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Schistosoma mansoni and soil-transmitted helminths among preschool-aged children in Chuahit, Dembia district, Northwest Ethiopia: prevalence, intensity of infection and associated risk factors
© Alemu et al. 2016
Received: 13 August 2015
Accepted: 12 February 2016
Published: 23 May 2016
Intestinal schistosomiasis and soil-transmitted helminthiasis are the major public health problems globally. Compared with any other age group, pre-school aged children and school-aged children are the most exposed. There are few studies showing the burden of intestinal schistosomiasis, and soil-transmitted helminthiasis among pre-school aged children in Ethiopia. Hence, this study aimed to assess the prevalence of schistosoma mansoni and soil-transmitted helminths and associated risk factors among preschool aged children of Chuahit and surrounding Kebeles, Northwest Ethiopia.
A community based cross sectional study was conducted from February 2 to March 27 2015. Four hundred one preschool-aged children were included in the study by using two stage cluster sampling technique. Pretested structured questionnaire was employed to collected data via face-to-face interview technique. A single stool specimen was collected, and a portion of the sample was processed by Kato Katz method.
Of the total children, 141 (35.2 %) harbored one or more intestinal helminthes. Schistosoma mansoni was found in 45 (11.2 %) of preschool age children. Ascaris lumbricoides was the predominant isolate, 77 (19.2 %) followed by S. mansoni, 45 (11.2 %). The least parasites isolated were Tania species, 2 (0.5 %). After adjusting for other variables, being mothers who did not have the habit of washing hands after toilet (AOR = 7.3, 95%CI: 2.97–17.95), being occupationally housewife mothers (AOR = 8.9, 95%CI: 2.27–25.4), using protected spring water as a main family source of water (AOR = 3.9, 95%CI: 1.2–12.3) and child habit of not wearing shoe (AOR = 1.91, 95%CI: 1.01–3.64) were significantly associated with high prevalence of soil-transmitted helminthiasis among preschool-age children in Chuahit.
The current study showed that relatively higher level of STH and S. mansoni among preschool-aged children in Chuahit. This finding calls for a need of public health education, promotion of women education and provision of safe water to reduce the burden of soil-transmitted intestinal helminthiasis and schistosomiaisis.
Intestinal schistosomiasis and soil-transmitted helminthiasis are the major medical and public health problems in many parts of the world. Schistosomiasis remains a serious public health concern in sub-Saharan Africa (SSA) and approximately one-third of the 192 million cases of schistosomiasis in the SSA are caused by Schistosoma mansoni, the causal agent of intestinal schistosomiasis .
Soil-transmitted helminths (STH) of major concern to humans are Ascaris lumbricoides, Trichuris trichiura, Necator americanus and Ancylostoma duodenale. Infection results from ingestion of eggs and contact with fecally contaminated soil, and occurs primarily in areas where the sanitation is poor sanitation and water supplies are unsafe. The latest estimates indicate that more than 2 billion people are infected with these parasites .
Schistosomiasis is a chronic Neglected Tropical parasitic disease (NTD) caused by schistosome species (S. haematobium, S. mansoni, S. japonicum, S. mekongi and S. intercalatum) found in fresh water, and human beings that come into contact with fresh water containing fresh water snails are at risk for infection. Two hundred forty million people are already infected with schistosomiasis and 700 million are at risk in 74 countries. Schistosomiasis ranks the second most common parasitic disease, and it is the fatal NTD killing an estimated 280,000 people each year in the African region alone in which more than 90 % of the cases occur . Recognizing the public health impact of schistosomiasis and soil-transmitted helminthiasis, the World Health Organization (WHO) has set a minimum target for the control of morbidity due to these parasitic worm infections, urging member states to regularly treat at least 75 % of all school-aged children (SAC) at risk of morbidity .
Control of STH and intestinal Schistosomiasis at population intervention level primarily bases on regular anti-helminthic and praziquantel treatment, health education, improving sanitation standards and developing a control strategy. These population based intervention are better than individual treatment and environmental measures like snail control in areas where Schistosomiasis common . In developing countries, however, control measures are difficult to implement due to inadequate clear water supply, poor sanitation and limited access to education. As a result, intestinal helminthic infection remains a significant health problem in these regions .
Ethiopia has one of the lowest quality-drinking water supply and latrine coverage in the world [6, 7]. As a result, Schistosomiasis and STH are endemic in many parts of Ethiopia, and the intestinal form of schisosomiasis caused by S. mansoni is more widely distributed in the country compared to the urinary form caused by S. hamatobium which is limited to some lowland areas of Ethiopia .
Morbidity caused by S. mansoni and STH is commonly associated with heavy infection intensities. Compared with any other age group, preschool-aged children (PSAC) and (SAC) are the most exposed groups, and they harbor the greatest numbers of intestinal worms resulting in diarrhea, loss of appetite, weight loss, growth retardation, malnutrition, anemia, cognitive defects and hepatosplenomegaly in chronic cases which may lead to sever heath problem and mortality later in life [9–11].
Schistosomiasis in African PSAC has been previously unnoticed but much better recognized in recent years. Although increasing evidence showing that treatment with praziquantel is safe, beneficial, and could be delivered within ongoing public health interventions, PSAC do not have satisfactory access to this drug, and there is a treatment gap [12, 13]. Most mass drug administration (MDA) campaigns have been implemented in sub-Saharan Africa treating millions of SAC for schistosomiasis with praziquantel (PZQ). But PSAC (≤7 years) have been every time excluded from access to such kind of medication . The reason behind is the belief that PSAC would not yet been exposed to infested freshwater bodies, thus the extent and severity of schistosomiasis is not sufficiently understood and documented in this age class . Recent studies showed that the prevalence of schistosome infections is high among PSAC whose parents have high levels of contact with water [13, 16]. Studies which were conducted in Mali, Niger, Sudan, Uganda and Zimbabwe showed that PSAC are at high risk of schistosomiasis, and prevalence of the infection ranged from 18 to 63 % which implies that PSAC were at high-risk in areas where schistosomiasis is endemic 
In Ethiopia, intestinal parasitic infections are highly prevalent: 5.01 million are infected with schistosomiasis and 37.5 million to be at risk. The burden and intensity of infection vary from locality to locality.. The estimated number of peoples infected with hookworm, A.lumbricoides and T.trichiura respectively were 11 million, 26 million and 21 million respectively . A study done in Wondo Genet, Ethiopia showed that the prevalence of T.trichiura, S.mansoni, A.lumbricoides, Hymenolepis nana, and hookworm infections were 74.7, 37.2, 25.7, 4.5, and 5.9 %, respectively . In another similar study done in Wonji Shoa, Ethiopia, the prevalence of T.trichiura, S.mansoni, A. lumbricoides, Hymenolepis nana, and hookworm infections were 2.9, 8.8, 4.6, 10.4, 0.8 % respectively .
Most previous studies conducted in Ethiopia were focusing on school-age children and only few studies reported intestinal helminths infections among preschool-aged children. Thus, the current study was undertaken to assess the prevalence of S.mansoni, STH infections and associated risk factors among preschool-aged children in Denbia district, North West Ethiopia.
Study design, area and population
A Community based cross-sectional study was conducted in preschool aged children living in Chuahit, Dembia District, North West Ethiopia, from February 2 to March 27, 2015. Chuahit is found in North Gondar Zone of Amhara Region of Ethiopia and is located 789 kms Northwest of the capital city Addis Ababa. It is one of the four small rural town found in Dembia District. Under its administrative area, it comprises nine kebeles. Four rivers namely Tanti Kura, Ambizina, Ambagenin and Chigero flow through it. The average temperature and humidity are 28 °C and 22 % respectively. PSAC who were under the age of seven years old were the source population . PSAC who had been living in Chuahit for at least 6 months before the study began and who had no history of having been treated with Praziquantel (PZQ) and anti-helminthic drug in the past 4 weeks were included.
Sample size determination and sampling technique
The required sample size was determined by using single population proportion formula with the following assumptions: prevalence (p) of 15.5 % from a previous study , 95 % confidence level, 5 % margin of error, design effect of 2. Accordingly, the minimum sample size (n) was found to be 401. A multi-stage sampling procedure was utilized to select study participants. At the first stage, two kebeles (Derena and Meskele kerestos) were selected randomly by simple random sampling from nine kebeles. At the second sampling stage, numbers of households included in each kebeles were determined by proportional allocation according to the total number of households found in each kebeles. Then, systematic sampling method was employed to select the households. The sampling interval was calculated by dividing the total households to the number of households to be included in the sample for each kebeles. The initial household interviewed was randomly selected by lottery method and the next households were selected at that interval. Whenever more than one eligible children were found in the same selected household, only one of them was chosen using the lottery method. In case no eligible candidate was identified in a selected household, the next household was selected keeping the interval constant afterwards. According to Chuahit administrative health office report, 6,947 PSAC were estimated to reside in Chuahit; of whom 781 and 523 were residing in Derena and Meskele kerestos respectively. Furthermore, 2,820 households (1462 in Derena and 1358 in Meskele kerestos) were found in the selected kebeles. Two hundred eight and 193 households were selected from the Derena and Meskele kerestos kebeles respectively. Likewise, 208 and 193 PSAC were participated in the study from Derena and Meskele kerestos kebeles respectively.
Data collection and processing
Data were collected by pretested structured Amharic version questionnaire using interview technique. Health extension workers were recruited for data collection and supervised by the Principal Investigator. Before data collection, data collectors were assigned to each Kebeles. Then each data collector conducted a house-to house survey. During the survey, the data collectors first asked the parents of PSAC whether or not any PSAC present or not in the household. When PSAC was found, the data collectors interviewed parents or caretakers after obtaining written informed consent. Repeat visits were conducted for those individuals who were not available during the first visit. At each data collection spot, full explanation about the aim of the research was given to the parents or caretakers of PSAC before the interview.
Sample collection and laboratory procedures
A single stool specimen of about 5 g was collected from each study participant using clean, dry and leak proof plastic container labeled with unique identification number. A portion of the sample was processed by Kato Katz method using a template holding 41.7 mg of stool . Examination for hookworm was performed within one hour of stool collection and Kato slide preparation. The slides were left for 24 h to clear for easy visualization of S. mansoni and other helminthes eggs. After 24 h, two experienced laboratory technologists examined each slides independently. Whenever the result of the two laboratory technologists discorded, the third experienced laboratory technologist examined the slides. Results of the laboratory investigation were recorded on a format prepared for this purpose. Infection intensity of the STHs and S. mansoni was estimated by multiplying the total number of eggs counted by 24, which gives as the eggs per gram (epg) of stool. Besides, the species specific classes of infection intensity with S.mansoni and STH were classified as light, moderate and heavy per the threshold set by WHO .
Data management and analysis
Data were entered in to and analyzed by statistical package for social sciences (SPSS) statistical software version 20. Study findings were explained in words, tables and other statistical summary techniques. Binary logistic regression model was used to identify factors associated with infection of S. mansoni and STHs. Multiple logistic regressions was fitted to control the possible effect of confounders, and finally the variables having independent association with dependent variables were identified on the basis of odd ratio (OR) with 95 % confidence interval (CI) and P-value less than 0.05.
The study was conducted after ethical approval was obtained from institutional ethical review committee of College of Medicine and Health Sciences, University of Gondar. Moreover, letter of support was secured from the Woreda health office and each Kebele administrations. Following an explanation of the purpose, the benefits and the possible risks of the study, written consent was obtained from parents/care takers of PSAC, which assured that the participation was on voluntarily basis. Children who were positive for S. mansoni and STHs were treated by referring them to Chuahit health center.
Socio-demographic characteristics of study participants
Socio-demographic characteristics of PSAC in Chuahit, Northwest Ethiopia, 2015
Age (in months)
Marital status of mothers
Educational status of mothers
Read and write
Occupation of mothers
Prevalence of S. mansoni and STHs
Prevalence of intestinal helminthiasis among PSAC in Chuahit, Northwest Ethiopia, 2015
One or more parasitic infection
Single parasitic infection
Double parasitic infection
x 2(p value)
x 2(p value)
Infection intensity of S. mansoni and STHs
Intensity of infection in PSAC with S.mansoni and soil-transmitted helminthic infection in Chuahit, Northwest Ethiopia, 2015
Class of infection intensity
Risk factor analysis for soil-transmitted helminthiasis
Bivariate ad multivariate logistic regression analysis of soil-transmitted helminthiasis in relation to selected variables among PSAC in Chuahit, Northwest Ethiopia, 2015
Presence of soil-transmitted helminthiasis
COR(95 % CI)
AOR(95 % CI)
Marital status of mothers
Educational status of mothers
Read and write
Occupation of mothers
Shoe wearing habit of the child
Not at all
Source of water
Hand washing habit after toilet
Risk factor analysis for S. mansoni
Bivariate and multivariate logistic regression analysis of intestinal Schistosomiasis in relation with selected variables among PSAC in Chuahit, Northwest Ethiopia, 2015
Presence of intestinal Schistosomiasis
COR(95 % CI)
AOR(85 % CI)
Sex of child
Age of child (in Months)
Habit of bringing child to river
Habit of washing children in the river
Habit of washing children with freshly fetched water at home
Habit of bringing children to irrigation sites
Child’s swimming habit in river
Child’s swimming frequency per week
Habit of child crossing river with bare foot
Distance of home from the river
Mothers knowledge about S. mansoni and STH
Of the total 401 mothers (aged 20 up to 52 years) interviewed, 324 (80.8 %) and 166 (41.4 %) of (them had never heard about intestinal schistosomiasis and soil-transmitted helminthiasis respectively. For those mothers had ever heard of these parasitic infections, their major source of information was health professionals. From, mothers of PSAC interviewed about ways of transmission of intestinal schistosomiasis, 85 % of them responded that intestinal schistosomiasis cannot be transmitted by swimming or bathing in the river, crossing river with bare foot, washing clothes in river and fishing in river. Regarding preventive methods of intestinal schistosomiasis, 380 (94.8 %) of mothers did not know ways of prevention of intestinal schistosomiasis Regarding the symptoms of intestinal schistosomiasis, almost all the mothers, 377 (94 %) did not know the symptoms of the disease. Nearly half and two-third of the mothers responded that they did not know about ways of transmission and the preventive methods of STH respectively.
The prevalence of one or more intestinal helminths infections observed among the study participants was 141 (35.2 %). This finding is lower than study conducted in different area of Ethiopia namely; Methara (89 %) , Wondo Genet (85.1 %) , Tigray (48.1 %) , but higher than a report from Wonji Shoa (15.5 %) . In this study, infection with one or more helminths increases as age increases which is in agreement with studies conducted in Ethiopia and Kenya [20, 25].
In the present study, the prevalence of S. mansoni infections was (11.2 %). This is in agreement with previous study carried out in Sierra Leone (11.2 %) . In contrary, this finding is lower that studies done Methara (29 %) , Wondo Genet (37.2 %) , Niger (43.8 %) , Cote d’Ivoire (25 %) , Kenya (17.6 %)  and Uganda (39.3 %) . On the other hand, this finding is higher than studies conducted in Tigray (1 %) , Wonji Shoa (8.8 %) , Ghana (0 %)  and Uganda (7 %) . Difference in water source, time of survey, environmental and socio-economic factors may account for this variation. Of the total 45 PSAC who were positive for S. mansoni 32 (71.1 %) and 13 (28.9 %), 0 % had light moderate and heavy infection respectively. However, a report from Niger  showed that 17.3, 23.8, 2.7 %,of PSAC were light, moderate and heavily infected respectively. No a statistically significant association was observed between prevalence of S. mansoni and age of PSAC in the current study. This is in contrast with a study conducted in Wonji Shoa  showing statistically significant association between S.mansoni and age of PSAC. Relatively higher prevalence of S. mansoni infection in the present study was observed. Therefore including praziquantel treatment in the deworming program as per the WHO guidelines would be essential to decrease the burden of these diseases in this age group .
In the current, the overall prevalence of STH infection was found to be 22.9 %. A. lumbricoides (19.2 %) was the predominant parasite. This finding was in agreement with a report from Sierra Leone (17.2 %) . However, this is lower than similar reports from Wondo Genet (25.7 %)  and Methara (40 %) , and higher than a study conducted in Wonji Shoa (4.6 %) , Cote d’Ivoire (3.1 %)  and Uganda (0.7 %) . The prevalence of T. trichiura in the present study was 1.7 %, which is much more lower than studies carried out in Methara (67 %)  and Wondo Genet (74.7 %) . The high tolerance of parasites’ eggs and larval stages to the variation of the soil temperature has been described as a key factor for the high transmission and prevalence of these parasites in the area .
The majority of PSAC mothers were not heard of intestinal schistosomiasis, 324 (80.8 %) and STH, 235 (58.6 %). Similar to the current study, a study conducted in Malawi reported that the awareness of mother’s about schistosomiasis was very poor, 97 % of the parents had little or no knowledge of the disease .
Even though it was not statistically significant in multivariate logistic regression (but significant in bivariate analysis), the habit of washing children in the river increases the prevalence of S.mansoni. Another study conducted in Cote d’Ivoire showed that children staying at home with their elders found 2 times more likely to be positive for S. mansoni than those who were accompanying their mothers during daily livelihood activities . Both of these findings indicated that PSAC are at higher risk of infection with S. mansoni. However, by focusing treatment upon the school-aged population, World Health Assembly (WHA) resolution 54.19 neglects PSAC, thus preventing them from benefiting from the praziquantel treatment given to their older peers, and hence creating a potential health inequity .
In the present study, the greater proportion of the mothers of PSAC bring children to the river,(50.9 %) and washed them in the river (47.9 %). This is in line with a study conducted in Niger , the majorities of mothers (76.3 %) were accompanied by their children to the canal or the pond and washed them with the contaminated water.
The major limitation of this study is that prevalence and infection intensity of STHs and S. mansoni were determined by examination of single stool specimen from each study participants. Thus, we could not access the intra and inter-stool variation of egg output. Furthermore, a single Kato-Katz template was examined for each of the stool specimens that might affect the accuracy of the egg count. Moreover, we could not include all modifiable risk factors in this study.
The current study has demonstrated that intestinal helmenthiasis and Schistosomiasis were prevalent in varying degree among PSAC in the study area. Maternal habit of not washing hands after toilet, being housewife maternal occupation, the use of protected spring water as a main family source of water and child habit of not wearing shoe were significantly associated with high prevalence of soil-transmitted helminthiasis.. The study also revealed that mothers of PSAC in the study area had limited knowledge on ways of transmission, symptom of the disease and preventive methods of S. mansoni. It is, therefore, important to consider including PSAC in ongoing public-health interventions such as the Expanded Programme on Immunization (EPI) and praziquantel mass drug administration (PZQ-MDA) programmes because they are set to suffer from the significant morbidity effects of chronic schistosomiasis. It is important to provide health education for behavior change to avoid contaminating water for the whole village community. It is also advisable to design and implement strategies that enhance access to education and safe water to reduce the burden of soil-transmitted helminthiasis and schistosomiaisis.
We acknowledge the study participants, mothers of PSAC and Health extension workers.
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- Hotez PJ, Kamath A. Neglected tropical diseases in sub-Saharan Africa: review of their prevalence, distribution, and disease burden. PLoS Negl Trop Dis. 2009;3(8):e412.View ArticlePubMedPubMed CentralGoogle Scholar
- WHO. Soil-transmitted helminthiases:eliminating as public health problem soil-transmitted helminthiases in children: progress report 2001–2010 and strategic plan 2011–2020. 2012.Google Scholar
- CDC. Neglected Tropical diseases,The Burden of Schistosomiasis (Schisto, Bilharzia, Snail Fever), CDC report. 2011Google Scholar
- WHO Expert Committee. Prevention and control of schistosomiasis and soil-transmitted helminthiasis. WHO technical report series, 2002.Google Scholar
- Albonico M, Montresor A, Crompton DW, Savioli L. Intervention for the control of soil-transmitted helminthiasis in the community. Adv Parasitol. 2006;61:311–48.View ArticlePubMedGoogle Scholar
- Abera K, Ahmed A. An overview of environmental health status in Ethiopia with particular emphasis to its organisation, drinking water and sanitation: a literature survey. Ethiop J Health Dev. 2005;19(2):89–103.Google Scholar
- Noyer C, Brandt L. Parasitic infections of the gastrointestinal tract. Curr Gastroenterol Rep. 1999;1(4):282–91.View ArticlePubMedGoogle Scholar
- Kloos H. The ecology of health and disease in Ethiopia. Zein ZA, editor: Ministry of Health; 1993.Google Scholar
- Tchuenté L-AT. Control of Schistosomiasis and Soil-Transmitted Helminthiasis in Sub-Saharan Africa: Challenges and Prospects. In: Rodriguez-Morales AJ, editor. Current Topics in Tropical Medicine. 2012.Google Scholar
- Stephenson LS, Latham MC, Ottesen E. Malnutrition and parasitic helminth infections. Parasitology. 2000;121(S1):S23–38.View ArticlePubMedGoogle Scholar
- CDC. Global Heath Division of Parasitic Disease and Malaria. 2014.Google Scholar
- Stothard JR, Sousa-Figueiredo JC, Betson M, Bustinduy A, Reinhard-Rupp J. Schistosomiasis in African infants and preschool children: let them now be treated. Trends Parasitol. 2013;29(4):197–205.View ArticlePubMedPubMed CentralGoogle Scholar
- Odogwu S, Ramamurthy N, Kabatereine N, Kazibwe F, Tukahebwa E, Webster J, Fenwick A, Stothard J. Schistosoma mansoni in infants (aged < 3 years) along the Ugandan shoreline of Lake Victoria. Ann Trop Med Parasitol. 2006;100(4):315–26.Google Scholar
- Sousa-Figueiredo JC, Betson M, Stothard JR. Treatment of schistosomiasis in African infants and preschool-aged children: downward extension and biometric optimization of the current praziquantel dose pole. International health. 2012;4(2):95–102.View ArticlePubMedPubMed CentralGoogle Scholar
- Garba A, Barkiré N, Djibo A, Lamine MS, Sofo B, Gouvras AN, et al. Schistosomiasis in infants and preschool-aged children: infection in a single Schistosoma haematobium and a mixed S. Haematobium–S. Mansoni foci of niger. Acta Trop. 2010;115(3):212–9.View ArticlePubMedGoogle Scholar
- Ekpo UF, Laja-Deile A, Oluwole AS, Sam-Wobo SO, Mafiana CF. Urinary schistosomiasis among preschool children in a rural community near Abeokuta. Niger Parasit Vectors. 2010;3:58.View ArticleGoogle Scholar
- WHO. Report of a Meeting to Review the Results of Studies on the Treatment of Schistosomiasis in Preschool-age Children. Geneva: WHO; 2010.Google Scholar
- Deribe K, Meribo K, Gebre T, Hailu A, Ali A, Aseffa A, Davey G. The burden of neglected tropical diseases in Ethiopia, and opportunities for integrated control and elimination. Parasit Vectors. 2012;5:240.Google Scholar
- Nyantekyi LA, Legesse M, Belay M, Tadesse K, Manaye K, Macias C, et al. Intestinal parasitic infections among under-five children and maternal awareness about the infections in Shesha Kekele, Wondo Genet. Southern Ethiopia Ethiop J Health Dev. 2010;24(3):185–90.Google Scholar
- Degarege A, Erko B. Prevalence of intestinal parasitic infections among children under five years of Age with emphasis on Schistosoma mansoni in Wonji Shoa sugar estate. Ethiopia PloS one. 2014;9(10), e109793.View ArticlePubMedGoogle Scholar
- Katz N, Chaves A, Pellegrino J. A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. Rev Inst Med Trop Sao Paulo. 1972;14(6):397.PubMedGoogle Scholar
- Montresor A, Crompton DWT, Hall A, Bundy DAP, Savioli L. Guidelines for the Evaluation of Soil-Transmitted Helminthiasis and Schistosomiasis at Community Level. Geneva: WHO; 1998. WHO/CTD/SIP/98.1.Google Scholar
- Birrie H, Baicha F, Abebe F. Intestinal parasitoses among under-fives in two communities in Ethiopia. Ethiop J Health Dev. 1998;12:63–7.Google Scholar
- Asfaw ST, Giotom L. Malnutrition and enteric parasitoses among under-five children in Aynalem village. Tigray Ethiop J Health Dev. 2000;14(1):67–75.Google Scholar
- Brooker S, Peshu N, Warn P, Mosobo M, Guyatt H, Marsh K, Snow R. The epidemiology of hookworm infection and its contribution to anaemia among pre-school children on the Kenyan coast. Trans R Soc Trop Med Hyg. 1999;93(3):240–6.Google Scholar
- Hodges MH, Paye J, Koroma MM, Nyorkor ED, Fofonah I, Zhang Y. High level of Schistosoma mansoni infection in pre-school children in Sierra Leone highlights the need in targeting this age group for praziquantel treatment. Acta Trop. 2012;124(2):120–5.View ArticlePubMedGoogle Scholar
- Coulibaly JT, N’Gbesso YK, N’Guessan NA, Winkler MS, Utzinger J, N’Goran EK. Epidemiology of Schistosomiasis in Two high-risk communities of South Côte d’Ivoire with particular emphasis on Pre-school–aged children. AmJTrop Med Hyg. 2013;89(1):32–41.View ArticleGoogle Scholar
- Verani JR, Abudho B, Montgomery SP, Mwinzi PN, Shane HL, Butler SE, Karanja DM, Secor WE. Schistosomiasis among young children in Usoma, Kenya. AmJTrop Med Hyg. 2011;84(5):787–91.Google Scholar
- Nalugwa A, Olsen A, Tukahebwa M, Nuwaha F. Intestinal schistosomiasis among preschool children along the shores of Lake Victoria in Uganda. Acta Trop. 2015;142:115–21.View ArticlePubMedGoogle Scholar
- Bosompem K, Bentum IA, Otchere J, Anyan W, Brown C, Osada Y, Takeo S, Kojima S, Ohta N. Infant schistosomiasis in Ghana: a survey in an irrigation community. Tropical Med Int Health. 2004;9(8):917–22.Google Scholar
- Poole H, Terlouw DJ, Naunje A, Mzembe K, Stanton M, Betson M, Lalloo DG, Stothard JR. Schistosomiasis in pre-school-age children and their mothers in Chikhwawa district, Malawi with notes on characterization of schistosomes and snails. Parasit Vectors. 2014;7(1):153.Google Scholar