Efficacy and safety of topical administration of selamectin for treatment of ear mite infestation in rabbits

Tom L. McTier Pfizer Animal Health, Veterinary Medicine Research and Development, Groton, CT 30604.

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J. Alexander Hair Nu Era Farms, Stillwater, OK 74071.

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Douglas J. Walstrom Pfizer Animal Health, Lee's Summit, MO 64081.
Present address is 204 SE Williamsburg Dr, Blue Springs, MO 64014.

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Leland Thompson Pfizer Animal Health, Lee's Summit, MO 64081.
Present address is 1205 Vintage Club Dr, Duluth, GA 30097.

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Abstract

Objective—To evaluate the efficacy and safety of topical administration of selamectin in rabbits naturally infested with Psoroptes cuniculi.

Design—Randomized controlled trial.

Animals—48 mixed-breed domestic rabbits with active P cuniculi mite populations and clinical ear lesions.

Procedures—Rabbits were randomly allocated to 1 of 6 treatment groups. On day 0, rabbits in groups 1 and 2 were given vehicle, rabbits in groups 3 and 4 were given selamectin at a dose of 6 mg/kg (2.7 mg/lb), and rabbits in groups 5 and 6 were given selamectin at a dose of 18 mg/kg (8.2 mg/lb). On day 28, rabbits in groups 2, 4, and 6 were given a second dose of vehicle or selamectin. Otoscopic examinations were performed and ear lesion size was measured weekly for 8 weeks. Quantitative viable mite counts were performed on day 56.

Results—On days 7 through 56, lesion sizes for all selamectin-treated groups were significantly lower than sizes for control groups; there were no significant differences in lesion sizes among selamectintreated groups. All rabbits in the 2 control groups had viable adult P cuniculi mites for the duration of the study, as determined by otoscopic examination, whereas all rabbits in the 4 selamectin-treated groups were free from P cuniculi mites on days 7 through 56. No adverse reactions associated with selamectin treatment were observed.

Conclusions and Clinical Relevance—Results suggest that topical application of selamectin at a dose of 6 or 18 mg/kg can completely eliminate mites from rabbits naturally infested with P cuniculi. (J Am Vet Med Assoc 2003;223:322–324)

Abstract

Objective—To evaluate the efficacy and safety of topical administration of selamectin in rabbits naturally infested with Psoroptes cuniculi.

Design—Randomized controlled trial.

Animals—48 mixed-breed domestic rabbits with active P cuniculi mite populations and clinical ear lesions.

Procedures—Rabbits were randomly allocated to 1 of 6 treatment groups. On day 0, rabbits in groups 1 and 2 were given vehicle, rabbits in groups 3 and 4 were given selamectin at a dose of 6 mg/kg (2.7 mg/lb), and rabbits in groups 5 and 6 were given selamectin at a dose of 18 mg/kg (8.2 mg/lb). On day 28, rabbits in groups 2, 4, and 6 were given a second dose of vehicle or selamectin. Otoscopic examinations were performed and ear lesion size was measured weekly for 8 weeks. Quantitative viable mite counts were performed on day 56.

Results—On days 7 through 56, lesion sizes for all selamectin-treated groups were significantly lower than sizes for control groups; there were no significant differences in lesion sizes among selamectintreated groups. All rabbits in the 2 control groups had viable adult P cuniculi mites for the duration of the study, as determined by otoscopic examination, whereas all rabbits in the 4 selamectin-treated groups were free from P cuniculi mites on days 7 through 56. No adverse reactions associated with selamectin treatment were observed.

Conclusions and Clinical Relevance—Results suggest that topical application of selamectin at a dose of 6 or 18 mg/kg can completely eliminate mites from rabbits naturally infested with P cuniculi. (J Am Vet Med Assoc 2003;223:322–324)

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