Peer-reviewed veterinary case report
Spinosad chewable tablets to treat and control fleas on dogs in Europe
By Wolken, S et al.·Published in The Veterinary record·2012·University of Veterinary Medicine Hannover, Germany·View original on PubMed →
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Original publication title: Evaluation of spinosad for the oral treatment and control of flea infestations on dogs in Europe.
- Species:
- dog
Plain-English summary
A group of dogs in Europe with flea infestations were treated with a new chewable tablet called spinosad to see how well it worked compared to an older treatment. The results showed that spinosad was very effective, reducing flea numbers by about 97% within the first month and up to 99.6% after three months. In comparison, the older treatment, selamectin, was less effective, with flea reductions of only 88.5% to 91% in the same timeframe. This suggests that spinosad is a strong option for controlling fleas in dogs.
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Abstract
The novel ectoparasiticide spinosad is a naturally occurring mixture of spinosyns A and D formed during a fermentation process. The spinosyns are tetracyclic macrolides with a unique ring system. Their mode of action differs from that of other commercially available insecticides. Laboratory and field trials were conducted to evaluate the use of spinosad in a chewable tablet at a dose range of 45 to 70 mg/kg for the treatment and control of flea infestations on dogs in Europe. Laboratory studies with artificially infested dogs confirmed persistent activity against Ctenocephalides felis of higher than 99 per cent at three weeks post-treatment with values of 96.5 to 97.8 per cent at four weeks. Two multicentric field trials with naturally infected client-owned animals in five European countries used selamectin as comparator. Monthly doses were given during the summer when many homes were heavily infested. Households with spinosad-treated dogs showed cumulative benefits with flea burdens reduced by about 97 per cent at 14 and 30 days and by 99.6 per cent at 60 and 90 days. Corresponding figures for selamectin were significantly lower (P<0.05) at all time points: between 88.5 and 91 per cent at 14 and 30 days, then 97.8 and 98.2 per cent at 60 and 90 days. Thus, the performance of spinosad compared favourably with that of the established reference product.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/22141112/