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首页> 外文期刊>Transactions of the Royal Society of Tropical Medicine and Hygiene >A randomized double-blind placebo-controlled field trial of ivermectin and albendazole alone and in combination for the treatment of lymphatic filariasis in Ghana.
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A randomized double-blind placebo-controlled field trial of ivermectin and albendazole alone and in combination for the treatment of lymphatic filariasis in Ghana.

机译:伊维菌素和阿苯达唑单独或联合治疗加纳淋巴丝虫病的随机双盲安慰剂对照田间试验。

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摘要

The efficacy and safety of single-dose ivermectin (150-200 micrograms/kg) and albendazole (400 mg) treatment administered separately or in combination for Wuchereria bancrofti infections were assessed in 1996-98 in a randomized double-blind placebo-controlled field trial in Ghana: 1425 individuals from 4 lymphatic filariasis-endemic villages, 340 of whom were microfilaria (mf)-positive before treatment, were randomized into 4 groups to receive albendazole alone, ivermectin alone, combination of albendazole and ivermectin, or placebo, respectively. Individuals were followed for 5 days after treatment to record any adverse reactions, and the effect of treatment on microfilaraemia was monitored in night-blood samples after 3, 6 and 12 months. Treatment efficacy was analysed for 236 mf-positive individuals who had > or = 100 mf/mL of blood and who were also present for examination at 12 months after treatment. Compared to the placebo group, the ivermectin and combination groups both showed statistically significant reductions in geometric mean mf intensities at the follow-up examinations (to 6.7% and 0.9%, 9.9% and 6.9%, and 21.7% and 11.4% of pre-treatment levels, respectively, at 3, 6 and 12 months after treatment). Compared to the ivermectin group, however, the reduction in the combination group was significantly greater only at 3 months after treatment, but not after 6 or 12 months. The albendazole group showed a slow but non-significant reduction over the same period. Adverse reactions were few and mostly mild (no severe reactions were recorded), and no significant differences were observed between the treatment groups. Both ivermectin and combination treatment thus appeared effective and safe for treatment of lymphatic filariasis, but the difference in efficacy was minor and the study did not provide clear evidence for the combination drug therapy, as compared to ivermectin therapy alone, to be superior for control of lymphatic filariasis.
机译:在随机双盲安慰剂对照田间试验中,于1996-98年评估了单剂量伊维菌素(150-200微克/千克)和阿苯达唑(400毫克)单独或联合治疗对班氏克氏杆菌感染的疗效和安全性。在加纳:来自4个淋巴丝虫病流行村的1425名患者(其中340名在治疗前微丝aria(mf)阳性)被随机分为4组,分别接受阿苯达唑,伊维菌素单独,阿苯达唑和伊维菌素的组合或安慰剂治疗。对个体进行治疗后随访5天,以记录任何不良反应,并在3、6和12个月后的夜间血液样本中监测治疗对微丝蛋白血症的影响。分析了血液中≥100 mf / mL且在治疗后12个月也曾接受检查的236 mf阳性个体的治疗效果。与安慰剂组相比,伊维菌素组和联合组在随访检查中均显示出几何平均mf强度的统计学显着降低(分别为6.7%和0.9%,9.9%和6.9%,以及21.7%和11.4%)。治疗水平分别在治疗后3、6和12个月)。但是,与伊维菌素组相比,联合治疗组的减少仅在治疗后3个月显着增加,而在6或12个月后则没有。在同一时期,阿苯达唑组显示出缓慢但无明显减少。不良反应很少,多数为轻度反应(未记录严重反应),各治疗组之间未观察到明显差异。因此,伊维菌素和联合治疗均对淋巴丝虫病有效,安全,但疗效差异很小,与单独使用伊维菌素治疗相比,该研究并未提供联合药物治疗的明显证据,优于后者。淋巴丝虫病。

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