Nguyen N L, Moulia-Pelat J P, Glaziou P, Martin P M, Cartel J L
Institut Territorial de Recherches Médicales Louis Malardé, Papeete, Tahiti, Polynésie Française.
Trans R Soc Trop Med Hyg. 1994 Jul-Aug;88(4):461-4. doi: 10.1016/0035-9203(94)90434-0.
In April and October in 1991-1993, 5 supervised single doses of ivermectin were given to inhabitants aged > or = 3 years in a Polynesian district: the first 3 treatments were with 100 micrograms/kg and the 2 latter with 400 micrograms/kg. At each treatment, about 97% of the eligible population (899) were treated and blood samples were collected just before treatment from 96% of the 613 inhabitants aged > or = 15 years. Following the 5 successive treatments, adverse reactions were observed in, respectively, 23.8, 13, 6.2, 13.6 and 7.9% of the microfilariae (mf) carriers, and in less than 1% of amicrofilaraemic subjects. Neither the frequency nor the intensity of adverse reactions was significantly different between single doses of 100 micrograms/kg and 400 micrograms/kg. Although the geometric mean microfilaraemia (GMM) was reduced, the mf carrier prevalence remained unchanged before and after 3 mass treatments with 100 micrograms/kg (21.4 and 20.7% respectively), and the mf recurrence rate 6 months after each dose of 100 micrograms/kg was roughly stable (respectively, 34.3%, 21.6% and 31.2% of the initial GMM). In contrast, after one dose round of 400 micrograms/kg, the mf carrier prevalence decreased significantly to 14.9% (P < 10(-6)), and the mf recurrence rate dropped to 9.9% (P < 10(-3)) of the initial GMM. These results confirm the safety and the effectiveness of 400 micrograms/kg of ivermectin for lymphatic filariasis control.
在1991年至1993年的4月和10月,在一个波利尼西亚地区,对3岁及以上居民给予5次监督下的单剂量伊维菌素:前3次治疗剂量为100微克/千克,后2次为400微克/千克。每次治疗时,约97%符合条件的人群(899人)接受了治疗,并且在治疗前从613名15岁及以上居民中的96%采集了血样。在连续5次治疗后,分别在23.8%、13%、6.2%、13.6%和7.9%的微丝蚴(mf)携带者中观察到不良反应,而在无微丝蚴血症的受试者中观察到的不良反应不到1%。100微克/千克和400微克/千克单剂量之间不良反应的频率和强度均无显著差异。尽管几何平均微丝蚴血症(GMM)有所降低,但在3次100微克/千克的群体治疗前后,mf携带者患病率保持不变(分别为21.4%和20.7%),并且每次100微克/千克剂量后6个月的mf复发率大致稳定(分别为初始GMM的34.3%、21.6%和31.2%)。相比之下,在一轮400微克/千克剂量后,mf携带者患病率显著降至14.9%(P < 10^(-6)),mf复发率降至初始GMM的9.9%(P < 10^(-3))。这些结果证实了400微克/千克伊维菌素用于控制淋巴丝虫病的安全性和有效性。