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敌百虫治疗和预防人体血吸虫病感染的现场试验。

Field trial of metrifonate in the treatment and prevention of schistosomiasis infection in man.

作者信息

Jewsbury J M, Cooke M J, Weber M C

出版信息

Ann Trop Med Parasitol. 1977 Mar;71(1):67-83. doi: 10.1080/00034983.1977.11687163.

Abstract

A field trial was set up to test the prophylactic properties of the organophosphorous drug metrifonate (Bilarcil Bayer AG). Subjects were rural African children living in an area of Rhodesia where Schistosoma haematobium and S. mansoni are highly endemic. The trial was conducted in three stages, a preliminary period of therapy followed by two six-month periods of prophylaxis. Parasitological and haematological tests were carried out monthly and major assessments (including clinical examinations) were carried out prior to the start of the trial and at the end of each of the three stages. Drug was given to the appropriate groups at a dose rate of 7-5 mg/kg once per fortnight for three doses during the therapy stage and four-weekly during the prophylaxis stage. Results with S. haematobium were very good. A 60% cure-rate was observed six weeks aection was obtained in those children continuing to receive the drug as a prophylactic, even during the season of highest transmission; intensities of infection in those who became infected were very low. Infection rates in the treated but unprotected group rose steadily from 40% at week 11 to 95% at week 70. There was a sigificant effect upon the intensity of S. mansoni infections only when pre- and post-trial data were compared. Apart from the anticipated (and previously reported) depression of plasma cholinesterase values no side effects were recorded. Drug tolerance and acceptibility were very high. It is likely that the costs of a year's protection against S. Haematobium using metrifonate will be significantly lower than protection by molluscicidal techniques or single courses of treatment with established drugs.

摘要

开展了一项现场试验,以测试有机磷药物敌百虫(拜耳公司的Bilarcil)的预防特性。研究对象是生活在罗德西亚一个地区的非洲农村儿童,那里埃及血吸虫和曼氏血吸虫高度流行。试验分三个阶段进行,先是一个初步治疗期,随后是两个为期六个月的预防期。每月进行寄生虫学和血液学检测,在试验开始前和三个阶段的每个阶段结束时进行主要评估(包括临床检查)。在治疗阶段,以7.5毫克/千克的剂量率每两周给适当的组服用一次药物,共服用三剂;在预防阶段,每四周服用一次。对于埃及血吸虫,结果非常好。六周时观察到60%的治愈率,即使在传播高峰期,继续接受该药物预防的儿童也有60%得到治愈;感染的儿童感染强度非常低。在接受治疗但未得到保护的组中,感染率从第11周的40%稳步上升至第70周的95%。只有在比较试验前后的数据时,才发现对曼氏血吸虫感染强度有显著影响。除了预期的(以及先前报道的)血浆胆碱酯酶值降低外,未记录到任何副作用。药物耐受性和可接受性非常高。使用敌百虫进行一年的埃及血吸虫预防的成本可能会显著低于使用杀螺技术或使用现有药物进行单疗程治疗的成本。

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