Gholami Mohammad Hossein, Derakhshanfar Amin, Gholami Tahereh
Faculty of Veterinary Medicine, Islamic Azad University of Kazerun, Kazerun, Iran.
Department of Comparative Biomedical Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
J Adv Vet Anim Res. 2023 Sep 30;10(3):516-521. doi: 10.5455/javar.2023.j705. eCollection 2023 Sep.
This study aimed to evaluate a new drug combination for small ruminant respiratory diseases to find a better treatment protocol for the potential replacement of older methods.
A total of 6,886 animals received common respiratory disease therapies out of 15,845 animals that had respiratory disorders. The new combination therapy technique treated the remaining animals (8,968). The animals were given an oral suspension of triclabendazole or levamisole at an initial dosage of 0.2 ml/kg body weight (BW). The following day, 0.2 mg/kg of 1% ivermectin was subcutaneously administered. Then, on the third and fifth days of treatment, a subcutaneous injection of 30 mg/kg BW of florfenicol (30%) was administered. The survival and recovery rates for both groups were tracked throughout a 6-month period of observation. Postmortem and histopathological signs were also assessed.
In the group of the novel combination therapy, group A, clinical, postmortem, and histopathological signs were significantly reduced compared to group B. Clinical signs and mortality in group A were 90% and 93% lower than in group B, respectively. Animals that received the new combination therapy were healed of their disease and stayed immune for 6 months.
This novel therapy demonstrated significant efficacy against respiratory diseases in a 10-year field study. The paper proved that the protocol introduced could be a new therapeutic approach.
本研究旨在评估一种用于小反刍动物呼吸道疾病的新型药物组合,以寻找一种更好的治疗方案,有可能替代旧方法。
在15845只患有呼吸道疾病的动物中,共有6886只接受了常见的呼吸道疾病治疗。新型联合治疗技术治疗了其余的动物(8968只)。给动物口服三氯苯达唑或左旋咪唑混悬液,初始剂量为0.2毫升/千克体重(BW)。第二天,皮下注射0.2毫克/千克的1%伊维菌素。然后,在治疗的第三天和第五天,皮下注射30毫克/千克体重的氟苯尼考(30%)。在6个月的观察期内跟踪两组的存活率和恢复率。还评估了死后和组织病理学体征。
在新型联合治疗组A中,与B组相比,临床、死后和组织病理学体征显著减轻。A组的临床体征和死亡率分别比B组低90%和93%。接受新型联合治疗的动物疾病痊愈,并保持6个月的免疫力。
在一项为期10年的实地研究中,这种新型疗法对呼吸道疾病显示出显著疗效。本文证明所引入的方案可能是一种新的治疗方法。