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保定的目的是要控制烈性犬的攻击性行为,从而保证人的安全。而保定器械在使用过程中也不能损伤到犬本身,要在其使用过程中尽量减少犬的应激。保定器械应具备实用性,即材质要牢靠、大小要适中、使用要方便,重复使用时犬接受保定的成功率要高。最后,还应考虑到是否便于消毒、所占场地大小等一系列相关问题。 相似文献
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在对藏獒等性格暴烈的犬进行检查或诊治时,为防止犬意外伤人,采用一些简单的物品进行保定非常实用。现根据笔者长期从事畜牧兽医工作的经验,将用过的几种常用保定方法简介如下。 相似文献
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犬、猫在诊疗时,可能会咬伤或抓伤医疗人员,或由于骚动而影响治疗操作。因此,应给予适当的保定。犬、猫对主人有较强的依恋性,所以保定时最好由主人共同参与操作。尤其是犬、猫,当由主人抱在胸前更有利于检查和治疗。犬、猫保定的方法很多,有以语言、人力、器械、药物等方法控制犬、猫,限制其防卫活动,确保人和犬猫的安全。 相似文献
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笔者经过多年的实践 ,自制了一种适用于犬戴的铁丝“笼头” ,很好地解决了犬的保定问题。经过 40多个场 (户 ) 6 80多条犬的实际应用 ,收到了很好的效果 ,现将此法介绍如下。笼头的制作与使用 :取直径 1mm、长约 1m的细铁丝 1根 ,将两头交叉在铁丝的中部挽成一个与犬嘴大小相符的圆圈。再从交叉处开始 ,2段铁丝各向相反方向缠绕 1/4周 ,起加固笼头圈的作用。剩余铁丝每段约长 2 0cm为宜 ,作为笼头的 2条系带。使用时 ,饲养人员边抚摸犬头边将笼头圈套在犬嘴巴上。然后拉住 2条系带 ,从两耳后上升到脑顶 ,在枕脊前打结。注意事项 :笼头… 相似文献
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《中国兽医学报》2016,(5):734-738
为了更好的了解我国东北地区犬细小病毒的流行情况,采用F81细胞从来自长春某宠物医院疑似患有肠炎的犬粪便样品中分离出1株病毒,经形态学、血清学、动物回归试验和分子生物学鉴定,分离的病毒为犬细小病毒new CPV-2b型,命名为CPV JL13-1。对该病毒主要结构蛋白VP2基因进行克隆测序和基因进化分析表明,CPV JL13-1分离株VP2基因与GenBank上提交的其他41株犬细小病毒株核苷酸和氨基酸均有较高的同源性,分别为98.6%~99.5%和97.6%~99.5%,其中核苷酸和氨基酸同源性最高的均为B-2004株。本研究为犬细小病毒分子流行病学调查和疫苗的研究奠定基础。 相似文献
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为了解决宠物门诊中的烈性犬保定问题,以Φ6′镀锌自来水管为主要材料设计、焊制脱卸式活动围栏,并在临床实践中不断改进和观察应用效果。结果表明,该围栏对于各种体格的烈性犬均具有可靠的保定效果,对人和犬均十分安全,而且操作简单,容易清洗和消毒。 相似文献
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J E Smith E Mahaffey P Board 《Journal of the American Veterinary Medical Association》1978,172(6):701-703
A solution consisting of ascorbate phosphate, citric acid, sodium citrate, sodium phosphate, and dextrose was developed to extend the shelf life of canine blood stored for transfusion. The 24-hour poststorage viability remained above 70% for 6 weeks of storage at 4 C. The concentration of 2,3 diphosphoglycerate remained constant for 3 weeks, then declined slowly. After 6 weeks of storage, the 2,3 diphosphoglycerate content was still sufficiently high to allow adequate dissociation of oxygen from oxyhemoglobin in vivo. It was concluded that blood stored up to 6 weeks in this solution would be safe to use for transfusion. 相似文献
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新型的食品和饲料添加剂--茶多酚的研究与应用 总被引:4,自引:0,他引:4
本文简述了生理活性物质茶多酚的理化特性与生物学活性;剖析了茶多酚的作用机理;阐述了茶多酚的研究与应用进展;并展望了茶多酚在食品和饲料工业及畜牧业中的应用前景。 相似文献
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Yasuhiro Fukuyama Tetsushi Tezuka Atsushi Kawabata Takuya Maruo 《The Veterinary quarterly》2016,36(3):176-182
In veterinary medicine, the management of malignant skin wounds is highly challenging. We conducted a study on seven case animals (four dogs and three cats) which presented with malignant skin wounds. All seven animals had signs and symptoms which were controlled following treatment with a modified Mohs paste. Upon obtaining informed consent from their owners, the animals requiring management of malignant wounds were enrolled in this study. The modified Mohs paste was prepared by mixing zinc chloride, zinc oxide starch powder, glycerin, and distilled water. The modified Mohs paste was topically applied to and left to remain on the malignant wounds for one hour, under controlled conditions. Once the paste was removed, the wounds were irrigated with a solution of sterile saline. At the first examination, the wounds of each animal were observed for signs of exudate, malodor, and bleeding. In every case, visible improvement was observed immediately after the modified Mohs paste treatment. Specifically, the size of the malignant wounds, and the number of times the dressing gauze required changing, significantly decreased (p < 0.05 and p < 0.01, respectively). The open malignant skin wounds caused by mammary gland tumors disappeared in two cases. The Mohs paste has been shown to be a viable option for the palliative treatment in canine and feline malignant skin wound management. 相似文献
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S.D. FOLZ S. GENG L.H. NOWAKOWSKI J R. R.D. CONKLIN 《Journal of veterinary pharmacology and therapeutics》1978,1(3):199-204
A total of forty-eight dogs were utilized to titrate and evaluate the activity of a new miticide, amitraz. The treatment was applied dermally and evaluated for efficacy against experimentally induced Demodex canis and Sarcoptes scabiei infestations. Five different concentrations (2000, 1000, 500, 250, 125 p.p.m.) of the active drug, N'—(2, 4-dimethylphenyl)N—{[(2, 4-dimethylphenyl) imino] methyl} -N-methyl-methanimidamide, were tested. The activity of amitraz was compared to a standard treatment, placebo treatment, and no treatment.
A single dermal treatment with amitraz (all concentrations) indicated activity against both D. canis and S. scabiei. The lowest concentration of active drug (125 p.p.m.) was significantly less efficacious than the four higher concentrations (250, 500, 1000, 2000 p.p.m.). At the 250 p.p.m. (or higher) level the effectiveness of this new miticide was comparable to the standard treatment. The data indicate the 250 p.p.m. concentration is the optimal level and the recommended dilution for treatment of mange mites. Drug reactions related to amitraz were not observed. 相似文献
A single dermal treatment with amitraz (all concentrations) indicated activity against both D. canis and S. scabiei. The lowest concentration of active drug (125 p.p.m.) was significantly less efficacious than the four higher concentrations (250, 500, 1000, 2000 p.p.m.). At the 250 p.p.m. (or higher) level the effectiveness of this new miticide was comparable to the standard treatment. The data indicate the 250 p.p.m. concentration is the optimal level and the recommended dilution for treatment of mange mites. Drug reactions related to amitraz were not observed. 相似文献
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Larson LJ Schultz RD 《Veterinary therapeutics : research in applied veterinary medicine》2007,8(4):305-310
A group of client-owned dogs and a group of dogs at a commercial kennel were evaluated for duration of antibody responses against canine parvovirus type 2 (CPV-2) and canine adenovirus type 1 (CAV-1) after receiving a combination vaccine containing recombinant canarypox-vectored canine distemper virus (CDV) and modified-live CPV-2, CAV-2, and canine parainfluenza virus, with (C6) or without (C4) two serovars of Leptospira (Recombitek C4 or C6, Merial). Duration of antibody, which correlates with protective immunity, was found to be at least 36 months in both groups. Recombitek combination vaccines can confidently be given every 3 years with assurance of protection in immunocompetent dogs against CPV-2 and CAV-1 as well as CDV. This allows this combination vaccine, like other, similar modified- live virus combination products containing CDV, CAV-2, and CPV-2, to be administered in accordance with the recommendations of the American Animal Hospital Association Canine Vaccine Task Force. 相似文献