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注射用多拉菌素在拉丁美洲治疗和控制人皮蝇感染中的疗效。

Efficacy of injectable doramectin in the therapy and control of Dermatobia hominis infestations in Latin America.

作者信息

Muniz R A, Cerqueira-Leite R, Coronado A, Soraci O, Umehara O, Moreno J, Errecalde J

机构信息

Animal Health Group, Pfizer Inc, Groton, CT 06340, USA.

出版信息

Vet Parasitol. 1995 Dec;60(3-4):265-71. doi: 10.1016/0304-4017(95)00793-x.

DOI:10.1016/0304-4017(95)00793-x
PMID:8747909
Abstract

Three studies were conducted in Latin America, one in Brazil, one in Venezuela and one in Argentina, using a common protocol to investigate the efficacy of a single subcutaneous injection of doramectin at 200 micrograms kg-1 (1 ml per 50 kg) for the treatment and control of Dermatobia hominis infestations in cattle raised under commercial conditions. In each study, two groups of 20 animals each were allocated on the basis of D. hominis nodules present 24 h before treatment to a treated group (T1), or to a control group (T2) which received saline solution at 1 ml per 50 kg of live weight. All cattle were injected in the mid-dorsal cervical region and examined on treatment day and 2, 7, 15 and 30 days post-treatment (p.t.). At each observation day the number of D. hominis nodules was counted and the viability of the larvae inside them was assessed and recorded. Treatment with doramectin was 100% effective in eliminating D. hominis larvae and in controlling the re-establishment of the parasite under field conditions of continuous reinfestation. During the first 48 h p.t., dead larvae of different ages were found outside or partially outside the nodules in animals of the doramectin groups. After 48 h p.t., no live larvae were found inside existing nodules, nor did new nodules develop in animals of the doramectin groups in any of the three studies. When compared with nodule counts in the control group on the same observation day or with parasite burdens on the same animal before treatment, doramectin-treated animals began to eliminate parasitic nodules at 48 h p.t. Efficacy reached 100% at 7 days p.t. and remained at 100% on subsequent observation days (P < 0.05). None of the doramectin-treated animals exhibited any clinical signs of adverse reaction to medication.

摘要

在拉丁美洲开展了三项研究,一项在巴西,一项在委内瑞拉,一项在阿根廷,采用通用方案调查皮下注射200微克/千克(每50千克体重注射1毫升)多拉菌素单次给药对商业养殖条件下牛的人皮蝇感染进行治疗和控制的效果。在每项研究中,根据治疗前24小时存在的人皮蝇结节,将每组20只动物分为治疗组(T1)或对照组(T2),对照组接受每50千克活体重1毫升的盐溶液。所有牛均在颈背部中部进行注射,并在治疗当天以及治疗后2、7、15和30天进行检查。在每个观察日,对人皮蝇结节的数量进行计数,并评估和记录其中幼虫的活力。在持续再感染的田间条件下,多拉菌素治疗在消除人皮蝇幼虫和控制寄生虫重新感染方面的有效率为100%。在治疗后的头48小时内,多拉菌素组动物的结节外或部分在结节外发现了不同年龄的死亡幼虫。治疗48小时后,在现有结节内未发现活幼虫,在三项研究中的任何一项中,多拉菌素组动物也未出现新的结节。与同一天观察日对照组的结节计数或治疗前同一动物的寄生虫负荷相比,多拉菌素治疗的动物在治疗后48小时开始消除寄生结节。治疗后7天疗效达到100%,在随后的观察日保持在100%(P<0.05)。所有接受多拉菌素治疗的动物均未表现出对药物的任何临床不良反应迹象。

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