Reason for performing study: Using an adjustable heart bar shoe model of foot pain, the objective of this study was to test the hypothesis that the combined use of phenylbutazone (PBZ) and flunixin meglumine (FM) would prove more efficacious in alleviating lameness than either drug alone. Materials and methods: One hour after induction of lameness at weekly intervals, 8 healthy adult Thoroughbred horses randomly underwent one of 4 i.v. treatments: saline (SAL) placebo (1ml/45kg bwt), PBZ (4.4mg/kg bwt), FM (1.1mg/kg bwt) or PBZ+FM (at the same dosages as given individually). Heart rate (HR) and lameness score (LS) responses were assessed in a blinded manner every 20min for 5h after lameness induction and then hourly for 12h after treatment. Jugular venous blood samples were obtained at -1, 0, 0.05, 1, 2, 4, 6, 8, 10 and 12h and subsequently analysed for drug concentrations. Repeated measures ANOVA and post hoc Tukey's test were used to identify analgesic effects at a significance level of P<0.05. Results: Heart rate was lower in all nonsteroidal anti-inflammatory drug (NSAID)-treated trials from 2h to 10h post treatment (P<0.05). Analgesic effects of FM and PBZ+FM, as evidenced by decreases in HR, lasted for 12h post treatment (P<0.05). Lameness score decreased earlier in PBZ and PBZ+FM trials than in FM trials (P<0.05) and the analgesic effect on LS lasted for 12h post treatment for all NSAID trials (P<0.05). Peak PBZ plasma concentration was 73.7±6.0 and 77.9±5.5μg/ml. Peak FM concentration was 12.0±0.8 and 13.7±1.0μg/ml Conclusions: It was concluded that the combination of PBZ+FM was not more effective than either PBZ or FM alone. These data do not support the hypothesis that the combination is more efficacious at these dosages than either drug alone in this model of acute foot pain.
- Nonsteroidal anti-inflammatory drug
- Plasma concentration
ASJC Scopus subject areas