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在乌干达进行的一项关于伊维菌素单独使用及与阿苯达唑联合使用治疗链尾丝虫感染的随机双盲现场试验。

A randomised, double-blind field trial of ivermectin alone and in combination with albendazole for the treatment of Mansonella perstans infections in Uganda.

作者信息

Asio Santa Maria, Simonsen Paul E, Onapa Ambrose W

机构信息

Kyambogo University, P.O. Box 1, Kyambogo, Kampala, Uganda.

出版信息

Trans R Soc Trop Med Hyg. 2009 Mar;103(3):274-9. doi: 10.1016/j.trstmh.2008.10.038. Epub 2008 Dec 9.

Abstract

The effect of a single dose of ivermectin alone (150-200microg/kg body weight) or in combination with albendazole (total of 400mg) in Mansonella perstans infection was assessed in a randomised, double-blind field trial in two endemic communities in Mukono and Luwero districts of Uganda. No side effects were observed or reported during the first 7 days after treatment. The effect on microfilaraemia was analysed among individuals with >or=20 microfilariae (mf) per 100mul of blood at baseline, who took the treatment and who attended follow-up examinations at 6 months and 12 months after treatment (48 and 46 in Mukono and 48 and 40 in Luwero for the ivermectin and combination treatment, respectively). In both communities, the combination treatment appeared slightly more effective than ivermectin alone, but the difference was not statistically significant. Both drug regimens were more effective in Luwero than in Mukono, probably owing to different diets in the two areas. However, in general both treatment regimens in both communities had limited effect on microfilarial intensities, and only one individual (given combination treatment in Luwero) was mf-negative at 6 months and 12 months after treatment. [ClinicalTrials.gov identifier: NCT00215280].

摘要

在乌干达穆科诺区和卢韦罗区的两个流行社区进行了一项随机、双盲现场试验,评估单剂量伊维菌素(150 - 200微克/千克体重)单独使用或与阿苯达唑联合使用(总量400毫克)对链尾曼森线虫感染的影响。治疗后的前7天未观察到或报告有副作用。对基线时每100微升血液中微丝蚴数≥20条、接受治疗且在治疗后6个月和12个月参加随访检查的个体(穆科诺区伊维菌素组和联合治疗组分别为48例和46例,卢韦罗区分别为48例和40例)的微丝蚴血症情况进行了分析。在两个社区中,联合治疗似乎比单独使用伊维菌素略有效,但差异无统计学意义。两种药物治疗方案在卢韦罗区比在穆科诺区更有效,这可能是由于两个地区的饮食不同。然而,总体而言,两个社区的两种治疗方案对微丝蚴强度的影响都有限,治疗后6个月和12个月时只有1例个体(卢韦罗区接受联合治疗者)微丝蚴呈阴性。[ClinicalTrials.gov标识符:NCT00215280]

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