RESUMEN
Beginning with the 2004-05 influenza season, the Advisory Committee on Immunization Practices (ACIP) recommended that all children aged 6-23 months receive influenza vaccinations annually. Other children recommended to receive influenza vaccinations include those aged 6 months-18 years who have certain high-risk medical conditions, those on chronic aspirin therapy, those who are household contacts of persons at high risk for influenza complications, and, since 2006, all children aged 24-59 months. Previously unvaccinated children aged <9 years need 2 doses administered at least 1 month apart to be considered fully vaccinated. This report assesses influenza vaccination coverage among children aged 6-23 months during the 2005-06 influenza season by using data from six immunization information system (IIS) sentinel sites. The findings demonstrate that vaccination coverage with 1 or more doses varied widely (range: 6.6% to 60.4%) among sites, with coverage increasing from the preceding influenza season in four of the six sites. However, <23% of children in five of the sites were fully vaccinated, underscoring the need for increased measures to improve the proportion of children who are fully vaccinated.
Asunto(s)
Programas de Inmunización , Vacunas contra la Influenza/administración & dosificación , Sistemas de Información Administrativa , Sistemas de Registros Médicos Computarizados , Vacunación/estadística & datos numéricos , Humanos , Lactante , Estaciones del Año , Estados Unidos/epidemiología , Vacunación/normasRESUMEN
Three studies were conducted to evaluate the persistent efficacy of doramectin injectable solution against experimental challenges with infective larvae of Cooperia punctata and Dictyocaulus viviparus. In each study, four groups of ten randomly-assigned calves, negative for trichostrongyle-type eggs on fecal examination, were treated subcutaneously in the midline of the neck with saline (1 ml/50 kg) on Day 0 or doramectin (200 microg/kg = 1 ml/50 kg) on Day 0, 7, or 14. Two additional calves from the same pool of animals were randomly assigned as larval-viability monitors and received no treatment. On Days 14-28, approximately 1000 and 50 infective larvae of Cooperia spp. and D. viviparus, respectively, were administered daily by gavage to each animal in Groups T1-T4. On Day 28, the two larval-viability monitor calves were inoculated in a similar manner with a single dose of approximately 30000 and 2000 larvae of Cooperia spp. and D. viviparus, respectively. Equal numbers of calves from each treatment group were killed on Days 42-45, as well as the two viability monitor animals to enumerate worm numbers. A 2% or 5% aliquot of small intestinal contents and washings were examined for worm quantification and identification, while 100% of the lung recoveries were quantified and identified. For each study and across the three studies, geometric mean worm recoveries for each treatment group were calculated from the natural log transformed data (worm count + 1) and were used to estimate percentage reduction. In the three studies, doramectin injectable solution was 97.5% efficacious against lungworms for up to 28 days and was 99.8% efficacious in reducing infection resulting from challenge with infective larvae of C. punctata for at least 28 days post-treatment.
Asunto(s)
Antihelmínticos/uso terapéutico , Enfermedades de los Bovinos/tratamiento farmacológico , Infecciones por Dictyocaulus/tratamiento farmacológico , Ivermectina/análogos & derivados , Tricostrongiloidiasis/veterinaria , Animales , Antihelmínticos/administración & dosificación , Antihelmínticos/normas , Bovinos , Dictyocaulus/efectos de los fármacos , Femenino , Florida , Idaho , Inyecciones Subcutáneas/veterinaria , Intestino Delgado/parasitología , Ivermectina/administración & dosificación , Ivermectina/normas , Ivermectina/uso terapéutico , Pulmón/parasitología , Masculino , Minnesota , Distribución Aleatoria , Trichostrongyloidea/efectos de los fármacos , Tricostrongiloidiasis/tratamiento farmacológicoRESUMEN
Two studies were conducted in North America to evaluate the persistent efficacy of doramectin injectable solution against experimental challenge with infective larvae of Ostertagia ostertagi. In both studies, four groups of 10 randomly-assigned calves, negative for trichostrongyle-type eggs on fecal examination, were treated subcutaneously in the midline of the neck with saline (1 ml 50 kg-1) on Day 0 or doramectin (200 micrograms kg-1 = 1 ml 50 kg-1) on Day 0, 7, or 14. Two additional calves from the same pool of animals were randomly assigned as larval-viability monitors and received no treatment. Beginning on Day 14 and continuing through Day 28, the 40 treated calves each were given approximately 1000 infective larvae of O. ostertagi by gavage daily; the two larval-viability monitors were inoculated in a similar manner with approximately 30,000 larvae as a single dose on Day 28. Animals were slaughtered on Day 42 in one study and on Days 42, 43, or 46 in the second. The abomasum from each calf was harvested and processed for worm recovery. A 2% aliquot of abomasal contents plus wash was examined for worm quantification and identification. Geometric mean O. ostertagi burdens were calculated from the log (O. ostertagi count + 1) and were used to estimate percentage reduction. In both studies, doramectin injectable solution was > or = 99.6% efficacious in reducing infection resulting from challenge with infective larvae of O. ostertagi for at least 21 days posttreatment; by 28 days posttreatment, efficacy was 87.3% in one study and 99.7% in the other.
Asunto(s)
Antihelmínticos/uso terapéutico , Enfermedades de los Bovinos , Ivermectina/análogos & derivados , Ostertagiasis/veterinaria , Animales , Bovinos , Heces/parasitología , Femenino , Ivermectina/uso terapéutico , Larva , Masculino , Orquiectomía , Ostertagia/aislamiento & purificación , Ostertagiasis/tratamiento farmacológico , Recuento de Huevos de ParásitosRESUMEN
During 1989-1990, the United States Department of Agriculture (USDA) meat inspection records were used to determine the distribution and incidence of liver flukes (Fasciola hepatica and Fascioloides magna) in Montana cattle. Of the cows and bulls slaughtered in USDA-inspected packing plants during a 12 month time period, 17.24% had livers that were condemned because of liver flukes. This was a 12% increase over USDA liver condemnations reported for 1973. Infected animals have been reported from 26 counties in Montana, mostly located in the south-central and western half of the state. Forty-nine percent of the 2.4 million cattle in Montana are raised in these counties. Lymnaeid snail species that may serve as intermediate hosts for Fasciola hepatica were found in most of the counties where liver flukes were reported. The principal vectors believed to be responsible for the transmission of Fasciola hepatica in Montana are species of the genus Fossaria. Stagnicola montanensis and Lymnaea stagnalis, which may serve as intermediate hosts for this parasite have also been collected. A known intermediate host for Fascioloides magna, Stagnicola caperata, was also found in several locations.
Asunto(s)
Enfermedades de los Bovinos/epidemiología , Vectores de Enfermedades , Fascioliasis/veterinaria , Fascioloidiasis/epidemiología , Caracoles/parasitología , Mataderos , Animales , Bovinos , Fascioliasis/epidemiología , Femenino , Inspección de Alimentos , Masculino , Carne/normas , Montana/epidemiologíaRESUMEN
22,23-Dihydroavermectin B1a (I) is determined in animal plasma over the concentration range 5-60 ng/ml by reverse-phase high-performance liquid chromatography (HPLC) with UV photometric detection. Prior to HPLC the sample is isolated by gravity-fed adsorption column chromatography on Florisil. The delta 2 isomer of I (designated as compound III) is used as an internal standard, and the conversion of I to this isomer by base hydrolysis is described. An accuracy of 2 ng/ml (mean deviation) and a precision in the range of 1-3 ng/ml (standard deviation) were observed for the method. The limit of detection is 2 ng/ml based on the background observed for normal cattle plasma. The method is applicable to bioavailability studies of I at usual therapeutic concentrations.
Asunto(s)
Ivermectina/análogos & derivados , Lactonas/sangre , Animales , Bovinos , Cromatografía Líquida de Alta Presión/métodos , Isomerismo , Microquímica , Espectrometría de Fluorescencia , Factores de TiempoRESUMEN
An analytical method is described for the determination of the avermectins in plasma based upon high-performance liquid chromatography of fluorescent derivatives of these compounds. The analyte is isolated by adsorption chromatography on Florisil, dehydrated in an acetic anhydride-pyridine mixture, and the fluorophore is further separated by chromatography on silica gel in advance of introduction into a reversed-phase system. This method, which can be applied to samples containing as little as 0.2 ng drug per ml, has an accuracy of 5% mean relative error and a precision of 8% relative standard deviation. A study and discussion of several factors which affect the analytical reaction are included.