Abstract

BackgroundLymphatic filariasis (LF) control in most countries of sub-Saharan Africa is based on annual mass drug administration (MDA) with a combination of ivermectin and albendazole, in order to interrupt transmission. However, attaining and maintaining high treatment coverage has been a challenge in many LF control programmes. This study was designed to elucidate reasons for continued transmission of LF in an endemic area of Tanga, northeastern Tanzania, where control activities based on MDA had been in place for eight years by the time of this study in 2012.MethodsA cross-sectional questionnaire survey was conducted in three sentinel villages used for monitoring the impact of MDA on LF transmission. A total of 747 individuals were interviewed, out of which 172 (23.0%), 27 (3.6%) and 49 (6.5%) had been shown to have circulating filarial antigens (CFA), microfilaraemia (MF) and LF gross lesions, respectively, prior to the interviews.ResultsThe interviewed population had a mean age of 33.7 years and a male to female ratio of 0.8. Males, individuals aged 30 years and above, peasants/fishermen and recent immigrants to the study communities were significantly more affected (CFA, MF and/ or LF gross lesions) than the other population groups. However, drug uptake rates were not significantly different between LF affected (those with CFA, MF and/ or LF gross lesions) and non-affected individuals. Likewise, drug uptake rates were not significantly different across different demographic parameters of the study population, some of which differed significantly in the level of infection. Moreover, it was found that misconceptions on how LF can be acquired were still evident, linking its transmission to witchcraft, heredity and sexual behaviour.ConclusionsThe findings indicated that misconceptions about LF and its transmission still existed despite eight years of control activities in the area. Improved communication on the rationale of MDA and an enhanced drug delivery strategy that is adapted to the local settings and targeting important demographic groups that serve as reservoir of infection will help in reaching the elimination target within a reasonable timeframe.

Highlights

  • Lymphatic filariasis (LF) control in most countries of sub-Saharan Africa is based on annual mass drug administration (MDA) with a combination of ivermectin and albendazole, in order to interrupt transmission

  • LF was targeted for global elimination following a World Health Assembly resolution passed in 1997, and subsequently in 2000 the World Health Organization (WHO) launched the Global Programme to Eliminate Lymphatic Filariasis (GPELF) with a target of eliminating the disease by 2020 [6, 7]

  • The findings of the present study showed that reported drug uptake rates were not significantly different among those affected and non-affected

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Summary

Introduction

Lymphatic filariasis (LF) control in most countries of sub-Saharan Africa is based on annual mass drug administration (MDA) with a combination of ivermectin and albendazole, in order to interrupt transmission. In sub-Saharan Africa, LF is caused by Wuchereria bancrofti and transmitted by Anopheles and Culex mosquitoes [2] In this region, it has been estimated that more than 45 million people are affected by LF [3]. The drug combination reduces the density of microfilariae in the blood and thereby the level of disease transmission in endemic areas For this strategy to be effective, a high treatment coverage (estimated to range from 65– 90%) successively for at least five to six years (corresponding to the life-span of the adult worms) is necessary [8, 9]

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