Chu K K, Cohen N D, Stanley S D, Wang N
Department of Statistics, College of Science, Texas A&M University, College Station 77843-4475, USA.
Am J Vet Res. 2001 Sep;62(9):1349-53. doi: 10.2460/ajvr.2001.62.1349.
To estimate the probability of concurrently exceeding thresholds for plasma concentration of furosemide and urine specific gravity after IV administration of furosemide in horses.
12 mature healthy Thoroughbred (n = 6) or Quarter Horse (6) mares.
Venous blood was collected from each horse prior to and 0.25, 0.5, 0.75, 1, 2, 3, 4, 4.5, 5, and 6 hours after IV administration of 250 mg (first experiment) or 500 mg (second experiment) of furosemide. Urine was collected hourly between 1 and 6 hours after administration of furosemide at both doses. Concentrations of furosemide were determined by use of an ELISA. Concentration of furosemide and urine specific gravity was modeled as a function of time, accounting for inter- and intrahorse variabilities. On the basis of pharmacokinetic and specific gravity data, the probability of exceeding a concentration of 100 ng of furosemide/ml as a function of time was determined, using a semiparametric smooth functional averaging method. A bootstrap approach was used to assess the inherent variation in this estimated probability.
The estimated probability of exceeding the threshold of 100 ng of furosemide/ml and urine specific gravity < 1.012 was approximately 0% between 4.0 and 5.5 hours after IV administration of 250 mg of furosemide/horse, and ranged from 0 to 1% between 4 and 5.5 hours after IV administration of 500 mg of furosemide/horse. The probability of a horse being falsely identified as in violation of regulatory concentrations was inversely associated with time.
Coupling plasma furosemide concentration with urine specific gravity testing will greatly reduce the chance that some horses are misclassified as being in violation of regulatory concentrations.
评估静脉注射速尿后,马血浆中速尿浓度和尿比重同时超过阈值的概率。
12匹成熟健康的纯种马(n = 6)或夸特马(6匹)母马。
在每匹马静脉注射250毫克(第一次实验)或500毫克(第二次实验)速尿之前以及注射后0.25、0.5、0.75、1、2、3、4、4.5、5和6小时采集静脉血。在两种剂量的速尿给药后1至6小时内,每小时收集尿液。使用酶联免疫吸附测定法测定速尿浓度。将速尿浓度和尿比重建模为时间的函数,同时考虑马之间和马体内的变异性。根据药代动力学和比重数据,采用半参数平滑函数平均法确定超过100纳克速尿/毫升浓度随时间变化的概率。采用自助法评估该估计概率的固有变异性。
静脉注射250毫克速尿/匹马后4.0至5.5小时内,超过100纳克速尿/毫升阈值且尿比重<1.012的估计概率约为0%;静脉注射500毫克速尿/匹马后4至5.5小时内,该概率范围为0至1%。马匹被错误判定违反监管浓度的概率与时间呈负相关。
将血浆速尿浓度与尿比重检测相结合,将大大降低一些马匹被误判违反监管浓度的可能性。