Assessment Of Performance And Impact Of A Two-Year Nationwide Schistosomiasis Haematobia Control Programme In Burkina Faso (2004 - 2005)

Abstract

Schistosoma haematobium infection or schistosomiasis haematobia or urinary schistosomiasis is the most common form of schistosomiasis affecting more than 60 million people in 46 sub-Saharan Africa countries. Symptoms and signs include chronic pain, anaemia, inflammation, haematuria, fibrosis and calcification of the bladder and the urinary and genital tracts, and ultimately bladder cancer. The disease is spreading as a result of increase in irrigation and water impoundment schemes that favours colonization by Bulinus spp. snail vectors. Treatment with praziquantel can prevent the development of chronic morbidity and forms the basis of the WHO-recommended preventive chemotherapy strategy for control of schistosomiasis. With this strategy, populations groups at-risk, especially school-age children, are treated at regular intervals, at frequencies determined by the levels of disease transmission. Treatment activities are usually carried out in schools which provide easy access to school-age children; nonenrolled school-age children, which can be many especially in rural areas, might however be left untreated. Issues of costs, manpower, expertise and the vast geographical areas have limited the implementation of disease control interventions in many countries to either small-scale or pilot projects. Most intervention programmes have also lacked a monitoring and evaluation framework which is key to achieving sustainability of control programmes. Thus most studies have reported on performance and impact extrapolated from results of small scale interventions. In 2003 the Ministry of Health of Burkina Faso opted to implement a nation-wide intervention to cover all school-age children irrespective of educational status, with support from the Schistosomiasis Control Initiative-Imperial College London, and the Bill & Melinda Gates Foundation. This decision offered the opportunity, and the subject of thesis, to investigate the performance and impact of a nation-wide programme relying on large-scale administration of praziquantel to control urinary schistosomiasis. A characteristic of this programme was its coordination by the Ministry of Health and use of only local human resources for its implementation that combined both school-based and community-based channels. The programme targeted each child eligible for treatment within a timeframe of 12 months during 2004-2005 in all 13 administrative regions of Burkina Faso. The present study investigated the programme's performance in terms of coverage and costs, and measured infection and morbidity indicators to determine its impact using both longitudinal cohorts and cross-sectional studies. Children aged 6-14 years were randomly selected from 16 sentinel schools in four regions located in the different ecological areas of Burkina Faso and were recruited into the longitudinal cohort at baseline, approximately six months before treatment. Infection indicators such as prevalence, intensity of infection and the proportion of heavy-intensity infections, as well as morbidity indicators such as haemoglobin concentration, anaemia status, microhaematuria and nutritional indexes, were all measured using recommended protocols. The study also measured these indicators cross-sectionally in newly enrolled children one year post-treatment to assess the quality of the community-based delivery channel and in school children randomly selected and matched by age and sex to those in the cohort in the second year, to validate the results obtained for the longitudinal study. A total of 3,322,564 school-age children were treated which was equivalent to a coverage of90.8% of the eligible population. 39.9% of the children were treated through schools whilst the majority, 60.1 %, through the community delivery channel. The total costs of the programme amounted to US$ 1,067,284, made up of delivery cost (US$ 325,936) and drug costs (US$ 741,348). The delivery cost per child treated was US$ 0.098 and the full cost of treating each child was US$ 0.32l. Out of 1,727 children recruited in the original baseline longitudinal cohort, 1,131 and 763 were followed up in the first and second years respectively, thus 596 and 368 respectively dropped out. Children that dropped out in the first year were mostly males (P<0.004), older (P<O.OOl), more wasted (P<O.OOl) and more stunted (P<O.OOl) than those who remained in the cohort. The parasitological parameters however did not differ significantly between the two groups. Similarly, there were more male (P<0.05) and older (P<0.01) children among the drop outs of the second follow-up. A significant increase in Hb concentration from 109.7g/l at baseline to 112.5g/l, and a reduction in prevalence of from 65.8% to 61.6%, were observed. Absence of haem aturi a increased from 50.4% to 89.5%. No significant changes were observed with nutritional indicators (wasting and stunting). The prevalence of infection decreased significantly from 59.6% to 6.2% at the first follow up and increased to 7.7% in the second year. Similarly the mean intensity of infection decreased from 94.2 eggsllOml to 1.0 eggsllOml and increased to 6.8 eggsllOml at the first and second follow-up respectively. The proportion of heavy-intensity infections was reduced from 25% to 0.4% after year one and remained below 2% at the end of the second year. A significant reduction of infection indicators 1 and 2 years posttreatment was also registered by the two cross-sectional study components. A combined school- and community-based drug distribution strategy was effective in attaining high coverage rates of all school-age children in communities, and inclusion of the community component did not significantly increase the budget. Drug costs were significant and fluctuations in cost of praziquantel might have a significant impact on overall costs of the intervention. The analysis of the recurrent costs suggests that delivery costs are expected to decrease further with each subsequent round of treatment. A calendar of retreatment with single administration of praziquantel every two years or more would be sufficient to control morbidity associated with urinary schistosomiasis, but will require further research. For sustainable intervention programmes, savings from the reduction in treatment frequency should be invested into strengthening the monitoring and evaluation of programme, which is usually not accorded the needed importance. This would allow for fine-tuning of the intervention strategies as programme implementation progresses. The monitoring and evaluation should be mainly based on cross-sectional surveys conducted at biennial intervals and include all children irrespective of educational status, with the aim of verifying that children in both school and communities have actually been targeted by the disease control intervention.

Description

Thesis (PhD)

Keywords

Schistosomiasis Haematobia, Burkina Faso

Citation