Evaluation of Levetiracetam as Adjunctive Treatment for Refractory Canine Epilepsy: A Randomized, Placebo-Controlled, Crossover Trial

被引:54
|
作者
Munana, K. R. [1 ]
Thomas, W. B. [2 ]
Inzana, K. D. [3 ]
Nettifee-Osborne, J. A. [1 ]
McLucas, K. J. [2 ]
Olby, N. J. [1 ]
Mariani, C. J. [1 ]
Early, P. J. [1 ]
机构
[1] N Carolina State Univ, Coll Vet Med, Dept Clin Sci, Raleigh, NC 27607 USA
[2] Univ Tennessee, Coll Vet Med, Dept Small Anim Clin Sci, Knoxville, TN USA
[3] Virginia Tech, Dept Small Anim Clin Sci, Virginia Maryland Reg Coll Vet Med, Blacksburg, VA USA
关键词
Clinical pharmacology; CNS disorders; Dog; Epilepsy; Neurology; Seizures; ANTIEPILEPTIC DRUGS; PHARMACOKINETICS; DOGS; EFFICACY; TOLERABILITY; SEIZURES; SAFETY; SINGLE;
D O I
10.1111/j.1939-1676.2011.00866.x
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: There is little evidence-based information available to guide treatment of refractory epilepsy in dogs. The antiepileptic drug levetiracetam (LEV) is administered to dogs, although its safety and efficacy are unknown. Objective: To evaluate the safety and efficacy of LEV as adjunctive therapy for refractory epilepsy in dogs. Animals: Thirty-four client-owned dogs with idiopathic epilepsy. Methods: Randomized, blinded trial involving dogs resistant to phenobarbital and bromide. Dogs received LEV (20 mg/kg PO q8h) or placebo for 16 weeks, and after a 4-week washout were crossed over to the alternate treatment for 16 weeks. Owners kept records on seizure frequency and adverse events. Hemogram, chemistry profile, urinalysis, and serum antiepileptic drug concentrations were evaluated at established intervals. Results: Twenty-two (65%) dogs completed the study. Weekly seizure frequency during the 1st treatment period decreased significantly during LEV administration relative to baseline (1.9 +/- 1.9 to 1.1 +/- 1.3, P = .015). The reduction in seizures with LEV was not significant when compared to placebo (1.1 +/- 1.3 versus 1.5 +/- 1.7, P = .310). The most common adverse event was ataxia, with no difference in incidence between LEV and placebo (45 versus 18%, P = .090). No changes in laboratory parameters were identified and owners reported an improved quality of life (QOL) with LEV compared to placebo (QOL score 32.7 +/- 4.3 versus 29.4 +/- 4.5, P = .028). Conclusions and Clinical Importance: Adjunctive treatment with LEV appears safe in epileptic dogs. Efficacy of LEV over placebo was not demonstrated, although the power of the study was limited. Further evaluation of LEV as treatment for epilepsy in dogs is warranted.
引用
收藏
页码:341 / 348
页数:8
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