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伊维菌素治疗盘尾丝虫病的对照试验和剂量探索研究。

Controlled trial and dose-finding study of ivermectin for treatment of onchocerciasis.

作者信息

White A T, Newland H S, Taylor H R, Erttmann K D, Keyvan-Larijani E, Nara A, Aziz M A, D'Anna S A, Williams P N, Greene B M

出版信息

J Infect Dis. 1987 Sep;156(3):463-70. doi: 10.1093/infdis/156.3.463.

Abstract

Ivermectin, given as a single oral dose, has shown considerable promise as a new treatment for onchocerciasis. We assessed the safety and efficacy of ivermectin and tried to determine the optimal dose. Two hundred Liberians received 100, 150, or 200 micrograms of ivermectin/kg or placebo and were followed up for 12 months. Therapy was associated with only minimal systemic and ocular side effects. A 200-micrograms/kg dose was associated with greater systemic reaction than was a 100-micrograms/kg dose. Each treatment group had significant reduction in skin microfilaria counts by day 3 and a decrease of approximately 95% at three months. At three months the proportion of persons with no microfilariae in a specimen of skin was significantly less in the 100-micrograms/kg group than in the 150-micrograms/kg or 200-micrograms/kg groups. At 12 months, the level of microfilariae in skin was still reduced approximately 80%. Significant reduction in ocular involvement was seen in all groups. These results confirm that single-dose ivermectin is effective and well-tolerated and suggest that 150 micrograms of ivermectin/kg may be the optimal dose for initial therapy.

摘要

伊维菌素单次口服给药,作为盘尾丝虫病的一种新疗法已显示出可观的前景。我们评估了伊维菌素的安全性和疗效,并试图确定最佳剂量。200名利比里亚人分别接受了每千克体重100、150或200微克的伊维菌素或安慰剂治疗,并随访12个月。治疗仅伴有轻微的全身和眼部副作用。每千克体重200微克剂量组的全身反应比每千克体重100微克剂量组更明显。每个治疗组在第3天时皮肤微丝蚴计数均显著减少,3个月时减少约95%。3个月时,每千克体重100微克剂量组皮肤标本中无微丝蚴者的比例显著低于每千克体重150微克或200微克剂量组。12个月时,皮肤中的微丝蚴水平仍降低约80%。所有组的眼部病变均有显著减轻。这些结果证实单次剂量伊维菌素有效且耐受性良好,并表明每千克体重150微克的伊维菌素可能是初始治疗的最佳剂量。

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