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1.
J Vet Intern Med ; 31(3): 901-906, 2017 05.
Artigo em Inglês | MEDLINE | ID: mdl-28421633

RESUMO

BACKGROUND: There is conflicting data regarding the efficacy of tulathromycin for the treatment of foals with bronchopneumonia. HYPOTHESES: Tulathromycin is effective for the treatment of bronchopneumonia in foals and noninferior to the combination of azithromycin and rifampin. ANIMALS: A total of 240 foals on a farm endemic for infections caused by Rhodococcus equi. METHODS: In a controlled, randomized, and double-blinded clinical trial, foals with ultrasonographic pulmonary lesions (abscess score 10-15 cm) were allocated to 3 groups: 1-tulathromycin IM q 7 days (n = 80); 2-azithromycin-rifampin, orally q24h (n = 80); or 3-untreated controls (n = 80). Physical examination and thoracic ultrasonography were performed by individuals unaware of treatment group assignment. Foals that worsened were considered treatment failures and removed from the study. RESULTS: The proportion of foals that recovered was significantly higher for foals treated with tulathromycin (70 of 79) or azithromycin-rifampin (76 of 80) compared to that of control foals (22 of 80). The difference in the percentage of efficacy of azithromycin-rifampin versus tulathromycin was 6.4% (90% CI = -0.72-13.5%). Given that the confidence interval crossed the predetermined noninferiority limit of 10%, the null hypothesis that the response rate in the azithromycin-rifampin group is superior to that of the tulathromycin group could not be rejected. Resolution of ultrasonographic lesions occurred faster in foals treated with azithromycin-rifampin than in foals treated with tulathromycin. CONCLUSION AND CLINICAL IMPORTANCE: Tulathromycin was effective for the treatment of bronchopneumonia in foals at this farm but not as effective as the combination of azithromycin-rifampin.


Assuntos
Antibacterianos/uso terapêutico , Broncopneumonia/veterinária , Dissacarídeos/uso terapêutico , Compostos Heterocíclicos/uso terapêutico , Doenças dos Cavalos/tratamento farmacológico , Infecções por Actinomycetales/tratamento farmacológico , Infecções por Actinomycetales/veterinária , Animais , Azitromicina/administração & dosagem , Azitromicina/uso terapêutico , Broncopneumonia/tratamento farmacológico , Broncopneumonia/microbiologia , Método Duplo-Cego , Quimioterapia Combinada/veterinária , Feminino , Cavalos , Masculino , Rhodococcus equi/efeitos dos fármacos , Rifampina/administração & dosagem , Rifampina/uso terapêutico , Resultado do Tratamento
2.
Dev Biol (Basel) ; 125: 133-40, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16878470

RESUMO

Since 1956, red foxes (Vulpes vulpes) and, to a lesser extent, golden jackals (Canis aureus), have been the primary vectors maintaining endemic wildlife rabies in Israel. Starting in the autumn of 1998, oral rabies vaccination campaigns have been conducted in Israel targeting these two wildlife species, with increasing yearly geographical extension. Significant data have been accumulated from an area of approximately 5,200 km2 in Northern Israel. In the spring of 2003 the project was extended to 14,000 km2 and in the autumn to 21,000 km2, covering almost all inhabited areas in Israel and the West Bank. A total of two million RABORAL V-RG (Merial) vaccine-filled baits were distributed bi-annually by plane or helicopter at 14-19 baits km2. Since the onset of oral vaccination activities in 1998, annual bait acceptance in the vaccination zones has been demonstrated by biomarker detection (with tetracycline) in 55 % (429/783) of bone samples of target animals submitted for diagnosis. In 1999 to 2004, vaccine contact and induction of immunity in animals collected from the vaccination zones were reflected by seroconversion in 66 of 284 animals (23 %). By the year 2004, rabies cases declined sharply in all progressively vaccinated areas.


Assuntos
Raposas , Vacina Antirrábica/farmacologia , Raiva/prevenção & controle , Vacinação , Administração Oral , Animais , Raposas/virologia , História do Século XX , História do Século XXI , Humanos , Israel , Chacais/virologia , Raiva/epidemiologia , Raiva/história , Raiva/veterinária , Vacina Antirrábica/história , Vacinação/história , Vacinação/métodos , Vacinação/veterinária
3.
Stress ; 7(2): 119-26, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15512856

RESUMO

Phosphatidylserine, derived from cow brains, has been shown previously to dampen the ACTH and cortisol response to physical stress. Further research investigated the influence of soy lecithin phosphatidylserine supplementation on mood and heart rate when faced with an acute stressor. In this study, we investigated the effects of soy lecithin phosphatidic acid and phosphatidylserine complex (PAS) supplementation on pituitary adrenal reactivity (ACTH, cortisol) and on the psychological response (Spielberger State Anxiety Inventory stress subscale) to a mental and emotional stressor. Four groups of 20 subjects were treated for three weeks with daily dosages of either 400 mg PAS, 600 mg PAS, 800 mg PAS, or placebo before exposure to the Trier Social Stress Test (TSST). Treatment with 400 mg PAS resulted in a pronounced blunting of both serum ACTH and cortisol, and salivary cortisol responses to the TSST, but did not affect heart rate. The effect was not seen with larger doses of PAS. With regard to the psychological response, 400 mg PAS seemed to exert a specific positive effect on emotional responses to the TSST. While the placebo group showed the expected increase in distress after the test, the group treated with 400 mg PAS showed decreased distress. These data provide initial evidence for a selective stress dampening effect of PAS on the pituitary-adrenal axis, suggesting the potential of PAS in the treatment of stress related disorders.


Assuntos
Glycine max/química , Ácidos Fosfatídicos/farmacologia , Fosfatidilcolinas/farmacologia , Fosfatidilserinas/farmacologia , Sistema Hipófise-Suprarrenal/metabolismo , Estresse Psicológico/metabolismo , Estresse Psicológico/psicologia , Hormônio Adrenocorticotrópico/sangue , Adulto , Relação Dose-Resposta a Droga , Método Duplo-Cego , Combinação de Medicamentos , Feminino , Humanos , Hidrocortisona/sangue , Hidrocortisona/metabolismo , Masculino , Ácidos Fosfatídicos/administração & dosagem , Fosfatidilcolinas/administração & dosagem , Fosfatidilserinas/administração & dosagem , Sistema Hipófise-Suprarrenal/efeitos dos fármacos , Saliva/metabolismo
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