Monitoring the impact of a national school based deworming programme on soil-transmitted helminths in Kenya: the first three years, 2012 – 2014
© The Author(s). 2016
Received: 17 November 2015
Accepted: 4 July 2016
Published: 25 July 2016
In 2012, the Kenyan Ministries of Health and of Education began a programme to deworm all school-age children living in areas at high risk of soil-transmitted helminths (STH) and schistosome infections. The impact of this school-based mass drug administration (MDA) programme in Kenya is monitored by the Kenya Medical Research Institute (KEMRI) as part of a five-year (2012–2017) study. This article focuses on the impact of MDA on STH infections and presents the overall achieved reductions from baseline to mid-term, as well as yearly patterns of reductions and subsequent re-infections per school community.
The study involved a series of pre- and post-intervention, repeat cross-sectional surveys in a representative, stratified, two-stage sample of schools across Kenya. The programme contained two tiers of monitoring; a national baseline and mid-term survey including 200 schools, and surveys conducted among 60 schools pre- and post-intervention. Stool samples were collected from randomly selected school children and tested for helminth infections using Kato-Katz technique. The prevalence and mean intensity of each helminth species were calculated at the school and county levels and 95 % confidence intervals (CIs) were obtained by binomial and negative binomial regression, respectively, taking into account clustering by schools.
The overall prevalence of STH infection at baseline was 32.3 % (hookworms: 15.4 %; Ascaris lumbricoides: 18.1 %; and Trichuris trichiura: 6.7 %). After two rounds of MDA, the overall prevalence of STH had reduced to 16.4 % (hookworms: 2.3 %; A. lumbricoides: 11.9 %; and T. trichiura: 4.5 %). The relative reductions of moderate to heavy intensity of infections were 33.7 % (STH combined), 77.3 % (hookworms) and 33.9 % (A. lumbricoides). For T. trichiura, however, moderate to heavy intensity of infections increased non-significantly by 18.0 % from baseline to mid-term survey.
The school-based deworming programme has substantially reduced STH infections, but because of ongoing transmission additional strategies may be required to achieve a sustained interruption of transmission.
Helminth infections are a major public health problem and cause mal-nutrition and cognitive impairment [1–4], with school children typically experiencing the heaviest burden of disease . Soil-transmitted helminths (STH: Ascaris lumbricoides, Trichuris trichiura, and the hookworms Necator americanus and Ancylostoma duodenale) are among the diseases classified by the World Health Organization as neglected tropical diseases (NTDs) . STH are endemic in nearly 166 countries globally  with majority of them now implementing mass drug administration (MDA) programmes, either through school-based deworming (SBD) or lymphatic filariasis control programmes [8, 9].
STH affects more than two billion people worldwide. Recent estimates suggest that A. lumbricoides infects 1.2 billion people, T. trichiura 795 million, and hookworms (Ancylostoma duodenale and Necator americanus) 740 million . The greatest numbers of STH infections occur in sub-Saharan Africa, the Americas, China and East Asia. Warm climates and adequate moisture are essential for the hatching or embryonation of STH eggs in the environment or development of larvae.
Infection is associated with ingestion of eggs from contaminated soil (A. lumbricoides and T. trichiura) or by active penetration of the skin by larvae in the soil (hookworms) . People infected with STHs produce a wide range of symptoms that include intestinal manifestations (diarrhoea, abdominal pain), general malaise and weakness that may affect working and learning capacities, and impaired physical growth. Hookworms cause chronic intestinal blood loss that result in anaemia. An important epidemiological feature is their highly aggregated distribution; the majority of patients harbour low intensity of infections, while only few individuals harbour very heavy infections .
Although school-based deworming has many benefits for treated children, it does not prevent re-infections, which can occur rapidly after treatment, particularly for A. lumbricoides and T. trichiura. Hence, there is a need for frequent and consistent MDA to maximise the benefit of preventive chemotherapy .
In 2012, the Kenyan Ministries of Health and Education began a school-based deworming program in 66 districts (now sub-counties) identified as having a high prevalence of STH and schistosome infections in four regions (Western, Nyanza, Rift Valley and Coast). According to the Kenyan National School Health Policy, treatment is administered to all school-age children, including those out of school, based on the prevalence and intensity of STH and schistosome infections in the area in order to reduce infection. The goal of the school-based deworming programme is to reduce the prevalence of moderate to heavy infections to < 1 % such that the infections are no longer of public health importance . The programme is embedded within the National Multi-Year Strategic Plan for the Control of Neglected Tropical Diseases, which was launched in 2011, and lays the basis for a comprehensive strategy for the integration of neglected tropical disease control efforts .
The impact of the Kenyan school-based deworming programme on STH and schistosome infections is being monitored through to 2017 with specific objectives outlined elsewhere , and includes pre-post intervention and repeated cross-sectional surveys as outlined in Additional file 1: Figure S1. Our analysis herein presents the findings on STH infections in 200 schools surveyed for baseline (2012) and mid-term (2014) assessment and in 60 schools surveyed yearly from 2012 to 2015 in the above mentioned regions. The results for schistosome infections are not reported due to the inconsistency in the delivery of praziquantel treatment caused by logistical challenges.
The specific aims of this study were to (i) determine the overall achieved reductions in infections from baseline to mid-term; (ii) determine the yearly patterns of treatment impact and re-infections per school community; and (iii) determine the impact on infections of high intensity (moderate or heavy infections).
Monitoring and evaluation (M&E) of the STH programme includes a series of pre- and post-intervention, repeat cross-sectional surveys in a representative, stratified, two-stage sample of schools across Kenya. Sub-county stratification was based on both geography and anticipated infection prevalence. There are two tiers of monitoring: (i) a national baseline, mid-term (after two MDA rounds) and end-term survey (after four MDA rounds) including 200 schools in 20 sub-counties from 16 counties, that aimed to establish an accurate national measurement of infection levels and monitor long term changes in worm infection levels; and (ii) surveys conducted in 60 of the 200 schools before and 3–5 weeks after the deworming activity (pre-post surveys) to evaluate reductions in infections that can be directly attributed to programme implementation (Additional file 1: Figure S1) .
A sample size of 200 schools for the baseline, mid-term and end-term assessment was determined to be adequate to detect a 5 % change in prevalence across years, assuming a power of β = 0.8 and test size α = 0.05, and considering the anticipated variance in prevalence .
Number of schools (children) sampled in each region for each tier of monitoring
Baseline, mid-term & endterm
Baseline surveys in 200 schools were conducted between January and April 2012 and year 1 (Y1) post-MDA surveys were conducted in 60 schools between September 2012 and May 2013. In year 2 (Y2), the pre-MDA surveys took place between May 2013 and February 2014 and the post-MDA surveys took place between July 2013 and April 2014. Mid-term surveys in year 3 (Y3) were carried out between March 2014 and February 2015, followed by post-MDA surveys in October 2014 and July 2015. In each school, 18 children (9 girls and 9 boys) were sampled randomly from each of the six classes; one Early Childhood Development (ECD) class and classes 2–6 using random number tables, for a total of approximately 108 children per school. Information was captured electronically during the interviews using Open Data Kit (ODK) for android-based smartphones  that stored, provisionally checked and later transmitted data to KEMRI headquarters in Nairobi.
Selected schools were visited one week prior to the survey date to explain the purpose of the survey to head teachers and school committees, and permission was sought at the school-level. Parental consent from parents/guardians of children in ECD and classes 2–6 was based on passive, opt-out consent rather than written opt-in consent. Selected children were asked to provide stool samples which were examined in duplicate for the presence of STH eggs by two different technicians using the Kato-Katz method; any discrepancies were resolved by a third senior technician. Ten percent of all samples were re-examined by a senior technician. The presence of each infection was recorded as eggs per gram of stool. Within the national deworming programme, all participants received treatment with albendazole (400 mg) for STH infection according to World Health Organization (WHO) guidelines .
The overall prevalence of each helminth species and STH combined was calculated at the school and county level and the 95 % confidence intervals (CIs) were obtained by binomial regression taking into account school clusters. Mean egg counts were expressed as arithmetic mean eggs per gram of feaces (epg) and since the distribution of egg counts was overdispersed, 95 % CIs were obtained using negative binomial regression models taking into account school clusters. Infection intensities were classified into light, moderate and heavy infections according to WHO guidelines (Additional file 1: Table S1) and the prevalence of each infection class together with 95 % CIs were obtained using binomial regression adjusting for clustering by schools. The relative reductions in prevalence and intensity of each STH species and light to heavy infections from Y1 baseline to Y3 Pre-MDA were calculated using multivariable mixed effects models with random intercepts for schools and counties and P-values were obtained using Wald test. We also estimated the absolute reductions in prevalence of each STH species using multivariable mixed effects models. All statistical analyses were carried out using STATA version 14.0 (STATA Corporation, College Station, TX, USA). Graphs were developed using the ggplot package implemented in R . School locations were mapped using ArcGIS Desktop version 10.2.2 software (Environmental Systems Research Institute Inc., Redlands, CA, USA). Hotspot analysis for STH infections at the school level was carried out using the ArcGIS’s cluster and outlier analysis tool, a school was identified as a significant hotspot for any of the STH based on the Anselin Local Moran’s I statistic .
Number of schools (children) examined in each survey
Year 1 (2012)
Year 2 (2013)
Year 3 (2014)
Reduction of infections from baseline to mid-term assessment
In the baseline survey, the overall prevalence of combined STH infection in the 199 schools was 32.3 % (95 % CI: 30.0–34.8). A. lumbricoides was the most common STH species, with 18.1 % (95 % CI: 15.8–20.7) of children infected, followed by hookworms with 15.4 % (95 % CI: 13.6–17.6) and T. trichiura with 6.7 % (95 % CI: 5.4–8.2). In the mid-term survey, the combined STH prevalence was reduced to 16.4 % (95 % CI: 14.4–18.6); with A. lumbricoides reduced to 11.9 % (95 % CI: 10.2–13.9), hookworms to 2.3 % (95 % CI: 1.8–3.0) and T. trichiura to 4.5 % (95 % CI: 3.4–6.0). These translated to a relative reduction in the prevalence of combined STH of 49.3 % (Wald test: Z = -13.69, P < 0.001), with species-specific relative reductions of 85.0 % (Wald test: Z = -14.65, P < 0.001) for hookworm, 34.0 % (Wald test: Z = -8.81, P < 0.001) for A. lumbricoides and 32.3 % (Wald test: Z = -3.91, P < 0.001) for T. trichiura.
Overall prevalence (P, %), mean intensity (epg), relative reductions % (Wald test: Z-statistic, P-value) and absolute reductions % (Wald test: Z-statistic, P-value) of STHs: Baseline and mid-term
P % (95 % CI)
P% (95 % CI)
49.3 (Z = -13.69, P < 0.001)
15.9 (Z = -16.95, P < 0.001)
85.0 (Z = -14.65, P < 0.001)
13.1 (Z = -13.92, P < 0.001)
34.0 (Z = -8.81, P < 0.001)
6.1 (Z = -8.15, P < 0.001)
32.3 (Z = -3.91, P < 0.001)
2.1 (Z = -4.36, P < 0.001)
epg (95 % CI)
epg (95 % CI)
IRR % (Z-statistic, P-value)
87.1 (Z = -6.60, P < 0.001)
42.1 (Z = -7.98, P < 0.001)
49.5 (Z = -1.11, P = 0.267)
Additional file 1: Table S2 presents the baseline and mid-term prevalence of each STH species and relative reductions by county. At baseline, hookworm prevalence was between 20 and 50 % in Bungoma, Busia, Kakamega, Migori, Kilifi and Kwale counties; A. lumbricoides prevalence was between 20 and 50 % in Bomet, Kericho, Kisii, Narok, Nyamira, Bungoma, Kakamega and Vihiga counties; and T. trichiura prevalence was between 20 and 50 % in Narok County only. Only two counties (Narok and Vihiga) had prevalence of any STH above 50 %. Relative reductions in prevalences were higher for hookworms with seven counties recording > 90 % reductions; for A. lumbricoides only two counties (Mombasa and Taita Taveta) recorded > 90 % reductions while Kilifi showed 81.6 % reduction. Similarly, relative reductions for T. trichiura were greater than 90 % in only one county. Baseline and mid-term mean intensity of each STH species and relative reductions by county are presented in (Additional file 1: Table S3).
Reduction of moderate to heavy intensity infection from baseline to mid-term assessment
Prevalence of light, moderate and heavy mean intensity of infections [% (95 % CI)] in Y1 and Y3 and relative reductions % (Wald test: Z-statistic, P-value)
Relative reduction (%)
55.1 (Z = -14.17, P < 0.001)
32.7 (Z = -6.47, P < 0.001)
75.1 (Z = -2.20, P = 0.028)
85.2 (Z = -15.25, P < 0.001)
86.9 (Z = -4.11, P < 0.001)
61.7 (Z = -1.62, P = 0.105)
34.1 (Z = -6.87, P < 0.001)
33.9 (Z = -6.79, P < 0.001)
34.6 (Z = -4.56, P < 0.001)
Increase (58.4 %) (Z = 1.70, P = 0.088)
94.0 (Z = -1.98, P = 0.047)
Patterns of annual treatment impact and re-infections
Relative and absolute reduction, % (Wald test: Z-statistic, P-value), in prevalence and mean intensity of infection: Baseline to Y3 pre-MDA
Relative reduction (%)
Relative reduction (%)
Relative reduction (%)
Absolute reduction (%)
Y1 to Y2
Y2 to Y3
Y1 to Y3
Y1 to Y3
42.3 (Z = -7.33, P < 0.001)
14.3 (Z = -2.10, P = 0.035)
50.6 (Z = -9.02, P < 0.001)
16.8 (Z = -11.46, P < 0.001)
36.6 (Z = -5.02, P < 0.001)
15.7 (Z = -1.45, P = 0.148)
46.6 (Z = -5.05, P < 0.001)
72.6 (Z = -6.37, P < 0.001)
45.8 (Z = -3.07, P = 0.002)
85.2 (Z = -8.15, P < 0.001)
14.0 (Z = -8.12, P < 0.001)
71.7 (Z = -3.60, P < 0.001)
66.3 (Z = -3.21, P = 0.001)
90.4 (Z = -6.36, P < 0.001)
35.2 (Z = -6.06, P < 0.001)
1.0 (increase)a (Z = 0.20, P = 0.843)
34.4 (Z = -6.17, P < 0.001)
6.7 (Z = -5.37, P < 0.001)
35.8 (Z = -4.66, P < 0.001)
14.5 (Z = -1.30, P = 0.192)
45.1 (Z = -4.66, P < 0.001)
5.9 (Z = -0.43, P = 0.671)
40.5 (Z = -3.46, P = 0.001)
44.0 (Z = -3.86, P < 0.001)
2.4 (Z = -3.46, P < 0.001)
45.5 (increase)a (Z = 1.35, P = 0.176)
44.3 (Z = -2.14, P = 0.033)
19.0 (Z = -1.06, P = 0.290)
For hookworms and A. lumbricoides, higher reductions in prevalence and intensity of infections were observed after the first MDA than the second MDA. Specifically, after the first MDA, prevalence for STH combined were significantly reduced by 42.3 % with species-specific reductions of 72.6 % for hookworms, 35.2 % for A. lumbricoides and 5.9 % (non-significant) for T. trichiura. However, during the second MDA, the relative reductions for each species were all significant except A. lumbricoides which instead showed re-infection. The absolute reductions in infections after two rounds of MDA for all of the species were as follows: STH combined (16.8 %); hookworms (14.0 %); A. lumbricoides (6.7 %); and T. trichiura (2.4 %).
Absolute increase, % (Wald test: Z-statistic, P-value), in prevalence (PI) and mean intensity of infection (II): Re-infections between different rounds of MDA
Y2 pre-MDA vs Y1 post-MDA
Y3 pre-MDA vs Y2 post-MDA
Y3 pre-MDA vs Y1 post-MDA
13.9 (Z = -19.40, P < 0.001)
11.1 (Z = -20.80, P < 001)
12.5 (Z = -19.58, P < 0.001)
616 (Z = 44.18, P < 0.001)
504 (Z = 38.96, P < 001)
524 (Z = 39.20, P < 0.001)
3.8 (Z = -17.44, P < 0.001)
2.3 (Z = -16.62, P < 0.001)
2.8 (Z = -18.11, P < 0.001)
12 (Z = 9.32, P < 0.001)
5 (Z = 5.87, P < 0.001)
7 (Z = 8.13, P < 0.001)
7.4 (Z = -19.63, P < 0.001)
7.2 (Z = -19.18, P < 0.001)
7.5 (Z = -19.19, P < 0.001)
590 (Z = 41.97, P < 0.001)
493 (Z = 38.26, P < 0.001)
507 (Z = 38.02, P < 0.001)
4.7 (Z = -13.60, P < 0.001)
2.8 (Z = -17.36, P < 0.001)
3.7 (Z = -15.20, P < 0.001)
13 (Z = 5.61, P < 0.001)
6 (Z = 6.46, P < 0.001)
10 (Z = 5.46, P < 0.001)
STH infections hotspots
Hotspot analysis was performed to investigate if any school locations had exceptionally high STH infection levels (hotspots) during baseline and after two rounds of MDA (mid-term). During the baseline, 3/199 (1.5 %) schools (two from Homabay and one from Kisii counties), were identified as hotspots for hookworms, and 2/199 (1.0 %) schools, (both from Vihiga County), as hotspots for T. trichiura infection. No hotspots were reported for A. lumbricoides during baseline. After two rounds of MDA, only one school in Vihiga County was identified as hotspot for T. trichiura infection while no hotspots were found for hookworms and A. lumbricoides infections.
School treatment coverage (%) by county
Total schools targeted
Schools treated (Coverage %)
Total schools targeted
Schools treated (Coverage %)
Total schools targeted
Schools treated (Coverage %)
School-based deworming for the control of STH has been identified as one of the most cost-effective health interventions both in theory and practice [22–24]. Currently, an increasing number of STH endemic countries in the world, including Kenya , are implementing school-based deworming programmes and this paper presents the results of the impact of the first three years of the programme.
During baseline, observed prevalences were 32.3, 15.4, 18.1 and 6.7 %, with mean intenisties of 1756, 63, 1659 and 33 epg for STH combined, hookworms, A. lumbricoides and T. trichiura, respectively. Baseline STH combined prevalence was lower than those reported from other national school-based deworming programmes in Ethiopia (41 % ); Thailand (70 % ) and Ghana (36.3 % ). In this study, we found that A. lumbricoides was the most common STH followed by hookworms and T. trichiura. This reiterates evidence from previous reports around the world that suggest A. lumbricoides as being more prevalent compared to the other helminth infections [27, 28].
The prevalences of STH combined and each worm type after two rounds of treatment dropped to 16.4, 2.3, 11.9 and 4.5 % with mean intensities of 985, 8, 960 and 17 epg for STH combined, hookworms, A. lumbricoides and T. trichiura, respectively. Relative reductions of infections after two rounds of MDA were of; 50.6, 85.2, 34.4 and 44.0 %, respectively, for the prevalence, and 46.6, 90.4, 45.1 and 19.0 %, respectively, for the mean intensity. The reductions reported here are substantially higher than what was reported after seven years of deworming in Myanmar . Further, our results corroborate other studies carried out in Kenya , which indicated a gradual decrease of observed combined STH prevalence over time across the country, with populations experiencing lower observed prevalence of infection in more recent years. The mid-term assessment showed that in overall the annual deworming is most effective against hookworms (reduction in intensity ≥ 90 %) but less effective against A. lumbricoides (reduction < 45 %) and T. trichiura (reduction < 44 %); a probable reflection of the higher rates of re-infection for A. lumbricoides and T. trichiura. The larger impact on hookworms has been highlighted previously in a review on STH infections in school-age children in sub-Saharan Africa .
The observed overall substantial decline in species-specific infections may be attributable to the direct impact of the school-based deworming programme, school health interventions, urbanisation and general improvements in socio-economic status, with associated improvements in living conditions, water, sanitation and hygienic (WASH) behaviour. For example, comparison of Demographic and Health Surveys from 1989 and 2009 reveals that access to an improved water source has risen nationally from 36.0 to 63.0 % of households . Such secular changes are probably not unique to Kenya and it is likely that much of Africa has experienced a gradual decline in the prevalence of parasitic diseases, including helminth infections .
During the baseline, the observed prevalence and intensity of all STH species were highest in Western Kenya while in Coast pockets of high prevalence of hookworms were observed. In Y3 mid-term, there was substantial reduction of hookworms and T. trichiura across all counties. This finding agrees with a study by Pullan et al. , which spatially modeled the transmission of soil- transmitted helminths and showed that MDA was most warranted in the western and coastal areas of the country.
The prevalence and mean intensity of species-specific infections varied considerably by region, county and school levels. At baseline, Narok and Vihiga were the only counties which showed > 50 % prevalence of any STH. Relative reductions in prevalence showed that impact of MDA against A. lumbricoides was satisfactory (reduction ≥ 90 %) in only two counties, Mombasa and Taita Taveta, while it was satisfactorily effective for hookworms (reduction ≥ 90 %) in seven counties and for T. trichiura (reduction ≥ 90 %) in only one county. Further, at the individual level, patterns of infection and intensity varied by age-group and sex of the children.
Patterns of annual treatment impact and re-infections per school community were analysed in 59 schools using pre-post MDA surveys. The observed impact of the deworming programme between baseline and the mid-term assessment is determined by immediate reductions in infections after Y1 and Y2 treatment deliveries followed by re-infections between the treatments. Immediate infection reductions are likely to be influenced by the treatment coverage, which itself can be influenced by the broader context of the programme, such as quality of education and health systems, infrastructure and capacity to deliver health services and the economic situation. The rate of re-infection per school community is likely to be influenced by general risk factors for STH infections such as environmental conditions, WASH and socio-economic conditions and baseline infection levels .
In this study, we report re-infection rates of ≤ 8 % for each STH species after two rounds of MDA, with A. lumbricoides showing the highest rates of re-infection, followed by T. trichiura and hookworms. A recent meta-analysis showed that after MDA, the prevalence of STH infections rapidly recovers in most endemic areas: six months post-treatment, the prevalence of all three species reached or exceeded half the initial level; and at 12 months post-treatment follow-up, the prevalence of A. lumbricoides and T. trichiura usually returned to levels close to the initial pre-treatment, while levels of hookworm re-infection continued to fluctuate at about half pre-treatment level . Rates of re-infections after treatment are influenced by species-specific characteristics, such as the life expectancy of the adult worm, the underlying intensity of transmission, environmental conditions that influence the development and survival of the free-living stages in the external environment, the relative rate of infection of different age groups, and drug efficacy [9, 32].
Notwithstanding the occurrence of re-infection, the first three years of intervention have been successful in reducing infections of moderate to heavy intensity, as well as the overall prevalence of STH infections. After the two rounds of MDA, infections of moderate intensity were significantly reduced by 32.7, 86.9 and 33.9 % for STH combined, hookworms and A. lumbricoides, respectively while they increased non-significantly for T. trichiura by 58.4 %. Other national control programmes have reported similar reductions, especially for any STH infections; particularly, after seven years of deworming in Myanmar, reduction of the infections of moderate to heavy intensity for any STH reduced from 18.5 % to less than 7 % . In our study, we did not report cases of heavy infections for A. lumbricoides since their values were truncated at 24,000 epg; however, heavy infections for both hookworms and T. trichiura showed 0.1 % prevalence at baseline.
Lastly, this study points out the existence of STH transmission hotspots in the study area. During the baseline survey, three schools from Homabay and Kisii counties and two schools from Vihiga County were reported as transmission hotspots for hookworm and T. trichiura infections respectively but after two rounds of MDA, only one school was reported as hotspot for T. trichiura infection. These hotspot schools were only found in western Kenya, suggesting that the prevailing environmental conditions in the area, such as climate, soil moisture and relative atmospheric humidity, might favour transmission of these STH parasites. The substantial reduction of the number of detected hotspots after two rounds of MDA suggests the efficacy of albendazole.
We recognize that our study was not without limitations, the diagnosis was based on routine parasitological procedures and a single stool sample may underestimate the prevalence of helminth infection . Moreover, the M&E programme does not follow-up individual children. Therefore, re-infections were estimated as the increase in infection levels by schools which may be influenced by variations in individual infections.
Our study provides robust evidence for the impact of the Kenya national school-based deworming programme on STH infections. After three years of implementation, the programme is associated with reduction of moderate to heavy mean intensity of STH infection, but because of re-infection due to ongoing transmission, infection levels are yet to fall to very low levels. Additional intervention strategies may be required to interrupt transmission of STH. This study’s data can be useful in contextualizing the impact produced by other deworming programmes worldwide.
CIFF, Children’s Investment Fund Foundation; CIs, confidence intervals; ECD, early childhood education; KEMRI, Kenya medical research institute; M&E, monitoring and evaluation; MDA, mass drug administration; NTDs, neglected tropical diseases; ODK, open data kit; SBD, school-based deworming; STH, soil transmitted helminths; WASH, water, sanitation and hygiene; WHO, World Health Organization; Y1, year 1; Y2, year 2; Y3, year 3
The authors are grateful to the Neglected Tropical Disease Unit, Ministry of Health, Nairobi, Kenya and the County ministries of health and education for their on-going support for this work. We would like to thank the school children, school teachers, sub-county education officials and the sub-county health management team for their support. We would like to specially thank all the members of the study team and field personel for their dedication. The study was funded by CIFF. CO is supported by CIFF through KEMRI - ESACIPAC as Statistician. SJB is supported by a Wellcome Trust Senior Fellowship in Basic Biomedical Science (098045) which also supports RLP and BN. This paper is published with the permission of the Director, KEMRI.
The financial support for this research has been provided through the grant number 208 by Children’s Investment Fund Foundation (CIFF). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Availability of data and material
The datasets supporting the conclusions of this article are included within the article and its additional files. Epidemiological data: We make available school-level datasets from each of the survey rounds (Additional file 2: Dataset 1). In these datasets, individual-level STH infection and demographic information were aggregated at the school level. School level treatment coverage: Information on treatment coverage, as reported by the schools, was obtained from Evidence Action, an international non-governmental organization, who provides technical support to government programmes.
CO participated in the data collection, analysis and developed the draft manuscript. CM designed the study. All other authors played an important role in data collection (JK, ES), data analysis (BN) and interpretation of findings (SJB, BN, JVG, MCF, RLP and CM). All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The study protocol received ethical approval from the KEMRI’s Scientific Steering Committee and the Ethics Review Committee (SSC No. 2206). Additional approval was provided by the appropriate county-level health and education authorities, who were briefed about the surveys. At the school level, parental consent was based on passive, opt-out consent rather than written opt-in consent owing to the low risk and routine nature of the study procedure. Individual assent was obtained from each child before participation in the surveys.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Booth M, Bundy DA. Comparative prevalences of Ascaris lumbricoides, Trichuris trichiura and hookworm infections and the prospects for combined control. Parasitology. 1992;105:151–7.View ArticlePubMedGoogle Scholar
- Bundy DA, Golden MH. The impact of host nutrition on gastrointestinal helminth populations. Parasitology. 1987;95:623–35.View ArticlePubMedGoogle Scholar
- Stoltzfus RJ, Albonico M, Chwaya HM, Savioli L, Tielsch J, Schulze K, et al. Hemoquant determination of hookworm-related blood loss and its role in iron deficiency in African children. Am J Trop Med Hyg. 1996;55:399–404.PubMedGoogle Scholar
- Watkins WE, Pollitt E. “Stupidity or worms”: do intestinal worms impair mental performance? Psychol Bull. 1997;121:171–91.View ArticlePubMedGoogle Scholar
- Cairncross S, Valdmanis V. Chapter 41 Water supply, sanitation and hygiene promotion. In: Dean TJ, Joel GB, Anthony RM, George A, Mariam C, David BE, Prabhat J, Anne M, Philip M, editors. Disease control priorities in developing countries. Washington DC: World Bank; 2006. p. 771–92.Google Scholar
- World Health Organization. Accelerating work to overcome the global impact of neglected tropical diseases: a roadmap for implementation. Washington: WHO; 2012. p. 1–42.Google Scholar
- Pullan RL, Smith JL, Jasrasaria R, Brooker SJ. Global numbers of infection and disease burden of soil-transmitted helminth infections in 2010. Parasit Vectors. 2014;7:37.View ArticlePubMedPubMed CentralGoogle Scholar
- World Health Organization. Soil-transmitted helminthiases: estimates of the number of children needing preventive chemotherapy and number treated, 2009. Wkly Epidemiol Rec. 2011;86:257–67.Google Scholar
- Nikolay B, Mwandawiro CS, Kihara JH, Okoyo C, Cano J, Mwanje MT, et al. Understanding heterogeneity in the impact of national neglected tropical disease control programmes: evidence from school-based deworming in Kenya. PLoS Negl Trop Dis. 2015;9:e0004108.Google Scholar
- WHO. World Health Statistics 2012. http://books.google.com/books?hl=en&lr=&id=osms0oMN_qwC&oi=fnd&pg=PA7&dq=World+Health+Statistics&ots=iZU1J3AqjI&sig=sIBAWCK7qn9DYyQU_cHVERTK4Ks\nww.who.int. Accessed 09 July 2016.
- Vandemark LM, Jia T-W, Zhou X-N. Social science implications for control of helminth infections in Southeast Asia. Adv Parasitol. 2010;73:137–70.View ArticlePubMedGoogle Scholar
- Holland CV. Predisposition to ascariasis: patterns, mechanisms and implications. Parasitology. 2009;136:1537–47.View ArticlePubMedGoogle Scholar
- Jia T-W, Melville S, Utzinger J, King CH, Zhou X-N. Soil-transmitted helminth reinfection after drug treatment: a systematic review and meta-analysis. PLoS Negl Trop Dis. 2012;6:e1621.View ArticlePubMedPubMed CentralGoogle Scholar
- CIFF. Kenya National School-Based Year 1 (2012–2013) Results Deworming Programme. 2013: https://ciff.org/documents/17/Kenya_National_SchoolBased_Deworming_Programme_Year1_evaluation.pdf. Accessed 09 July 2016.
- Mwandawiro CS, Nikolay B, Kihara JH, Ozier O, Mukoko D a, Mwanje MT, et al. Monitoring and evaluating the impact of national school-based deworming in Kenya: study design and baseline results. Parasit Vectors. 2013;6:198.View ArticlePubMedPubMed CentralGoogle Scholar
- Pullan RL, Gething PW, Smith JL, Mwandawiro CS, Sturrock HJW, Gitonga CW, et al. Spatial modelling of soil-transmitted helminth infections in Kenya: a disease control planning tool. PLoS Negl Trop Dis. 2011;5:e958.View ArticlePubMedPubMed CentralGoogle Scholar
- Brooker S, Kabatereine NB, Smith JL, Mupfasoni D, Mwanje MT, Ndayishimiye O, et al. An updated atlas of human helminth infections: the example of East Africa. Int J Health Geogr. 2009;8:42.View ArticlePubMedPubMed CentralGoogle Scholar
- Open Data Kit. Available from: http://opendatakit.org/. Accessed 09 July 2016.
- Crompton DWT. Preventive chemotherapy in human helminthiasis: coordinated use of anthelminthic drugs in control interventions: a manual for health professionals and programme managers. Geneva: World Health Organization; 2006.Google Scholar
- Wickham, Hadley. ggplot2: elegant graphics for data analysis. Springer Science and Business Media; 2009.Google Scholar
- Anselin L. Local indicators of spatial association—LISA. Geogr Anal. 1995 [accessed on: 27 Feb 2016]; Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1538-4632.1995.tb00338.x/full. Accessed 09 July 2016.
- PCD. The health and nutritional status of schoolchildren in Africa: evidence from school-based health programmes in Ghana and Tanzania. Trans R Soc Trop Med Hyg. 1998;92:254–61.Google Scholar
- Brooker S, Miguel EA, Moulin S, Luoba AI, Bundy DA, Kremer M. Epidemiology of single and multiple species of helminth infections among school children in Busia District, Kenya. East Afr Med J. 2000;77:157–61.PubMedGoogle Scholar
- Getachew M, Tafess K, Zeynudin A, Yewhalaw D. Prevalence soil-transmitted helminthiasis and malaria co-infection among pregnant women and risk factors in Gilgel Gibe Dam area, southwest Ethiopia. BMC Res Notes. 2013;6:263.View ArticlePubMedPubMed CentralGoogle Scholar
- Boel M, Carrara VI, Rijken M, Proux S, Nacher M, Pimanpanarak M, et al. Complex interactions between soil-transmitted helminths and malaria in pregnant women on the Thai-Burmese border. PLoS Negl Trop Dis. 2010;4:e887.View ArticlePubMedPubMed CentralGoogle Scholar
- Yatich NJ, Yi J, Agbenyega T, Turpin A, Rayner JC, Stiles JK, et al. Malaria and intestinal helminth co-infection among pregnant women in Ghana: prevalence and risk factors. Am J Trop Med Hyg. 2009;80:896–901.PubMedGoogle Scholar
- De Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, Savioli L. Soil-transmitted helminth infections: updating the global picture. Trends Parasitol. 2003;19:547–51.View ArticlePubMedGoogle Scholar
- Hotez PJ, Brindley PJ, Bethony JM, King CH, Pearce EJ, Jacobson J. Helminth infections: the great neglected tropical diseases. J Clin Invest. 2008;118:1311–21.View ArticlePubMedPubMed CentralGoogle Scholar
- Tun A, Myat SM, Gabrielli AF, Montresor A. Control of soil-transmitted helminthiasis in Myanmar: results of 7 years of deworming. Trop Med Int Health. 2013;18:1017–20.View ArticlePubMedGoogle Scholar
- Uneke CJ. "Soil transmitted helminth infections and schistosomiasis in school age children in sub-Saharan Africa: efficacy of chemotherapeutic intervention since World Health Assembly Resolution 2001." Tanzan J Health Res. 2010;1(12): 86–99.Google Scholar
- Macro ICF. Kenya Demographic and Health Survey 2008-09. KNBS; 2010.Google Scholar
- Anderson R, Truscott J, Hollingsworth TD. The coverage and frequency of mass drug administration required to eliminate persistent transmission of soil-transmitted helminths. Philos Trans R Soc B. 2014;369:20130435–5.Google Scholar
- Krauth SJ, Coulibaly JT, Knopp S, Traor M, N’Goran EK, Utzinger J. An in-depth analysis of a piece of shit: Distribution of Schistosoma mansoni and hookworm eggs in human stool. PLoS Negl Trop Dis. 2012;6(12):e1969.Google Scholar