Navrongo Health Research Centre, Navrongo, Ghana.
Trop Med Int Health. 2011 Sep;16(9):1112-9. doi: 10.1111/j.1365-3156.2011.02814.x. Epub 2011 Jun 20.
To compare (i) side effects associated with the simultaneous adminstration of praziquantel, albendazole and ivermectin with side affects associated with albendazole and ivermectin only and (ii) coverage by volunteers distributing three or two drugs.
Two-arm comparative study in northern Ghana integrated praziquantel distribution into an existing lymphatic filariasis and onchocerciasis control programme using Community Directed Distributors. The control arm continued to distribute only ivermectin and albendazole. Dosages of ivermectin and praziquantel were based on height. Treatment was directly observed, and all two/three drugs were co-administered. Adverse effects were recorded based on passive surveillance. Parasitological, anthropometric and haematological data were collected at baseline.
Prevalence of Schistosoma haematobium infection among 1001 (boys: 47.9% girls: 52.1%) school-age children (6-15 years) [intervention: 30.0% (CI: 23.1-34.2); control: 23.0% (CI: 18.9-27.0)], mean haemoglobin, weight and age were similar among the intervention and control groups. While 1676 (99.1%) compounds in the control area were visited and 15,020 (96.58%) people were treated, only 1375 (88.5%) compounds in the intervention area were visited and 8454 (80.97%) people treated (P < 0.001). The numbers of adverse effects were similar (intervention: 50/6896; control: 130/15,020). The most reported adverse effects was headache (intervention: 14/50; control: 13/130), followed by body weakness, which was reported more from the intervention group (intervention: 13/50, 95% CI: 14.6-40.3; control: 6/130, 95% CI: 1.7-9.8]. Sixty-six per cent (6896/10,441) of the eligible population received praziquantel.
Reported adverse events were mild and managed at the subdistrict level with no cases of hospitalization; intensive health education will, however, be required to improve coverage.
比较(i)同时给予吡喹酮、阿苯达唑和伊维菌素与仅给予阿苯达唑和伊维菌素相关的副作用,以及(ii)志愿者分发三种或两种药物的覆盖率。
在加纳北部,采用社区定向分销商将吡喹酮的分发纳入现有的淋巴丝虫病和盘尾丝虫病控制规划,进行了一项双臂比较研究。对照组继续仅分发伊维菌素和阿苯达唑。伊维菌素和吡喹酮的剂量基于身高。治疗是直接观察的,所有三种/两种药物都同时给予。根据被动监测记录不良反应。在基线时收集寄生虫学、人体测量学和血液学数据。
在 1001 名(男孩:47.9%;女孩:52.1%)学龄儿童(6-15 岁)中,曼氏血吸虫感染的患病率为 30.0%(95%CI:23.1-34.2);对照组为 23.0%(95%CI:18.9-27.0)[干预组:30.0%(95%CI:23.1-34.2);对照组:23.0%(95%CI:18.9-27.0)]。干预组和对照组的平均血红蛋白、体重和年龄相似。在对照组,有 1676 个(99.1%)化合物被访问,有 15020 人(96.58%)接受了治疗,而在干预组,只有 1375 个(88.5%)化合物被访问,有 8454 人(80.97%)接受了治疗(P<0.001)。不良反应的数量相似(干预组:50/6896;对照组:130/15020)。最常见的不良反应是头痛(干预组:14/50;对照组:13/130),其次是身体虚弱,干预组报告的更多(干预组:13/50,95%CI:14.6-40.3;对照组:6/130,95%CI:1.7-9.8]。符合条件的人群中有 66%(6896/10441)接受了吡喹酮治疗。
报告的不良事件是轻微的,并在分区一级进行了管理,没有住院治疗的病例;然而,需要进行强化健康教育,以提高覆盖率。