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清除剂量的伊维菌素和单次高剂量伊维菌素及乙胺嗪治疗班氏吴策线虫微丝蚴血症的疗效比较

Comparative efficacy of clearing-dose and single high-dose ivermectin and diethylcarbamazine against Wuchereria bancrofti microfilaremia.

作者信息

Addiss D G, Eberhard M L, Lammie P J, McNeeley M B, Lee S H, McNeeley D F, Spencer H C

机构信息

Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control, Atlanta, Georgia.

出版信息

Am J Trop Med Hyg. 1993 Feb;48(2):178-85. doi: 10.4269/ajtmh.1993.48.178.

DOI:10.4269/ajtmh.1993.48.178
PMID:8447520
Abstract

To compare the efficacy and tolerability of various combinations of low- and high-dose ivermectin and diethylcarbamazine (DEC), 59 persons with Wuchereria bancrofti microfilaremia were enrolled in a double-blinded six-arm clinical trial in Leogane, Haiti. On day 1, study participants were treated with low clearing doses of ivermectin, DEC, or placebo; on day 5 they received 200-400 micrograms/kg of ivermectin or 6 mg/kg of DEC. Adverse reactions, which were generally mild, occurred more frequently with ivermectin than with DEC. One year after treatment, the geometric mean microfilarial density returned to 0.9% of pretreatment levels for persons who received a total of 420 micrograms/kg of ivermectin. This rate was significantly lower than 5.6% for persons who were treated with 220 micrograms/kg of ivermectin (P = 0.02) and 9.3% for those receiving 6 or 7 mg/kg of DEC (P = 0.006). Persons treated with a clearing dose of ivermectin followed by 6 mg/kg of DEC also had low microfilarial densities (1.7% of pretreatment levels), suggesting an additive or synergistic effect of the two drugs. The addition of a clearing dose neither reduced the severity of adverse reactions nor improved the efficacy of high-dose ivermectin. Community-based intervention trials are now warranted to determine the feasibility and effectiveness of mass chemotherapy with single high-dose ivermectin for the prevention and control of lymphatic filariasis.

摘要

为比较低剂量和高剂量伊维菌素与乙胺嗪(DEC)不同组合的疗效和耐受性,59名班氏吴策线虫微丝蚴血症患者参与了在海地莱奥甘进行的一项双盲六组临床试验。第1天,研究参与者接受低清除剂量的伊维菌素、DEC或安慰剂治疗;第5天,他们接受200 - 400微克/千克的伊维菌素或6毫克/千克的DEC。不良反应一般较轻,伊维菌素组比DEC组更频繁出现。治疗一年后,接受总共420微克/千克伊维菌素的患者,其微丝蚴密度几何均值降至治疗前水平的0.9%。这一比例显著低于接受220微克/千克伊维菌素治疗患者的5.6%(P = 0.02)以及接受6或7毫克/千克DEC治疗患者的9.3%(P = 0.006)。先接受清除剂量伊维菌素然后接受6毫克/千克DEC治疗的患者微丝蚴密度也较低(治疗前水平的1.7%),表明两种药物有相加或协同作用。添加清除剂量既未降低不良反应的严重程度,也未提高高剂量伊维菌素的疗效。现在有必要开展基于社区的干预试验,以确定单次高剂量伊维菌素大规模化疗预防和控制淋巴丝虫病的可行性和有效性。

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