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The magnitude of Schistosoma mansoni and its associated risk factors among Sebatamit primary school children, rural Bahir Dar, Northwest Ethiopia: a cross-sectional study
BMC Research Notes volume 12, Article number: 447 (2019)
The aim of this study was to determine the magnitude of Schistosoma mansoni and its associated risk factors in the study area.
Of 422 school children, 223 (52.8%) and 199 (47.2%) were males and females, respectively. The Overall prevalence of Schistosoma mansoni infection was 24.9% (105/422). Seventy-five out of 422 (71.4%) of the infected individuals showed light infections. The overall mean intensity of Schistosoma mansoni in the study was 106.16 eggs per gram of stool. Age (p = 0.013), swimming habit (p = 0.001), participating in irrigational activities (p = 0.03) and washing clothes in the river (p = 0.039) were factors associated with Schistosoma mansoni infection.
Schistosomiasis is a disease caused by trematode worms of the genus Schistosoma . The three medically important Schistosoma species (Schistosoma spp.) are Schistosoma mansoni (S. mansoni), Schistosoma hematobium (S. hematobium) and Schistosoma japonicum (S. japonium) . Among these, S. hematobium is the cause of urinary schistosomiasis and the other two cause intestinal schistosomiasis . It is one of the most prevalent neglected tropical diseases (NTDs) and a major public health problem in 77 developing countries in tropics and subtropics . Over 240 million people are infected and 700 million people are at risk of schistosomiasis worldwide .
In Africa, schistosomiasis due to S. mansoni and S. haematobium are the second most common NTDs after hookworm infection . In sub-Saharan Africa, over 3000,000 deaths occur annually due to schistosomiasis . In Ethiopia, 37.3 million people are living in schistosomiasis endemic areas, comprising 3.4 million pre-school children, 12.3 million school-aged children, and 21.6 million adults . As a result, the magnitude and impact of schistosomiasis infection is high in Ethiopia even though several control methods have been conducted.
In North West Ethiopia, different data have indicated that there is high prevalence of S. mansoni in the region including 89.9% in Sanja General elementary school , 82.8% in Sanja and Ewukat Amba primary school , 56.6% in Tach Armachio district , 37% in Zarima town of Gonder , 20.6% in Gorgora town , 14.3% in Ethiopian Orthodox church students around Lake Tana  and 2.8% in Bahir Dar Shimbit elementary school .
In our study area, the school children are at risk for S. mansoni due to their contact to Abay and Andassa Rivers for their daily activities like swimming, fetching, washing clothes and agricultural activities like irrigation. Therefore the objective of this study was to determine the magnitude of S. mansoni in and its associated factors Sebatamit primary school children.
Methods and materials
Study design and area
A school-based cross-sectional study was conducted at Sebatamit primary school from April to May, 2018. The school is located 7 km from Bahir Dar city which is the capital city of Amhara Regional State. The altitude of the area is 1820 m above sea level. The annual temperature of the area is 11–29 °C. The residents at the study area use Abbay and Andassa Rivers for recreational, irrigation, drinking and cooking purposes.
Sample size determination and sampling technique
Sample size was determined using 50% prevalence since there was no study conducted regarding this topic in the area, 95% CI, 5% margin of error with 10% non-response rate; hence using single proportion formula, 422 students were included in the study. The total number of children from grade 1–8 in the school was 1734. There were four sections in each grade. Then, proportional allocation formula was used to determine to the number of children sampled from each grade. Hence, the numbers of students sampled from grade 1–8, respectively were: 65, 62, 58, 55, 59, 43, 46 and 34 having a total of 422 children. Then, by using class rosters as a sampling frame, systematic sampling technique was used to select the sections from each grade and the school children from the selected sections.
Stool sample collection for parasitological examination
Each of the school children was informed to provide total of 2 g of stool sample. Then, the stool samples were preserved with 10% formalin and transported to Bahir Dar University Microbiology and Parasitology teaching Laboratory for Kato-Katz. Moreover, standardized questionnaires were used to collect data on socio-demographic characteristics of the study participants and associated risk factors of S. mansoni infection.
Parasitological stool examination by Kato Katz technique
For Kato-Katz technique, two Kato slides were prepared for every school children’s stool sample using fixed quantity of sieved 41.7 mg of stool on a punched template . They were then mounted on slides and covered with malachite green impregnated cellophane. The slides were observed within 1 h under the microscope at a magnification of 10× objective. The mean total number of eggs was expressed as eggs per gram (EPG) of stool.
Ten percent of the examined Kato-Katz slides were randomly selected and re-examined at the end by qualified laboratory technologist who were blind for the first result. Finally, all results were documented on log book by its unique ID number and copied to the questionnaire by principal investigators.
Data were analyzed using SPSS version 23. The associated risk factors for S. mansoni infection were first analyzed by bivariate logistic regression. Then, to control the possible confounding factors, variables with p value < 0.2 were adjusted by multivariate logistic by stepwise variable selection. Finally, variables with p value < 0.05 were considered as statistically significant.
Ethical clearance was obtained from Bahir Dar University College of Medicine and Health Sciences institutional review board (IRB) and approved with protocol number 070/18-04 on 04 April 2018 prior to start the study. Permission letter was obtained from Bahir Dar city education department and Sebatamit primary school director office. Informed written consent was obtained from the children’s parents and assent was obtained from the children. Those school children who were positive for S. mansoni were treated accordingly.
Sociodemographic characteristics of the study participants
Out of 422 school children, 223 (52.8%) and 199 (47.2%) were males and were females, respectively. The age of the school children ranged from 7 to 18 years with the mean age of 11.5 year. Two hundred sixty out of 422 (53.6%), 150/422 (35.5%) and 46/422 (10.9%) of the school children were from 11 to 14, 7 to 10 and 15 to 18 years age group, respectively. Most of the school children were from grades 1–4 accounted 240/422 (56.9%) followed by 182/422 (43.1%) from grades 5–8.
The prevalence of S. mansoni infection
One hundred five children were found to be positive to S. mansoni infection giving an overall prevalence of 24.9%. The males were found to be more infected than the females with 66 (15.6%) of the males being infected. The age group with the highest prevalence value for S. mansoni infection was between 11 and 14 years with 66 (15.6%) of them found to be infected while the least prevalence of 1.4% was among 6 children in the age group 15–18 years as shown in Table 1.
Intensity of S. mansoni infection
Out of 105 school children, 75 (71.4%), 25 (23.8%) and 5 (4.8%) had light, moderate and heavy infections, respectively according to WHO classification . Thirty (76.6%), 7 (17.9%) and 2 (5.2%) of female students had light, moderate and heavy infections, respectively where as 45 (68.2%), 18 (27.3%) and 3 (4.5%) of male students had light, moderate and heavy infections, respectively. The age group with the highest light infections was between 11 and 14 years with 48 (72.7%) while the least was between 15 and 18 years with 4 (66.8%). Both 7–10 and 11–14 years had similar moderate infections with 8 (24.2%) and 16 (24.2%), respectively while the highest heavy infections, 1 (16.6%) was found in 15–18 years.
Analysis of risk factors associated with S. mansoni infection
Among the potential associated risk factors of S. mansoni infection, swimming habit (p = 0.001), irrigational activities (p = 0.005) and washing clothes in the river (p = 0.045) were statistically significant with S. mansoni infection in bivariate logistic regression analysis. However, factors like crossing the river on bare foot and open defecation were not statistically significant (p > 0.05). From sociodemographic factors, sex of the children (p = 0.018) and age of the children (p = 0.046) were statistically associated in bivariate logistic regression analysis. But academic level of the students was not statistically significant (p = 0.23) as shown in Table 2.
All bivariate results that had p-value < 0.2 were subjected to multivariate logistic regression model to control possible confounding factors as shown in Table 2. After adjustment to multivariate logistic regression model, sex of the school children (p = 0.659) was not statistically significant. The school children from 11 to 14 years were 3.2 more likely to be infected with S. mansoni than those who were from 15 to 18 years (AOR = 3.2, 95% CI 1.274–8.151, p = 0.013). The odds of being infected by S. mansoni among school children who swam was 2.8 more likely as compared to those who did not (AOR = 2.8, 95% CI 1.702–4.699, p = 0.001). The school children who participated in irrigational activities were 1.675 more likely to be infected with S. mansoni than those who did not (AOR = 1.675, 95% CI 1.050–2.671, p = 0.030). The school children who washed their clothes in the river were 1.711 more likely to be infected with S. mansoni than those who didn’t (AOR = 0.1.711, 95% CI 1.028–2.851, p = 0.039) as shown in Table 3.
In this study, the overall prevalence of S. mansoni infection was 24.9%. This prevalence was slightly in with other studies such as 24% in Jimma , 23.9% in Mekelle , 26.5% in Democratic Republic of Congo . However, the prevalence of this study found to be lower compared to other findings in different parts of Ethiopia; including 73.7% in Bushulo village of Southern Ethiopia , 31% along lake Hawassa of Southern Ethiopia , 58.6% in Wolaita Zone , 67.6% in Horo Guduru Wollega , 73.9% and 42.4% in Tigray [23, 24], 37% in Zarima town of Gondar , 89.9% in Sanja General elementary school of Gondar , 82.8% in Sanja and Ewukat Amba primary school Gondar of , 56.6% in Tach Armachiho district of Gonde , 60.5% in Kenya , 84.01% in Tanzania .
The variations in the prevalence in this study might be due to some factors such as: the presence of fast running rivers (Abay and Andassa) in the area leading to low availability of vector snails that are mainly found to prefer stagnant or slow-moving water bodies ; the sociodemographic and other factors (immune status); the distance of the study area to the source of water may be a major cause of variation in prevalence; sample size..
On the other hand, the prevalence of this study was higher than 119 (20.6%) in Gorgora town , 14.3% in Ethiopian Orthodox church students around Lake Tana  and 2.8%) in Bahir Dar Shimbit elementary school . The reason for these variations might be due to poor sanitation; in our study area greater than 50% of the study participants had no latrine in their home.
In our study, most of infections were light infections. This is in line with the study done in Jimma zone  and Mekelle city . However, the highest moderate infections were observed in Sanja town [8, 9] and in Gorgora town  whereas in Wolayita zone  the highest heavy infections were observed. The difference in infection intensity could have been due to the frequency of exposure to contaminated water, the burden of the adult worms in hosts and immune status of the study participants.
In this study regarding the associated factors to S. mansoni infection, sex as an associated factor to S. mansoni infection was not retained on the multivariate analysis though it was significant in bivariate analysis which was similar to the findings from different parts of Ethiopia [8, 9 and 22]. Contrasting findings on S. mansoni infection among males and females were identified. Higher prevalence of S. mansoni infection among males was reported in Jimma Zone  and Wolayita Zone , whereas the study conducted in Gorgora and Mekelle [12, 17] reported the opposite findings (higher prevalence in females than males). These differences might be due to the difference in the exposure status of both sexes to cercarial contaminated water source.
The school children who were from 11 to 14 years were 3.2 more likely to be infected with S. mansoni infection than those in 15–18 years. This finding is in line with the study done in Gorgora , Jimma zone , Mekelle  and Kenya . This could be due to higher rate of water contact activities for recreational purposes and for bathing by the school children within 11–14 years and the concomitant immunity to re-infection in school children aged 15–18 years. Swimming habit, participation in irrigational activities and washing clothes in the river were factors associated with S. mansoni infection.
The overall prevalence of S. mansoni infection in the present study was 24.9%. Majority of the infections were light infection with mean intensity of 106.6 EPG. Age; swimming habit, irrigational activities, washing clothes in the river were the factors associated with S. mansoni infection. However, deworming program and community awareness should be strengthened to control S. mansoni infection.
We did not include associated factors and sociodemographic factors like awareness of the study. Participants about schistosomiasis, occupational status of parents, and religion of the study participants and residence of the participants.
Availability of data and materials
All data and material were obtained from Google Scholar, Pub Med and Med Line data bases.
adjusted odds ratio
crude odds ratio
eggs per gram of stool
institutional review board
neglected tropical diseases
Satoskar AR, Simon GL, Hotez PJ, Tsuji M. Medical parasitology. Austin: Landes Bioscience; 2009.
Brown DS. Freshwater snails of Africa and their medical importance. Boca Raton: CRC Press; 2014.
Bruun B, Aagaard-Hansen J. The social context of schistosomiasis and its control: an introduction and annotated bibliography. Geneva: World Health Organization; 2008.
Hotez PJ, Asojo OA, Adesina AM. Nigeria: “Ground Zero” for the High Prevalence Neglected Tropical Diseases. PLoS Negl Trop Dis. 2012;6(7):e1600.
Nagi S, Chadeka EA, Sunahara T, Mutungi F, Justin YK, Kaneko S, et al. Risk factors and spatial distribution of Schistosoma mansoni infection among primary school children in Mbita District, Western Kenya. PLoS Negl Trop Dis. 2014;8(7):e2991.
Adenowo AF, Oyinloye BE, Ogunyinka BI, Kappo AP. Impact of human schistosomiasis in sub-Saharan Africa. Braz J Infect Dis. 2015;19(2):196–205.
Federal Democratic Republic of Ethiopia Ministry of Health. Second Edition of Ethiopia National Master Plan for neglected tropical diseases. Ethiopia: Addis Ababa; 2016.
Worku L, Damte D, Endris M, Tesfa H, Aemero M. Schistosoma mansoni infection and associated determinant factors among school children in Sanja Town, Northwest Ethiopia. J Parasitol Res. 2014;1:1. https://doi.org/10.1155/2014/792536.
Alebie G, Erko B, Aemero M, Petros B. Epidemiological study on Schistosoma mansoni infection in Sanja area, Amhara region, Ethiopia. Parasites Vectors. 2014;7(1):15.
Yimer M, Abera B, Mulu W. Soil transmitted helminths and Schistosoma mansoni infections in elementary school children at Tach Armachiho district, North-west Ethiopia. J Appl Sci Res. 2014;2(2):43–53.
Alemu A, Atnafu A, Addis Z, Shiferaw Y, Teklu T, Mathewos B, et al. Soil transmitted helminths and Schistosoma mansoni infections among school children in Zarima town, Northwest Ethiopia. BMC Infect Dis. 2011;11(1):189.
Essa T, Birhane Y, Endris M, Moges A, Moges F. Current status of Schistosoma mansoni infections and associated risk factors among students in Gorgora town, Northwest Ethiopia. Int Sch Res Notes Infect Dis. 2012. https://doi.org/10.5402/2013/636103.
Bitew AA, Abera B, Seyoum W, Endale B, Kiber T, Goshu G, et al. Soil-Transmitted helminths and Schistosoma mansoni infections in Ethiopian Orthodox Church Students around Lake Tana, Northwest Ethiopia. PLoS ONE. 2016;11(5):e0155915.
Getnet A, Worku S. The Association between major helminth infections (Soil-Transmitted Helminthes and Schistosomiasis) and anemia among School Children in Shimbit Elementary School, Bahir Dar, Northwest Ethiopia. Am J Health Res. 2015;3(2):97–104.
Katz N, Chaves A, Pellegrino J. A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. Rev Inst Med Trop São Paulo. 1972;14:397–400.
Bajiro M, Dana D, Ayana M, Emana D, Mekonnen Z, Zawdie B, et al. Prevalence of Schistosoma mansoni infection and the therapeutic efficacy of praziquantel among school children in Manna District, Jimma Zone, southwest Ethiopia. Parasites Vectors. 2016;9(1):560.
Assefa A, Dejenie T, Tomass Z. Infection prevalence of Schistosoma mansoni and associated risk factors among schoolchildren in suburbs of Mekelle city, Tigray, Northern Ethiopia. Momona Ethiop J Sci. 2013;5(1):174–88.
Khonde Kumbu R, Mbanzulu Makola K, Bin L. Prevalence of Schistosoma mansoni infection in four health areas of Kisantu health zone, Democratic Republic of the Congo. Adv Med. 2016. https://doi.org/10.1155/2016/6596095.
Terefe A, Shimelis T, Mengistu M, Hailu A, Erko B. Schistosomiasis mansoni and soil-transmitted helminthiasis in Bushulo village, southern Ethiopia. Ethiop J Health Dev. 2011;25(1):46–50.
Tadege B, Shimelis T. Infections with Schistosoma mansoni and geohelminths among school children dwelling along the shore of the lake Hawassa, southern Ethiopia. PLoS ONE. 2017;12(7):e0181547.
Alemayehu B, Tomass Z, Wadilo F, Leja D, Liang S, Erko B. Epidemiology of intestinal helminthiasis among school children with emphasis on Schistosoma mansoni infection in Wolaita zone, Southern Ethiopia. BMC Public Health. 2017;17(1):587.
Haile S, Golassa L, Mekonnen Z. Prevalence of Schistosoma mansoni and effectiveness of Praziquantel in school children in Finchaa valley, Ethiopia. J Parasitol Vector Biol. 2012;4(3):25–30.
Abebe N, Erko B, Medhin G, Berhe N. Clinico-epidemiological study of Schistosoma mansoni in Waja-Timuga, district of Alamata, Northern Ethiopia. Parasites Vectors. 2014;7(1):158.
Desta H, Bugssa G, Demtsu B. The current status of Schistosoma mansoni infection among school children around Hizaty Wedicheber Microdam in Merebmieti, Ethiopia. J Bacteriol Parasitol. 2014;5(5):1.
Odiere MR, Rawago FO, Ombok M, Secor WE, Karanja DM, Mwinzi PN, et al. High prevalence of schistosomiasis in Mbita and its adjacent islands of lake Victoria, western Kenya. Parasites Vectors. 2012;5(1):278.
Munisi DZ, Buza J, Mpolya EA, Kinung’hi SM. Intestinal schistosomiasis among primary schoolchildren in two on-shore communities in Rorya district, Northwestern Tanzania: prevalence, intensity of infection and associated risk factors. J Parasitol Res. 2016;1:1. https://doi.org/10.1155/2016/1859737.
Fao.org. Three overviews on Environment and Aquaculture in the Tropics and Sub-tropics. [Online]. http://www.fao.org/3/ad002e/ad002e03.htm. Accessed 20 Jul 2019.
We would like to express great thanks to Sebatamit school director and staffs. Our appreciation also goes to all data collectors and finally we would like to thank all the school children who participated in this study.
Ethics approval and consent to participate
The study was approved by Bahir Dar University, college of medicine and health sciences institutional review board (IRB) (070/18-04). Informed written consent was obtained from the children’s parents and assent was obtained from the children.
Consent for publication
The authors declare that they have no competing interests.
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Workineh, L., Yimer, M., Gelaye, W. et al. The magnitude of Schistosoma mansoni and its associated risk factors among Sebatamit primary school children, rural Bahir Dar, Northwest Ethiopia: a cross-sectional study. BMC Res Notes 12, 447 (2019) doi:10.1186/s13104-019-4498-3
- Rural Bahir dar
- Sebatamit primary school
- Schistosoma mansoni