Abstract

BackgroundThe World Health Organization recommends that schistosomiasis be treated through Mass Drug Administration (MDA). In line with this recommendation, Zimbabwe commenced a national helminth control program in 2012 targeting schoolchildren throughout the country for 6 years. This study, part of a larger investigation of the impact of helminth treatment on the overall health of the children, determined the effect of annual praziquantel treatment on schistosome infection and morbidity in a cohort of children during Zimbabwe’s 6-year national helminth control program.Methodology/Principal findingsA school-based longitudinal study was carried out in 35 sentinel sites across Zimbabwe from September 2012 to November 2017. The sentinel sites were selected following a countrywide survey conducted in 280 primary schools. Schistosoma haematobium was diagnosed using the urine filtration technique. Schistosoma mansoni was diagnosed using both the Kato-Katz and formol-ether concentration techniques. S. haematobium morbidity was determined through detection of macro and microhaematuria. A cohort of children aged 6–15 years old was surveyed annually before MDA and 6 weeks post treatment. Maximum treatment coverage reached 90% over the 6 rounds of MDA. At baseline S. haematobium infection prevalence and intensity were 31.7% (95% CI = 31.1–32.2) and 28.75 eggs/10ml urine (SEM = 0.81) respectively, while S. mansoni prevalence and intensity were 4.6% (95% CI = 4.4–4.8) and 0.28 eggs/25mg (SEM = 0.02). Prior to the 6th round of MDA, S. haematobium infection prevalence had reduced to 1.56% (p<0.001) and infection intensity to 0.07 (SEM 0.02). Six weeks later after the 6th MDA, both were 0. Similarly the prevalence of S. haematobium morbidity as indicated by haematuria also fell significantly from 32.3% (95% CI = 29.9–34.6) to 0% (p< 0.0001) prior to the final MDA. For S.mansoni, both prevalence and intensity had decreased to 0 prior to the 6th MDA. After 6 rounds of annual MDA, prevalence and intensity of both schistosome species decreased significantly to 0% (p< 0.0001).ConclusionZimbabwe’s helminth control program significantly reduced schistosome infection intensity and prevalence and urogenital schistosomiasis morbidity prevalence in a cohort of school-aged children, moving the schistosome prevalence in the children from moderate to low by WHO classification. These findings will inform the design of the country’s next stage interventions for helminth control and eventual elimination.

Highlights

  • Zimbabwe is endemic to several of the neglected tropical diseases (NTDs) as listed by the World Health Organization (WHO) [1]

  • Data from this study revealed high schistosomiasis prevalence in 55 districts and soil transmitted helminths occurring in 47 districts, with 33 districts being endemic to both types of NTDs

  • Following 6 annual rounds of Mass Drug Administration (MDA), the prevalence of S. haematobium decreased significantly to 0% (p

Read more

Summary

Introduction

Zimbabwe is endemic to several of the neglected tropical diseases (NTDs) as listed by the World Health Organization (WHO) [1]. From the very first community survey in Zimbabwe, Rhodesia, in 1932 [3], Zimbabwe has had programs to control schistosomiasis [4] These programs have targeted workers and schoolchildren using several approaches including treatment of infected people (first with tartar emetic and praziquantel(PZQ)), improving water and sanitation, snail control and education/awareness campaigns [4]. The World Health Organization recommends that schistosomiasis be treated through Mass Drug Administration (MDA) In line with this recommendation, Zimbabwe commenced a national helminth control program in 2012 targeting schoolchildren throughout the country for 6 years. The national survey indicated the different districts in the country which fell in the WHO classification of heavy, moderate and low schistosome endemicity based on the infection levels in the school children [15] Following this national survey, annual MDAs were carried out in September 2012, October 2013, January 2015, November 2015, November 2016 and November 2017. The children in the cohort study described here were treated during these MDAs

Objectives
Results
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