Evaluating the Bias of Two Point-of-Care Glucometers for Calves and Ewes: Awareness for Ruminant Practitioners

Author:

Flynn Ryan1,Cremerius Haley1,Ebner Lisa2,Mulon Pierre-Yves1ORCID,Garcia Jessica1,Bennett Kailee1,Gerbert Jessica2,Harvill Lainey1,Escher Olivia1,Cantrell Channing1,Soto-Gonzalez Windy1,Rahn Rebecca R.1,Olivarez Jeff D.3,Yuan Lingnan3,Mochel Jonathan P.4ORCID,Kreuder Amanda J.5,Smith Joe13

Affiliation:

1. Large Animal Clinical Sciences, University of Tennessee College of Veterinary Medicine, Knoxville, TN 37996, USA

2. Richard A. Gillespie College of Veterinary Medicine, Lincoln Memorial University, Harrogate, TN 37752, USA

3. Biomedical Sciences, Iowa State University College of Veterinary Medicine, Ames, IA 50011, USA

4. Department of Pathology, University of Georgia College of Veterinary Medicine, Athens, GA 30602, USA

5. Veterinary Microbiology and Preventive Medicine, Iowa State University College of Veterinary Medicine, Ames, IA 50011, USA

Abstract

(1) Background: Multiple point-of-care (POC) glucometers are in use in veterinary medicine, but few are compared to each other. This leaves the potential for clinicians to be unaware of the effect of bias when comparing results from different POC glucometers. (2) Methods: Samples from healthy calves and ewes were simultaneously compared with two POC veterinary glucometers, the Precision Xtra and the AlphaTrak2, under both the “canine” and “feline” settings. The results of each sample were statistically analyzed with linear regression and Bland–Altman analysis. (3) Results: 170 samples from healthy calves and 108 samples from healthy ewes were available for comparison. Calves: The AT2 consistently overestimated blood glucose concentrations when compared to the PX device with the calves. Correlationt with the PX was r = 0.8496 (canine setting) and r = 0.8861 (feline setting). Both the canine and feline settings demonstrated a consistent bias (41.11 and 33.64 mg/dL, respectively). Ewes: The AT2 consistently overestimated blood glucose concentrations when compared to the PX device with the ewes. Correlation with the PX was R = 0.4710 (canine setting) and R = 0.7269 (feline setting). Both the canine and feline settings demonstrated a consistent bias (21.23 and 14.54 mg/dL, respectively). (4) Clinicians should be aware of the potential for consistent bias when evaluating calf and sheep blood glucose concentrations as the AT2 device, at both settings, overestimated blood glucose compared to the previously validated PX. This reliability appears to change when the values are farther from the normal ranges, which should be considered when making clinical decisions based on data from these devices.

Funder

Large Animal Clinical Sciences

Publisher

MDPI AG

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