Intestinal schistosomiasis and geohelminths of Ukara Island, North-Western Tanzania: prevalence, intensity of infection and associated risk factors among school children
© Mugono et al.; licensee BioMed Central. 2014
Received: 26 September 2014
Accepted: 18 December 2014
Published: 23 December 2014
Schistosoma mansoni and soil-transmitted helminths (STH) are among the most prevalent and highly neglected tropical diseases in Tanzania. However, little is known on the distribution of these infections in rural settings, especially in the island areas on Lake Victoria. Identifying the local risk factors of S. mansoni and soil-transmitted helminths is one step towards understanding their transmission patterns and will facilitate the design of cost-effective intervention measures. The present study was therefore conducted to determine the prevalence, intensity of infection and risk factors associated with S. mansoni and soil-transmitted helminth infections among school children in Ukara Island.
This was a cross sectional study which enrolled 774 school children aged 4-15 years in 5 primary schools in Ukara Island, North-Western Tanzania. Single stool samples were collected, processed using the Kato Katz technique and examined for eggs of S. mansoni and geohelminths under a light microscope. A pre-tested questionnaire was used to collect socio-demographic information.
Overall, 494/773 (63.91%, 95% CI; 45.19-90.36) of the study participants were infected with S. mansoni and the overall geometrical mean eggs per gram (GM-epg) of feaces were 323.41epg (95% CI: 281.09 – 372.11). The overall prevalence of soil-transmitted helminth (STH) was 6.73% (n = 52/773, 95% CI = 4.39 – 10.32) with the most prevalent species being hookworms, 5.69% (n = 44/773, 95% CI; 3.68 – 8.79). Location of school in the study villages (P < 0.0001), parent occupation, fishing (P < 0.03) and reported involvement in fishing activities (P < 0.048) remained significantly associated with the prevalence and intensity of S.mansoni infection.
Schistosoma mansoni infection is highly prevalent in the islands whereas the prevalence of soil-transmitted helminths is low. The risk of infection with S. mansoni and the intensity of infection increased along the shorelines of Lake Victoria. These findings call for the need to urgently implement integrated control interventions, starting with targeted mass drug administration.
KeywordsSchistosoma mansoni Soil-transmitted helminths Ukara Island North-Western Tanzania
The Sub-Saharan Africa (SSA) region is endemic to schistosomiasis and soil-transmitted helminth (STH), with many areas reaching high transmission levels ,. Of the 249 millions cases of schistosomiasis occurring in 78 endemic countries of the world, 90% (192 million cases) occurs in SSA ,. An estimated 779 million individuals live in areas potentially risky for the transmission of schistosomiasis . In the SSA region, S. mansoni and S. haematobium are known to cause intestinal and urogenital schistosomiasis, with the former being focally distributed and the later widely distributed -. For the soil-transmitted helminths (STH), an estimated 198 million people are infected with hookworm, 173 million with A. lumbricoides and 162 million with T. trichura in SSA ,. Chronic infection with soil-transmitted helminths results into malnutrition, micronutrient deficiencies, poor cognitive function and school absenteeism , whereas chronic infection with S. mansoni results in hepatomegaly, hepatosplenomegaly and poor growth in children . Despite the serious health impact resulting from these infections and their predominance in areas of poverty, their geographical distribution especially in rural remote areas of SSA, remains unknown ,.
In Tanzania, S. mansoni and STH are increasingly becoming major public health concerns, especially among communities living along the Lake Victoria shores, in the North-Western regions of the country . Despite the implementation of a control program in these areas, more than 80% of the school children aged < 15 years are infected with S. mansoni and one of the STH species -. The geographical distribution of these infections has been described in the region by different methods ,. Predictive maps have been generated to guide control programs in the areas but these maps have a limitation in clearly predicting the distribution of these infections due to focal nature of transmission of these infections, especially S. mansoni which depends on distribution of its intermediate hosts ,. Thus, there is a paucity of data on the micro-geographical and micro-epidemiological information of these diseases in remote and hard to reach areas . In addition, despite the fact that communities living along the Lake Victoria shores have been known for many years to be highly endemic to S. mansoni and STH , some have never been reached by control programs, especially the ones residing on the islands of Lake Victoria. Therefore, epidemiological data remain sparse and incomplete. The availability of local epidemiological data would be beneficial for public health authorities and would allow the identification of the high-risk groups and transmission sites. This data would in turn become critical for developing sound and targeted control interventions to reduce the burden of these infections in the rural communities.
In that context, the present study aimed at studying the prevalence of S. mansoni and geohelminths and further understanding their associated risk factors in Ukara islands, where there has been up to date inadequate research on the epidemiology of intestinal schistosomiasis and soil-transmitted helminths. Identifying the local risk factors of S. mansoni and STH infection represents one step towards a better understanding of the transmission patterns, which will subsequently facilitate the design of cost effective intervention measures.
Ukara is an island located on the Lake Victoria and is part of the Ukerewe district, Mwanza region, North-Western Tanzania. The island has a total population of 34,181 according to the national census of 2012 . It is divided into four wards, namely Bwisya, Bukungu, Nyamanga and Bukiko. There are eight villages: Bwisya, Nyang’ombe, Bukungu, Chifule, Nyamanga, Chibasi, Bukiko and Kome. There are 12 government-owned primary schools. The main socio-economic activities carried out by the inhabitants of the island include fishing, subsistence farming, livestock keeping and small scale businesses. At the time this study was conducted, no control program was in place against intestinal helminth infections.
Study design, population and inclusion criteria
A cross-sectional study was conducted among school going children aged 4-15 years focusing on determining the prevalence of infection with STH and S. mansoni and their associated risk factors. Children were included in the study if parents/guardians had given written informed consented for them to participate in the study and if assent had been obtained from the children. Teachers were involved to educate parents and children on the importance and risks of participating in the study. Children with a history of taking anthelmintic medication in the past three months were excluded from the study.
Sample size determination and sampling procedures
The sample size was calculated as described elsewhere ,, considering the prevalence of S. mansoni infection of 60% in the island of Ukerewe , at 95% confidence interval and margin error of 5%. A design effect of 1.5 was considered for the variation in prevalence between schools. A minimum sample of 609 school children was needed for this study.
A simple random sampling method was used to select the villages with a primary school to participate in the study. The number of school children selected from each school was determined by the probability proportional to size of the school and the class population. Systematic sampling, using the class registers as the sampling frame was used, where the names of the children were arranged in alphabetical order. The sampling interval was obtained by dividing the total population in the class with the number of children to be investigated in that class (N/n). After obtaining a start from a table of random numbers, the same interval was kept until the required number of children in each class was obtained.
Questionnaire: socio-demographic and assessment of risk factors
A pre-tested Kiswahili translated questionnaire was used to collect demographic, socio-economic activities of parents/guardians, hygiene practices and KAP (knowledge, attitudes and practices). This was done in an attempt to describe the potentially relevant factors associated with the transmission of S. mansoni and STH among study participants. The questionnaire was initially developed in English and then translated to Kiswahili and back-translated by a different person who was blinded to the original questionnaire.
Stool sample collection and examination of S. mansoni and soil-transmitted helminths
A single stool sample was collected from all study participants. Two Kato Katz thick smears were prepared from different parts of the single stool sample using a template of 41.7 mg (Vestergaard Frandsen, Lausanne, Switzerland) , following a standard protocol . Within 30-60 minutes of slides preparation, Kato Katz smears were examined for the presence of STH eggs, specifically hookworms. After 24 hours, the smears were independently examined for S. mansoni eggs by two experienced laboratory technicians . For quality assurance, a random sample of 10% of the negative and positive Kato Katz thick smears were re-examined by a third technician.
The collected data were entered into a data base using Epi data version 3.1. Data analysis was done using STATA version 12.0 (Stata corp, Chicago). The prevalence of S. mansoni 95% confidence interval (95% CI) was obtained by binomial logistic regression taking into account clustering by schools. The comparison of prevalence by demographic factors for S. mansoni infection was tested for significance using χ2 or fisher exact test where appropriate. The age variable was described as mean ± standard deviations. The arithmetic mean of S. mansoni egg counts for each participant was calculated from the counts of two Kato Katz thick smears and multiplied by 24 to obtain individuals’ eggs per gram of faeces . S. mansoni egg counts were over dispersed so were logarithmically transformed prior to analysis. The geometric mean intensity eggs per gram of faeces (GM-epg) of S. mansoni infection were obtained as the antilog of the mean of the transformed egg counts. The comparison of geometric mean egg counts for S. mansoni between various demographic factors was undertaken using t-tests and ANOVA. The intensity of infection was categorized as: 1-99 epg, 100-399 epg, ≥400 epg defined as low, moderate and heavy intensities of infection respectively . To determine the factors associated with S. mansoni infection and intensities, multiple linear and multivariable logistic regression models were used, controlling for other explanatory variables. The model building strategy was to first identify potential factors at bivariate/linear regressions level and include these factors in the multivariable/multiple linear regression level. Factors with P-value < 0.2 were identified at bivariate level and were considered for the final model. Stepwise backward procedures were used to determine whether these variables were independent factors of intensity of S. mansoni infection by using adjusted odds ratios (AOR) for linear models and the 95% confidence interval (CI).
Ethical approval was obtained from the joint Ethical and Review Committee of Bugando Medical Centre and Catholic University of Health and Allied Sciences. The study received further clearance from the district administrative authorities (District Education Officer, Medical Officer, Executive Officer) and division authorities at Ukara Island. Kiswahili translated informed assent and consent forms were used to obtain parents/guardians consent for the children to participate in the study and assent of the children. For illiterate parents, a thumb print was used to sign the assent and consent forms after a clear description of the study objectives and their acceptance for their children to participate. All study participants who were infected with S. mansoni and STH were treated with praziquantel (40 mg/kg) and albendazole (400 mg) according to WHO and country guidelines .
Demographic characteristics of the study population
Demographic information of school children participated in the study from Ukara Island, North-Western Tanzania (n = 774)
Age (in years)
4 - 7
8 - 10
11 - 15
Occupational of parents
Overall prevalence of Schistosoma mansoni and soil transmitted helminth infections
Overall, 66.11% (n = 511/773, 95% CI = 62.76 -69.45) of the study participants were infected with at least one of the parasites investigated in the present study. The overall prevalence of S. mansoni was 63.91% (n = 494/773, 95% CI = 60.51 - 67.30). The overall prevalence of soil transmitted helminths was 6.73% (n = 52/773, 95% CI = 4.95 – 8.49) with the prevalent species of the STH being hookworm 5.69% (n = 44/773, 95% CI = 4.06 –7.32). Other STH helminth observed was A. lumbricoides, 1.03% (n = 8/773, 95% CI = 0.32- 1.75).
Prevalence of Schistosoma mansoni stratified by demographic characteristics
Prevalence of Schistosoma mansoni stratified by demographic characteristics of the study participants
46.79 – 92.51
41.90 – 90.69
Age (in years)
4 – 7
57.68 – 86.19
8 – 10
40.94 – 98.22
11 – 15
39.91 – 78.22
69.70 – 83.56
56.97 – 70.17
93.72 – 99.57
44.70 – 61.09
12.59 – 34.91
52.65 – 64.53
76.96 – 80.63
Presence of toilet at home/school
56.91 – 70.32
65.15 – 71.73
64.04 – 70.62
26.59 – 70.62
53.99 – 71.00
60.47 – 67.89
Intensity of Schistosoma mansoni and soil-transmitted helminths
Intensity of S. mansoni infection stratified by demographic factors of the study participants
Age (in years)
4 – 7
259.29 – 419.08
8 – 10
307.69 – 461.03
11 - 15
154.65 – 298.84
Presence of toilet at home/school
Of all the children found infected with any of the STH observed in the study, the majority had a light to moderate intensity of infection.
Factors associated with Schistosoma mansoni infection and intensity
Factors associated with Schistosoma mansoni infection among school children in Ukara Island, North-Western Tanzania
Age (in years)
4 - 7
0.95 – 1.98
0.74 – 1.79
8 – 10
1.25 – 2.85
0.79 – 2.09
11 - 15
0.98 - 2.59
2.24 – 6.74
33.82 - 257.19
3.46 – 10.95
5.59 – 18.38
The results of multiple linear regression revealed that fishing as parents occupations (AOR = 1.20, 95% CI; 1.02-1.42, P < 0.03), reportedly involved in paddy cultivation (AOR = 1.45,95% CI: 1.004-2.10, P < 0.048) and the location of the schools at Nyamanga (AOR = 1.75,95% CI; 1.37 – 2.24, P < 0.0001), Kome (AOR = 7.52, 95% CI; 5.78-9.75, P < 0.0001), Mubule (AOR = 2.22,95% CI; 1.73 – 2.86, P < 0.0001) and Chifule (AOR = 3.91,95% CI; 3.03-5.04, P < 0.0001) villages P < 0.0001) along the shorelines of Lake Victoria remained significantly associated with the intensity of S. mansoni infection (P < 0.0001) Additional file 1. The prevalence of STH was very low to allow the analysis of factors associated with STH in the present study population.
Prevalence of Schistosoma mansoni and soil-transmitted helminth infection
The overall prevalence of S.mansoni observed in the present study was similar to the prevalence of 64.3% reported among school children along the Lake shore in Sengerema district, North-Western Tanzania , but slightly higher compared to studies in Mbita Island in Western Kenya (60.5%)  and Sesse islands on Lake Victoria in Uganda (58.1%) . In addition, the prevalence and intensity of S. mansoni infections varied significantly by demographic characteristics of the study participants. The prevalence and intensity of infection varied by age of the study participants, gender, village of residence and parental occupation. In endemic areas, it is usually acknowledged that S. mansoni intensities of infection show a peak at the age group 6-19 years and, thereafter, the intensities decline gradually with an increased age -. Similarly, in the present study, the youngest age groups had the highest intensity of infection. Our study further showed that in the study area, infection with S. mansoni starts at a young age (probably < 4 years of age). If these children are not treated in time , by the time they start school, they may have developed significant morbidities .
We observed an inverse relationship between the proximity to the lake and S. mansoni prevalence and intensity of infection in the study areas, with schools located closest to Lake Victoria having the highest prevalence compared to schools which were located away from the Lake shores. Our observations were consistent with the results of Handzel et al who observed the decrease in prevalence of S. mansoni with increasing distance from the Lake Victoria shore . The school located nearest the lake (750 meters) had a mean prevalence of 80% which decreased to 20% at a distance of 4-13 km from the lake shore . Similarly, in Mbita and its adjacent islands, schools located in close proximity to Lake Victoria had the highest prevalence of S. mansoni,,.
The overall prevalence of soil-transmitted helminths observed in the present study population was very low compared to 12.4% , 16.2%  and 42.5%%  reported from Western Kenya. Of all the soil-transmitted helminths observed in the present study, hookworms were the most predominant species, although their prevalence was very low as compared to data reported by previous studies in North-Western Tanzania which quoted a prevalence of 38%  and 37%  and in Western Kenya (42.5%) . Along the Lake Victoria shores in Western Kenya and North-Western Tanzania, hookworms appear to be the predominant species and other soil-transmitted helminths areas are rarely found. Two previous studies in North-Western Tanzania reported a prevalence of <1% of A. lumbricoides, T. trichiura and E. vermicularis,. The high tolerance of hookworms’ 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 the infected children had a light to moderate infection intensity of these helminths infections. This observation was consistent with data from previous studies which observed that most of the individuals infected with soil-transmitted helminths normally excrete a low number of eggs ,-.
Intensity of S. mansoni infections
Epidemiological surveys along the Lake Victoria have shown that school children are carrying the highest intensity of infection as compared to other age groups , and male individuals are more heavily infected ,. In the present study, the majority of the study participants infected with S. mansoni had light to moderate intensities and only a few were heavily infected with S. mansoni. Male individuals had the highest infection intensity as compared to female individuals. The difference in intensity of infection between sexes is mainly associated with the variation of exposure to risk areas and the time spent in water sources . Male individuals tend to spend more time in water sources compared to female individuals . A high exposure is associated with swimming and sometime fishing in male children and can result in the maintenance of a high prevalence and intensity of infection into adulthood ,.
The focal nature of S. mansoni transmission along the present study area appears to influence intensity of infection. We have observed variations in the intensity of infection between schools, with schools located along the lake shores having the highest intensity of infection as compared to schools which were located away from the lake. Similar findings have been reported in Ssese island on the Lake Victoria shore in Uganda  and in Western Kenya ,-.
Risk factors associated with intensity and S. mansoni infection
In S. mansoni endemic areas, gender, age group, geographical location and occupation are some of the well-described demographic factors reported to be associated with infection and intensities ,-. Similarly, our findings showed that S. mansoni infection was mainly associated with the younger age group (4 - 10 years). In addition, parental occupation, especially involvement in fishing, the location of the school and a reported history of visiting the lake regularly were significantly associated with S. mansoni infection. However, on a multivariable analysis, only the location of schools remained associated with S. mansoni infection. As explained above, the proximity to the lake shores was associated with an increased risk of high infection in the present study area. In Sesse Island, in Uganda, a combination of malacological and parasitological surveys revealed that S. mansoni infection was only occurring in certain parts of the island . The same applied in Western Kenya ,. The present study did not include malacological surveys and these surveys are recommended in future studies in the area.
Conversely, a multiple linear regression model revealed that being male and the location of the schools along the shorelines of Lake Victoria remained significantly associated with the intensity of S. mansoni infection. Similar results have been described elsewhere in sub-Saharan Africa ,. A heavy intensity of infection was mainly seen in male individuals. The schools location along the shorelines of Lake Victoria mainly defines the level of exposure and transmission of the disease in the study area. Children attending schools located in villages which had close proximity to the lake, had highest intensities and appeared to be more exposed to cercariae infested water as compared to those who were living away from the lake shore ,,.
Schistosoma mansoni infection is highly prevalent in the Ukara Island whereas the prevalence of soil-transmitted helminths is low. The risk of infection with S. mansoni and the intensity increased along the shorelines of Lake Victoria. These findings reveal an actual presence of intestinal schistosomiasis in remote areas which have not been covered by any control program. Moreover, these findings call for the need to urgently implement integrated control interventions covering school going children of all ages, starting with targeted mass drug administration in relation to specific location of the villages.
We appreciate teachers, parents and schoolchildren who participated in this study and the technical work of the National Institute for Medical Research. We acknowledge the financial support from the Ukerewe District Council, in particular the Office of the District Executive Director.
HDM is supported by the Training Health Researchers into Vocational Excellence in East Africa (THRiVE) Programme funded by Wellcome Trust, grant number 087540, we acknowledge their support.
- Hotez PJ, Kamath A: Neglected tropical diseases in sub-saharan Africa: review of their prevalence, distribution, and disease burden. PLoS Neg Trop Dis. 2009, 3 (8): e412-10.1371/journal.pntd.0000412.View ArticleGoogle Scholar
- Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J: Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis. 2006, 6 (7): 411-25. 10.1016/S1473-3099(06)70521-7.View ArticlePubMedGoogle Scholar
- van der Werf MJ, de Vlas SJ, Brooker S, Looman CW, Nagelkerke NJ, Habbema JDF, Engels D: Quantification of clinical morbidity associated with schistosome infection in sub-Saharan Africa. Acta Trop. 2003, 86 (2): 125-39. 10.1016/S0001-706X(03)00029-9.View ArticlePubMedGoogle Scholar
- WHO: Soil-transmitted helminthiases. Eliminating soil-transmitted helminthiases as a public health problem in children: progress report 2001–2010 and strategic plan 2011–2020. 2012, World Health Organisation; 2012, GenevaGoogle Scholar
- Hotez PJ, Fenwick A, Savioli L, Molyneux DH: Rescuing the bottom billion through control of neglected tropical diseases. Lancet. 2009, 373 (9674): 1570-5. 10.1016/S0140-6736(09)60233-6.View ArticlePubMedGoogle Scholar
- McCreesh N, Booth M: Challenges in predicting the effects of climate change on Schistosoma mansoni and Schistosoma haematobium transmission potential. Trends Parasitol. 2013, 29 (11): 548-55. 10.1016/j.pt.2013.08.007.View ArticlePubMedGoogle Scholar
- Mazigo HD, Nuwaha F, Kinung’hi SM, Morona D, Pinot De Moira A, Wilson S, Heukelbach J, Dunne DW: Epidemiology and control of human schistosomiasis in Tanzania. Parasit Vectors. 2012, 5: 274-10.1186/1756-3305-5-274.PubMed CentralView ArticlePubMedGoogle Scholar
- Mazigo HD, Waihenya R, Lwambo NJ, Myone LL, Mahande AM, Seni J, Zinga M, Kapesa A, Kweka EJ, Mshana SE, Heukelbach J, Mkoji GM: Co-infections with Plasmodium falciparum, Schistosoma mansoni and intestinal helminths among schoolchildren in endemic areas of northwestern Tanzania. Parasit Vectors, 19(3):44.,Google Scholar
- Kardorff R, Gabone RM, Mugashe C, Obiga D, Ramarokoto CE, Mahlert C, Spannbrucker N, Lang A, Gunzler V, Gryseels B, Ehrich JH, Doehring E. Schistosoma mansoni-related morbidity on Ukerewe Island, Tanzania: clinical, ultrasonographical and biochemical parameters.Trop Med Int Health 1997, 2(3):230–9.,View ArticlePubMedGoogle Scholar
- Scheich EL, Hofer L, Kaatano G, Foya J, Odhiambo D, Igogote J, Lwambo N, Ekamp H, Karst K, Haussinger D, Richter J. Hepatosplenic morbidity due to Schistosoma mansoni in schoolchildren on Ukerewe Island, Tanzania. Parasitol Res 2012, 110(6):2515–20.,View ArticlePubMedGoogle Scholar
- Clements AC, Lwambo NJ, Blair L, Nyandindi U, Kaatano G, Kinung’hi S, Webster JP, Fenwick A, Brooker S: Bayesian spatial analysis and disease mapping: tools to enhance planning and implementation of a schistosomiasis control programme in Tanzania. Trop Med Intern Health. 2006, 11 (4): 490-503. 10.1111/j.1365-3156.2006.01594.x.View ArticleGoogle Scholar
- Brooker S, Kabatereine NB, Gyapong JO, Stothard JR, Utzinger J: Rapid mapping of schistosomiasis and other neglected tropical diseases in the context of integrated control programmes in Africa. Parasitol. 2009, 136 (13): 1707-18. 10.1017/S0031182009005940.View ArticleGoogle Scholar
- Tanzania National Bureau of Statistics: Tanzania Populations census. 2000 Tanzania government. 2002Google Scholar
- 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, 2014: 792536-10.1155/2014/792536.PubMed CentralView ArticlePubMedGoogle Scholar
- Alebie G, Erko B, Aemero M, Petros B: Epidemiological study on Schistosoma mansoni infection in Sanja area, Amhara region, Ethiopia. Parasit Vectors. 2014, 7: 15-10.1186/1756-3305-7-15.PubMed CentralView ArticlePubMedGoogle Scholar
- Katz N, Chaves A, Pellegrino J: A simple device for quantitative stool thick-smear technique in Schistosomiasis mansoni. Rev Inst MedTrop Sao Paulo. 1972, 14 (6): 397-400.Google Scholar
- WHO: Prevention and control of schistosomiasis and soil-transmitted helminthiasis. World Health Organ Tech Rep Ser. 2002, 912: i-Google Scholar
- Odiere MR, Rawago FO, Ombok M, Secor WE, Karanja DM, Mwinzi PN, Lammie PJ, Won K: High prevalence of schistosomiasis in Mbita and its adjacent islands of Lake Victoria, western Kenya. Parasit Vectors. 2012, 5: 278-10.1186/1756-3305-5-278.PubMed CentralView ArticlePubMedGoogle Scholar
- Standley CJ, Adriko M, Besigye F, Kabatereine NB, Stothard RJ: Confirmed local endemicity and putative high transmission of Schistosoma mansoni in the Sesse Islands, Lake Victoria, Uganda. Parasit Vectors. 2011, 4: 29-10.1186/1756-3305-4-29.PubMed CentralView ArticlePubMedGoogle Scholar
- Butterworth AE: Immunological aspects of human schistosomiasis. Brit Med Bull. 1998, 54 (2): 357-68. 10.1093/oxfordjournals.bmb.a011693.View ArticlePubMedGoogle Scholar
- Gryseels B: Human resistance to Schistosoma infections: age or experience?. Parasitol Today. 1994, 10 (10): 380-4. 10.1016/0169-4758(94)90226-7.View ArticlePubMedGoogle Scholar
- Stothard JR, Sousa-Figueiredo JC, Betson M, Bustinduy A, J R-R: Schistosomiasis in African infants and preschool children:let them now be treated. Trends Parasitol. 2013, 29 (4): 197-205. 10.1016/j.pt.2013.02.001.PubMed CentralView ArticlePubMedGoogle Scholar
- Handzel T, Karanja DM, Addiss DG, Hightower AW, Rosen DH, Colley DG, Andove J, Slutsker L, Secor WE: Geographic distribution of schistosomiasis and soil-transmitted helminths in Western Kenya: implications for anthelminthic mass treatment. Am J Trop Med Hyg. 2003, 69 (3): 318-23.PubMedGoogle Scholar
- Sang HC, Muchiri G, Ombok M, Odiere MR, Mwinzi PN: Schistosoma haematobium hotspots in south Nyanza, western Kenya: prevalence, distribution and co-endemicity with Schistosoma mansoni and soil-transmitted helminths. Parasit Vectors. 2014, 7: 125-10.1186/1756-3305-7-125.PubMed CentralView ArticlePubMedGoogle Scholar
- Nagi S, Chadeka EA, Sunahara T, Mutungi F, Justin YKD, Ichinose Y, Njenga SM, Shimada M, Hamano S: 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.,PubMed CentralView ArticlePubMedGoogle Scholar
- Odiere MR, Opisa S, Odhiambo G, Jura WG, Ayisi JM, Karanja DM, Mwinzi PN: Geographical distribution of schistosomiasis and soil-transmitted helminths among school children in informal settlements in Kisumu City, Western Kenya. Parasitology. 2011, 138 (12): 1569-77. 10.1017/S003118201100059X.View ArticlePubMedGoogle Scholar
- Lwambo NJ, Siza JE, Brooker S, Bundy DA, Guyatt H: Patterns of concurrent hookworm infection and schistosomiasis in schoolchildren in Tanzania. Trans R Soc Trop Med Hyg. 1999, 93 (5): 497-502. 10.1016/S0035-9203(99)90349-8.View ArticlePubMedGoogle Scholar
- Booth M, Vennervald BJ, Kabatereine NB, Kazibwe F, Ouma JH, Kariuki CH, Muchiri E, Kadzo H, Ireri E, Kimani G, Mwatha JK, Dunne DW: Hepatosplenic morbidity in two neighbouring communities in Uganda with high levels of Schistosoma mansoni infection but very different durations of residence. Trans R Soc Trop Med Hyg 2004, 98(2):125–36.,View ArticlePubMedGoogle Scholar
- Abdel-Latif Z, Abdel-Wahab MF, El-Kady NM: Evaluation of portal hypertension in cases of hepatosplenic schistosomiasis using ultrasound. J Clin Ultrasound. 1981, 9 (8): 409-12. 10.1002/jcu.1870090802.View ArticlePubMedGoogle Scholar
- Scott JT, Diakhate M, Vereecken K, Fall A, Diop M, Ly A, De Clercq D, de Vlas SJ, Berkyens D, Kestens L, Gryseels B: Human water contacts patterns in Schistosoma mansoni epidemic foci in northern Senegal change according to age, sex and place of residence, but are not related to intensity of infection. Trop Med Int Health 2003, 8(2):100–8.,View ArticlePubMedGoogle Scholar
- Barreto ML: Geographical and socioeconomic factors relating to the distribution of Schistosoma mansoni infection in an urban area of north-east Brazil. Bull World Health Organ. 1991, 69 (1): 93-102.PubMed CentralPubMedGoogle Scholar
- Berhe N, Medhin G, Erko B, Smith T, Gedamu S, Bereded D, Moore R, Habte E, Redda A, Gebre-Michael T: Variations in helminth faecal egg counts in Kato–Katz thick smears and their implications in assessing infection status with < Schistosoma mansoni. Acta Trop. 2004, 92 (3): 205-12. 10.1016/j.actatropica.2004.06.011.View ArticlePubMedGoogle Scholar
- Boisier P, Ramarokoto CE, Ravoniarimbinina P, Rabarijaona L, Ravaoalimalala V: Geographic differences in hepatosplenic complications of schistosomiasis mansoni and explanatory factors of morbidity. Trop Med Intern Health. 2001, 6 (9): 699-706. 10.1046/j.1365-3156.2001.00781.x.View ArticleGoogle Scholar
- Opisa S, Odiere MR, Jura WG, Karanja DM, Mwinzi PN: Malacological survey and geographical distribution of vector snails for schistosomiasis within informal settlements of Kisumu City, western Kenya. Parasit Vectors. 2011, 4: 226-10.1186/1756-3305-4-226.PubMed CentralView ArticlePubMedGoogle Scholar
- Berhe N, Myrvang B, Gundersen SG: Intensity of Schistosoma mansoni, hepatitis B, age, and sex predict levels of hepatic periportal thickening/fibrosis (PPT/F): a large-scale community-based study in Ethiopia. Am J Trop Med Hyg. 2007, 77 (6): 1079-86.PubMedGoogle Scholar
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