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阿苯达唑和伊维菌素增加剂量及用药频率对马拉维北部班氏吴策线虫微丝蚴清除率影响的随机对照临床试验

Randomised controlled clinical trial of increased dose and frequency of albendazole and ivermectin on Wuchereria bancrofti microfilarial clearance in northern Malawi.

作者信息

Tafatatha Terence T, Ngwira Bagrey M, Taegtmeyer Miriam, Phiri Amos J, Wilson Trevor P, Banda Louis G, Piston Wilson N, Koole Olivier, Horton John, French Neil

机构信息

Karonga Prevention Study, Chilumba, Karonga district, Malawi Centre for Neglected Tropical Diseases, Liverpool School of Tropical Medicine, Liverpool, UK

Karonga Prevention Study, Chilumba, Karonga district, Malawi London School of Hygiene & Tropical Medicine, London, UK.

出版信息

Trans R Soc Trop Med Hyg. 2015 Jun;109(6):393-9. doi: 10.1093/trstmh/trv027. Epub 2015 Apr 15.

Abstract

BACKGROUND

In Africa, albendazole and ivermectin are currently used in combination for annual mass drug administration (MDA) for lymphatic filariasis (LF) elimination. Rapid and sustained clearance is desirable for public health impact and elimination of LF. Increasing the dose and/or frequency of albendazole and ivermectin treatment may be more effective in clearing microfilariae than standard MDA.

METHODS

We conducted a randomised controlled open label trial in northern Malawi comparing three modified treatment groups to standard dosage of ivermectin and albendazole in adults with confirmed circulating LF antigen and microfilaria. Participants were followed-up every 6 months for 2 years for repeat microfilarial counts and safety assessments.

RESULTS

A total of 1851 adults were screened and 70 with microfilarial counts >80 microfilariae/ml were randomised. All treatment groups achieved a significant reduction of microfilariae levels by 12- and 24-months of follow-up. Doubling the standard dose and administering it twice yearly showed a non-significant tendency towards faster and more complete clearance. There were no serious adverse reactions.

CONCLUSIONS

In this small study, all regimens effectively cleared microfilaria. Standard treatment may be adequate in settings like Malawi but not in all endemic settings and larger studies are required to demonstrate benefit of higher dosages. [ClinicalTrials.gov identifier: NCT01213576].

摘要

背景

在非洲,阿苯达唑和伊维菌素目前联合用于每年的大规模药物给药(MDA)以消除淋巴丝虫病(LF)。为了对公共卫生产生影响并消除LF,需要快速且持续的清除。增加阿苯达唑和伊维菌素治疗的剂量和/或频率在清除微丝蚴方面可能比标准MDA更有效。

方法

我们在马拉维北部进行了一项随机对照开放标签试验,将三个改良治疗组与伊维菌素和阿苯达唑的标准剂量用于确诊有循环LF抗原和微丝蚴的成年人进行比较。参与者每6个月随访一次,持续2年,以重复进行微丝蚴计数和安全性评估。

结果

共筛查了1851名成年人,70名微丝蚴计数>80条/毫升的患者被随机分组。所有治疗组在随访12个月和24个月时微丝蚴水平均显著降低。将标准剂量加倍并每年给药两次显示出更快和更完全清除的不显著趋势。没有严重的不良反应。

结论

在这项小型研究中,所有方案均有效清除了微丝蚴。在马拉维这样的地区,标准治疗可能足够,但并非在所有流行地区都足够,需要更大规模的研究来证明更高剂量的益处。[ClinicalTrials.gov标识符:NCT01213576]

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