Article Versions
Export Article
Cite this article
  • Normal Style
  • MLA Style
  • APA Style
  • Chicago Style
Open Access Peer-reviewed

Prevalence, Peculiarities and Patterns of Urogenital Schistosomiasis and Hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria

Peletu B.J., Ofoezie I.E., Ikwuka A.O.
American Journal of Public Health Research. 2023, 11(2), 56-61. DOI: 10.12691/ajphr-11-2-3
Received January 18, 2023; Revised February 20, 2023; Accepted March 02, 2023

Abstract

Background: Schistosomiasis, Leprosy, Leishmaniasis, Malaria, Trypanosomiasis and Filariasis are the six major tropical diseases, specially targeted for control by the Special Program for Research and Training on Tropical Diseases of the United Nations Development Programme (UNDP), World Bank and World Health Organization. Out of the above six diseases, schistosomiasis is the second most important tropical diseases, second only to malaria. The distribution of schistosomiasis cuts across 76 countries in Africa, Latin America and Asia. Schistosoma hematobium endemicity cuts across 54 countries. Aim: To study the prevalence, peculiarities and patterns of urogenital schistosomiasis and hematuria in Owena Reservoir Area for an effective, affordable and sustainable schistosomiasis control in the area. Materials and methods: Owena Reservoir Area consists of Owena, Kajola and Baiken communities. A school-based cross-sectional technique was used for urine collection and quantification of Schistosoma hematobium eggs which involved 624 pupils in March 2014 and 591 pupils in April 2015. Risk factors, socio-demographic variables were collected using questionnaires. Urine samples were examined for Schistosoma hematobium eggs using sedimentation by gravity cum centrifugation. The urine samples obtained from the pupils were divided into two separate 30ml universal sterling plastic bottles with conical bottom. The first of the two 30ml universal sterling plastic bottles were examined for Schistosoma hematobium eggs using sedimentation by gravity cum centrifugation. The second of the two 30ml universal sterling plastic bottles were assessed for gross hematuria through visual observation of bloody urine while non-bloody samples were examined for micro-hematuria using one strip of commercially prepared chemical reagent strips COMBUR-9 prepared and marketed by Acun Laboratory USA which was dipped into each urine sample and the color change was matched with standard by the side of the container of the reagent strips. Results: Out of the 624 pupils examined in March 2014, 256 (41.0%) were positive for Schistosoma hematobium eggs in urine, while in April 2015, 381 (64.5%) out of 591 were positive. Prevalence of hematuria in the three communities shows that in Owena community the age group 21 – 30 had the highest prevalence (49.2%); in Kajola, the age group 5-10 had the highest prevalence (46.2%); while in Baiken community, the age group 5-10 had the highest prevalence (55.5%) – with 95% Confidence Interval in all cases. Conclusion: Macrohematuria was identified as a sensitive and specific diagnostic technique for identifying people infected with Schistosoma hematobium in the three communities. This parameter may be recommended as a cost saving diagnostic approach during future control efforts, with reference to the April 2015 peculiarities and patterns of infection shown by this study.

1. Introduction

Schistosomiasis is a snail-borne, parasitic infection caused by blood-dwelling (hence, called blood fluke) trematode worms of the genus Schistosoma 1. The infection is now commonly known as bilharziasis, swimmer’s itch, snail fever, katayama fever, blood fluke, Tsargiyya in Hausa, Atosiaja in Yoruba languages of Nigeria 2, 3, 4, 5, 6. The characteristic symptom of blood in urine (hematuria) results from the entry of blood and eggs into the human urinary bladder as a result of the bursting of veins, due to clogging of the venus plexus which prevent blood flow 6, 7, 8.

Schistosomiasis remains an important public health problem globally with approximately 779 million estimated to be at risk 6, 9. Within sub-saharan Africa, Nigeria is the country with highest prevalence of human schistosomiasis with about 29 million reported cases in 2008 9, 10. It is perhaps the most important disease associated with man-made lake and irrigation projects in tropical countries 3, 11, 12.

There is evidence for a link between the occurrence of human urogenital schistosomiasis and several factors such as knowledge, attitude, perception, behavioural, cultural and religious practices, primary occupation, educational level, household income. All these factors go a long way to influence the transmission of urogenital schistosomiasis in any endemic settlement 13, 14, 15.

Information on urogenital schistosomiasis transmission and human water contact pattern in Ondo State is scanty despite widespread distribution in some of its neighbouring states 13. Infections among the people could be managed through chemotherapy. Chemotherapeutic control is used to reduce morbidity in human populations. Out of all the drugs often recommended on their basis of minimal side effects and efficacy, praziquantel is the most widely used, because it is effective against all the species of schistosomes, easily affordable and well tolerated 13.

Urogenital schistosomiasis is highly endemic in three communities (Owena, Kajola and Baiken) of Ondo State, Nigeria 16. There is a need for sustainable controls targeted towards behavioral modifications by mass sensitization and provision of pipe-borne water facilities and modern toilet systems with a view to discouraging people from having contact with cercacriae-infected water bodies 16.

The aim of this study is to determine the prevalence, peculiarities and patterns of urogenital schistosomiasis and hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria with a view to fashioning out sustainable control strategies of the disease in the study area.

2. Materials and Methods

The study was carried out in Owena Reservoir and its adjoining three randomly selected communities (Owena, Kajola and Baiken) which are rural to semi-urban settlements in Ondo East Local Goverment Area, Ondo State, Nigeria (Figure 1) and lies between latitudes 700' – 70301N and longitudes 50001-50301E. Further illustrations are presented in the map of Owena showing Owena Reservoir, Owena Dam and the eight sampling sites of Owena, Kajola and Baiken Communities (Figure 2).

  • Figure 1. Map of Ondo East Local Government Area, Ondo State, Nigeria, showing Owena Reservoir Area, the three sampled communities (Owena, Baiken and Kajola), Owena Dam, Owena River and the eight sampling sites (Source: Adapted from Map of Ondo East L.G.A., Ondo State, Nigeria - Igboloro and Associates (Planners, Architects and Engineers), No. 3 Ayodele Awodeyi Street, Ketu, Lagos State, Nigeria (2012))
2.1. Urine Collection and Quantification of Schistosoma hematobium Eggs

A school-based cross-sectional technique was used for urine collection and quantification of Schistosoma hematobium eggs 6, 9. This is on the basis that children, especially school age children represent the prime reservoir for the schistosome parasites and children are more amenable to mass chemotherapy than adults 14, 17. From the three studied riverian communities, (Owena, Kajola and Baiken), three schools (one from each of the communities) were selected on the basis of their proximity to the water bodies 11. These schools include Owena Communitiy Grammar School, Owena; Ebenezer Anglican Primary School, Kajola; and St. Peter’s Roman Catholic Mission Primary School, Baiken.

Urine collection and examination for Schistosoma hematobium eggs were carried out in March 2014 and April 2015. In 2014, urine samples were collected from a total of 624 school age children in the three communities combined. In 2015, urine samples were collected from the same, above named schools to the total of 591 (made up of 295 males and 296 females). The collection and examination of urine samples were carried out using the sedimentation by gravity cum centrifugation technique as described by 3, 18, 19, 20, 21. Each pupil was given a clean, dry, labelled, wide-mouthed, plastic urine container (300-500ml) to provide a urine sample between the hours of 10am and 12pm GMT, the best time interval of eggs deposit in the bladder 14, 22. The urine sample provided was thoroughly mixed before two 10ml sub-samples were transferred into two separate 30ml universal sterlin plastic bottles with conical bottom 5, 11, 19.

Immediately after dividing the sample into two sub-samples, the first of the two sub-samples was preserved with a view to preventing the eggs from hatching 6, 18 while the second sub-sample was assessed for macrohematuria and microhematuria. Visual observation (the physical appearance of the urine samples color) was used to assess macrohematuria with the positivity based on a bloody red color of the urine, and negativity based on non-bloody color of the urine 18, 23. Microhematuria was immediately determined using one strip of commercially prepared chemical reagent strip COMBUR-9, marketed and prepared by Acon Laboratory, USA, which was dipped into each urine sample and the color change was matched with standard colors by the side of the container of the reagent strips.

Results indicating positive hematuria were characterized as change of the color of the reagent strip from yellow to light green as light hematuria; to deep green as moderate hematuria or to deeper green as heavy hematuria. Negative hematuria indicated no color change of the reagent strip. However, all the positive or negative hematuria results were recorded as either green color change or no color change respectively. Other variables such as sex, weight, height, religion, tribe of each pupil were determined. Height was measured with a calibrated pole, with individuals standing barefoot on the flat, cemented floors of their classrooms. Body weight was determined using a standard bathroom scale. Religion, tribe and other variables were determined by oral interview of each pupil.

2.2. Ethical Approval and Informed Consent

Approval for this study was gotten from the Research and Ethics Committee of the Obafemi Awolowo University (OAU), Ile-Ife, Osun State, Nigeria concerning postgraduate studies and research. Laboratory studies were carried out in accordance with the recommendations of the manufacturers of diagnostic test kits and systems using modern laboratory technologies and with due observance of the ethical principles of the Declaration of Helsinki (DoH) in 2013 concerning human research. Verbal informed consents were gotten as this study was carried out in a rural setting and with very low literacy rate of study participants.

3. Results and Discussion

3.1. Prevalence and Intensity of Hematuria in Owena, Kajola and Baiken communities

In Owena community, the age group that had the highest rate of blood in urine (hematuria) was 21-30 years with 49.2%. The least rate of hematuria was seen in age group 16–20 years with 37.8%.

In Kajola community, age group with the highest rate was 5-10 years with 46.2%, 44.0% was observed in 11-15 years, whereas 16-20 years and 21-30 years age groups had no blood in urine.

In Baiken community, the age group with the highest prevalence was 11-15 years with 56.2%. Prevalence rate of 55.5% was noted in 5-10 years, whereas 16-20 years and 21-30 years age groups had no blood in urine.

From the above, the community with the highest prevalence of hematuria in the 11-15 years was Baiken at 56.2%, and the least was Owena at 39.8% (Table 1).

3.2. Peculiarities and Patterns of Hematuria in Owena, Kajola and Baiken Communities

The people in other endemic areas of Nigeria have been found to be commonly ignorant of factors influencing Schistosoma hematobium transmission to humans, and hardly know that schistosomiasis is a major public health problem 5, 6, 24 which is confirmed by the present study. The highly age-dependent exposure in the communities indicates that this may play an important role towards eradicating urogenital schistosomiasis within the three communities. It has now been generally accepted that the strategies of schistosome control should aim at reduction in the infected snail density, wading through infected fresh water bodies unprotected, environmental contamination of streams, rivers, reservoirs, lakes, ponds, dams, and embankments, to a low level of public health implication 5, 6, 23, 25, 26, 27. The overall pattern of Schistosoma hematobium eggs per 10ml of urine in the three communities also shows that this was sex dependent and age dependent.

In this study, the age group with the highest prevalence was 11-15 years in 2014 (55.38%) and in 2015 (26.25%). The prevalence of infection was also sex dependent. The prevalence of infection for males was 43.59% in 2014 and 71.86% in 2015, and for females, it was 37.03% in 2014 and 57.0% in 2015. This is because more males took part in more complete water contact activities such as swimming, bathing with higher duration of contact, than the females in the communities. Those in 11-15 years age group got themselves involved in swimming, bathing than other groups. Most of the females were not always allowed to swim in the river, with the ignorant belief that the only source of water supply in the communities could be contaminated if women under menstruation wash or bath in the water body.

Baiken is the remotest of the communities from the Owena Reservoir Dam with very few pipe borne water supply. The sources of water supply for 55.65% of Baiken residents are rivers, streams, indicating that they have the highest exposure of water contact than other communities. It may be suggested that though the two communities Owena and Kajola may be treated of schistosomiasis, Baiken residents should be mostly treated in terms of duration and intensity of treatment. Prevalence, peculiarities and patterns of schistosomiasis and hematuria were also compared to a community ranking and important diseases in the three studied communities done in another study 16 (Table 2).

4. Conclusion

Urogenital schistosomiasis and its concomitant hematuria are prevalent in Owena, Kajola and Baiken communities of Ondo East Local Government Area, Ondo State, Nigeria. In all three communities of Owena, Kajola and Baiken, schistosomiasis would be most difficult to treat and/or eradicate in Baiken community. Efforts by stakeholders should be geared towards implementing full control strategies such as provision of pipe borne water, modern toilet facilities, regular chemotherapy controls to the school age children and adults of age group 21–30 years.

Acknowledgments

Special thanks to the authorities of the primary schools who permitted this study to be carried out within the three communities and to all participants of this study.

Conflict of Interest

The authors guarantee responsibility for everything published in this manuscript, as well as the absence of a conflict of interest and the absence of their financial interest in performing this research and writing this manuscript.

References

[1]  Weinland. Digenea Schistosomatidae and the intermediate snail host general. Revue de Zoologie Africaine Tervuren. 1858; 100: 137-152.
In article      
 
[2]  Ahmad MM, Abubakar MM, Lawal M, Shuaibu I, Tijani AM. Urinary and Intestinal schistosomiasis among primary school aged children in Dutse, Jigawa State, Nigeria. International Journal of Biological Sciences (IJBS). 2015; 2(1): 15-22.
In article      
 
[3]  Ofoezie IE. Human health and sustainable water resources development in Nigeria: schistosomiasis in artificial lakes. Natural Resources Forum. 2002; 26: 150-160.
In article      View Article
 
[4]  Oladejo SO, Ofoezie IE. Unabated Schistosomiasis in Erinle river dam, Osun State, Nigeria: evidence of neglect of environmental effects of developments. Journal of Tropical Medicine and International Health. 2006: 11(6): 843-850.
In article      View Article  PubMed
 
[5]  Ugbomoiko US, Ofoezie IE, Okoye IC, Heukelbach J. Factors associated with urinary schistosomiasis in two peri-urban communities in South-western Nigeria. Annals of Tropical Medicine and Parasitology. 2010; 104(5): 409-419.
In article      View Article  PubMed
 
[6]  World Health Organization. Updated Facts on Schistosomiasis. 2015.
In article      
 
[7]  Ekpo UF, Akintunde L, Oluwole AS, Sam-Wobo SO, Mafiama E. Urinary schistosomiasis among pre-school children in a rural community near Abeokuta, Nigeria. Parasite and Vector. 2012; 3: 58.
In article      View Article  PubMed
 
[8]  Peletu BJ. Schistosoma Intermediate Host Profile, Ecological Variations and Human Factors Influencing Schistosomiasis Transmission in Owena Reservoir Area, Ondo State, Nigeria. PhD Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 2016: 217.
In article      
 
[9]  Babatunde TA, Asaolu SO, Sowemimo OA. Urinary schistosomiasis among pre-school and school aged children in two peri-urban communities in Southwest Nigeria. Journal of Parasitology and Vector Biology. 2013; S17: 96-110.
In article      
 
[10]  Hotex PJ, Kamath A. Neglected Tropical Diseases in sub-Saharan Africa: Review of their Prevalence, Distribution, and Disease Burden. PLuS Neglected Tropical Diseases. 2009; 3: e412.
In article      View Article  PubMed
 
[11]  Oladejo SO. Assessment of Schistosomiasis using Geographic Information System/Remote Sensing in Osun State, Southwest, Nigeria. PhD Thesis, University of Ibadan, Nigeria. 2011.
In article      
 
[12]  Lengeler C, Utzinger J, Tanner M. Questionnaires for rapid screening of schistosomiasis in sub-Saharan Africa. Bull. World Health Organ. 2002; 80: 235-242.
In article      
 
[13]  Peletu BJ, Ofoezie IE, Ikwuka AO. Urogenital schistosomiasis transmission and human water contact patterns in Aponmu-Lona river basin, Idanre, Ondo State, Nigeria. Donn. J. Med. Med. Sci. 2020; 6(1): 1-8.
In article      
 
[14]  World Health Organization. Urine Filtration technique for S. haematobium infection. Geneva, Switzerland. 2014.
In article      
 
[15]  Peletu BJ. Ecology of Fresh Water Snails Transmitting Schistosoma haematobium in Aponmu-Lona River Basin, Idanre, Ondo State, Nigeria. MSc Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 2010.
In article      
 
[16]  Peletu BJ, Ofoezie IE, Ikwuka AO. Attitude, Knowledge, Perception, Behavioural, Cultural and Religious Practices Influencing Transmission of Urogenital Schistosomiasis in Owena, Kajola and Baiken Communities Bordering Owena Reservoir/Dam, Ondo East Local Government Area, Ondo State, Nigeria. European Journal of Medical and Health Sciences. 2023; 5(1): 23-30.
In article      View Article
 
[17]  Ibironke OA, Phillips AE, Garba A, Lamine SM, Shiff C. Diagnosis of Schistosoma haematobium by detection of specific DNA fragments from filtered urine samples. The American Journal of Tropical Medicine and Hygiene. 2011; 84(6): 998.
In article      View Article  PubMed
 
[18]  Amaechi EC. Urinary schistosomiasis among school age children in some rural communities of Abia state, South Eastern Nigeria. Animal Research International. 2014; 11(2): 1953-1957.
In article      
 
[19]  Asaolu SO, Ofoezie IE. A simple method for concentrating eggs of Schistosoma haematobium in the urine. The Nigerian Journal of Parasitology. 1990; 9(11): 47-50.
In article      
 
[20]  Otuneme OG, Akinkuade FO, Obebe OO, Usiobeigbe OS, Faloye TG, Olasebikan AS, Akinleye WA, Koku OD. A study on the prevalence of Schistosoma haematobium and Schistosoma intercalatum in a rural community of Ogun State, Nigeria. South East Asia Journal of Public Health. 2015; 4(1): 67-71.
In article      View Article
 
[21]  Ishaleku D, Yako AB, Usman D, Azamu SA. Schistosoma haematobium infection among school children in Keffi Town, Nasarawa State, Nigeria. Scholarly J. Med. 2012; 2(7): 104-7.
In article      
 
[22]  Banji BB, Mann A, Nma EM, Obi PV, Ezeako IA. Prevalence of schistosomiasis and other intestinal Helminth parasite among school children in Bida, Niger State, Nigeria. European Journal of Scientific Research. 2011; 621-626.
In article      
 
[23]  Ugbomoiko SO. The prevalence, incidence and distribution of human urinary schistosomiasis in Edo state, Nigeria. Nigerian Journal of Parasitology. 2000; 21: 314.
In article      
 
[24]  Ofoezie IE, Christenses NO, Madsen H. Water contact patterns and behavioural knowledge of schistosomiasis in Southwest Nigeria. Journal of Biosocial Science. 1998; 30: 245-259.
In article      View Article  PubMed
 
[25]  Jordan P, Webbe G, Sturrock RF. Human schistosomiasis, Wallingford CAB International. 1993: 159-193.
In article      
 
[26]  Ofoezie IE. A Study of Urinary Schistosomiasis Transmission in Resettlement Communities bordering Oyan River Dam, Ogun State, Nigeria. PhD Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 1995; 273.
In article      
 
[27]  Jordan P, Webbe G. Epidemiology, In: Jordan P, Webbe G, Sturrock RF (ed) Human schistosomiasis, Wallingford CAB International, 1993; 159-193.
In article      
 

Published with license by Science and Education Publishing, Copyright © 2023 Peletu B.J., Ofoezie I.E. and Ikwuka A.O.

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/

Cite this article:

Normal Style
Peletu B.J., Ofoezie I.E., Ikwuka A.O.. Prevalence, Peculiarities and Patterns of Urogenital Schistosomiasis and Hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria. American Journal of Public Health Research. Vol. 11, No. 2, 2023, pp 56-61. https://pubs.sciepub.com/ajphr/11/2/3
MLA Style
B.J., Peletu, Ofoezie I.E., and Ikwuka A.O.. "Prevalence, Peculiarities and Patterns of Urogenital Schistosomiasis and Hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria." American Journal of Public Health Research 11.2 (2023): 56-61.
APA Style
B.J., P. , I.E., O. , & A.O., I. (2023). Prevalence, Peculiarities and Patterns of Urogenital Schistosomiasis and Hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria. American Journal of Public Health Research, 11(2), 56-61.
Chicago Style
B.J., Peletu, Ofoezie I.E., and Ikwuka A.O.. "Prevalence, Peculiarities and Patterns of Urogenital Schistosomiasis and Hematuria in Owena Reservoir Area, Ondo East Local Government Area, Ondo State, Nigeria." American Journal of Public Health Research 11, no. 2 (2023): 56-61.
Share
  • Figure 1. Map of Ondo East Local Government Area, Ondo State, Nigeria, showing Owena Reservoir Area, the three sampled communities (Owena, Baiken and Kajola), Owena Dam, Owena River and the eight sampling sites (Source: Adapted from Map of Ondo East L.G.A., Ondo State, Nigeria - Igboloro and Associates (Planners, Architects and Engineers), No. 3 Ayodele Awodeyi Street, Ketu, Lagos State, Nigeria (2012))
  • Figure 2. Map of Owena showing Owena Reservoir, Owena Dam, Owena River and the eight sampling sites of Owena, Baiken and Kajola communities (Source: Adapted from Map of Ondo East L.G.A., Ondo State, Nigeria - Igboloro and Associates (Planners, Architects and Engineers), No. 3 Ayodele Awodeyi Street, Ketu, Lagos State, Nigeria (2012))
  • Table 1. Prevalence of hematuria in Owena, Kajola and Baiken communities (between March 2014 and April 2015)
  • Table 2. Community ranking and important diseases in the three studied communities (Owena, Kajola and Baiken)
[1]  Weinland. Digenea Schistosomatidae and the intermediate snail host general. Revue de Zoologie Africaine Tervuren. 1858; 100: 137-152.
In article      
 
[2]  Ahmad MM, Abubakar MM, Lawal M, Shuaibu I, Tijani AM. Urinary and Intestinal schistosomiasis among primary school aged children in Dutse, Jigawa State, Nigeria. International Journal of Biological Sciences (IJBS). 2015; 2(1): 15-22.
In article      
 
[3]  Ofoezie IE. Human health and sustainable water resources development in Nigeria: schistosomiasis in artificial lakes. Natural Resources Forum. 2002; 26: 150-160.
In article      View Article
 
[4]  Oladejo SO, Ofoezie IE. Unabated Schistosomiasis in Erinle river dam, Osun State, Nigeria: evidence of neglect of environmental effects of developments. Journal of Tropical Medicine and International Health. 2006: 11(6): 843-850.
In article      View Article  PubMed
 
[5]  Ugbomoiko US, Ofoezie IE, Okoye IC, Heukelbach J. Factors associated with urinary schistosomiasis in two peri-urban communities in South-western Nigeria. Annals of Tropical Medicine and Parasitology. 2010; 104(5): 409-419.
In article      View Article  PubMed
 
[6]  World Health Organization. Updated Facts on Schistosomiasis. 2015.
In article      
 
[7]  Ekpo UF, Akintunde L, Oluwole AS, Sam-Wobo SO, Mafiama E. Urinary schistosomiasis among pre-school children in a rural community near Abeokuta, Nigeria. Parasite and Vector. 2012; 3: 58.
In article      View Article  PubMed
 
[8]  Peletu BJ. Schistosoma Intermediate Host Profile, Ecological Variations and Human Factors Influencing Schistosomiasis Transmission in Owena Reservoir Area, Ondo State, Nigeria. PhD Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 2016: 217.
In article      
 
[9]  Babatunde TA, Asaolu SO, Sowemimo OA. Urinary schistosomiasis among pre-school and school aged children in two peri-urban communities in Southwest Nigeria. Journal of Parasitology and Vector Biology. 2013; S17: 96-110.
In article      
 
[10]  Hotex PJ, Kamath A. Neglected Tropical Diseases in sub-Saharan Africa: Review of their Prevalence, Distribution, and Disease Burden. PLuS Neglected Tropical Diseases. 2009; 3: e412.
In article      View Article  PubMed
 
[11]  Oladejo SO. Assessment of Schistosomiasis using Geographic Information System/Remote Sensing in Osun State, Southwest, Nigeria. PhD Thesis, University of Ibadan, Nigeria. 2011.
In article      
 
[12]  Lengeler C, Utzinger J, Tanner M. Questionnaires for rapid screening of schistosomiasis in sub-Saharan Africa. Bull. World Health Organ. 2002; 80: 235-242.
In article      
 
[13]  Peletu BJ, Ofoezie IE, Ikwuka AO. Urogenital schistosomiasis transmission and human water contact patterns in Aponmu-Lona river basin, Idanre, Ondo State, Nigeria. Donn. J. Med. Med. Sci. 2020; 6(1): 1-8.
In article      
 
[14]  World Health Organization. Urine Filtration technique for S. haematobium infection. Geneva, Switzerland. 2014.
In article      
 
[15]  Peletu BJ. Ecology of Fresh Water Snails Transmitting Schistosoma haematobium in Aponmu-Lona River Basin, Idanre, Ondo State, Nigeria. MSc Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 2010.
In article      
 
[16]  Peletu BJ, Ofoezie IE, Ikwuka AO. Attitude, Knowledge, Perception, Behavioural, Cultural and Religious Practices Influencing Transmission of Urogenital Schistosomiasis in Owena, Kajola and Baiken Communities Bordering Owena Reservoir/Dam, Ondo East Local Government Area, Ondo State, Nigeria. European Journal of Medical and Health Sciences. 2023; 5(1): 23-30.
In article      View Article
 
[17]  Ibironke OA, Phillips AE, Garba A, Lamine SM, Shiff C. Diagnosis of Schistosoma haematobium by detection of specific DNA fragments from filtered urine samples. The American Journal of Tropical Medicine and Hygiene. 2011; 84(6): 998.
In article      View Article  PubMed
 
[18]  Amaechi EC. Urinary schistosomiasis among school age children in some rural communities of Abia state, South Eastern Nigeria. Animal Research International. 2014; 11(2): 1953-1957.
In article      
 
[19]  Asaolu SO, Ofoezie IE. A simple method for concentrating eggs of Schistosoma haematobium in the urine. The Nigerian Journal of Parasitology. 1990; 9(11): 47-50.
In article      
 
[20]  Otuneme OG, Akinkuade FO, Obebe OO, Usiobeigbe OS, Faloye TG, Olasebikan AS, Akinleye WA, Koku OD. A study on the prevalence of Schistosoma haematobium and Schistosoma intercalatum in a rural community of Ogun State, Nigeria. South East Asia Journal of Public Health. 2015; 4(1): 67-71.
In article      View Article
 
[21]  Ishaleku D, Yako AB, Usman D, Azamu SA. Schistosoma haematobium infection among school children in Keffi Town, Nasarawa State, Nigeria. Scholarly J. Med. 2012; 2(7): 104-7.
In article      
 
[22]  Banji BB, Mann A, Nma EM, Obi PV, Ezeako IA. Prevalence of schistosomiasis and other intestinal Helminth parasite among school children in Bida, Niger State, Nigeria. European Journal of Scientific Research. 2011; 621-626.
In article      
 
[23]  Ugbomoiko SO. The prevalence, incidence and distribution of human urinary schistosomiasis in Edo state, Nigeria. Nigerian Journal of Parasitology. 2000; 21: 314.
In article      
 
[24]  Ofoezie IE, Christenses NO, Madsen H. Water contact patterns and behavioural knowledge of schistosomiasis in Southwest Nigeria. Journal of Biosocial Science. 1998; 30: 245-259.
In article      View Article  PubMed
 
[25]  Jordan P, Webbe G, Sturrock RF. Human schistosomiasis, Wallingford CAB International. 1993: 159-193.
In article      
 
[26]  Ofoezie IE. A Study of Urinary Schistosomiasis Transmission in Resettlement Communities bordering Oyan River Dam, Ogun State, Nigeria. PhD Thesis, Obafemi Awolowo University, Ile-Ife, Nigeria. 1995; 273.
In article      
 
[27]  Jordan P, Webbe G. Epidemiology, In: Jordan P, Webbe G, Sturrock RF (ed) Human schistosomiasis, Wallingford CAB International, 1993; 159-193.
In article