Cutolo André Antonio, Santos Anderson Tintino dos, Allegretti Silmara Marques
Departamento de Biologia Animal, Instituto de Biologia, Universidade Estadual de Campinas, Cidade Universitária Zeferino Vaz, Rua Monteiro Lobato 255, Campinas, SP, Brazil.
Rev Bras Parasitol Vet. 2011 Apr-Jun;20(2):171-5.
Twenty horses naturally infected with nematodes were included in a blind, controlled field study on efficacy and safety of an oral 2% ivermectin formulation at a dose of 0.2 mg.kg(-1). Horses were divided into treated and non-treated (control) groups with ten animals each based on preliminary counts of eggs per gram of feces (EPG). Stool samples were collected after treatment for identification of nematode species. Clinical evaluations and EPG counts were performed on days 0, +5, +14 and +19. Nineteen nematode species were identified: Coronocyclus ulambajari, Craterostomum acuticaudatum, Cyathostomum catinatum, Cyathostomum pateratum, Cylicocyclus brevicapsulatus, Cylicocyclus insigne, Cylicocyclus leptostomum, Cylicocyclus nassatus, Cylicocyclus ultrajectinus, Cylicocyclus spp., Cylicostephanus calicatus, Cylicostephanus longibursatus, Cylicostephanus poculatus, Habronema muscae, Habronema spp., Parascaris equorum, Poteriostomum imparidentatum, Oxyuris equi and Triodontophorus spp. The mean EPG counts of treated and non-treated (control) groups on Days �15, 0, +5, +14 and +19 were 1925, 1340, 0, 12.5, 0, 1470, 790, 875, 1605 and 1240 respectively. The efficacy of treatment on Days +5, +14 and +19 was 100, 99.2 and 100% respectively, with a significant difference compared to the control group (p < 0.01). The product was considered to be safe with no findings of clinical significant changes during the study.
20匹自然感染线虫的马被纳入一项关于口服2%伊维菌素制剂(剂量为0.2毫克/千克)疗效和安全性的双盲对照现场研究。根据每克粪便中虫卵(EPG)的初步计数,将马分为治疗组和未治疗(对照)组,每组10只动物。治疗后收集粪便样本以鉴定线虫种类。在第0、+5、+14和+19天进行临床评估和EPG计数。鉴定出19种线虫:乌兰巴贾里冠状环线虫、尖尾杯口线虫、卡氏杯环线虫、父杯环线虫、短囊环行线虫、显著环行线虫、细口环行线虫、鼻状环行线虫、超射环行线虫、环行线虫属、杯状环纹线虫、长囊环纹线虫、杯状环纹线虫、蝇柔线虫、柔线虫属、马副蛔虫、不等口线虫、马尖尾线虫和三齿线虫属。治疗组和未治疗(对照)组在第-15、0、+5、+14和+19天的平均EPG计数分别为1925、1340、0、12.5、0、1470、790、875、1605和1240。在第+5、+14和+19天的治疗效果分别为100%、99.2%和100%,与对照组相比有显著差异(p<0.01)。该产品被认为是安全的,在研究期间未发现具有临床意义的显著变化。