Abstract

BackgroundIndia has made great progress towards the elimination of lymphatic filariasis. By 2015, most endemic districts had completed at least five annual rounds of mass drug administration (MDA). The next challenge is to determine when MDA can be stopped. We performed a simulation study with the individual-based model LYMFASIM to help clarify this.MethodsWe used a model-variant for Indian settings. We considered different hypotheses on detectability of antigenaemia (Ag) in relation to underlying adult worm burden, choosing the most likely hypothesis by comparing the model predicted association between community-level microfilaraemia (Mf) and antigenaemia (Ag) prevalence levels to observed data (collated from literature). Next, we estimated how long MDA must be continued in order to achieve elimination in different transmission settings and what Mf and Ag prevalence may still remain 1 year after the last required MDA round. The robustness of key-outcomes was assessed in a sensitivity analysis.ResultsOur model matched observed data qualitatively well when we assumed an Ag detection rate of 50 % for single worm infections, which increases with the number of adult worms (modelled by relating detection to the presence of female worms). The required duration of annual MDA increased with higher baseline endemicity and lower coverage (varying between 2 and 12 rounds), while the remaining residual infection 1 year after the last required treatment declined with transmission intensity. For low and high transmission settings, the median residual infection levels were 1.0 % and 0.4 % (Mf prevalence in the 5+ population), and 3.5 % and 2.0 % (Ag prevalence in 6–7 year-old children).ConclusionTo achieve elimination in high transmission settings, MDA must be continued longer and infection levels must be reduced to lower levels than in low-endemic communities. Although our simulations were for Indian settings, qualitatively similar patterns are also expected in other areas. This should be taken into account in decision algorithms to define whether MDA can be interrupted. Transmission assessment surveys should ideally be targeted to communities with the highest pre-control transmission levels, to minimize the risk of programme failure.Electronic supplementary materialThe online version of this article (doi:10.1186/s13071-016-1768-y) contains supplementary material, which is available to authorized users.

Highlights

  • India has made great progress towards the elimination of lymphatic filariasis

  • The purpose of our study is to assess the required duration of mass drug administration (MDA) to achieve elimination and the associated 1-year post-treatment values of Mf and Ag prevalence associated with successful elimination, both for the community as a whole and for 6–7 year children only

  • The observed data show considerable variation around the model-predicted values, which can be explained by sampling variation due to relatively small sample sizes in the data compounded by variation in the age-composition of the study sample and geographic variation in underlying transmission conditions

Read more

Summary

Introduction

By 2015, most endemic districts had completed at least five annual rounds of mass drug administration (MDA). The recommended strategy is to treat entire at-risk populations annually through mass drug administration (MDA) with a single dose of ivermectin and albendazole (IVM + ALB) in sub-Saharan Africa or with diethylcarbamazine and albendazole (DEC + ALB) in other regions, including India, for a minimum of 5 years with effective population coverage of treatment [1, 3]. By 2015, most endemic districts have completed the WHO recommended minimum of five annual effective (i.e. at least 65 % treatment coverage) rounds of MDA with the diethylcarbamazine-albendazole drug-combination (DEC + ALB) [4]. The key challenge now is to determine whether this effort has been sufficient to interrupt transmission, so that MDA can safely be stopped in all treated areas [5, 6]. Effective monitoring and evaluation are essential to assess whether elimination programmes are on track and whether infection levels have been brought below the critical threshold

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call