with ciCa 2+ in adult cattle in our study with different clinical disorders.An overlooked physicochemical phenomenon is that an increase in serum cCl directly increases the number of chloride ions bound to bovine albumin, 22 and the increased chloride binding displaces calcium from adjacent electrostatic binding sites, thereby increasing serum ionized Ca 2+ concentration. 23The positive association between blood cCl and ciCa 2+ in our study is consistent with previous findings obtained from dogs, cats, and neonatal calves, where ciCa 2+ increased as serum or plasma cCl increased. 4,17,21Chloride ions are bound in a salt-type manner to positively charged guanidium and ε-amino groups in The results of multivariable analysis of the association between selected blood, plasma, or serum analytes of blood ionized calcium (iCa 2+ ) concentration with blood ionized calcium concentration in 265 adult cattle with different clinical disorders.albumin despite the net negative charge of albumin at physiologic pH, 24 with 3 chloride ions being electrostatically bound to bovine albumin at physiologic pH. 22The effect of chloride binding to albumin on ciCa 2+ does not appear to be because of the effect of a decrease in plasma pH because of a decrease in SID because plasma cCl was positively correlated with plasma cNa (r = 0.70) and plasma cK (r = 0.55) in our study, indicating minimal change in plasma SID and therefore plasma pH because of large changes in plasma cCl.Similar to our study, the effect of chloride ions on ciCa 2+ was observed to be independent of its effect on pH in critically ill neonatal calves. 4In accordance with our results, diet-induced increases in plasma cCl by feeding an acidogenic ration in dairy cows during early lactation was accompanied by an increase in ciCa 2+ but no change ctCa. 25Moreover, in cows with parturient paresis, IV administration of CaCl 2 resulted in higher serum iCa 2+ concentrations than when the same amount calcium was administered as calcium borogluconate despite the fact that no difference was observed in ctCa. 12Taken together, these findings indicate that clinical evaluation of ctCa in sick adult cattle would benefit from simultaneous evaluation of blood chloride concentration, because of the direct effect of plasma cCl on iCa 2+ binding to albumin.
Current recommendations are that for clinical application, ciCa 2+ and blood pH should be measured simultaneously and within 15 minutes in samples kept at room temperature or 4 hours in samples collected in iced water, and ciCa 2+ reported as actual and adjusted to a pH of 7.40. 26Correction for pH compensates for preanalytical pH alterations associated with incorrect anaerobic handling of the sample and loss of CO 2 through the wall of the polypropylene syringe during storage.A decrease in pH most likely increases ciCa 2+ through pH-induced changes in net imidazole charge in specific histidine groups in albumin, resulting in a localized change in charge distribution that decreases iCa 2+ binding.In multivariable regression analysis, comparison of actual pH vs pH-corrected values for iCa 2+ indicated a pH-independent effect of chloride binding to albumin on ciCa 2+ in that changes in chloride concentration had the same proportional effect on ciCa 2+ whether ciCa 2+ was actual or corrected to a pH of 7.40.
Taken together, our results and that of a previous study in calves 4 indicate that clinically relevant changes in plasma cCl exert a greater effect on ciCa 2+ than clinically relevant changes in plasma pH.
A negative association between venous blood pH and ciCa 2+ was identified in critically ill neonatal calves. 4Moreover, venous blood pH had the second largest effect after plasma tCa concentrations on ciCa 2+ , and venous blood pH explained 19% of the variation of ciCa 2+ in those calves. 4Univariable regression in our study also indicated a negative association between venous blood pH and ciCa 2+ in adult cattle, but the association was weak in the multivariable regression model.Our results suggest that the effect of venous blood pH on ciCa 2+ in sick adult cattle is lower than that previously appreciated. 4e median venous blood pH in ill neonatal calves was 7.31, ranging from 6.9 to 7.54 in that study 4  in critically ill neonatal calves. 4In that study, the range for blood cK was 2.1-11.5 mmol/L (median, 4.6 mmol/L).Serum cK was positively associated with ciCa 2+ in dogs and cats, but the association was weak relative to that of tCa, Cl, and albumin 17,21  showed that serum albumin concentration had a significant but weak effect relative to ctCa, venous blood pH, and cCl on ciCa 2+ .In that study, serum albumin concentration was not a significant predictor of ciCa 2+ in a stepwise multivariable regression model. 4Serum albumin concentration had an influence on ciCa 2+ in dogs 17 and cats. 21Species differences in the number of calcium binding sites on albumin and net albumin charge could play a role in the observed differences.
The iCa 2+ percentage of ctCa has been investigated primarily in clinically healthy cattle and constituted 51% in 141 clinically healthy cows. 7In that study, calcium concentrations were measured within 2 hours after blood collection. 7The percentage of serum iCa 2+ was determined as 43% in clinically healthy cows in different stages of lactation where most samples were analyzed within 24 hours, but some measurements were performed within 4 days. 9Mean plasma iCa 2+ percentage was 57% at parturition and then decreased to 53% at peak lactation in clinically healthy Holstein and Jersey cows. 27Use of serum or plasma samples for the determination iCa 2+ and time from sample collection to analysis might have influenced the blood iCa 2+ percentage in the studies noted above.Blood iCa 2+ % in ctCa changed from 49.6% to 47.2% depending on dietary cation-anion difference at prepartum period in clinically healthy cows.In that study, blood iCa 2+ measurements were made within 30 minutes of sampling. 25In another study, blood iCa 2+ % in ctCa was approximately 52% at prepartum day 3 and then increased to approximately 54% at parturition in cows fed with a dietary cation-anion difference of À7 where ciCa 2+ was measured within 1 hour of sample collection. 28The range of blood iCa 2+ percentage was 35 to 61% in 950 critically ill neonatal calves. 4Blood iCa 2+ concentration and ctCa measurement methods in the previous 3 studies were similar to those of our study.In our study, the range of blood iCa 2+ percentage in sick adult cattle (24%-69%) was wider than that of critically ill neonatal calves. 4Moreover, the median ciCa 2+ of sick adult cattle was higher than that of sick neonatal calves (54% vs 47%).It has been suggested that approximately 50% of calcium in bovine blood exists in the ionized form.This assumption has been based on previous studies performed on clinically healthy cattle.In our study, blood iCa 2+ percentages in ctCa of 100 of 265 cattle were >55%.The results of our study indicated that the assumption noted above might not be valid for sick cattle.Moreover, we observed lower median iCa 2+ % in ctCa in cattle with gastrointestinal disorders than in cattle with other system diseases but its median value still was >50% in these cattle.
A potential limitation of our study was the failure to measure plasma biochemical variables that have been associated in other studies with ciCa 2+ .Serum nonesterified fatty acids and beta-hydroxybutyric acid concentrations are negatively correlated with iCa 2+ % in clinically healthy periparturient dairy cows. 29Serum magnesium and plasma L-lactate concentrations are associated with ciCa 2+ in critically ill neonatal calves. 4Serum creatinine, urea nitrogen, cholesterol, and triglyceride concentrations are associated with ciCa 2+ in dogs and cats. 17,21It is well known that calcium metabolism disorders are an important problem during the postpartum period.In our study, 26 out of 240 cows were within 3 weeks postpartum.This limited number of early lactating cows is partly associated with the selection criteria which excluded cows that previously received calcium treatment to limit interference of treatment with study findings.Therefore, additional studies appear indicated, especially in periparturient dairy cows, to investigate the association of analytes such as nonesterified fatty acids, beta-hydroxybutyric acid, phosphorus, and magnesium on ciCa 2+ .
In conclusion, ctCa measurements failed to accurately predict ciCa 2+ status in ill adult cattle.The ciCa 2+ had a positive relationship with ctCa, plasma cCl and cK, and with ctCa and plasma cCl, accounting for 63% of the variation on ciCa 2+ .Our results showed that venous blood pH and serum albumin concentration are not significant predictors of ciCa 2+ in sick adult cattle.Accurate clinical evaluation of calcium status using ctCa measurements in adult cattle with clinical disorders would benefit from simultaneous evaluation of cCl and possibly cK because hypochloremia, hypokalemia, and hypocalcemia are common concurrent electrolyte disorders in sick adult cattle, particularly cattle with primary gastrointestinal tract diseases.

ACKNOWLEDGMENT
No funding was received for this study.

3. 5 |
Relationships among venous blood pH, chloride, sodium, potassium, serum total calcium, albumin, globulin, and blood ionized calcium The individual relationships between ciCa 2+ and ctCa, and serum albumin concentrations, venous blood pH, and plasma cCl are shown in Figure 2. Correlations among ciCa 2+ , venous blood pH, ctCa, serum albumin concentrations, serum globulin concentrations, F I G U R E 1 The distribution of blood ionized calcium (iCa 2+ ) concentration by age category in sick adult cattle.
The range, median, and interquartile range of venous blood pH, ionized calcium, plasma chloride, sodium, potassium, serum total calcium, total protein, albumin, and globulin concentrations in 265 sick adult cattle.
17sults of univariable analyses of the association of selected blood, plasma, or serum analytes with blood ionized calcium (iCa 2+ ) concentration in 265 adult cattle with different diseases.differentclinicaldisorders.In our study, the diagnostic discordance between ctCa and ciCa 2+ was 30.2%, indicating that ctCa measurements did not correctly predict iCa 2+ status in at least 30.2% of cattle with different disorders.Similarly, diagnostic discordance of ctCa in dogs previously was determined as 27.0%16or 18.5%.In the latter study, 80% of dogs had normal ciCa 2+ concentrations.17Inour study, the diagnostic discordance between ctCa measurements and Abbreviations: CI, confidence interval; iCa 2+ , ionized calcium; tCa, serum total calcium.with tle.From a clinical view, the use of ctCa measurements instead of ciCa 2+ determination may cause misclassification of calcium status in cattle with clinical disorders.Thus, ciCa 2+ measurements should be performed whenever available.
whereas the median of venous blood pH in sick adult cattle was 7.48, ranging from 7.16 to 7.65 in our study.Moreover, in our study, venous blood pH results of 180 of 265 cattle were >7.46.Higher venous blood pH of sick adult cattle might be an explanation for this finding.Plasma cK was positively associated with ciCa 2+ in sick adult cattle in our study, accounting for 9% of the variation in ciCa 2+ .The range for blood cK was 1.8-5.4mmol/L (median, 3.6 mmol/L) in adult cattle.Plasma cK was not significantly associated with ciCa 2+ Differences in blood cK may account for the different associations between plasma cK and ciCa 2+ between ill neonatal and sick adult cattle.
In our study, serum albumin concentration was significantly associated with ciCa 2+ , but serum albumin concentration accounted for only 1% of the variation in ciCa 2+ of adult cattle with different clinical disorders.This finding indicates that clinical evaluation of ctCa in sick adult cattle does not require simultaneous evaluation of serum albumin concentration.In critically ill calves, univariate regression analyses Sébastien Buczinski serves as Consulting Editor for Experimental Design and Statistics for the Journal of Veterinary Internal Medicine.He was not involved in review of this manuscript.No other authors declare a conflict of interest.OFF-LABEL ANTIMICROBIAL DECLARATION Authors declare no off-label use of antimicrobials.INSTITUTIONAL ANIMAL CARE AND USE COMMITTEE (IACUC) OR OTHER APPROVAL DECLARATION Approved by the Firat University Ethics Committee on Animal Experimentation, Protocol Number: 2019/123, Decision Number: 179.