Dueger E L, Moro P L, Gilman R H
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California Davis, Davis, California 95616,
Antimicrob Agents Chemother. 1999 Sep;43(9):2263-7. doi: 10.1128/AAC.43.9.2263.
A blinded, randomized placebo-controlled trial assessed the efficacy and safety of oxfendazole for the treatment of ovine hydatid disease. Cyst fertility and parasite viability were measured following daily, weekly, and monthly treatment schedules with 30 mg of oxfendazole per kg of body weight. The 12-week trial was conducted in 215 adult sheep in the central Peruvian Andes and was masked for both treatment group and scheduling. In this trial oxfendazole significantly reduced protoscolex viability relative to controls in all treatment groups. In the daily, weekly, and monthly groups, 100, 97, and 78% of sheep, respectively, were either cured or improved following treatment, compared to 35% cured or improved animals in the control group. However, daily dosing at 30 mg of oxfendazole per kg proved highly toxic to sheep, resulting in a 24% death rate in the daily group as compared to a 4 to 6% mortality rate in all other groups. If found safe in humans, oxfendazole may prove to be a useful and inexpensive treatment for cestode infections in humans. This study suggests that a staggered dosing regimen of oxfendazole, and possibly other benzimidazoles, may be as efficacious as daily treatment regimens for hydatidosis while decreasing both the cost and adverse effects associated with daily dosing.
一项双盲、随机、安慰剂对照试验评估了奥芬达唑治疗绵羊包虫病的疗效和安全性。按照每日、每周和每月的治疗方案,以每千克体重30毫克奥芬达唑进行治疗,之后测量包囊繁殖力和寄生虫活力。这项为期12周的试验在秘鲁中部安第斯山脉的215只成年绵羊身上进行,治疗组和治疗方案均采用盲法。在该试验中,相对于对照组,奥芬达唑在所有治疗组中均显著降低了原头蚴的活力。在每日、每周和每月治疗组中,分别有100%、97%和78%的绵羊在治疗后治愈或病情改善,而对照组中治愈或病情改善的动物为35%。然而,每千克体重30毫克奥芬达唑的每日给药对绵羊毒性极高,导致每日治疗组的死亡率为24%,而其他所有组的死亡率为4%至6%。如果在人体中被证明是安全的,奥芬达唑可能被证明是一种治疗人类绦虫感染的有用且廉价的方法。这项研究表明,奥芬达唑以及可能的其他苯并咪唑类药物的错开给药方案,对于包虫病可能与每日治疗方案一样有效,同时可降低每日给药的成本和不良反应。