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1.
Vet Rec ; 152(4): 105-8, 2003 Jan 25.
Artigo em Inglês | MEDLINE | ID: mdl-12572939

RESUMO

The clinical efficacy of a recombinant feline interferon (IFN) (type omega) was evaluated under field conditions for the treatment of dogs with parvoviral enteritis. In this multicentric, double-blind, placebo-controlled trial, 94 dogs from one to 28 months old were randomly assigned to two groups which were treated intravenously either with IFN (2.5 million units/kg) or placebo once a day for three consecutive days, and monitored for clinical signs and mortality for 10 days. Each dog received individual supportive treatment The data from 92 interpretable cases (43 IFN-treated and 49 placebo) showed that the clinical signs of the IFN-treated animals improved significantly in comparison with the control animals, and that there were only three deaths in the IFN group compared with 14 deaths in the placebo group (P = 0.0096) corresponding to a 4.4-fold reduction. Alternative analyses of the data taking into account the prior vaccination status of the dogs against canine parvovirus suggested that the IFN therapy resulted in a 6.4-fold reduction in mortality (P = 0.044) in the unvaccinated cohort, a significant reduction when compared with the vaccinated cohort.


Assuntos
Doenças do Cão/tratamento farmacológico , Enterite/tratamento farmacológico , Enterite/veterinária , Interferon Tipo I/uso terapêutico , Infecções por Parvoviridae/tratamento farmacológico , Infecções por Parvoviridae/veterinária , Parvovirus Canino , Animais , Temperatura Corporal , Doenças do Cão/imunologia , Doenças do Cão/virologia , Cães , Enterite/imunologia , Enterite/virologia , Feminino , Imunoterapia , Interferon Tipo I/efeitos adversos , Interferon Tipo I/imunologia , Masculino , Infecções por Parvoviridae/imunologia , Taxa de Sobrevida , Fatores de Tempo , Resultado do Tratamento , Vacinas Virais/imunologia
2.
J Small Anim Pract ; 42(10): 491-4, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11688524

RESUMO

The clinical application of a new method for using the insect growth regulator, pyriproxyfen, for controlling flea populations in cat-owning homes is evaluated for the first time. In a multicentric, controlled and randomised trial, 107 flea-infested cats were treated with a minimum dose of 10 mg/kg bodyweight pyriproxyfen as a 10 per cent spot-on application on two occasions, with a three-month interval between doses. For comparison, 99 cats received lufenuron suspension orally, once a month, for six months. Flea counts decreased significantly over time in each group and were significantly lower in the pyriproxyfen group than in cats treated with the reference product. The percentage of 'zero-flea' cats increased from 49 per cent on day 30 to 88 per cent on day 180 in the pyriproxyfen group and from 30 to 71 per cent in the lufenuron group at the same time points (P<0.05). Appropriately timed topical applications of pyriproxyfen, therefore, offer a method of flea control in the domestic environment.


Assuntos
Doenças do Gato/prevenção & controle , Ectoparasitoses/veterinária , Inseticidas/administração & dosagem , Piridinas/administração & dosagem , Sifonápteros , Administração Cutânea , Administração Oral , Animais , Benzamidas/administração & dosagem , Gatos , Esquema de Medicação , Ectoparasitoses/prevenção & controle , Feminino , França , Alemanha , Masculino , Resultado do Tratamento
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