Effectiveness of a pre-treatment snack on the uptake of mass treatment for schistosomiasis in Uganda: a cluster randomized trial.

BACKGROUND: School-based mass treatment with praziquantel is the cornerstone for schistosomiasis control in school-aged children. However, uptake of treatment among school-age children in Uganda is low in some areas. The objective of the study was to examine the effectiveness of a pre-treatment snack on uptake of mass treatment. METHODS AND
FINDINGS: In a cluster randomized trial carried out in Jinja district, Uganda, 12 primary schools were randomized into two groups; one received education messages for schistosomiasis prevention for two months prior to mass treatment, while the other, in addition to the education messages, received a pre-treatment snack shortly before mass treatment. Four weeks after mass treatment, uptake of praziquantel was assessed among a random sample of 595 children in the snack schools and 689 children in the non-snack schools as the primary outcome. The occurrence of side effects and the prevalence and mean intensity of Schistosoma mansoni infection were determined as the secondary outcomes. Uptake of praziquantel was higher in the snack schools, 93.9% (95% CI 91.7%-95.7%), compared to that in the non-snack schools, 78.7% (95% CI 75.4%-81.7%) (p = 0.002). The occurrence of side effects was lower in the snack schools, 34.4% (95% CI 31.5%-39.8%), compared to that in the non-snack schools, 46.9% (95% CI 42.2%-50.7%) (p = 0.041). Prevalence and mean intensity of S. mansoni infection was lower in the snack schools, 1.3% (95% CI 0.6%-2.6%) and 38.3 eggs per gram of stool (epg) (95% CI 21.8-67.2), compared to that in the non-snack schools, 14.1% (95% CI 11.6%-16.9%) (p = 0.001) and 78.4 epg (95% CI 60.6-101.5) (p = 0.001), respectively.
CONCLUSIONS: Our results suggest that provision of a pre-treatment snack combined with education messages achieves a higher uptake compared to the education messages alone. The use a pre-treatment snack was associated with reduced side effects as well as decreased prevalence and intensity of S. mansoni infection. TRIAL REGISTRATION: www.ClinicalTrials.gov NCT01869465

RCT Entities:   Population Interventions Outcomes

Introduction

Schistosomiasis is a major global public health problem especially in sub-Saharan Africa [1]–[3]. The disability-adjusted life-years (DALYs) loss attributable to schistosomiasis and soil transmitted helminthiasis (STHs) combined (44 million) are more than those due to malaria (36 million) and close to those due to tuberculosis (47 million) [4]–[7]. According to the Global Burden of Disease Study (2010), schistosomiasis alone is responsible for an estimated 3.3 million DALYs [8].

Control strategies recommended by WHO for long-term morbidity control of schistosomiasis include provision of safe and effective anti-schistosomal drugs such as praziquantel, and preventive measures focusing on health education, clean water, and adequate sanitation [2],[3],[9]–[11]. In many developing countries in sub-Saharan Africa including Burkina Faso, Ghana, Mali, Niger, Ivory Coast, and Tanzania, regular chemotherapy with praziquantel is implemented as the main strategy for schistosomiasis control with varying levels of success [11]–[13]. The target is to provide regular treatment of at least 75% of school-age children at risk of morbidity in order to keep the worm burden in individuals low and confined [3]. In these countries, praziquantel is mainly delivered through school-based health programs at low cost [14]–[16].

In Uganda, school-based mass drug administration (MDA) for schistosomiasis is the main approach that was adopted by the national schistosomiasis control program and is currently implemented in more than 38 districts within regions surrounding large lakes and rivers [17]. The success of the school-based strategy was based on the premise that schools are widely distributed particularly in the rural areas with high enrollment and attendance rates, that teachers are willing to administer the drugs to the children, and that the children will accept the treatment. The benefit of this approach has been documented [18]–[20]. However, studies undertaken among school children have reported low uptake of praziquantel [21]–[23]. The fear of treatment and low school-attendance rates were highlighted as some of the major contributors to the low uptake. Praziquantel is generally perceived to be a strong drug that causes transient sickness and occasional fatalities and resistance to take the drug has been reported [24]–[27]. In a particular study conducted in Jinja district in Uganda, the fear of side effects of praziquantel, lack of knowledge about schistosomiasis prevention, and lack of teacher support to distribute treatment were the major factors thought to underpin the low uptake [23].

Due to the risk of side effects and the difficulties of administering a large number of tablets to individuals, drug administration should be accompanied by precautionary measures before mass treatment is rolled out [28]. The administration of praziquantel should be accompanied by concomitant administration of food to reduce the risk of side effects of the drug [29]–[31]. Considerable reductions in occurrence of side effects and high treatment coverage have been reported by large-scale national control programs where special feeding programs for the children to mitigate the side effects were provided [31],[32]. The Ugandan Government's policy under the universal primary education program requires that parents and care takers of children take responsibility for feeding their children while at school [33],[34]. In many parts of the country, children go to school in the morning without a meal because many parents cannot afford to meet the cost of a daily meal for their children while at school [34]. This situation implies that in schools where annual mass treatment for schistosomiasis is implemented, most children take the treatment on empty stomachs with the risk of widespread side effects [23],[35],[36]. In this study, we hypothesized that provision of a pre-treatment snack in combination with education messages for schistosomiasis prevention would improve uptake as well as reduce the occurrence of side effects attributable to praziquantel. It was anticipated that the improved uptake would reduce the prevalence and intensity of schistosomiasis infection.

Materials and Methods

Ethical Considerations

The study protocol was approved by Makerere University College of Health Sciences Higher Degrees, Research and Ethics Committee and granted ethical clearance by the Uganda National Council for Science and Technology. One month prior to the study, the objectives and the procedures of the study were explained to the district health and education authorities and to the parents or guardians of all children in the schools through half-day meetings held at the district health headquarters and the respective schools. During the meetings held in schools, written informed consent was obtained from the parents or guardians of all the children. Assent to participate in the study was obtained from all children. Children identified with schistosomiasis and/or STH were treated with praziquantel and/or albendazole.

Study Setting

The study was carried out in 12 primary schools in Walukuba division, Jinja district of south eastern Uganda between May and July 2013. Intestinal schistosomiasis is highly endemic in the area. School-based mass treatment for schistosomiasis is implemented in the division on an annual basis as a standalone intervention. In 2013, mass treatment was conducted in June. Prior to mass treatment, the Vector Control Division of the Ministry of Health conducted refresher training for members of the district health team and the district education office. The district then cascaded training and supervision duties to the sub-county health assistants and inspector of schools who in turn, trained and supervised the school teachers. In addition, awareness of schistosomiasis control was communicated through radio talk shows and radio spot messages. The drugs, tally sheets and registers were distributed to the primary schools after the training. During mass treatment, a central location in each school was organized for drug administration. Children were invited according to their grade, to receive treatment. Praziquantel was distributed according to the height of the child using a standard dose pole, which provides a simple and reasonably accurate estimate of weight [37]. These activities were supported through a parallel structure within the Ministry of Health with external funding from the United States Agency for International Development (USAID) channelled through Research Triangle Institute (RTI) International.

Study Design, Stratification, and Randomization

This was a cluster randomized trial during which 12 primary schools were grouped into two strata of six schools each according to the 2012 uptake levels of praziquantel; low (<55%) uptake and high (≥55%) uptake [38]. From each stratum, the schools (clusters) were randomized into two groups of six schools each; the snack and the non-snack group using a computer generated program in STATA 10.0 (Figure 1). A cluster design was adopted for logistical convenience since the study evaluates unblinded interventions that would otherwise cause resentment or contamination if they were to be provided for some children but not others in the same schools. Stratification was aimed at creating a good balance in participant characteristics in terms of uptake levels of praziquantel in each group (Figure 1). Randomization was performed by an independent statistician.

Figure 1

Study profile showing stratification and randomization of the schools to the intervention groups and the selection of children for assessment after mass treatment.

The Interventions

This included a pre-treatment snack. In addition, education messages for schistosomiasis prevention were provided.

The pre-treatment snack

The snack consisted of mango juice and doughnuts. These were considered safe for consumption, were locally available at low cost, could be easily transported to the schools, stored, and distributed to the children during mass treatment. Each child in the snack schools received 500 ml of mango juice and a doughnut shortly before swallowing praziquantel during mass treatment. A total of 2,833 children in six primary schools received the snack. Ingredients of the mango juice included vitamin C, fruit flavors from concentrate, sugar, water, citric acid, color E 110, and preservative E 221. The 500 ml bottles of mango juice are certified by the Uganda national bureau of standards and were considered safe for human consumption. The doughnuts were made of wheat flour, baking powder, sugar, and cooking oil. A local manufacturer was contracted to make, pre-pack, and distribute the snack to the schools. The snack was distributed by the class teachers who also distributed and recorded the treatment in separate registers.

The education messages

In addition to the pre-treatment snack, education messages for schistosomiasis prevention were provided. These were developed by the authors in collaboration with the district health and education sectors. The messages were tailored to the knowledge gap established earlier [23] and included the following aspects: (i) dangers of schistosomiasis infection; (ii) acquisition of infection from contaminated water; (iii) prevention of acquiring the infection by avoiding unnecessary water contact; (iv) taking preventive treatment (praziquantel) annually to avoid getting serious disease; (v) taking the treatment with food in order to avoid the side effects of the drugs. The head teachers and school teachers in charge of health and sanitation were trained in the above aspects of schistosomiasis prevention through a two-day workshop, during which the print materials of the messages were also distributed. School children in both the snack and the non-snack group received a 30-minute session of the above messages, twice a week for two months, prior to mass treatment. A total of 5,920 children in the 12 primary schools received the messages. The trained teachers delivered the messages in both the local language of Lusoga and English through face to face interactions with the children during school assemblies.

Costs

The total cost of providing the pre-treatment snack and education messages was estimated at US$0.6 and US$0.1 per child, respectively.

Sample Size

The sample size used in this study was based on that required to detect an increase in uptake from 49% registered in 2012 [38] to the recommended 75% [3]. At 90% power and a 95% CI, the sample size required to detect this difference was 79 in the snack schools and 79 in the non-snack schools (STATA 10.0). This sample size was adjusted by 10% non-response to 87. Because of the cluster design, a design effect of 6.3 from a previous study [23] was applied to obtain a minimum sample size of 548 in the snack schools and 548 in the non-snack schools.

Sampling, Eligibility Criteria, and Data Collection

Sampling and data collection were conducted one month after mass drug administration. The study schools were pre-visited to obtain updated school populations. Probability proportion to size of the school and grade populations was used to determine the number of children selected from each school and grade in the two groups. Children were randomly selected from grades 4–6 using systematic sampling. Children were considered eligible for the study if they had been enrolled or attended class at the school for more than six months prior to data collection and were present at school during mass treatment. Experienced research assistants, all blinded to the children's intervention groups conducted face to face interviews with each selected child using structured questionnaires. Throughout data collection, the research assistants were not made aware of the intervention groups. Stool specimens from each child were concurrently collected, processed, and examined for S. mansoni infection. Children who failed to provide stool specimens for examination were replaced by randomly selecting an equal number of children from grades 4–6. A total of 12 children did not provide stool specimens and were replaced. Throughout the stool collection procedure, boys and girls were separated. The data were made available and shared with the national Vector Control Division, Ministry of Health.

Measures

Measures were determined at both the cluster and individual levels. The primary outcome was uptake of mass treatment. The secondary outcomes were occurrence of side effects, knowledge of schistosomiasis prevention, and prevalence and intensity of S. mansoni infection in the two groups. In addition, the socio-demographic characteristics of the children were also assessed. The proportion of children who received education messages and a snack prior to mass treatment in the two groups was calculated. Uptake of praziquantel was defined as having received and swallowed the drug during mass treatment, which was measured through self-report. Children who reported to have swallowed treatment were asked if they developed any side effects after swallowing the drug. The socio-demographic characteristics assessed included age, sex, school name, grade (year), and distance of residence/school from the lake. Knowledge of schistosomiasis prevention was measured on a score scale of 1–3. The children were asked the different ways through which the infection can be transmitted and prevented, including taking preventive treatment. For each of the correct responses, a score of 1 was awarded. Children who mentioned at least one correct method of transmission and two correct methods of prevention scored an aggregate of 3 and were regarded as having correct knowledge of schistosomiasis prevention.

Stool examination for diagnosis of S. mansoni infection

On two consecutive days, early morning stool specimens were collected from each child. From each specimen, two slides were prepared using the modified Kato-Katz thick smear technique [39] with a 41.7 mg template. Two experienced technicians, all blinded to the children's intervention groups, examined the slides under the microscope (10×). An independent technician read a random 10% of stool slides and the results were compared. If there was a discrepancy of more than 5%, the slides were read again by two independent technicians until counts harmonized. However, all results concurred with those of the third technician. The egg counts were found to be over dispersed and thus were logarithmically transformed and intensities reported as geometric mean intensity (GMI) of eggs per gram of stool (epg) among positives only. In case of the presence of soil transmitted helminthiasis (STH) infections on the slides, this was registered so the child could be treated.

Data Management and Statistical Analysis

Double data entry and validation was performed in EpiInfo software (version 7.1.2; Centers for Disease Control and Prevention, Atlanta (Georgia), US). After internal consistency checks, the cleaned dataset was exported to STATA 10.0 for analysis. To determine whether the groups were comparable in terms of uptake and prevalence and intensity of S. mansoni infection, the uptake levels and prevalence and intensity of S. mansoni infection in a random sample of another set of children in the same schools during a previous mass treatment of 2012 were compared. However, since the children were selected at random in both studies, it is possible that some of the children examined in 2012 could have been re-examined in 2013. Differences in the demographic and descriptive variables between the groups were compared using chi squared tests for dichotomized or categorical variables. Student's t-test was used to compare mean intensity of S. mansoni infection. To adjust for clustering, comparisons with test statistics based on chi squared tests were divided by the design effect, while test statistics based on the t-test were divided by the square root of the design effect [40],[41]. To evaluate the effect of the snack on uptake, a logistic regression mixed effects model allowing for fixed (school-level) and participant-level random effects was applied. ANOVA was used to compare the effect of the snack on mean intensity infection with regard to sex and age. All the analyses were planned prior to the study.

Quality Control

Experienced research assistants who were fluent in the local language of Lusoga were recruited and trained in data collection methods. The questionnaires were translated into Lusoga and then back translated to ensure consistency in meaning. They were then pre-tested in one of the schools in a non-study area for purposes of clarity, validation, suitability, and logical flow of the questions. Interviews with the children were held in a private and quiet environment within the school premises. Data were checked for completeness and accuracy before leaving the field and consequently, no data were missing. The first author closely supervised the research assistants during data collection.

Results

Baseline Characteristics

A total of 1,284 children in 12 primary schools were assessed: 595 (46.3%) in the snack schools and 689 (53.7%) in the non-snack schools. The mean age was 11.3 years (standard deviation [SD] 1.7) and 11.7 years (SD 1.6) in the snack and non-snack schools, respectively. The majority 317 (53.3%) in the snack schools and 365 (53.0%) in the non-snack schools were aged between 12 and 16 years. Children in both groups were comparable in terms of age group, sex, distance from area of residence to the lake, and knowledge of schistosomiasis prevention (p>0.05) (Table 1). The uptake levels and prevalence and intensity of S. mansoni infection in a random sample of children in the same schools during a previous mass treatment of 2012 were also comparable. Uptake of praziquantel in the snack schools was 46.5% while that in the non-snack schools was 51.0% (p = 0.57). The prevalence of S. mansoni infection in snack schools was 34.4% compared to 30.9% in the non-snack schools (p = 0.64) and the intensity of S. mansoni infection was 115.9 epg and 120.5 epg in the snack and non-snack schools (p = 0.26), respectively (Table 2) [38].

Table 1

Baseline characteristics of the two intervention groups.

Characteristic	Non-snack Schools (n = 689) (%)	Snack Schools (n = 595) (%)	χ2a	p-Value
Age group
7–11 years	291 (42.2)	310 (52.1)	1.981	0.16
12–16 years	398 (57.8)	285 (47.9)	—	—
Sex
Female	343 (49.8)	296 (49.8)	0.00003	0.99
Male	346 (50.2)	299 (50.3)	—	—
Distance from area of residence to the lake
≤5 km	330 (47.9)	284 (47.7)	0.0035	0.98
>5 km	359 (52.1)	311 (52.3)	—	—
Knowledge of schistosomiasis prevention
Yes	595 (86.4)	500 (84.0)	0.2179	0.64
No	94 (13.6)	95 (16.0)	—	—

Adjusted for cluster design effect.

Table 2

Uptake of praziquantel, prevalence, and intensity of infection among a random sample of children in the same schools during the 2012 mass treatment.

Characteristic	Non-snack Schools (n = 543) (%)	Snack Schools (n = 477) (%)	Test Statistica	p-Value
Self-reported uptake of praziquantel
Yes	277 (51.0)	222 (46.5)	χ2 = 0.322	0.57
No	266 (48.9)	255 (53.5)	—	—
S. mansoni infection status (%)
Positive	168 (30.9)	164 (34.4)	χ2 = 0.217	0.64
Negative	375 (69.1)	313 (65.6)	—	—
Intensity of S. mansoni infection (epg)
GMI epg	120.5	115.9	t = −1.126	0.26

Adjusted for cluster design effect.

Proportion of children who received education messages and a pre-treatment snack

The majority of children in the snack 436 (73.3%) and non-snack schools 492 (71.4%) reported to have received education messages for schistosomiasis prevention prior to mass treatment (p = 0.766). A total of 519 (92.8%) and 270 (49.8%) children in the snack and non-snack schools, respectively, reported to have eaten something prior to mass treatment (p<0.001). The majority (92.7%) in the snack received mango juice and doughnuts while 48.2% in the non-snack schools reported to have taken maize porridge, 6.7% reported posho and beans, 5.2% mango juice and doughnut, and 40.0% reported other types of food including pancakes, bananas, cassava, bread, and dry tea.

Primary Outcome

Self-reported uptake of praziquantel

Uptake of praziquantel in the snack and non-snack schools was 93.9% and 78.7%, respectively (p = 0.002).

Secondary Outcomes

Occurrence of side effects and prevalence and intensity of S. mansoni infection

The children who reported to have developed side effects in the snack and non-snack schools were comparable in terms of age (p = 0.08) and sex (p = 0.55). The proportion of children who reported to have developed at least one side effect after swallowing praziquantel was 34.4% in the snack schools compared to 46.9% in the non-snack schools (p = 0.041). The occurrence of side effects among the infected children was 34 (7.6%) and that among the non-infected was 421 (92.4%) (p = 0.016). The most common reported side effects in both groups included abdominal pain, dizziness, diarrhea, and vomiting. Among the children who reported to have eaten something prior to mass treatment, 276 (36.3%) developed side effects compared to 163 (53.4%) among the children who did not eat anything (p<0.001).

The difference in prevalence of S. mansoni infection between the two groups was statistically significant (p = 0.001). The prevalence and GMI of S. mansoni infection was 1.3% and 38.3 epg and 14.1% and 78.4 epg in the snack and non-snack schools, respectively (Table 3). Children who reported to have taken praziquantel had a lower prevalence of infection, 60/1,101 (5.5%), compared to those who did not take praziquantel, 45/183 (24.6%) (prevalence ratio  = 1.83 [95% CI 1.60–2.10], p<0.001). Similarly, the GMI of infection was lower among children who reported to have taken praziquantel, 46.2 epg (95% CI 35.0–60.9) compared to those who reported not to have taken the drug, 106.1 epg (95% CI 74.7–150.6).

Table 3

Characteristics of the snack and non-snack schools after the interventions.

Variable	Non-snack Schools n = 689 (%)	Snack Schools n = 595 (%)	Test Statistica	p-Value
Received education messages prior to mass treatment (%)
Yes	492 (71.4)	436(73.3)	χ2 = 0.089	0.77
No	197 (28.6)	159 (26.7)	—	—
Eaten something prior to mass treatment (%)
Yes	270 (49.8)	519 (92.8)	χ2 = 39.825	<0.001
No	272 (50.2)	40 (7.2)	—	—
Type of food/snack taken prior to mass treatment (%)
Mango juice and doughnut	14 (5.2)	481 (92.7)	χ2 = 95.333	<0.001
Maize porridge	130 (48.2)	2 (0.4)	—	—
Posho and beans	18 (6.7)	12 (2.3)	—	—
Other (pancakes, bananas, cassava, bread, and dry tea)	108 (40.0)	24 (2.3)	—	—
Self-reported uptake of praziquantel (%)
Yes	542 (78.7)	559 (93.9)	χ2 = 9.683	0.002
No	147 (21.3)	36 (6.1)	—	—
Side effects attributable to praziquantel (%)
Yes	254 (46.9)	192 (34.4)	χ2 = 4.181	0.041
No	288 (53.1)	367 (63.6)	—	—
Reported side effects attributable to praziquantel (%)
Abdominal pain	133 (52.4)	109 (56.8)	χ2 = 0.738	0.947
Dizziness	61 (24.0)	45 (23.4)	—	—
Diarrhea	31 (12.2)	27 (14.1)	—	—
Vomiting	19 (7.5)	7 (3.6)	—	—
Other (headache, nausea)	10 (3.9)	4 (2.1)	—	—
S. mansoni infection status (%)
Positive	97 (14.1)	8 (1.3)	χ2 = 10.937	0.001
Negative	592 (85.9)	587 (98.7)	—	—
Intensity of S. mansoni infection (epg)
GMI epg	78.4	38.3	t = 18.54	0.001

Adjusted for cluster design effect.

Exploratory Outcomes

Through a step-wise forward selection method, covariates with p<0.2 from the unadjusted model (distance from area of residence to the lake, going to the lake, having received education messages prior to mass treatment, knowledge of schistosomiasis prevention, and intervention group) were considered for inclusion in the multivariable adjusted model. The covariates retained in the final model were belonging to the snack group (adjusted odds ratio [AOR] 4.61, 95% CI 2.48–8.58, p<0.001) and having received education messages prior to mass treatment (AOR 13.3, 95% CI 8.29–20.80, p<0.001) (Table 4).

Table 4

Estimated crude odds ratios and adjusted odds ratio and their 95% CI from the final logistic regression mixed-effects model.

Variable	COR (95% CI)	p-Value	AOR (95% CI)	p-Value
Distance from area of residence to the lake
≤5 km	1.59 (1.08–2.38)	0.022	1.00 (0.59–1.70)	0.99
Going to the lake
Yes	1.59 (1.07–2.38)	0.022	1.52 (0.87–2.68)	0.14
Correct knowledge of schistosomiasis prevention
Yes	4.44 (3.01–6.54)	<0.001	1.39 (0.68–2.94)	0.39
Sensitized about schistosomiasis prevention
Yes	12.2 (7.99–18.60)	<0.001	13.1 (8.29–20.80)	<0.001
Intervention
Snack group	4.19 (2.67–6.59)	<0.001	4.61 (2.48–8.58)	<0.001

Adjusted for age and sex.

COR, crude odds ratio.

Discussion

This study found that provision of a pre-treatment snack to school children increases uptake of mass treatment for schistosomiasis. The use of a pre-treatment snack is associated with reduced side effects attributable to praziquantel. The increased uptake in the snack group is associated with reduced prevalence and intensity of schistosomiasis infection among school children.

The self-reported uptake of praziquantel by children in the snack schools (93.9%) was considerably higher than in the non-snack schools (78.7%). A comparable high coverage (94.0%) among school children was achieved by the national control program in Sierra Leone where a special feeding program for the children was provided [32]. We ascribe the observed difference in uptake between the two groups to the pre-treatment snack. The provision of food is an incentive for children to participate in school activities including health intervention programs [42],[43]. The fact that praziquantel should be taken with food to mitigate the side effects was well known by the children because it was part of the education messages given to the children prior to mass treatment. In a previous mass treatment, more than two-thirds of the children reported fear of side effects as the major reason for non uptake of praziquantel [23]. In this study, more than half of the children in the non-snack schools did not take anything prior to mass treatment while the majority (92.8%) in the snack group received a snack before swallowing the drug. Thus, provision of a snack to mitigate the side effects of praziquantel could have motivated the children to take treatment.

Praziquantel is the current drug of choice for schistosomiasis control and is virtually the only anti-schistosomal drug readily available for treatment [28],[44],[45]. The drug is given orally, is effective as a single dose for the three major species of schistosomes, has a low toxicological profile, is well tolerated, and confers some resistance to re-infection [46]. However, praziquantel causes transient side effects of the gastro-intestinal and central nervous systems especially when the drug is taken on an empty stomach. Food high in carbohydrate content increases absorption of the drug from the gastro-intestinal tract, enhances its bioavailability, and lowers the odds of side effects [29]–[31]. Praziquantel undergoes first-pass metabolism through the cytochrome P450 pathway and only small amounts reach circulation. In the presence of high carbohydrate food, hydroxylation of the drug is inhibited and the renal clearance reduced, leading to increased plasma levels [29],[30]. By disrupting calcium ions' (Ca2+) homeostasis, praziquantel increases the permeability of the schistosome membranes to Ca2+ and the resultant rapid influx of Ca2+ causes paralysis of the parasites in a contracted state. The side effects experienced after taking the drug are a result of the contents released by the dead parasites and the subsequent host immune reaction. The frequency and severity of the side effects increase with increasing parasite burden [47]. In this study, the occurrence of side effects among the infected children was lower (7.6%) than among the non-infected children (92.4%). The observed difference could be attributable to the effect of the snack. Besides, the prevalence of S. mansoni infection among the children who took praziquantel was generally very low (5.6%). The major side effects reported after mass treatment in this study included abdominal pain, dizziness, diarrhea, and vomiting. Similar side effects have been reported in other studies [32],[47]–[49]. The lower occurrence of the side effects in the snack schools (34.4%) compared to the non-snack schools (46.9%) is probably attributable to the pre-treatment snack. However, even in the presence of a snack, more than a third of the children in the snack group reported to have experienced the side effects. A comparable proportion of children experiencing similar side effects after taking praziquantel with a snack was reported in Ghana (28%), Tanzania (31%) [48], and in Sierra Leon (30%) [50]. The probable explanation for the occurrence of side effects even when the drug is taken with food is the presence of moderate intensity of schistosomiasis infection among the children before treatment. Because the prevalence and intensity of infection in the snack and non-snack arm were comparable during the 2012 post mass treatment, the difference in the frequency of side effects between the two groups cannot be attributed to the difference in prevalence and intensity of infection with schistosomiasis.

The efficacy of praziquantel against adult schistosomes is indisputable [20],[51]–[53], and the reduction in prevalence and intensity of schistosomiasis infection depends on achieving and maintaining high treatment coverage [3],[28]. The lower prevalence and intensity of S. mansoni infection in the snack schools compared to the non-snack schools is probably due to the higher uptake of praziquantel in the snack schools compared to that in the non-snack schools.

Study Limitations

The study assessed uptake of praziquantel and side effects of the drug based on self-report. It is possible that children could have provided socially desirable answers. However, measures were undertaken to ensure fairly accurate self-report on uptake and side effects. First, the study was conducted four weeks after mass treatment, a period short enough to minimize recall bias. Secondly, the questionnaires used were pre-tested in one of the schools in a non-study area and none of the children interviewed failed to recall whether they had received treatment or not at the last mass distribution. Children were able to recall treatment because praziquantel tablets are unusually large, pungent, and unpalatable. Similar methods for measuring uptake of treatment have been successfully used in northern and south-eastern regions of Uganda [54]. Thirdly, a number of relationships corroborated evidence that self-report in our study is fairly accurate. For instance, among the children who reported uptake of praziquantel, more than 95% were able to recall and mention the true color of praziquantel and more than 96% were able to recall whether they experienced side effects with the drug or not. Lastly, the comparison of the self-reported uptake with the S. mansoni infection status and intensity validated the self-reported uptake as accurate. The prevalence of S. mansoni infections was lower in children who reported to have taken the drug compared to those who did not take the drug. Besides, the proportion of socially desirable answers was expected to be similar in both groups and should therefore have no effect on the direction of the conclusions regarding prevalence and intensity of infection attributable to the snack. Another limitation is the cost of the snack used in the study. It is not known whether alternative food such as maize porridge would be as effective as the doughnuts and mango juice and may need further testing.

Conclusion

This study shows that provision of a pre-treatment snack can improve uptake of mass treatment as well as reduce the side effects attributable to praziquantel treatment. The increased uptake significantly reduces the prevalence and intensity of S. mansoni infection in this age group. A detailed cost-effectiveness analysis of provision of locally available and relatively low cost food with comparable efficacy, such as maize porridge, during mass treatment for schistosomiasis should be undertaken and if found cost-effective, provision of food should be integrated into school-based mass treatment. This strategy may be applicable at the national level and other similar settings in sub-Saharan Africa to increase treatment coverage among school children.