TY - JOUR
T1 - Voltage changes in the lithium dilution cardiac output sensor after exposure to blood from horses given xylazine
AU - Ambrisko, T. D.
AU - Moens, Y.
N1 - Funding Information:
This work was supported by the Department for Companion Animals and Horses, University of Veterinary Medicine, Vienna, Austria, and the LiDCO Ltd, London, UK (donated LiDCO sensors).
PY - 2014/2
Y1 - 2014/2
N2 - BackgroundIn a previous in vitro study using saline medium, the authors showed that certain drugs changed the voltages of lithium dilution cardiac output (LiDCO) sensors and also influenced their accuracy in measuring lithium concentrations. These two parameters correlated and so we examined whether such drug-sensor interaction exists when LiDCO sensor was exposed to xylazine in blood.MethodsFive healthy adult warm-blood horses were injected with 0.5 mg kg-1 xylazine i.v. Physiological saline solution and venous blood were consecutively sampled through the same LiDCO sensor at 60, 45, 30, 15, and 0 min before and then 5, 15, 30, 45, and 60 min after xylazine injection. Sensor voltages were recorded and the differences between saline- and blood-exposed sensor voltages were compared at each time point.ResultsSaline-exposed sensor voltages continuously increased in a non-linear pattern during the experiment. Blood-exposed sensor voltages also increased in a similar pattern, but it was interrupted by an abrupt increase in voltage after xylazine injection. The differences between saline- and blood-exposed sensor voltages were 7 (6.1-8) mV [median (range)] before xylazine but decreased significantly at 5 and 15 min after xylazine treatment. The highest drug-induced voltage change was 3.4 (1.6-7) mV.ConclusionsThis study showed that exposure of a LiDCO sensor to blood after a single clinically relevant dose of xylazine in horses changed the voltages of the sensors for 15 min. Comparison of saline- and blood-exposed sensor voltages could become a tool to detect drug-sensor interactions.
AB - BackgroundIn a previous in vitro study using saline medium, the authors showed that certain drugs changed the voltages of lithium dilution cardiac output (LiDCO) sensors and also influenced their accuracy in measuring lithium concentrations. These two parameters correlated and so we examined whether such drug-sensor interaction exists when LiDCO sensor was exposed to xylazine in blood.MethodsFive healthy adult warm-blood horses were injected with 0.5 mg kg-1 xylazine i.v. Physiological saline solution and venous blood were consecutively sampled through the same LiDCO sensor at 60, 45, 30, 15, and 0 min before and then 5, 15, 30, 45, and 60 min after xylazine injection. Sensor voltages were recorded and the differences between saline- and blood-exposed sensor voltages were compared at each time point.ResultsSaline-exposed sensor voltages continuously increased in a non-linear pattern during the experiment. Blood-exposed sensor voltages also increased in a similar pattern, but it was interrupted by an abrupt increase in voltage after xylazine injection. The differences between saline- and blood-exposed sensor voltages were 7 (6.1-8) mV [median (range)] before xylazine but decreased significantly at 5 and 15 min after xylazine treatment. The highest drug-induced voltage change was 3.4 (1.6-7) mV.ConclusionsThis study showed that exposure of a LiDCO sensor to blood after a single clinically relevant dose of xylazine in horses changed the voltages of the sensors for 15 min. Comparison of saline- and blood-exposed sensor voltages could become a tool to detect drug-sensor interactions.
KW - anaesthesia, veterinary
KW - analgesic techniques, infusion
KW - horses
KW - measurement techniques, cardiac output
UR - http://www.scopus.com/inward/record.url?scp=84892756817&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84892756817&partnerID=8YFLogxK
U2 - 10.1093/bja/aet298
DO - 10.1093/bja/aet298
M3 - Article
C2 - 23996857
AN - SCOPUS:84892756817
SN - 0007-0912
VL - 112
SP - 367
EP - 369
JO - British Journal of Anaesthesia
JF - British Journal of Anaesthesia
IS - 2
ER -